Triboluminescence Phenomenon Based on the Metal Complex Compounds—A Short Review

Triboluminescence (TL) is a phenomenon of light emission resulting from the mechanical force applied to a substance. Although TL has been observed for many ages, the radiation mechanism is still under investigation. One of the exemplary compounds which possesses triboluminescent properties are copper(I) thiocyanate bipyridine triphenylphosphine complex [Cu(NCS)(py)2(PPh3)], europium tetrakis dibenzoylmethide triethylammonium EuD4TEA, tris(bipyridine)ruthenium(II) chloride [Ru(bpy)3]Cl2, and bis(triphenylphosphine oxide)manganese(II) bromide Mn(Ph3PO)2Br2. Due to the effortless synthesis route and distinct photo- and triboluminescent properties, these compounds may be useful model substances for the research on the triboluminescence mechanism. The advance of TL studies may lead to the development of a new group of sensors based on force-responsive (mechanical stimuli) materials. This review constitutes a comprehensive theoretical study containing available information about the coordination of metal complex synthesis methodologies with their physical, chemical, and spectroscopic properties.


Introduction
Triboluminescence (TL) may be obtained by rubbing, crushing, cracking, and grinding as a result of an external force interaction with the substance [1]. Thousands of TL compounds have been reported over the years. It has been estimated that due to the mechanical action, light emission can be observed in 36% of all inorganic compounds, 19% of organic compounds, 37% of aromatics, 70% of alkaloids, and probably about 50% of all crystalline substances [2]. The most well-known triboluminescent substances are sucrose [3], UO 2 (NO 3 ) 2 ·H 2 O [4], quartz [1], and ZnS [5]. Since the phenomenon was described hundreds of years ago, nowadays, a significant amount of TL compounds is known. However, the universal mechanism that would allow to define physical explanation for all cases of transformation mechanical energy into light has not been discovered yet.
The implementation perspectives of TL compounds are wide. The most outstanding idea is the application of mechanical stress-responsive materials as sensing elements for the new generation of force and damage sensors [11]. The external force-inducing

[Cu(NCS)(py) 2 (PPh 3 )] Complex
There are two main preparation methods of the [Cu(NCS)(py) 2 (PPh 3 )] complex currently described in the literature, i.e., one-and two-step processes [6,16]. Despite the superficial differences, the presented chemical reactions are based on the same general type of formation.
The first discussed synthesis method is a one-step process schematically presented in Figure 1. According to the provided literature information, 5 mL of hot pyridine containing dissolved CuSCN (0.121 g; 1.0 mmol) and PPh 3 (0.262 g; 1.0 mmol) were mixed for 3 h in 70 • C. It is important to maintain the temperature; otherwise, the [Cu(NCS)(py) 2 (PPh 3 )] complex will not form. Carrying out the synthesis at room temperature leads to the precipitation of the [Cu(NCS)(PPh 3 )] complex [6]. Afterward, the solution was slowly cooled down, and half of the solvent was evaporated under the fume hood. During the evaporation process, the pale yellow crystals started to precipitate, and they were subsequently filtered out [6]. It is optional to cleanse the product with toluene [16]. The explanation of TL, which would be comprehensive for all types of compounds, still has not been described. The advances in the triboluminescence phenomenon understanding will enable to design of the materials and systems exhibiting specific TL properties, which undoubtedly will pave the way for new implementation possibilities.

Synthesis of Triboluminescent Complex Compounds
One of the most significant advantages of this group of complex compounds is its relatively fast (several hours) and uncomplicated preparation. The accessible and cheap substrates and direct synthesis methods create new possibilities of process optimization. Further research may affect the future implementation of triboluminescent substances in various materials and areas.

3.1.[. Cu(NCS)(py)2(PPh3)] Complex
There are two main preparation methods of the [Cu(NCS)(py)2(PPh3)] complex currently described in the literature, i.e., one-and two-step processes [6,16]. Despite the superficial differences, the presented chemical reactions are based on the same general type of formation.
The first discussed synthesis method is a one-step process schematically presented in Figure 1. According to the provided literature information, 5 mL of hot pyridine containing dissolved CuSCN (0.121 g; 1.0 mmol) and PPh3 (0.262 g; 1.0 mmol) were mixed for 3 h in 70 °C. It is important to maintain the temperature; otherwise, the [Cu(NCS)(py)2(PPh3)] complex will not form. Carrying out the synthesis at room temperature leads to the precipitation of the [Cu(NCS)(PPh3)] complex [6]. Afterward, the solution was slowly cooled down, and half of the solvent was evaporated under the fume hood. During the evaporation process, the pale yellow crystals started to precipitate, and they were subsequently filtered out [6]. It is optional to cleanse the product with toluene [16]. The reaction yield can reach even 80-90%, and it is possible to obtain well-formed, colorless crystals by slowly cooling down the mixture from previously implemented higher temperature (80 °C) [1]. The one-step synthesis method is the most frequently repeated one [6,10,17].

EuD4TEA Complex
Hurt et al. were the first who synthesized the europium complex in 1966. They used anhydrous europium chloride as a source of europium(III) ions [7]. In 2011, the europium chloride was replaced with europium(III) nitrate to avoid chloride contamination in the solution [19]. This modification significantly reduced the cost of the synthesis and contributed to the improvement of TL properties of the europium(III) complex [19]. The The reaction yield can reach even 80-90%, and it is possible to obtain well-formed, colorless crystals by slowly cooling down the mixture from previously implemented higher temperature (80 • C) [1]. The one-step synthesis method is the most frequently repeated one [6,10,17].

EuD 4 TEA Complex
Hurt et al. were the first who synthesized the europium complex in 1966. They used anhydrous europium chloride as a source of europium(III) ions [7]. In 2011, the europium chloride was replaced with europium(III) nitrate to avoid chloride contamination in the solution [19]. This modification significantly reduced the cost of the synthesis and contributed to the improvement of TL properties of the europium(III) complex [19]. The discussed synthesis is presented in Figure 2 [20]. According to Fontenot R.S. et al. [20], to obtain the EuD 4 TEA complex, firstly, europium(III) nitrate (1.44 g, 4.0 mmol) was dissolved in 25 mL of heated anhydrous ethyl alcohol. Afterward, dibenzoylmethane (2.93 g, 13.0 mmol) and triethylamine (2 mL, 14.0 mmol) were added to the solution and heated up to obtain a clear solution. The mixture was left at room temperature to cool down. During a slow temperature decrease, TL crystals were formed. The following day, the product was filtered out and left to dry. discussed synthesis is presented in Figure 2 [20]. According to Fontenot R.S. et al. [20] obtain the EuD4TEA complex, firstly, europium(III) nitrate (1.44 g, 4.0 mmol) w dissolved in 25 mL of heated anhydrous ethyl alcohol. Afterward, dibenzoylmethane (2 g, 13.0 mmol) and triethylamine (2 mL, 14.0 mmol) were added to the solution and hea up to obtain a clear solution. The mixture was left at room temperature to cool dow During a slow temperature decrease, TL crystals were formed. The following day, product was filtered out and left to dry.  [20].
Furthermore, it is possible to modify the synthesis process of the TL europium co plex by using different solvents [21]. Dissolving europium(III) nitrate in acetonitrile acetone speeds up the synthesis, so it is not necessary to heat the solution. Using aceto leads to the precipitation of a small crystalline product, but after harvesting it and leav it to crystalize, well-formed crystals are obtained. The solvent has an impact on the int sity of triboluminescence and decay time of EuD4TEA [21]. Additionally, it was found t replacing anhydrous ethanol with laboratory ethanol has no impact on the TL results [2 Moreover, doping EuD4TEA complex with organic substances such as piperi DMMP, TEPS [20], uranium [22], or even multivitamin [23] affect TL properties, which a useful feature for further application as an element of sensors. The influence of orga dopants will be discussed in chapter 6.

