Lanthanum Ferrite Ceramic Powders: Synthesis, Characterization and Electrochemical Detection Application

The perovskite-type lanthanum ferrite, LaFeO3, has been prepared by thermal decomposition of in situ obtained lanthanum ferrioxalate compound precursor, LaFe(C2O4)3·3H2O. The oxalate precursor was synthesized through the redox reaction between 1,2-ethanediol and nitrate ion and characterized by chemical analysis, infrared spectroscopy, and thermal analysis. LaFeO3 obtained after the calcination of the precursor for at least 550–800 °C/1 h have been investigated by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM). A boron-doped diamond electrode (BDD) modified with LaFeO3 ceramic powders at 550 °C (LaFeO3/BDD) by simple immersion was characterized by cyclic voltammetry and tested for the voltammetric and amperometric detection of capecitabine (CCB), which is a cytostatic drug considered as an emerging pollutant in water. The modified electrode exhibited a complex electrochemical behaviour by several redox systems in direct relation to the electrode potential range. The results obtained by cyclic voltammetry (CV), differential-pulsed voltammetry (DPV), and multiple-pulsed amperometry proved the electrocatalytic effect to capecitabine oxidation and reduction and allowed its electrochemical detection in alkaline aqueous solution.


Synthesis of LaFe(C 2 O 4 ) 3 ·3H 2 O Oxalate Precursor and LaFeO 3
An aqueous solution containing lanthanum nitrate, iron nitrate, 1,2-ethanediol, and 2 M nitric acid in a molar ratio of 1:1:3:2 that assured the solution pH of 3 was heated for 20 min at about 100 • C in a water bath. The synthesis conditions related to acidic pH of 3 were set-up based on the stoichiometry of the redox reaction related to the molar ratio. The temperature of about 100 • C is aqueous solution boiling temperature and the reaction time of 20 min was considered as the time for consuming reactants. The obtained precursor was purified by washing with acetone and dried in air. VARIAN SpectrAA 110 atomic absorption spectrophotometer (Varian, Palo Alto, CA, USA) was used to determine the metal content and a Carlo Erba 1108 elemental analyzer (Carlo Erba, Milan, Italy) was used for carbon and hydrogen analyzing. LaFeC 6 22. The precursor was calcinated in air under the temperature range from 550 to 800 • C with a heating rate of 10 • C min −1 for time duration of one hour to get the LaFeO 3 ceramic powders.

Characterization of LaFe(C 2 O 4 ) 3 ·3H 2 O Oxalate Precursor and LaFeO 3
The comparative Fourier transform infrared spectroscopy (FTIR) spectra of the LaFeO 3 and oxalate precursor were recorded based on KBr pellets using a Jasco FT-IR spectrophotometer (Jasco, Tokyo, Japan) under the range of 4000-400 cm −1 . Thermal measurements (TG, DTG, DSC) were carried out in artificial air flow of 20 mL min −1 and heating rate of 10 K min −1 using a NETZSCH-STA 449C instrument (Netzsch, Selb, Germany) under the temperature range of 25-1000 • C, using alumina crucibles that were performed on the precursor. X-ray diffraction (XRD) analyses performed at room temperature by a Rigaku Ultima IV diffractometer (Rigaku Co., Tokyo, Japan), using Ni-filtered CuKα radiation (λ = 1.5418Ǻ) to characterize the phase purity and crystal structure of calcined powders. To refine the lattice parameters, the Rietveld method using the HighScore Plus 3.0e software (Rigaku Co., Tokyo, Japan) was applied. Scanning electron microscopy (FE-SEM), using a high-resolution FEI QUANTA INSPECT F microscope (FEI Co., Eindhoven, The Netherlands) with a field emission gun, was used to assess the size and the agglomeration tendency of the LaFeO 3 particles. In addition, transmission electron microscopy (TEM/HR-TEM) and selected area electron diffraction (SAED) investigations were performed for a high-accuracy assessment of the morphology and crystallinity degree of the constitutive LaFeO 3 particles. Moreover, a TecnaiTM G 2 F30 S-TWIN transmission electron microscope (FEI Co., Eindhoven, The Netherlands) was used to collect the bright-field and high-resolution images.

