Preparation and Properties of Cyanobacteria-Based Carbon Quantum Dots/Polyvinyl Alcohol/ Nanocellulose Composite

Blue luminescent carbon quantum dots (CQDs) were prepared from cyanobacteria by a hydrothermal method. The PL quantum yields of the obtained CQDs was 5.30%. Cyanobacteria-based carbon quantum dots/polyvinyl alcohol/nanocellulose composite films were prepared, which could emit bright blue under UV light. FTIR characterization showed that the composite films had hydroxyl groups on the surface and no new groups were formed after combining the three materials. The photoluminescence (PL) spectra revealed that the emission of the prepared CQDs was excitation dependent. Studies on the water resistance performance and light barrier properties of the composite films showed that they possessed higher water resistance properties and better UV/infrared light barrier properties. Therefore, we report the cyanobacteria-based carbon quantum dots/polyvinyl alcohol/nanocellulose composite films have the potential to be applied in flexible packaging materials, anti-fake materials, UV/infrared light barrier materials and so on.


Introduction
Cyanobacterial (CB) blooms found in many lakes, ponds and rivers have become a serious threat to human and animal health throughout the world [1]. Cyanobacteria are Gram-negative bacteria capable of producing a wide range of potent toxins-cyanotoxins-as secondary metabolites, which can cause acute and possibly chronic public health problems and fatal poisoning in aquatic and domestic animals [2,3]. Removing extensively accumulated cyanobacteria from the water is generally considered the most straightforward solution to CB blooms. As a result, scientists and entrepreneurs have paid close attention to the collected cyanobacteria. If the biomass in cyanobacteria can be reduced to a certain level, the problem of its environmental risk can be solved [4]. Given that cyanobacteria contain large amounts of plant proteins, amino acids and other extractable substances, people have tried to use the collected cyanobacteria as a biological resource to make value-added products, such as biofertilizer [5], high purity phycocyanin [1], activated carbon [6] and algae powder [7]. In this study, carbon quantum dots (CQDs) were extracted from collected cyanobacteria and used to produce fluorescent polyvinyl alcohol (PVA) films, which provides a new way to ameliorate cyanobacteria pollution.

Preparation of CNF
Cellulose nanofibers was extracted from coconut palm petiole and the steps were referred to the report of Zhao et al. [44].

Synthesis of CQDs
Cyanobacterial carbon quantum dots was synthesized with a hydrothermal method which was referred to Wang et al. [45]. The CY powder (1.5 g) was treated in a mixture of purified water/glycerol (3:1 by volume) under stirring at room temperature for 20 min. Then the mixture was transferred into a polytetrafluoroethylene-equipped stainless-steel autoclave (100 mL) and heated at 200 • C for 8 h in an oil bath. The resulted dark brown product which consisted of CQDs solution and black residue was filtered with a piece of microporous membrane (0.22 µm, pore size), resulting in cyanobacterial carbon quantum dots.
The solution drying method was used to calculate the concentration of the prepared cyanobacterial CQDs according to Equation (1): where C refers to the concentration of CQDs, M 1 refers to total mass (mg) of clean slides and cover slides and M 2 refers to the mass (mg) of dried carbon quantum dots dispersion with slide and cover glass, and V represents volume of CQDs. Finally, the concentration of CQDs was 175 mg/mL.

Characterization
A ZF-1 three-use ultraviolet analyzer (Hangzhou Qiwei Instrument Co., Ltd., Hangzhou, China) was used in this study to see if the produced CQDs and the corresponding films had fluorescence effects. Photoluminescence performance of the CQDs and films was investigated with a fluorescence spectrometer (Model LS-55, PerkinElmer, Waltham, MA, USA). The ultraviolet-visible spectroscopy (UV-vis) absorption spectra were recorded on a Lambda 950 spectropolarimeter (PerkinElmer). FT-IR spectra of the film samples were acquired with a Fourier transform spectrometer (NICOLET IS10, Thermo Scientific, Inc., Waltham, MA, USA) operating in the Smart iTR diamond ATR mode and the range from 500 cm −1 to 4000 cm −1 . Barrier properties of the films to light (200-2500 nm) was tested by a U-4001 spectrophotometer (Hewlett-Packard Co., Santa Clara, CA, USA). A cold field emission scanning electron microscope (Regulus 8200, Hitachi, Tokyo, Japan) was used to analysis the fracture morphology of the films. The water resistance of films was expressed by the water absorption. The samples with a size of 2 cm × 2 cm were first dried at 100 • C for 24 h, then weighed (W 1 ) and soaked in distilled water (50 mL) for 24 h. After drying its surface, the sample was weighted again (W 2 ), and the water absorption (A) of the sample was calculated by Equation (2):