3.3.[. Ru(bpy)3]Cl2 Complex
In some publications, authors used the purchased [Ru(bpy)3]Cl2 complex [24,25], hough it can be synthesized in several different ways. Sumana Bhar and Rajakumar A anthakrishnan prepared the Ru(II)-metal complex with 70% yield by following method in [8]. They dissolved 2,2′-bipyridine (0.234 g, 1.5 mmol) and anhydrous Ru (0.104 g, 0.5 mmol) in distilled water. Then, freshly prepared sodium phosphinate solut was added dropwise. The mixture was boiled for 30 min under reflux. During the re tion, the color of the solution gradually changed from bluish-green to orange-red. T solution with the crude product was filtrated and KCl (3.728 g, 0.05 mol) was added to filtrate. The mixture was heated up to the boiling point and stirred for a few minutes obtain a deep red solution. After cooling down to room temperature red product crys lized out of the solution. The crystals were filtered, then washed from the residual imp rities with ice-cold 10% aqueous acetone and acetone. In the end, the crystals were dried. The whole process is schematically presented in Figure 3. In the literature, similar synthesis routes can be found, in which some paramete such as reaction time, reducing agent, solvent, and inert gas, have been changed [25-2 Furthermore, it is possible to modify the synthesis process of the TL europium complex by using different solvents [21]. Dissolving europium(III) nitrate in acetonitrile or acetone speeds up the synthesis, so it is not necessary to heat the solution. Using acetone leads to the precipitation of a small crystalline product, but after harvesting it and leaving it to crystalize, well-formed crystals are obtained. The solvent has an impact on the intensity of triboluminescence and decay time of EuD 4 TEA [21]. Additionally, it was found that replacing anhydrous ethanol with laboratory ethanol has no impact on the TL results [21].
Moreover, doping EuD 4 TEA complex with organic substances such as piperine, DMMP, TEPS [20], uranium [22], or even multivitamin [23] affect TL properties, which is a useful feature for further application as an element of sensors. The influence of organic dopants will be discussed in chapter 6.

[Ru(bpy) 3 ]Cl 2 Complex
In some publications, authors used the purchased [Ru(bpy) 3 ]Cl 2 complex [24,25], although it can be synthesized in several different ways. Sumana Bhar and Rajakumar Ananthakrishnan prepared the Ru(II)-metal complex with 70% yield by following the method in [8]. They dissolved 2,2 -bipyridine (0.234 g, 1.5 mmol) and anhydrous RuCl 3 (0.104 g, 0.5 mmol) in distilled water. Then, freshly prepared sodium phosphinate solution was added dropwise. The mixture was boiled for 30 min under reflux. During the reaction, the color of the solution gradually changed from bluish-green to orange-red. The solution with the crude product was filtrated and KCl (3.728 g, 0.05 mol) was added to the filtrate. The mixture was heated up to the boiling point and stirred for a few minutes to obtain a deep red solution. After cooling down to room temperature red product crystallized out of the solution. The crystals were filtered, then washed from the residual impurities with ice-cold 10% aqueous acetone and acetone. In the end, the crystals were air-dried. The whole process is schematically presented in Figure 3. Furthermore, it is possible to modify the synthesis process of the TL europium plex by using different solvents [21]. Dissolving europium(III) nitrate in acetonitr acetone speeds up the synthesis, so it is not necessary to heat the solution. Using ace leads to the precipitation of a small crystalline product, but after harvesting it and lea it to crystalize, well-formed crystals are obtained. The solvent has an impact on the i sity of triboluminescence and decay time of EuD4TEA [21]. Additionally, it was found replacing anhydrous ethanol with laboratory ethanol has no impact on the TL results Moreover, doping EuD4TEA complex with organic substances such as pipe DMMP, TEPS [20], uranium [22], or even multivitamin [23] affect TL properties, wh a useful feature for further application as an element of sensors. The influence of org dopants will be discussed in chapter 6.

3.3.[. Ru(bpy)3]Cl2 Complex
In some publications, authors used the purchased [Ru(bpy)3]Cl2 complex [24,25 hough it can be synthesized in several different ways. Sumana Bhar and Rajakumar anthakrishnan prepared the Ru(II)-metal complex with 70% yield by following method in [8]. They dissolved 2,2′-bipyridine (0.234 g, 1.5 mmol) and anhydrous R (0.104 g, 0.5 mmol) in distilled water. Then, freshly prepared sodium phosphinate sol was added dropwise. The mixture was boiled for 30 min under reflux. During the tion, the color of the solution gradually changed from bluish-green to orange-red solution with the crude product was filtrated and KCl (3.728 g, 0.05 mol) was added t filtrate. The mixture was heated up to the boiling point and stirred for a few minut obtain a deep red solution. After cooling down to room temperature red product cry lized out of the solution. The crystals were filtered, then washed from the residual im rities with ice-cold 10% aqueous acetone and acetone. In the end, the crystals wer dried. The whole process is schematically presented in Figure 3. In the literature, similar synthesis routes can be found, in which some param such as reaction time, reducing agent, solvent, and inert gas, have been changed [25 In the literature, similar synthesis routes can be found, in which some parameters, such as reaction time, reducing agent, solvent, and inert gas, have been changed [25][26][27]. Frequently, the complex is given only as an intermediate product for which the yield is not given [2].

Mn(Ph 3 PO) 2 Br 2 Complex
This compound was synthetized in all known publications based on a method reported by Goodgame D.L. et al. [9]. The manganese complex with bromides and triphenylphosphine was prepared by the one-pot method shown in Figure 4. The phosphine oxide and manganous salt are mixed in a 2.2:1 molar ratio and then dissolved in 20-40 mL hot absolute ethanol. The mixture was left to cool down and precipitate crystals. The product was filtered out, washed with cold ethanol, and vacuum dried. The achieved yield was equal to 60% [9]. oxide and manganous salt are mixed in a 2.2:1 molar ratio and then dissolved in 20-40 mL hot absolute ethanol. The mixture was left to cool down and precipitate crystals. The product was filtered out, washed with cold ethanol, and vacuum dried. The achieved yield was equal to 60% [9].
Infrared spectroscopy (IR) analysis of the product showed signals of P-O stretching-1163 cm −1 and 1158 cm −1 , which confirms the presence of the phosphine oxide in the manganese(II) complex [9]. In the literature, another method was also described [25]. In fact, this method is an extension of the method described by Goodgame D.L. et al. [9]. First, 0.13 mol of triphenylphosphine oxide and 0.04 mol of MBr2 tetrahydrate were dissolved in hot ethanol. Reagents were exactly stirred and refluxed at 60 °C for 1 h. Next, the product was slowly cooled down to room temperature. The final mixture was filtered and left in the ambient conditions for few days. After that, precipitated light green crystals were filtered out, washed with cold anhydrous alcohol, and left to dry [25].
It is also possible to add some dopants to the crystals, for example HBr and HgCl2 [25]. In this case, in the first step, solutions of admixtures are added to the reaction mixture. The rest of the procedure is the same as for the synthesis of pure Mn(Ph3PO)Br2 [25].

Chemical and Structural Analysis
Analysis of the fundamental structural properties may give an opportunity to describe the details of the triboluminescence mechanism. Moreover, sufficient chemical and physical properties are necessary for the application of given compounds.