Electrochemical Detection Application
In order to easily test the electrochemical behaviour of LaFeO 3 in the presence of capecitabine, the commercial BDD electrode produced by Windsor Scientific Ltd. (Slough, UK). For electroanalytic use, with a boron content of about 0.1, it was modified by simple immersion in 5 mg mL −1 LaFeO 3 suspension. Unmodified and LaFeO 3 -modified boron-doped diamond electrode (LaFeO 3 /BDD) were electrochemically characterized and tested for detection using Autolab Pontentiostat/Galvanostat PGStat 302 (EcoChemie, Utrecht, The Netherlands) controlled with GPES 4.9 software (EcoChemie, Utrecht, The Netherlands) and a classical three-electrode cell. The saturated calomel electrode as a reference (SCE), the platinum electrode as a counter-electrode and the LaFeO 3 modified/unmodified boron-doped diamond electrode modified (LaFeO 3 /BDD and BDD) as working electrodes were used for the electrochemical applications. The LaFeO 3 /BDD electrode was prepared by simple immersion prior to each electrochemical experiment running. The reproducibility of the modified surface was checked after stabilization by cyclic voltammetry and confirmed by a complete overlay of the cyclic voltammograms.
After electrode immersion, 10 continuous repetitive cyclic voltammograms within the various potential ranges related to each application conditions were applied for the electrochemical stabilization of the electrode. The cyclic voltammetry, differential-pulsed voltammetry, and multiple-pulsed amperometry were applied for the electrochemical characterization and the detection applications.
All measurements were carried out in 0.1 M sodium hydroxide supporting electrolyte at room temperature without a temperature control.

Results and Discussion
The method of the synthesis of the oxalate complex compound is based on the oxidation reaction of 1,2-ethanediol by the nitrate ion.
Materials 2020, 13, x FOR PEER REVIEW 4 of 18 checked after stabilization by cyclic voltammetry and confirmed by a complete overlay of the cyclic voltammograms. After electrode immersion, 10 continuous repetitive cyclic voltammograms within the various potential ranges related to each application conditions were applied for the electrochemical stabilization of the electrode. The cyclic voltammetry, differential-pulsed voltammetry, and multiplepulsed amperometry were applied for the electrochemical characterization and the detection applications.
All measurements were carried out in 0.1 M sodium hydroxide supporting electrolyte at room temperature without a temperature control.

Characterization of LaFe(C2O4)3·3H2O Oxalate Precursor
The method of the synthesis of the oxalate complex compound is based on the oxidation reaction of 1,2-ethanediol by the nitrate ion.
The IR spectrum of oxalate precursor ( Figure 1a [43,44]. No other bands characteristic to the presence of the water and the oxalate anion can be noticed due to thermal decomposition of the precursor, known as the LaFe(C2O4)3·3H2O oxalate compound, which are further detailed and presented.  No other bands characteristic to the presence of the water and the oxalate anion can be noticed due to thermal decomposition of the precursor, known as the LaFe(C 2 O 4 ) 3 ·3H 2 O oxalate compound, which are further detailed and presented.
La(III)-Fe(III) oxalate trihydrate decomposes ( Figure 2) via three steps with the formation of a carbonate intermediate.
The first step of thermal decomposition of LaFe(C 2 O 4 ) 3 ·3H 2 O (25-160 • C, mass loss: found 11.10%, calcd. 10.53%) is associated with an endothermic effect, and the mass loss is attributed to the evolving of the lattice water [43].
The next decomposition step (160-280 • C) characterized by an endothermic effect is due to the degradation of the terminal oxalate anions (mass loss, found 10.40%, calcd. 10  The first step of thermal decomposition of LaFe(C2O4)3·3H2O (25-160 C, mass loss: found 11.10%, calcd. 10.53%) is associated with an endothermic effect, and the mass loss is attributed to the evolving of the lattice water [43].