Characterization of CQDs
The optical properties of the as-obtained CQDs under visible and UV light are shown in Figure 1a (inset). The CQDs appears brown and bright blue under visible and UV light, respectively. Even more interesting, in Figure 1a, when the wavelength of excitation increases from 360 to 440 nm, its emission intensity is different and the wavelength of the strongest emission peak of the CQDs is 450-525 nm. Moreover, when the excitation wavelength was 420 nm, the CQDs presented the strongest fluorescence intensity (36 a.u.), and a corresponding emission wavelength is 512 nm. This indicates that the PL spectrum of the CQDs displays excitation wavelength-dependent features. It means that the emission wavelength can be adjusted by changing the excitation wavelength. This property is useful for the future applications, such as an anti-fake packaging film, biological imaging and photocatalytic degradation [43]. This is similar to some of the other CQDs extracted from ascorbic acid [14] and soot [46]. The reasons why this phenomenon exists are still controversial. Lau et al. [47] and Xiao et al. [48] believed that the presence of different functional groups on the surface of carbon quantum dots can lead to multiple emission centers, with different ones dominating at different excitation wavelengths. Si et al. [49] further argued this point that if the functional groups on the surface of the carbon quantum dots are diverse, the emission centers will appear to be multiple, and the main emission center will change with the change of the excitation wavelength, which appears as excitation dependence. Zhang et al. [50] used (N-(2-aminoethyl)-3-aminopropyl) tris-(2-ethoxy) silane (KH791) as catalyzer, stabilizing and passivation agent, the prepared CQDs can be self-assembled in solution and exhibit excitation wavelength independent PL property. In addition, silane KH791 helps to enhance PL intensity of CQDs.
The PL quantum yields (QY) of CQDs was calculated by Equation (  and the reference. Here, quinine sulfate was used as the reference (QY = 54%) [52]. According to the PL spectra of the CQDs and the quinine sulfate, the QY of our CQDs is 5.30%. The UV-vis absorption spectrum of the CQDs is shown in Figure 1b. As shown, the CQDs have two obvious absorption peaks, located at 212 and 251 nm. The strong absorption peak at 212 nm is assigned to the presence of cysteine or the effect of the carbon skeleton compared to the UV-vis absorption of pure cysteine and carbon skeleton, respectively [9]. The absorption peak at 251 nm is caused by π-π* transitions of the conjugated system [9]. The PL quantum yields (QY) of CQDs was calculated by Equation (3) [51]: where, Qsam and Qref is the QY of the sample and the reference; Asam and Aref is the absorbance of the sample and the reference at an excitation wavelength; Nsam and Nref is the refractive indices of the sample and the reference medium; Isam and Iref is the integrated fluorescence intensities of the sample and the reference. Here, quinine sulfate was used as the reference (QY = 54%) [52]. According to the PL spectra of the CQDs and the quinine sulfate, the QY of our CQDs is 5.30%. The UV-vis absorption spectrum of the CQDs is shown in Figure 1b. As shown, the CQDs have two obvious absorption peaks, located at 212 and 251 nm. The strong absorption peak at 212 nm is assigned to the presence of cysteine or the effect of the carbon skeleton compared to the UV-vis absorption of pure cysteine and carbon skeleton, respectively [9]. The absorption peak at 251 nm is caused by π-π* transitions of the conjugated system [9].  [53], and 1661 cm −1 [54], respectively. Specifically, the absorption peak at 1566 cm −1 is associated with the C=C stretching vibration [55]. After the addition of CQDs, the intensity of the peak at 1566 cm -1 slightly increases, and then the intensity of the absorption peak gradually decreases with the increase of CQDs content. One reason may be related to the increasing amount of C=C, which exist in the skeleton of the CQDs [45]. The other reason for the result is possible that thermal treatment tends to facilitate the precursor to undergo dehydration, decomposition, polymerization and carbonization, and thus leads to the formation of carbon skeletons [45]. The absorption peak at 1446 cm −1 is ascribed to O-H and C-H bending vibrations [45], and the peak at 1332 cm −1 is attributed to O-H and C-H shaking vibrations. The absorption peaks at 1086 and 1042 cm −1 are attributed to the stretching vibrations of C-O-C and C-O, respectively. With the increase of CQDs content, the intensity of the absorption peak at 1042 cm −1 , which is the characteristic of cyanobacteria-derived CQDs, gradually increases [45,56]. The absorption peaks at 916 and 845 cm −1 correspond to -CH2 and C-C bending vibrations, respectively. Therefore, the FTIR spectrum of sample No.1 indicates that it mainly contains functional groups such as O-H, C-H and C=O.   [53], and 1661 cm −1 [54], respectively. Specifically, the absorption peak at 1566 cm −1 is associated with the C=C stretching vibration [55]. After the addition of CQDs, the intensity of the peak at 1566 cm −1 slightly increases, and then the intensity of the absorption peak gradually decreases with the increase of CQDs content. One reason may be related to the increasing amount of C=C, which exist in the skeleton of the CQDs [45]. The other reason for the result is possible that thermal treatment tends to facilitate the precursor to undergo dehydration, decomposition, polymerization and carbonization, and thus leads to the formation of carbon skeletons [45]. The absorption peak at 1446 cm −1 is ascribed to O-H and C-H bending vibrations [45], and the peak at 1332 cm −1 is attributed to O-H and C-H shaking vibrations. The absorption peaks at 1086 and 1042 cm −1 are attributed to the stretching vibrations of C-O-C and C-O, respectively. With the increase of CQDs content, the intensity of the absorption peak at 1042 cm −1 , which is the characteristic of cyanobacteria-derived CQDs, gradually increases [45,56]. The absorption peaks at 916 and 845 cm −1 correspond to -CH 2 and C-C bending vibrations, respectively. Therefore, the FTIR spectrum of sample No. 1 indicates that it mainly contains functional groups such as O-H, C-H and C=O.    Figure 3 shows the PL spectra of the composite films with different CQDs content. As shown in Figure 1a, when the excitation wavelength is 420 nm, the emission intensity of the prepared CQDs is the highest. Therefore, here we selected the light with a wavelength of 420 nm to excite the films to study their photoluminescent properties.   Figure 3 shows the PL spectra of the composite films with different CQDs content. As shown in Figure 1a, when the excitation wavelength is 420 nm, the emission intensity of the prepared CQDs is the highest. Therefore, here we selected the light with a wavelength of 420 nm to excite the films to study their photoluminescent properties.   Figure 3 shows the PL spectra of the composite films with different CQDs content. As shown in Figure 1a, when the excitation wavelength is 420 nm, the emission intensity of the prepared CQDs is the highest. Therefore, here we selected the light with a wavelength of 420 nm to excite the films to study their photoluminescent properties.  It is observed that the fluorescence spectra of all PVA/CNF/CQDs films present a similar changing trend. In general, the intensity of the strongest emission of film No. 2 is higher than that of a CQD solution. According to [57], the fluorescence of PVA at excitation wavelengths less than 420 nm is very weak. The excitation wavelength selected in this study is exactly 420 nm, and the amount of PVA is certain, so PVA has almost no effect on the fluorescence of the composite film. According to another paper [58], introducing CNF into the PVA/CQDs films can increase emission intensity, which explains why the intensity of the strongest emission of film No. 2 is higher than that of CQD solution.