4.1.[. Cu(NCS)(py)2(PPh3)] Complex
The crystallographic structure of a triboluminescent compound may have a crucial influence on the TL properties [18]. In the case of the described compound, the Cu + ion is surrounded by four electron-donor ligands: thiocyanate group, triphenylphosphine, and two pyridine molecules (Figure 5a,b). The coordination number is equal to 4. The NCSgroup is bonded with the central atom by one electron pair of nitrogen atom [28]. Infrared spectroscopy (IR) analysis of the product showed signals of P-O stretching-1163 cm −1 and 1158 cm −1 , which confirms the presence of the phosphine oxide in the manganese(II) complex [9]. In the literature, another method was also described [25]. In fact, this method is an extension of the method described by Goodgame D.L. et al. [9]. First, 0.13 mol of triphenylphosphine oxide and 0.04 mol of MBr 2 tetrahydrate were dissolved in hot ethanol. Reagents were exactly stirred and refluxed at 60 • C for 1 h. Next, the product was slowly cooled down to room temperature. The final mixture was filtered and left in the ambient conditions for few days. After that, precipitated light green crystals were filtered out, washed with cold anhydrous alcohol, and left to dry [25].
It is also possible to add some dopants to the crystals, for example HBr and HgCl 2 [25]. In this case, in the first step, solutions of admixtures are added to the reaction mixture. The rest of the procedure is the same as for the synthesis of pure Mn(Ph 3 PO)Br 2 [25].

Chemical and Structural Analysis
Analysis of the fundamental structural properties may give an opportunity to describe the details of the triboluminescence mechanism. Moreover, sufficient chemical and physical properties are necessary for the application of given compounds.

[Cu(NCS)(py) 2 (PPh 3 )] Complex
The crystallographic structure of a triboluminescent compound may have a crucial influence on the TL properties [18]. In the case of the described compound, the Cu + ion is surrounded by four electron-donor ligands: thiocyanate group, triphenylphosphine, and two pyridine molecules (Figure 5a,b). The coordination number is equal to 4. The NCS − group is bonded with the central atom by one electron pair of nitrogen atom [28]. The center of the molecule with Cu + ion has distorted tetrahedral geometry [28]. The summarized values of the bond lengths and angles are presented in Table 1. Copper complex crystallizes in the P21 space group, which is part of the monoclinic crystal system [28]. This structure is characterized by a lack of symmetry centers, which is essential to enable the triboluminescence phenomenon. The edge lengths of an oblique The center of the molecule with Cu + ion has distorted tetrahedral geometry [28]. The summarized values of the bond lengths and angles are presented in Table 1. S-C 1.638 (2) Cu-N-C 157.4 (2) C-N 1.168(3) N-C-S 179.5 (2) Copper complex crystallizes in the P21 space group, which is part of the monoclinic crystal system [28]. This structure is characterized by a lack of symmetry centers, which is essential to enable the triboluminescence phenomenon. The edge lengths of an oblique rectangular prism are as follows: The angle of a slope between the sides and base is equal to β = 116.9660(10) • [28]. Infrared spectroscopy (IR) was used to perform the structural analysis ( Figure 6a). The substance exhibits strong absorption of pyridine at 1594 cm −1 and two absorption peaks at 2065 and 748 cm −1 , which is characteristic of NCS ligand, where the moiety is linked to the copper via the Cu-N bond [6]. The signals localized at 1479 and 1434 cm −1 are characteristic of triphenylphosphine [6]. The solid-state NMR spectroscopy method was also used. 31 P CPMAS (cross-polarization magic-angle spinning) was also performed and confirmed the structure of the compound [10]. The obtained 31 P CPMAS parameters are as follows: ρ = −7.2; ∆ν 1 = 1537; ∆ν 2 = 1568; ∆ν 3 = 1581; <∆ν> = 1526; d = −11.00 Hz; dν Cu = 0.79 × 10 −9 .
The described copper complex exhibits sufficient thermal stability ( Figure 6b) up to the temperature of 75 °C. Above this value, the sample weight reduction is observed, which is related to the complex decomposition. The first step of the degradation process is based on one pyridine ligand detachment. Next, at a temperature range of 114-120 °C, the second pyridine moiety is being detached. The final step of the copper complex thermal degradation occurs in a range of 150-330 °C, where the PPh3 and CuNCS parts, are being separated. At the higher temperature, the colorless CuNCS is stable [6]. According to the literature [16], the melting point of the considered compound was observed at 165-167 °C.
The solubility of the copper complex was investigated as well. Its crystals dissolve in pyridine, chlorinated solvents, acetonitrile, DMSO [6], and chloroform [16]. However, the compound is resistant to moisture and air [6].

EuD4TEA Complex
The Eu 3+ ion is coordinated with eight dibenzoylmethane's oxygen atoms, so the coordination number of EuD4TEA is equal to 8 [29]. Those coordination bonds create tetrabidentate anionic europium(III) complex. To equalize the charge of the molecule the structure is protonated with triethylammonium molecule (Et3NH + ) [29]. The protonated tertiary ammonium group is responsible for its strong triboluminescent properties [7]. The molecule structure is presented in Figure 7a [29]. The hydrogen bonds between the Et3NH + group and oxygen have a strong impact on stabilizing the long-range structure of the complex. The EuD4TEA was investigated using scanning electron microscopy (SEM) [29]. The SEM imagine ( Figure 7b) represents a large agglomerate, which is built with smaller rectangular crystals. The size is characterized by Gaussian distribution (Figure 7c). According to the data, the average size estimates are 400-30 µm [29]. The described copper complex exhibits sufficient thermal stability ( Figure 6b) up to the temperature of 75 • C. Above this value, the sample weight reduction is observed, which is related to the complex decomposition. The first step of the degradation process is based on one pyridine ligand detachment. Next, at a temperature range of 114-120 • C, the second pyridine moiety is being detached. The final step of the copper complex thermal degradation occurs in a range of 150-330 • C, where the PPh 3 and CuNCS parts, are being separated. At the higher temperature, the colorless CuNCS is stable [6]. According to the literature [16], the melting point of the considered compound was observed at 165-167 • C.
The solubility of the copper complex was investigated as well. Its crystals dissolve in pyridine, chlorinated solvents, acetonitrile, DMSO [6], and chloroform [16]. However, the compound is resistant to moisture and air [6].

EuD 4 TEA Complex
The Eu 3+ ion is coordinated with eight dibenzoylmethane's oxygen atoms, so the coordination number of EuD 4 TEA is equal to 8 [29]. Those coordination bonds create tetrabidentate anionic europium(III) complex. To equalize the charge of the molecule the structure is protonated with triethylammonium molecule (Et 3 NH + ) [29]. The protonated tertiary ammonium group is responsible for its strong triboluminescent properties [7]. The molecule structure is presented in Figure 7a [29]. The hydrogen bonds between the Et 3 NH + group and oxygen have a strong impact on stabilizing the long-range structure of the complex. The EuD 4 TEA was investigated using scanning electron microscopy (SEM) [29]. The SEM imagine ( Figure 7b) represents a large agglomerate, which is built with smaller rectangular crystals. The size is characterized by Gaussian distribution (Figure 7c). According to the data, the average size estimates are 400-30 µm [29]. The structure of the EuD4TEA complex was solved and the space group was de as P21, which is part of the monoclinic crystal system. The coordination geome square-antiprismatic [29]. Details of molecule geometry are presented in Table 2.
The TL properties of the described EuD4TEA complex depend on the europium used in the synthesis [19]. The use of the europium(III) chloride not only extends the thesis time and increases the cost, but also deteriorates TL emission. Two of the same allel syntheses, which are differing only in the use of europium(III) salt, were made. I reaction ethanol was used as a solvent. TL spectra of the products were measured (F 8) [19]. The intensity of emission increased by 82% for EuD4TEA crystals doped wit ropium(III) nitrate. Moreover, the yield of synthesis increased, because the unnece step of washing out chlorides was omitted [19]. The structure of the EuD 4 TEA complex was solved and the space group was defined as P21, which is part of the monoclinic crystal system. The coordination geometry is square-antiprismatic [29]. Details of molecule geometry are presented in Table 2. The unit cell dimensions are as follows: • a = 9.0297(7) Å; The angle of a slope between sides and the base is equal to β = 91.323(3) • , and the volume is 5649.2(9) • Å 3 [29].
The TL properties of the described EuD 4 TEA complex depend on the europium salt used in the synthesis [19]. The use of the europium(III) chloride not only extends the synthesis time and increases the cost, but also deteriorates TL emission. Two of the same parallel syntheses, which are differing only in the use of europium(III) salt, were made. In the reaction ethanol was used as a solvent. TL spectra of the products were measured (Figure 8) [19]. The intensity of emission increased by 82% for EuD 4 TEA crystals doped with europium(III) nitrate. Moreover, the yield of synthesis increased, because the unnecessary step of washing out chlorides was omitted [19].