The next decomposition step (160-280 C) characterized by an endothermic effect is due to the degradation of the terminal oxalate anions (mass loss, found 10.40%, calcd. 10 [44,45]. The strong exothermic effect that characterizes the third step (280-550 C) is attributed to the oxidative degradation of CO 3 2− and the last C 2 O 4 2− with the formation of the lanthanum ferrite, which retains small amounts of carbon dioxide (mass loss: found 34.03%, calcd. 34.32%). In the temperature range of 550-700 C, the mass loss corresponds to the removal of carbon dioxide. Simultaneously, with this endothermicdecomposition step, an exothermic process of crystallization, involving the formation of the perovskite skeleton from an amorphous phase also takes place, so that, only a small and flattened endothermic peak, as a resultant of the two opposite processes, can be observed on the DSC curve [45,46]. The thermal analysis suggests the following sequence for decomposition of LaFe(C2O4)3·3H2O in static air atmosphere.

Characterization of LaFeO3 Powders
The room-temperature X-ray diffraction patterns presented in Figure 3a show that the asprepared precursor, as well as the powder that resulted after calcination at 500 C, are amorphous, while, in the powders obtained at higher temperatures (T  550 C), the main reflections specific to the LaFeO3 perovskite phase with orthorhombic Pbnm(62) structure were detected. For the powder calcined at 550 C, the broader profile and the lower intensity of the diffraction peaks as well as the higher background of the corresponding diffraction pattern suggested that a significant amount of an amorphous phase still persists in the sample. The increase of the annealing temperature from 550 The strong exothermic effect that characterizes the third step (280-550 • C) is attributed to the oxidative degradation of CO 2− 3 and the last C 2 O 2− 4 with the formation of the lanthanum ferrite, which retains small amounts of carbon dioxide (mass loss: found 34.03%, calcd. 34.32%). In the temperature range of 550-700 • C, the mass loss corresponds to the removal of carbon dioxide.
Simultaneously, with this endothermic decomposition step, an exothermic process of crystallization, involving the formation of the perovskite skeleton from an amorphous phase also takes place, so that, only a small and flattened endothermic peak, as a resultant of the two opposite processes, can be observed on the DSC curve [45,46].
The thermal analysis suggests the following sequence for decomposition of LaFe(C 2 O 4 ) 3 ·3H 2 O in static air atmosphere.

Characterization of LaFeO 3 Powders
The room-temperature X-ray diffraction patterns presented in Figure 3a show that the as-prepared precursor, as well as the powder that resulted after calcination at 500 • C, are amorphous, while, in the powders obtained at higher temperatures (T ≥ 550 • C), the main reflections specific to the LaFeO 3 perovskite phase with orthorhombic Pbnm(62) structure were detected. For the powder calcined at 550 • C, the broader profile and the lower intensity of the diffraction peaks as well as the higher background of the corresponding diffraction pattern suggested that a significant amount of an amorphous phase still persists in the sample. The increase of the annealing temperature from 550 to 800 • C induces the reduction of the amount of amorphous phase, concurrently with the gradual increase of the crystallintiy degree and purity of the perovskite phase reflected in the enhancement of intensity of the main diffraction lines of LaFeO 3 .    The results of the Rietveld analysis of the room temperature diffraction data of LaFeO 3 powders thermally treated at various temperatures in the temperature range of 550-800 • C are presented in Figure 3b-e. The quality of the samples is indicated by the parameters provided by the Rietveld refinement, R expected (R exp ), R profile (R p ), weighted R profile (R wp ), and goodness of fit (χ 2 ), which show values in good agreement with other literature data [56] ( Table 1).
The dependence of the lattice parameters, a, b, and c and, consequently, of the unit cell volume V, on the calcination temperature, exhibits a decreasing trend ( Table 1). The progress of the crystallization process involves a clear contraction of the unit cell, as shown in Figure 4a.