PL Spectra of the PVA/CNF/CQDs Films
With the increase of CQDs content, the intensity of the strongest emission of the PVA/CNF/CQDs films gradually weakens. This shows that the CQD content has a significant effect on the attenuation of the fluorescence intensity of composites, consistent with the conclusions of Ling [59]. One possible reason may be due to the π-π * and n-π * electron transitions improve after adding CQDs in PVA/CNF films, thus weakening the fluorescence intensity of the films [60]. The other possibility is due to the increase of electron-withdrawing group (carbonyl group) in the films, which can weaken the fluorescence [61]. For all PVA/CNF/CQDs films, when the excitation wavelength is 420 nm, the wavelength corresponding to the strongest emission is less than 512 nm, which is the wavelength for the CQDs itself, as shown in Figure 1a. We think that PVA and CNF reduce the density of the CQDs' luminous centers which causes the observed blue shift in the spectrum.
Moreover, the fluorescence spectra are clearly visible with convex peaks in the emission wavelength of 475 to 500 nm, which is the lipid oxidation fluorescence peak. The reason is that 2p2 non-bonding electrons of the oxygen atom occurs n-π * electron transition in the free hydroxyl group of the molecular conformation of PVA [61].

Water Resistance Performance of the PVA/CNF/CQDs Films
The water absorption performance of the prepared PVA/CNF and PVA/CNF/CQDs composite films is shown in Figure 4. In the PVA/CNF matrix, although hydrogen bonds are easily formed between CNF and PVA, there are still many free hydroxyl groups, which is confirmed in Figure 2, resulting in a high water absorption rate (119.6%). With the increase of CQDs from 0.1 to 4 mL, the water absorption rate of the PVA-based film decreases significantly from 119.6% to 42.0%, indicating that introducing a certain amount of CQDs into PVA/CNF matrix can improve the water resistance performance of the PVA-based films. One reason may be due to the reduction of porosity [62]. The other reason is when CQDs with many carboxyl groups are introduced, the decrease of free hydroxyl radicals is due to the reaction between hydroxyl and carboxyl groups. This leads to the decrease of water absorption of the films [63].
nm is very weak. The excitation wavelength selected in this study is exactly 420 nm, and the amount of PVA is certain, so PVA has almost no effect on the fluorescence of the composite film. According to another paper [58], introducing CNF into the PVA/CQDs films can increase emission intensity, which explains why the intensity of the strongest emission of film No.2 is higher than that of CQD solution.
With the increase of CQDs content, the intensity of the strongest emission of the PVA/CNF/CQDs films gradually weakens. This shows that the CQD content has a significant effect on the attenuation of the fluorescence intensity of composites, consistent with the conclusions of Ling [59]. One possible reason may be due to the π-π * and n-π * electron transitions improve after adding CQDs in PVA/CNF films, thus weakening the fluorescence intensity of the films [60]. The other possibility is due to the increase of electron-withdrawing group (carbonyl group) in the films, which can weaken the fluorescence [61]. For all PVA/CNF/CQDs films, when the excitation wavelength is 420 nm, the wavelength corresponding to the strongest emission is less than 512 nm, which is the wavelength for the CQDs itself, as shown in Figure 1a. We think that PVA and CNF reduce the density of the CQDs' luminous centers which causes the observed blue shift in the spectrum.
Moreover, the fluorescence spectra are clearly visible with convex peaks in the emission wavelength of 475 to 500 nm, which is the lipid oxidation fluorescence peak. The reason is that 2p2 non-bonding electrons of the oxygen atom occurs n-π * electron transition in the free hydroxyl group of the molecular conformation of PVA [61].

Water Resistance Performance of the PVA/CNF/CQDs Films
The water absorption performance of the prepared PVA/CNF and PVA/CNF/CQDs composite films is shown in Figure 4. In the PVA/CNF matrix, although hydrogen bonds are easily formed between CNF and PVA, there are still many free hydroxyl groups, which is confirmed in Figure 2, resulting in a high water absorption rate (119.6%). With the increase of CQDs from 0.1 to 4 mL, the water absorption rate of the PVA-based film decreases significantly from 119.6% to 42.0%, indicating that introducing a certain amount of CQDs into PVA/CNF matrix can improve the water resistance performance of the PVA-based films. One reason may be due to the reduction of porosity [62]. The other reason is when CQDs with many carboxyl groups are introduced, the decrease of free hydroxyl radicals is due to the reaction between hydroxyl and carboxyl groups. This leads to the decrease of water absorption of the films [63].

Light Barrier Property of the PVA-Based Films
The light transmittance of the PVA-based composites to the light at wavelengths between 200 and 2500 nm is shown in Figure 5a. The transmittance of the samples with CQDs (No. 2-No. 7) is lower than that of the sample without CQDs (No. 1), suggesting that the light barrier properties of the PVA/CNF films can be improved by introducing CQDs into PVA/CNF matrix.