4.3.[. Ru(bpy)3]Cl2 Complex
Ru(II)-metal complex is a valuable material for triboluminescence investigation, pecially due to the well-described structural properties [24,31,32]. The substance show strong absorption band around 2370 cm −1 , and several minor bands between 1500 cm and 1800 cm −1 (Figure 9a) [31]. Transition metal complexes are difficult to analyze by ma spectrometry mainly due to their tendency to reduction during ionization and low vo tility. Viswanatham Katta et al. analyzed the ions of transition metal complexes with el trospray ionization. They obtained spectra of [Ru(bpy)3]Cl2 (M = 641 g/mol) by el trospraying a 15 pmol/pL solution in acetonitrile. Figure 9b shows MS spectra with a lo level of collisional activation; the peak at m/z 285 corresponds to the Ru(bpy)3 2+ ion [3 Full 1 H NMR spectrum (400 MHz) of Ru(II)-metal complex in D2O was obtained at roo temperature. The clear signals coming from the 2,2′-bipyridine system were found (Figu 10) [24].

[Ru(bpy) 3 ]Cl 2 Complex
Ru(II)-metal complex is a valuable material for triboluminescence investigation, especially due to the well-described structural properties [24,31,32]. The substance shows a strong absorption band around 2370 cm −1 , and several minor bands between 1500 cm −1 and 1800 cm −1 (Figure 9a) [31]. Transition metal complexes are difficult to analyze by mass spectrometry mainly due to their tendency to reduction during ionization and low volatility.

4.3.[. Ru(bpy)3]Cl2 Complex
Ru(II)-metal complex is a valuable material for triboluminescence investigation, especially due to the well-described structural properties [24,31,32]. The substance shows a strong absorption band around 2370 cm −1 , and several minor bands between 1500 cm −1 and 1800 cm −1 (Figure 9a) [31]. Transition metal complexes are difficult to analyze by mass spectrometry mainly due to their tendency to reduction during ionization and low volatility. Viswanatham Katta et al. analyzed the ions of transition metal complexes with electrospray ionization. They obtained spectra of [Ru(bpy)3]Cl2 (M = 641 g/mol) by electrospraying a 15 pmol/pL solution in acetonitrile. Figure 9b shows MS spectra with a low level of collisional activation; the peak at m/z 285 corresponds to the Ru(bpy)3 2+ ion [32]. Full 1 H NMR spectrum (400 MHz) of Ru(II)-metal complex in D2O was obtained at room temperature. The clear signals coming from the 2,2′-bipyridine system were found ( Figure  10) [24].   Kian Sing Low et al. analyzed a few Ru and Fe complexes by X-ray diffractometer. In [Ru(bpy)3]Cl2, the ruthenium ion is surrounded by three bidentate bipyridyl ligands, which are electron donors. The coordination number of the central atom is equal to 6. The chemical structure and crystal-packing diagram are presented in Figure 11.     Table 3.

Mn(Ph 3 PO)Br 2 Complex
The described complex contains the Mn +II ion surrounded by two Br − ions and two triphenylphosphine oxide, which are bonded with the metal atom by oxygen atoms (Figure 12). The coordination number is equal to 4. Molecules of the Mn(Ph 3 PO) 2 Br 2 crystallize as a mononuclear structure in a polar space group P1, so the manganese(II) complex has a non-centrosymmetric structure. Cell parameters were defined as follows: The FTIR analysis of the products showed a peak at 1155 cm −1 , which stretching of the P=O group. Two bands at 3051 and 1595 cm −1 indicate the aromatic rings in triphenylphosphine. Another doublet signal at 726 and caused by Mn-O stretching and bending [25].  The FTIR analysis of the products showed a peak at 1155 cm −1 , which is caused by stretching of the P=O group. Two bands at 3051 and 1595 cm −1 indicate the presence of aromatic rings in triphenylphosphine. Another doublet signal at 726 and 686 cm −1 is caused by Mn-O stretching and bending [25].  The FTIR analysis of the products showed a peak at 1155 cm −1 , which is caus stretching of the P=O group. Two bands at 3051 and 1595 cm −1 indicate the presen aromatic rings in triphenylphosphine. Another doublet signal at 726 and 686 cm caused by Mn-O stretching and bending [25].

TL and PL of the [Cu(NCS)(py)2(PPh3)] Complex
The photoluminescent properties of the [Cu(NCS)(py)2(PPh3)] were first visual sessed. It is possible to observe strong photoluminescence of crystals with an excit wavelength of 365 nm. Claudio Pettinari et al. compared the photoluminescence pr ties of the several copper complexes, including [Cu(NCS)(py)2(PPh3)] [10]. Each of showed a broad absorption band localized at 370-490 nm. The maximum of the em band was observed at 496 nm ( Figure 13) [28]. Additionally, the authors measure emission decay time, which was 5.8 ns [10].  In another work, two emission bands were observed-at 479 nm and 587 nm [16]. All of the photoluminescence spectra presented in the literature coincide to a large extent; however, minor differences occurred. It may be due to the distinctions in the purity of the tested compounds, measurement conditions, and used apparatus.
The [Cu(NCS)(py) 2 (PPh 3 )] complex shows one of the strongest triboluminescent properties among the already known compounds, which makes their observation possible in daylight. The emitted light takes a blue-green color ( Figure 14) [6]. however, minor differences occurred. It may be d tested compounds, measurement conditions, and The [Cu(NCS)(py)2(PPh3)] complex shows properties among the already known compounds in daylight. The emitted light takes a blue-green The triboluminescence spectrum is shifted b to the photoluminescence one; thus, maximum e 13). The full width at half-maximum (FWHM) nm, which is 23 nm smaller than the same param ferences were noted between the intensity of th cence emission [28]. Measurements were perfor described in Section 7 of the article.

TL and PL of the Europium Complex
Under UV light irradiation, strong red phot is observed. The wavelength of the maximum em The triboluminescence spectrum is shifted by 10 nm towards lower energy compared to the photoluminescence one; thus, maximum emission of TL occurs at 500 nm ( Figure 13). The full width at half-maximum (FWHM) of the triboluminescence spectrum is 90 nm, which is 23 nm smaller than the same parameter of the PL. No other significant differences were noted between the intensity of the triboluminescence and photoluminescence emission [28]. Measurements were performed using a specially designed system described in Section 7 of the article.

TL and PL of the Europium Complex
Under UV light irradiation, strong red photoluminescence of the EuD 4 TEA complex is observed. The wavelength of the maximum emission is 612 nm, which corresponds to 5 D 0 → 7 F 2 transition in Eu 3+ ions. Additionally, transitions from 5 D 0 to 7 F 1 , 7 F 3 , and 7 F 4 occur [23].
The light emitted during the mechanical deformation of crystals takes a red color, and it is caused by the typical Eu 4+ -centered 5 D 0 → 7 F 0−4 transitions, but mainly 5 D 0 → 7 F 2 transitions (Figure 15b) [35]. The TL and PL spectra are presented in Figure 15a [35]. Maximum emission of TL occurs at 614 nm. The obtained spectra exhibit significant similarities; however, TL has a lower intensity. Due to the end of the spectrometer's measuring range, the signal coming from 5 D 0 → 7 F 4 transition has not been recorded [35]. The EuD4TEA exhibits one of the highest triboluminescence intensities among all currently known substances. The bright emission is noticeable in daylight and the intensity is 106% stronger than the most popular triboluminescent compound-ZnS:Mn [36]. The relative light yield of the europium(III) complex is 42 146 ± 7784 and ZnS:Mn 20 426 ± 1294 ( Figure 16). The described measurements were performed with samples made with europium(III) nitrate [36].