Even if the coarsening process evolves with the increase of annealing temperature, the values of the average crystallite size, also determined from the XRD data, are kept in the nanometric range, varying from 17.5 nm for the LaFeO 3 powder calcined at 550 • C to 36.7 nm in the case of the powder calcined at 800 • C. The significantly lower rate of increasing both the proportion of crystalline phase with respect to the amount of amorphous phase and the crystallite size with the temperature increase for LaFeO 3 particles investigated in this study, in comparison to the steeper increase of these characteristics in the case of BiFeO 3 powders calcined in the same temperature range reported earlier, which can be related to the higher refractoriness of lanthanum relative to that of Bi in the ferrite-type compounds [44]. As expected, the increase of the crystallite size determines a lattice relaxation proved by the clear decrease in the lattice micro-strains when increasing the calcination temperature ( Figure 4b). Therefore, the increase of the crystallite size involves the reduction in the inter-atomic spacing, which results in the contraction of the unit cell.     For all the powders under investigation, the FE-SEM analyses showed the clear tendency of the LaFeO 3 particles to form large (of few tens of microns), non-uniform (as shape and size) aggregates, with a spongeous aspect, as indicated by the FE-SEM overall images of Figure 5a,c,e,g.
The higher magnification FE-SEM images have taken in order to notice the structuring inside the aggregates showed that the powder calcined at 550 • C consists of very small-sized particles (most of them below 15 nm). The value of the average particle size is difficult to be estimated mainly because of the presence of a significant amount of amorphous phase (as XRD data indicated), which impeded the clear distinction of the particle's boundaries (Figure 5b). The structuring inside the aggregates becomes better highlighted in the case of the powders that resulted after annealing at 600 and especially at 700 • C (Figure 5d,f). The presence of the amorphous phase is still noticed along with the crystalline aggregates in the LaFeO 3 powder calcined at 600 • C (Figure 5d), while the aggregates of the powder calcined at 600 • C seems to consist of porous agglomerates of 300-500 nm, inside which nanometric particles (of 25-35 nm), linked together by necks and form 3D networks are observed (Figure 5f). Taking into account the values of the average crystallite size determined from the XRD data, one can assume that the nanoparticles of the LaFeO 3 powders resulted after annealing in the temperature range of 550-700 • C are single crystals. The FE-SEM detail image of Figure 5h indicates that the LaFeO 3 powder calcined at 800 • C consists of partially-sintered blocks, formed of nano-sized crystalline grains (with an average grain size <DG> = 69.4 nm) with well-defined boundaries and triple junctions, between which a small amount of intergranular porosity is detected. In some regions, the grain growth process, favored by the higher annealing temperature, induced a coalescence of some smaller grains, with the formation of the larger ones (of 200-300 nm) as well as the concurrent modification of some intergranular pores into intragranular pores (Figure 5h). Considering the value of the average crystallite size obtained from the XRD data, the values of the grain/particle size inside the agglomerates estimated from the FE-SEM observations suggest that the grains of the LaFeO 3 powder calcined at 800 • C exhibit a polycrystalline nature. Thus, we were able to estimate that the smaller grains consist of 2-3 crystallites, while the larger ones are formed from 6-10 crystallites. The HRTEM image of the LaFeO3 sample calcined at 550 °C indicate the presence of some small particles with sizes of 6.5-10 nm. Inside these particles, oriented fringes spaced at 1.60 Å corresponding to the crystalline plane (2 0 4) were noticed (Figure 6c). It is difficult to notice these small particles because they are usually embedded into an amorphous matrix. In the case of the powder calcined at 700 °C, the lower amount of amorphous phase allowed to better visualize the long-range ordered fringes, so that the HRTEM image clearly emphasizes long-range ordered fringes EDX (energy-dispersive X-ray analysis) analyses were also performed in order to determine the elemental composition of the LaFeO3 powders under investigation. The EDX spectra show only the presence of La, Fe, and O species, which indicates that no contamination took place during the powders processing (Figures 6e and 7e).   EDX (energy-dispersive X-ray analysis) analyses were also performed in order to determine the elemental composition of the LaFeO3 powders under investigation. The EDX spectra show only the presence of La, Fe, and O species, which indicates that no contamination took place during the powders processing (Figures 6e and 7e).   The HRTEM image of the LaFeO 3 sample calcined at 550 • C indicate the presence of some small particles with sizes of 6.5-10 nm. Inside these particles, oriented fringes spaced at 1.60 Å corresponding to the crystalline plane (2 0 4) were noticed (Figure 6c). It is difficult to notice these small particles because they are usually embedded into an amorphous matrix. In the case of the powder calcined at 700 • C, the lower amount of amorphous phase allowed to better visualize the long-range ordered fringes, so that the HRTEM image clearly emphasizes long-range ordered fringes spaced at 3.51 Å, corresponding to the crystalline plane (1 1 1) (Figure 7c).