Light Barrier Property of the PVA-Based Films
The light transmittance of the PVA-based composites to the light at wavelengths between 200 and 2500 nm is shown in Figure 5a. The transmittance of the samples with CQDs (No.2-No.7) is lower than that of the sample without CQDs (No.1), suggesting that the light barrier properties of the PVA/CNF films can be improved by introducing CQDs into PVA/CNF matrix. Furthermore, in order to investigate the barrier performance of the composite to light with different wavelengths, we described Figure 5a in sections according to different wavelengths, as shown in Figures 5b-d. In the range of ultraviolet light (wavelength ≤380 nm) and infrared light (wavelength ≥780 nm), compared with sample No.1 without CQDs, the transmittance of composite films with CQDs (No.2-No.7) is significantly reduced; however, in the range of visible light, introducing CQDs into PVA/CNF does not significantly enhance the barrier performance of the composite. It indicates that in PVA/CNF/CDQs films, the improvement of light resistance caused by CQDs is mainly concentrated in the ultraviolet regions. As explained in Section 3.1, CQDs have two obvious absorption peaks in the ultraviolet region, which means CQDs can absorb ultraviolet light. Therefore, with the increase of CQDs content in matrix, the UV light barrier properties of the composite are getting better and better, indicating that the greater the amount of CQDs in the PVA/CNF matrix, the more obvious the improvement of the composites' UV light barrier. Furthermore, in order to investigate the barrier performance of the composite to light with different wavelengths, we described Figure 5a in sections according to different wavelengths, as shown in Figure 5b-d. In the range of ultraviolet light (wavelength ≤380 nm) and infrared light (wavelength ≥780 nm), compared with sample No. 1 without CQDs, the transmittance of composite films with CQDs (No. 2-No. 7) is significantly reduced; however, in the range of visible light, introducing CQDs into PVA/CNF does not significantly enhance the barrier performance of the composite. It indicates that in PVA/CNF/CDQs films, the improvement of light resistance caused by CQDs is mainly concentrated in the ultraviolet regions. As explained in Section 3.1, CQDs have two obvious absorption peaks in the ultraviolet region, which means CQDs can absorb ultraviolet light. Therefore, with the increase of CQDs content in matrix, the UV light barrier properties of the composite are getting better and better, indicating that the greater the amount of CQDs in the PVA/CNF matrix, the more obvious the improvement of the composites' UV light barrier.

Conclusions
Cyanobacterial blooms represent a serious threat to the health of humans and animals around the world. In this work blue luminescent carbon quantum dots were prepared from cyanobacteria by a hydrothermal method. The PL quantum yields of the obtained CQDs was 5.30%. Cyanobacteria-based carbon quantum dots/polyvinyl alcohol/nanocellulose composite films were prepared, which could emit bright blue under UV light. The introduction of CQDs into the PVA/CNF film is expected to improve the water resistance performance and achieve good UV-light-barrier, anti-fake and high trasparency film materials, which have promising applications in the flexible packaging field.
FTIR characterization showed that the composite films had many hydroxyl groups on the surface and the spectra of samples No. [2][3][4][5][6][7] with CQDs are similar to that of No. 1, indicating that the introduction of CQDs into the composite PVA/CNF does not add new functional groups, that is to say, there are no new chemical reactions between CQDs and PVA/CNF.
The PL spectra revealed that the emission of prepared CQDs was excitation dependent and with the increase of CQDs content, the intensity of the strongest emission of the PVA/CNF/CQDs films gradually weakens.
Studies on the water resistance performance showed that the composite films possessed higher water resistance properties. With the increase of CQDs from 0.1 to 4 mL, the water absorption rate of the PVA-based film decreases significantly from 119.6% to 42.0%, indicating that introducing a certain amount of CQDs into the PVA/CNF matrix can improve the water resistance performance of the PVA-based films.
In the study of the light barrier properties of the PVA-based films, we found that with the increase of CQDs content in the matrix, the light barrier effect of the composite is getting better and better, indicating that the greater the amount of CQDs in PVA/CNF matrix, the more obvious the improvement of the composites' light barrier properties.
Therefore, we report the cyanobacteria-based carbon quantum dots/polyvinyl alcohol/nano-cellulose composite films have the potential to be applied in flexible packaging materials, anti-fake materials, UV/infrared light barrier materials and so on.