TL and PL of the [Ru(bpy)3]Cl2 Complex
Photoluminescent properties are observed in the [Ru(bpy)3]Cl2⋯6H2O complex because of the presence of the [Ru(bpy)3] 2+ cations [24]. Glyus L. Sharipov and Adis A. Tukhbatullin described fundamental spectroscopic properties of the obtained complex. The measured maximum of the emission upon 450 nm excitation wavelength was 519 nm [37]. The EuD 4 TEA exhibits one of the highest triboluminescence intensities among all currently known substances. The bright emission is noticeable in daylight and the intensity is 106% stronger than the most popular triboluminescent compound-ZnS:Mn [36]. The relative light yield of the europium(III) complex is 42 146 ± 7784 and ZnS:Mn 20 426 ± 1294 ( Figure 16). The described measurements were performed with samples made with europium(III) nitrate [36]. The EuD4TEA exhibits one of the highest triboluminescence intensities among all currently known substances. The bright emission is noticeable in daylight and the intensity is 106% stronger than the most popular triboluminescent compound-ZnS:Mn [36]. The relative light yield of the europium(III) complex is 42 146 ± 7784 and ZnS:Mn 20 426 ± 1294 ( Figure 16). The described measurements were performed with samples made with europium(III) nitrate [36].

TL and PL of the [Ru(bpy)3]Cl2 Complex
Photoluminescent properties are observed in the [Ru(bpy)3]Cl2⋯6H2O complex because of the presence of the [Ru(bpy)3] 2+ cations [24]. Glyus L. Sharipov and Adis A. Tukhbatullin described fundamental spectroscopic properties of the obtained complex. The measured maximum of the emission upon 450 nm excitation wavelength was 519 nm [37]. The lifetime of the excited ionic state marked as *N2, *[R(bpy)] 2+ was 40 µs (Figure 17). Kalyanasundaram K. reported the quantum yield of the described complex in an aqueous solution as 0.044 [38].

TL and PL of the [Ru(bpy) 3 ]Cl 2 Complex
Photoluminescent properties are observed in the [Ru(bpy) 3 ]Cl 2 · · · 6H 2 O complex because of the presence of the [Ru(bpy) 3 ] 2+ cations [24]. Glyus L. Sharipov and Adis A. Tukhbatullin described fundamental spectroscopic properties of the obtained complex. The measured maximum of the emission upon 450 nm excitation wavelength was 519 nm [37]. The lifetime of the excited ionic state marked as *N 2 , *[R(bpy)] 2+ was 40 µs (Figure 17). Kalyanasundaram K. reported the quantum yield of the described complex in an aqueous solution as 0.044 [38]. The triboluminescence spectrum of [Ru(bpy)3]Cl2 • 6H2O consists of two parts ( Figure  17). The first one comes from the emission of N2, while the second one is similar to the photoluminescence of the complex. The similarity of the TL and PL spectra is caused by the *[Ru(bpy)3] 2+ ion excitation; however, the excitation mechanisms are different [37]. The theories of the triboluminescence fundamentals are described in Section 2.
[Ru(bpy)3]Cl2⋯6H2O crystals are asymmetric [38], which makes this compound a particularly valuable material for TL investigation. According to one of the postulated theories, only centrosymmetric compounds exhibit triboluminescence, so the non-centrosymmetric crystal with strong triboluminescence sheds new light on the topic [38]. Moreover, the correlation between the degree of fragmentation and TL intensity has not been observed [37], which has been reported for centrosymmetric crystals [39].
Glyus L. Sharipov and Adis A. Tukhbatullin reported triboluminescence spectra in specific gas environments, such as neon and argon ( Figure 18). The obtained TL spectrum under neon exhibits intense emission corresponding to excited neon and, in addition, from N2 excitation. A similar effect is observed in the argon environment; however, the weak emission from excited *[Ru(bpy)3] 2+ ion (620 nm) is still visible. The ion emission in the neon environment is not reported due to a strong Ne emission. The observed nitrogen emission can be caused by N2 molecules absorbed on the surface of the material [37]. The triboluminescence spectrum of [Ru(bpy) 3 ]Cl 2 · 6H 2 O consists of two parts ( Figure 17). The first one comes from the emission of N 2 , while the second one is similar to the photoluminescence of the complex. The similarity of the TL and PL spectra is caused by the *[Ru(bpy) 3 ] 2+ ion excitation; however, the excitation mechanisms are different [37]. The theories of the triboluminescence fundamentals are described in Section 2.
[Ru(bpy) 3 ]Cl 2 · · · 6H 2 O crystals are asymmetric [38], which makes this compound a particularly valuable material for TL investigation. According to one of the postulated theories, only centrosymmetric compounds exhibit triboluminescence, so the noncentrosymmetric crystal with strong triboluminescence sheds new light on the topic [38]. Moreover, the correlation between the degree of fragmentation and TL intensity has not been observed [37], which has been reported for centrosymmetric crystals [39].
Glyus L. Sharipov and Adis A. Tukhbatullin reported triboluminescence spectra in specific gas environments, such as neon and argon ( Figure 18). The obtained TL spectrum under neon exhibits intense emission corresponding to excited neon and, in addition, from N 2 excitation. A similar effect is observed in the argon environment; however, the weak emission from excited *[Ru(bpy) 3 ] 2+ ion (620 nm) is still visible. The ion emission in the neon environment is not reported due to a strong Ne emission. The observed nitrogen emission can be caused by N 2 molecules absorbed on the surface of the material [37].
The TL spectrum was also collected in O 2 atmosphere ( Figure 19). The reported emission from N 2 was suppressed, while the emission from excited ion *[Ru(bpy) 3 ] 2+ was unchanged. On this basis, it was found that the excitation of the complex is not caused by absorption of the energy emitted by the excited N 2 molecules. The TL spectrum was also collected in O2 atmosphere ( Figure 19). The reported emission from N2 was suppressed, while the emission from excited ion *[Ru(bpy)3] 2+ was unchanged. On this basis, it was found that the excitation of the complex is not caused by absorption of the energy emitted by the excited N2 molecules.

TL and PL of the Manganese Complex
The excitation spectrum of the Mn(Ph3PO)Br2 contains a broad band between 250 and 350 nm. It is caused by π-π* transition in the compound [25]. Photoluminescence of the manganese(II) complex could be explained by using ligand field theory. The maximum emission is recorded at 510 nm, which is caused by 4 T1 → 6 A1 transition [9]. As a result of the mechanical interaction, green emission is observed. The excitation and PL spectra are  The TL spectrum was also collected in O2 atmosphere ( Figure 19). The reported emission from N2 was suppressed, while the emission from excited ion *[Ru(bpy)3] 2+ was unchanged. On this basis, it was found that the excitation of the complex is not caused by absorption of the energy emitted by the excited N2 molecules.

TL and PL of the Manganese Complex
The excitation spectrum of the Mn(Ph3PO)Br2 contains a broad band between 250 and 350 nm. It is caused by π-π* transition in the compound [25]. Photoluminescence of the manganese(II) complex could be explained by using ligand field theory. The maximum emission is recorded at 510 nm, which is caused by 4 T1 → 6 A1 transition [9]. As a result of the mechanical interaction, green emission is observed. The excitation and PL spectra are presented below (Figure 20).