For both powders, the high crystallinity degree of the randomly oriented particles is also pointed out by the bright spots, forming concentric diffraction rings, assigned to several crystalline planes of the perovskite LaFeO 3 phase in the specific SAED (selected area electron diffraction) patterns of Figures 6d and 7d. EDX (energy-dispersive X-ray analysis) analyses were also performed in order to determine the elemental composition of the LaFeO 3 powders under investigation. The EDX spectra show only the presence of La, Fe, and O species, which indicates that no contamination took place during the powders processing (Figures 6e and 7e).
The morphostructural properties of the LaFeO 3 are different functions of the calcination temperature, and the lowest particles were obatined at a relatively low temperature of 550 • C in comparison with other materials synthesized by the same method [43][44][45][46].

Electrochemical Characterization and Detection Application
Based on the morphostructural properties of LaFeO 3 ceramic powders, which were presented above and discussed in relation with the electroactivity capacity and electro-catalytical effect, for testing in electrochemical detection application LaFeO 3 synthesized at 550 • C. The comparative electrochemical behaviours of unmodified and LaFeO 3 -modified BDD electrodes in alkaline medium was studied by cyclic voltammetry (CV) and the results are presented in Figure 8a,b. It can be noticed that the oxidation and coupled reduction peak for LaFeO 3 /BDD, which can be attributed to Fe 2+/ Fe 3+ and Fe 3+ /Fe 4+ redox systems according to the literature [12]. In addition, capacitive component of the current is much larger in comparison with the unmodified BDD electrode, which is expected for the electrocatalyst electrode material. Thus, a depolarization effect toward the oxygen evolution reaction and a polarization effect on the hydrogen evolution reaction were manifested through LaFeO 3 on the BDD electrode surface. The electrocatalytic activity of the LaFeO 3 sample is relevant with the crystalline size and the rate of oxygen migration from bulk towards the surface [57,58], which relates to the applied potential range.
Both unmodified and LaFeO 3 /BDD electrodes were tested in the presence of 5 µM CCB and no signal was found at an unmodified BDD electrode (the results are not shown here). The behavior of the LaFeO 3 /BDD electrode in the presence of various CCB concentrations ranged from 2.5 to 22.5 µM is shown in Figure 9a and it can be noticed that the current grows with CCB concentration increasing for two potential values, which can be considered as detection potentials. The redox systems manifested to −0.4 V/SCE and +0.4 V/SCE showed a strong promoting effect and high stability towards the electrochemical oxidation of CCB. The linear dependence between the current and CCB concentration was found at the potential value of −0.4 V/SCE and 0.4 V/SCE (Figure 9b). Under this potential range, no increase of any cathodic reduction peak was noticed for the LaFeO 3 /BDD electrode, which informed that the CCB oxidation is not reversible.