TL and PL of the Manganese Complex
The excitation spectrum of the Mn(Ph 3 PO)Br 2 contains a broad band between 250 and 350 nm. It is caused by π-π* transition in the compound [25]. Photoluminescence of the manganese(II) complex could be explained by using ligand field theory. The maximum emission is recorded at 510 nm, which is caused by 4 T 1 → 6 A 1 transition [9]. As a result of the mechanical interaction, green emission is observed. The excitation and PL spectra are presented below (Figure 20). The photoluminescence efficiency of the manganese(II) complex can be affected by doping. HBr-doped compounds exhibit brighter emission and higher efficiency. On the other hand, a compound doped with HgCl2 performs weaker photoluminescence than an undoped complex. The decrease in emission could be caused by the presence of chlorine ions, which provide more non-radiative decay pathways [25].
The emission also decreases with the increase of surrounded gas pressure [40][41][42]. The measurements were performed with a modified Drickamer Type I high-pressure optical cell.
Mn(Ph3PO)2Br2 complex shows a strong triboluminescent. Emission maximum occurs at 510 nm. Triboluminescence spectrum shape is conforming to the photoluminescence spectrum (Figure 21) [41]. The emission lifetime of triboluminescence is equal to 602 µs [9]. Measurements were performed using a specially designed system described in Section 7.  The photoluminescence efficiency of the manganese(II) complex can be affected by doping. HBr-doped compounds exhibit brighter emission and higher efficiency. On the other hand, a compound doped with HgCl 2 performs weaker photoluminescence than an undoped complex. The decrease in emission could be caused by the presence of chlorine ions, which provide more non-radiative decay pathways [25].
The emission also decreases with the increase of surrounded gas pressure [40][41][42]. The measurements were performed with a modified Drickamer Type I high-pressure optical cell.
Mn(Ph 3 PO) 2 Br 2 complex shows a strong triboluminescent. Emission maximum occurs at 510 nm. Triboluminescence spectrum shape is conforming to the photoluminescence spectrum ( Figure 21) [41]. The emission lifetime of triboluminescence is equal to 602 µs [9]. Measurements were performed using a specially designed system described in Section 7. The photoluminescence efficiency of the manganese(II) complex can be affected by doping. HBr-doped compounds exhibit brighter emission and higher efficiency. On the other hand, a compound doped with HgCl2 performs weaker photoluminescence than an undoped complex. The decrease in emission could be caused by the presence of chlorine ions, which provide more non-radiative decay pathways [25].
The emission also decreases with the increase of surrounded gas pressure [40][41][42]. The measurements were performed with a modified Drickamer Type I high-pressure optical cell.
Mn(Ph3PO)2Br2 complex shows a strong triboluminescent. Emission maximum occurs at 510 nm. Triboluminescence spectrum shape is conforming to the photoluminescence spectrum (Figure 21) [41]. The emission lifetime of triboluminescence is equal to 602 µs [9]. Measurements were performed using a specially designed system described in Section 7.  Reprinted with permission from Elsevier [41].
Ligands in the complex structure have a significant impact on the luminescent properties. Interestingly, changing from Br − ions to Cl − causes the disappearance of the photoluminescence properties, although Mn(Ph 3 PO) 2 Cl 2 still possesses efficient triboluminescent properties (Figure 22). For the manganese(II) complex with chlorine anions as a ligand emission maximum is shifted to 520 nm [9].

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Ligands in the complex structure have a significant impact on the luminescent properties. Interestingly, changing from Br − ions to Cl − causes the disappearance of the photoluminescence properties, although Mn(Ph3PO)2Cl2 still possesses efficient triboluminescent properties (Figure 22). For the manganese(II) complex with chlorine anions as a ligand emission maximum is shifted to 520 nm [9].

Various Stimuli Affecting the Triboluminescence
The common method for TL measurements utilizes a drop tower, where a falling object with defined weight is a cracking sample. Then, generated radiation is collected by a dedicated spectrometer. The details of the TL measurement system are described in Section 7.
Regardless of the impact force, the maximum intensities oscillate at wavelength values close to 496 nm. The spectrum shape of [Cu(NCS)(py)2(PPh3)] complex also remains unchanged. For the larger impact force, a higher intensity of the triboluminescence is observed. Between the smaller applied force (0.98 N) and the largest one (4.98 N), more than twice higher TL intensity was observed ( Figure 23) [28,42].
Moreover, it has been shown that the TL emission depends on the crystallites size [28]. Each successive hit causes fragmentation of the crystalline material, which reflects the decrease of the triboluminescence intensity during the subsequent attempts [28]. The SEM pictures of the crystalline particles captured before the TL measurement and after the first, third, fifth, and eighth attempts are shown in Figure 23c. A Gaussian distribution was fitted for mean diameters, yielding results of 120 ± 20, 100 ± 15, 80 ± 12, 50 ± 10, and 30 ± 8 µm for the abovementioned hit numbers, respectively.

Various Stimuli Affecting the Triboluminescence
The common method for TL measurements utilizes a drop tower, where a falling object with defined weight is a cracking sample. Then, generated radiation is collected by a dedicated spectrometer. The details of the TL measurement system are described in Section 7.
Regardless of the impact force, the maximum intensities oscillate at wavelength values close to 496 nm. The spectrum shape of [Cu(NCS)(py) 2 (PPh 3 )] complex also remains unchanged. For the larger impact force, a higher intensity of the triboluminescence is observed. Between the smaller applied force (0.98 N) and the largest one (4.98 N), more than twice higher TL intensity was observed ( Figure 23) [28,42].
Moreover, it has been shown that the TL emission depends on the crystallites size [28]. Each successive hit causes fragmentation of the crystalline material, which reflects the decrease of the triboluminescence intensity during the subsequent attempts [28]. The SEM pictures of the crystalline particles captured before the TL measurement and after the first, third, fifth, and eighth attempts are shown in Figure 23c. A Gaussian distribution was fitted for mean diameters, yielding results of 120 ± 20, 100 ± 15, 80 ± 12, 50 ± 10, and 30 ± 8 µm for the abovementioned hit numbers, respectively.
Combining the polymer matrix with photoluminescent and triboluminescent compounds, and their influence on the examination of optical properties has been recently reported in the literature [28,42]. It was extensively investigated what kind of effect may influence the triboluminescence phenomenon when placing the [Cu(NCS)(py) 2 (PPh 3 )] complex in another material. The Cu(I) complex was used in composites with different polymers and also placed inside the hydrogels structures [28,42]. Combining the polymer matrix with photoluminescent and triboluminescent compounds, and their influence on the examination of optical properties has been recently reported in the literature [28,42]. It was extensively investigated what kind of effect may influence the triboluminescence phenomenon when placing the [Cu(NCS)(py)2(PPh3)] complex in another material. The Cu(I) complex was used in composites with different polymers and also placed inside the hydrogels structures [28,42].

Polymer Mats Coated with a Triboluminescent Compound
To create a material with the triboluminescent properties, crystalline particles of the Cu(I) complex were deposited on the surface of electrospinning mats, made of four polymers: poly(methyl methacrylate) (PMMA), polystyrene (PS), polyurethane (PU), and

Polymer Mats Coated with a Triboluminescent Compound
To create a material with the triboluminescent properties, crystalline particles of the Cu(I) complex were deposited on the surface of electrospinning mats, made of four polymers: poly(methyl methacrylate) (PMMA), polystyrene (PS), polyurethane (PU), and poly(vinylidene fluoride) (PVDF). Spectroscopic measurements of TL were performed with the same tower system, as in the case of pure crystalline material ( Figure 24). Depending on the used polymer, different emission intensities were obtained. Triboluminescence intensities for the first impact are 1200, 2500, 4000, and 2750 counts per second for materials based on PMMA, PS, PU, and PVDF, respectively [28]. For all used composites (polymer mats/copper complex crystals), the triboluminescence signal is visible when the same sample is mechanically treated several times. For PMMA, PS, PVDF, and PU, triboluminescence response was observed for three, five, six, and eight impacts, respectively. For all of the subsequent samples, maxima and spectra shape are the same, but the intensity gradually decreases as the composite becomes quenched [28]. In addition, composite mats were also fabricated by another method. In this alternative approach, called blending, the [Cu(NCS)(py)2(PPh3)] crystals were dissolved in a polymer solution, and the homogeneous mixture was used to make electrospinning mats. Interestingly, the composites prepared by the blending method exhibited none of TL response [42]. Probably, during the dissolving process, the molecules of the copper complex dispersed in the polymer, which led to the loss of the long-range crystal structure. Differences between these two techniques are also visible in the SEM pictures (Figure 25a,b) and under a fluorescence microscope (Figure 25c,d). During imaging with fluorescence microscopy (FM, λexc. = 365 nm), the samples of polymer substrates exhibited no luminescent properties, so the acquired colorful emission visible in the photos comes from the copper(I) complex. The surface impregnation process (Figure 25c) leads to creating local areas with higher intense emission, which is caused by advanced aggregation and complex particle deposition. For comparison, a composite obtained by blending (Figure 25d) shows a homogeneous luminescence over the entire surface of the fibers, which indicates dispersion of the copper(I) complex in the polymer matrix at the molecular level. This result implies an important connection between the crystalline structure and triboluminescent properties [28]. The PU fibers were the thinnest ones among the tested polymers. This probably contributed to the decrease in interfiber space, reduction of the sieving effect, and as a conse- Depending on the used polymer, different emission intensities were obtained. Triboluminescence intensities for the first impact are 1200, 2500, 4000, and 2750 counts per second for materials based on PMMA, PS, PU, and PVDF, respectively [28]. For all used composites (polymer mats/copper complex crystals), the triboluminescence signal is visible when the same sample is mechanically treated several times. For PMMA, PS, PVDF, and PU, triboluminescence response was observed for three, five, six, and eight impacts, respectively. For all of the subsequent samples, maxima and spectra shape are the same, but the intensity gradually decreases as the composite becomes quenched [28]. In addition, composite mats were also fabricated by another method. In this alternative approach, called blending, the [Cu(NCS)(py) 2 (PPh 3 )] crystals were dissolved in a polymer solution, and the homogeneous mixture was used to make electrospinning mats. Interestingly, the composites prepared by the blending method exhibited none of TL response [42]. Probably, during the dissolving process, the molecules of the copper complex dispersed in the polymer, which led to the loss of the long-range crystal structure. Differences between these two techniques are also visible in the SEM pictures (Figure 25a,b) and under a fluorescence microscope (Figure 25c,d). During imaging with fluorescence microscopy (FM, λ exc. = 365 nm), the samples of polymer substrates exhibited no luminescent properties, so the acquired colorful emission visible in the photos comes from the copper(I) complex. The surface impregnation process (Figure 25c) leads to creating local areas with higher intense emission, which is caused by advanced aggregation and complex particle deposition. For comparison, a composite obtained by blending (Figure 25d) shows a homogeneous luminescence over the entire surface of the fibers, which indicates dispersion of the copper(I) complex in the polymer matrix at the molecular level. This result implies an important connection between the crystalline structure and triboluminescent properties [28]. The PU fibers were the thinnest ones among the tested polymers. This probably contributed to the decrease in interfiber space, reduction of the sieving effect, and as a consequence, the deposition of more crystals. It is also possible that chemical affinity between the PU matrix and the copper(I) complex occurred [28]. The summarized parameters of enriched polymer triboluminescent mats are presented in Table 5.  In conclusion, it has been shown that the surface impregnation technique makes it possible to prepare homogeneous triboluminescent composites, where light emission depends on the polymer substrate type. Out of the used composites, the best triboluminescence properties were given by surface-impregnated PU. This shows that these materials can be applied in practice as, e.g., pressure sensors [11].
Apart from plane polymer mats, it is possible to receive three-dimensional polymeric  In conclusion, it has been shown that the surface impregnation technique makes it possible to prepare homogeneous triboluminescent composites, where light emission depends on the polymer substrate type. Out of the used composites, the best triboluminescence properties were given by surface-impregnated PU. This shows that these materials can be applied in practice as, e.g., pressure sensors [11].
Apart from plane polymer mats, it is possible to receive three-dimensional polymeric structures with triboluminescence emission [43]. Hydrogels can be used for this purpose. Samples were synthesized using acrylamide (AA), and its derivatives as monomer.
Solutions of N-(hydroxymethyl)acrylamide (NHMA) and N-isopropylacrylamide (NIPAM) were combined with N,N -methylenebisacrylamide (MBA) and ammonium persulphate (APS) as a reaction initiator, respectively. N,N,N ,N -tetramethylethyldiamine (TEMED) was used as a cross-linker of polymers. Then, the Cu(I) complex crystals were added. The solutions were poured into a Petri dish and left to polymerize overnight at room temperature [42].
The performed approach affected the TL properties. Namely, the growth of triboluminescence intensity was observed for all types of hydrogel samples compared to the pure Cu(I) complex. Moreover, the luminescence was more intense in the case of water treatment. The brighter light was emitted if the gel was placed underwater in a shorter time. Among monomers used in synthesis the NIPAM one was stood out, whose polymer matrix with Cu(I) complex achieved the highest TL emission time from all the investigated samples ( Figure 26). NIPAM and ligands of the copper(I) complex have typical hydrophobic properties. Hence, such an approach may enhance the total emission time [42].

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22 of 26 added. The solutions were poured into a Petri dish and left to polymerize overnight at room temperature [42]. The performed approach affected the TL properties. Namely, the growth of triboluminescence intensity was observed for all types of hydrogel samples compared to the pure Cu(I) complex. Moreover, the luminescence was more intense in the case of water treatment. The brighter light was emitted if the gel was placed underwater in a shorter time. Among monomers used in synthesis the NIPAM one was stood out, whose polymer matrix with Cu(I) complex achieved the highest TL emission time from all the investigated samples ( Figure 26). NIPAM and ligands of the copper(I) complex have typical hydrophobic properties. Hence, such an approach may enhance the total emission time [42]. The triboluminescence aberrations can also come from the optical properties of the utilized polymer medium, which could easily propagate, scatter, or refract the emitted light. Hydrogels have greater optical density and viscosity compared to the surrounding air environment. These parameters' growth intensifies triboluminescence emission. Moreover, the Cu(I) complex crystals suspended in the gel are separated from each other and kept a crystalline structure [42].

Dopant Implementation
Triboluminescent properties can be modified by the inclusion of organic dopants during the synthesis. Zeng X.R. et al. reported on a morphine-doped EuD4TEA complex exhibiting eight times higher triboluminescence than pure sample [43]. Moreover, the effect of piperine, DMMP, and TEPS doping was widely studied by Fontenot R.S. et al., who reported the influence of the dopants on TL yield, crystals morphology, synthesis time, and TL decay time [20]. The implementation of the piperine, which had been chosen due to its similarity to morphine, does not have a significant influence on the TL properties of the material. However, DMMP-doped material exhibits a 55% higher TL yield, whereas TEPS inclusion quenches the emission by 46% [20].
The measurements of photo-and triboluminescence show no influence of dopants on spectra. For both experiments shifts of the characteristic emission peaks are not observed. According to the authors, implemented dopants play the role of the co-activator Figure 26. TL intensity vs. water treatment duration presentation (a). Emission spectra before (b) and after (c) water treatment of hydrogel samples [42].
The triboluminescence aberrations can also come from the optical properties of the utilized polymer medium, which could easily propagate, scatter, or refract the emitted light. Hydrogels have greater optical density and viscosity compared to the surrounding air environment. These parameters' growth intensifies triboluminescence emission. Moreover, the Cu(I) complex crystals suspended in the gel are separated from each other and kept a crystalline structure [42].

Dopant Implementation
Triboluminescent properties can be modified by the inclusion of organic dopants during the synthesis. Zeng X.R. et al. reported on a morphine-doped EuD 4 TEA complex exhibiting eight times higher triboluminescence than pure sample [43]. Moreover, the effect of piperine, DMMP, and TEPS doping was widely studied by Fontenot R.S. et al., who reported the influence of the dopants on TL yield, crystals morphology, synthesis time, and TL decay time [20]. The implementation of the piperine, which had been chosen due to its similarity to morphine, does not have a significant influence on the TL properties of the material. However, DMMP-doped material exhibits a 55% higher TL yield, whereas TEPS inclusion quenches the emission by 46% [20].
The measurements of photo-and triboluminescence show no influence of dopants on spectra. For both experiments shifts of the characteristic emission peaks are not observed. According to the authors, implemented dopants play the role of the co-activator or quenching agents [20].
Broad possibilities of the complex properties modification by doping with organic compounds significantly extend the implementation perspective. Even inclusion of unusual sub-stances such as common multivitamin remarkably affects TL properties [23]. The influence of the series of organic compounds was widely described by Fontenot R.S. et al. [44].

Experimental Setup for the Triboluminescence Measurements
The TL measurement setup contains two fundamental elements: the first one is responsible for the force application and the second allows to perform the emitted radiation analysis. Although the TL measurement's methodology is simple and the triboluminescent compounds are omnipresent, there are no commercially available setups for this type of experiment. It causes the need for a framework design and manufacturing by each of the research groups. The most commonly used type of triboluminescence measurement system is based on a drop tower in which the dropping ball constitutes a source of the mechanical force ( Figure 27). The potential energy of the ball changes into kinetic energy, which is then transferred to the sample. By changing the height of the drop, it is possible to manipulate the energy of the interaction. The mechanical force implementation causes light emission. The emitted light is transferred via a fiber optic to a spectrometer, where induced radiation is collected and analyzed [36]. analysis. Although the TL measurement's methodology is simple and the triboluminescent compounds are omnipresent, there are no commercially available setups for this type of experiment. It causes the need for a framework design and manufacturing by each of the research groups. The most commonly used type of triboluminescence measurement system is based on a drop tower in which the dropping ball constitutes a source of the mechanical force ( Figure 27). The potential energy of the ball changes into kinetic energy, which is then transferred to the sample. By changing the height of the drop, it is possible to manipulate the energy of the interaction. The mechanical force implementation causes light emission. The emitted light is transferred via a fiber optic to a spectrometer, where induced radiation is collected and analyzed [36]. The undoubted advantage of the presented type of measurement system is an uncomplicated construction and its low manufacturing cost. The tunable height of the drop makes it possible to measure the influence of the conditions on the induced emission. As indicated in the previous part of the paper, the applied mechanical force is one of the stimuli which straightforwardly influences the triboluminescence properties [10,28]. Due to the simple setup construction, its modification is feasible. The drop tower can be used for both crystal powder and matrices doped with triboluminescent compounds. The implementation of the sealing system can allow for TL measurements in pure gas conditions. The significant influence of this stimulus has been observed previously [45]. However, the [Cu(NSC)(py)2(PPh3)] complex has not yet been tested in this way. The pure gas measurements may become an essential element of the triboluminescence mechanism description.

Perspectives of TL Implementation
Triboluminescent compounds have a wide range of applications. One of the most promising is designing a new group of mechanical force and stress sensors based on TL materials. An exemplary sensing system described by D. Olawale et al. is based on a manganese-doped zinc sulfide (ZnS:Mn) and can be used for concrete elements' damage monitoring [11]. The proposed solution uses the connected fiber optics system, which is covered with the TL material in specific areas. The structural damages lead to light genera- The undoubted advantage of the presented type of measurement system is an uncomplicated construction and its low manufacturing cost. The tunable height of the drop makes it possible to measure the influence of the conditions on the induced emission. As indicated in the previous part of the paper, the applied mechanical force is one of the stimuli which straightforwardly influences the triboluminescence properties [10,28]. Due to the simple setup construction, its modification is feasible. The drop tower can be used for both crystal powder and matrices doped with triboluminescent compounds. The implementation of the sealing system can allow for TL measurements in pure gas conditions. The significant influence of this stimulus has been observed previously [45]. However, the [Cu(NSC)(py) 2 (PPh 3 )] complex has not yet been tested in this way. The pure gas measurements may become an essential element of the triboluminescence mechanism description.

Perspectives of TL Implementation
Triboluminescent compounds have a wide range of applications. One of the most promising is designing a new group of mechanical force and stress sensors based on TL materials. An exemplary sensing system described by D. Olawale et al. is based on a manganese-doped zinc sulfide (ZnS:Mn) and can be used for concrete elements' damage monitoring [11]. The proposed solution uses the connected fiber optics system, which is covered with the TL material in specific areas. The structural damages lead to light generation, which is, in the next step, detected by an electronic system monitoring the whole network of fiber optics. The proposed solution may have particular use in registering seismic damages of buildings [11].
Moreover, wind flow can be used to achieve a mechanoluminescence response. Jeong et al. designed elastic-ML materials, which consists of the multicolored ZnS:Cu microparticles embedded in PDMS fiber. This composite can be applied in wind-activated, energetically independent displays and lightning systems [46]. N. Terasaki et al. researched mechanoluminescent nanoparticles, which can be useful in bioimaging. Followed by the triboluminescence generation with ultrasonic waves, the compound can monitor the work of the digestive system [13]. Triboluminescence can also be used as a light source for a fluorescent probe. Ceramic TL materials that stay inside the body, or cells activated by ultrasounds emit light, influence organic dye molecules [47]. Furthermore, using ultrasound techniques these compounds found the application in lightsupported therapies [13]. Additionally, the triboluminescent compounds have potential application in catalyzing photosensitive reactions. A method has been developed to synthesize stable SAOE-Zr-TiO 2 by TL generation in situ. The obtained hybrid material is based on europium doped strontium aluminate (SAOE) with TiO 2 nanoparticles [12].
The process of designing and manufacturing many types of solutions, especially sensors, is primarily based on the well-known materials' properties changes under the influence of an external stimulus. The development of TL-based devices and techniques is significantly straightened due to the unknown nature of the triboluminescence phenomenon. Obtaining new triboluminescent materials may shed new light on the possible definition of the mechanism of stress-induced light emission.

Conclusions
In this contribution, we have described the variety of transition metal coordination complexes, which are excellent examples to study the triboluminescent mechanism. In the article, we paid attention to synthesis routes, various spectroscopic product analyses, as well as TL and PL measurements discussion. Moreover, the triboluminescent properties dependent on external factors, for example, embedded in the polymer mats, were presented. We found that the described compounds do not require a complicated synthesis apparatus and procedure. It can be received in a common laboratory with a simple working fume hood. Mainly, the synthesis is just a one-or two-step procedure. As discussed in this short review compounds have appealing spectroscopic properties, such as significant and visible TL and PL, which leads to many practical applications. This could help in further research on the TL mechanism, which would allow defining universal explanation or clear division for all cases of transformation mechanical energy into the light in different class materials.
Development in this field is crucial for further implementation. Currently, there are promising results; however, without additional knowledge about the nature of the considered phenomenon, it is impossible to fully exploit the triboluminescence potential. Acknowledgments: The authors would like to thank Adam Matloch for his help with the preparation of the graphical abstract.