Taking into account that differential-pulsed voltammetry technique (DPV) exhibit the advantages of the higher sensitivity in comparison with CV, this technique was tested in various working conditions related to modulation amplitude and the step potential. The detection results depended by the direction of the applied potential scanning. No reproducible results were achieved for anodic scanning, which suggest that this technique is not appropriate for the CCB detection based on its oxidation process. However, very good results were reached by potential scanning in a cathodic sense under a modulation amplitude of 0.2 V and step potential of 0.05 V (Figure 10). Cathodic peak characteristics to CCB reduction was found at the potential value of −1.02 V/SCE, which should be due to the oxidation-based activation of the electrode surface. The cathodic peak current increased linearly with CCB concentration for two concentration ranges below 2.5 µM CCB and ranged from 2.5 µM to 17 µM CCB (see inset of Figure 10). that the oxidation and coupled reduction peak for LaFeO3/BDD, which can be attributed to Fe 2+/ Fe 3+ and Fe 3+ /Fe 4+ redox systems according to the literature [12]. In addition, capacitive component of the current is much larger in comparison with the unmodified BDD electrode, which is expected for the electrocatalyst electrode material. Thus, a depolarization effect toward the oxygen evolution reaction and a polarization effect on the hydrogen evolution reaction were manifested through LaFeO3 on the BDD electrode surface. The electrocatalytic activity of the LaFeO3 sample is relevant with the crystalline size and the rate of oxygen migration from bulk towards the surface [57,58], which relates to the applied potential range. Both unmodified and LaFeO3/BDD electrodes were tested in the presence of 5 µM CCB and no signal was found at an unmodified BDD electrode (the results are not shown here). The behavior of the LaFeO3/BDD electrode in the presence of various CCB concentrations ranged from 2.5 to 22.5 µM is shown in Figure 9a and it can be noticed that the current grows with CCB concentration increasing for two potential values, which can be considered as detection potentials. The redox systems manifested to −0.4 V/SCE and +0.4 V/SCE showed a strong promoting effect and high stability towards the electrochemical oxidation of CCB. The linear dependence between the current and CCB concentration was found at the potential value of −0.4 V/SCE and 0.4 V/SCE (Figure 9b). Under this potential range, no increase of any cathodic reduction peak was noticed for the LaFeO3/BDD electrode, which informed that the CCB oxidation is not reversible. Taking into account that differential-pulsed voltammetry technique (DPV) exhibit the advantages of the higher sensitivity in comparison with CV, this technique was tested in various working conditions related to modulation amplitude and the step potential. The detection results depended by the direction of the applied potential scanning. No reproducible results were achieved for anodic scanning, which suggest that this technique is not appropriate for the CCB detection based on its oxidation process. However, very good results were reached by potential scanning in a cathodic sense under a modulation amplitude of 0.2 V and step potential of 0.05 V (Figure 10). Cathodic peak characteristics to CCB reduction was found at the potential value of −1.02 V/SCE, which should be due to the oxidation-based activation of the electrode surface. The cathodic peak current increased linearly with CCB concentration for two concentration ranges below 2.5 µM CCB and ranged from 2.5 µM to 17 µM CCB (see inset of Figure 10). One of the most desired technique for electro-detection is chronoamperometry (CA) due to its simplicity and easy application, which was tested for the LaFeO 3 /BDD electrode in CCB detection. A very low signal was achieved (the results are not shown here), which led to testing three-levels potential based multiple-pulsed amperometry (MPA) as a variant of CA. The potential levels were selected based on the results of voltammetry techniques of both CV and DPV, considering the oxidation and reduction processes related to CCB. According to the literature [59], the oxidation steps of the CCB to 5"-deoxy-5-fluorocytudine and further to five fluorouracil and its reduction to dihydrofluorouracil should be considered based on the previous results of CV and DPV related to the potential range and scanning sense. Amperograms recorded by MPA are presented in Figure 11. The pulses were applied continuously using the following scheme: (a) −1.1 V/SCE for a duration of 50 ms, where CCB reduction occurred, (b) −0.4 V/SCE for a duration of 50 ms, where CCB oxidation occurred involving Fe 2+ /Fe 3+ redox system, (c) 0.4 V/SCE for a duration of 50 ms, where further CCB oxidation occurred involving Fe 3+ /Fe 4+ redox system besides an oxygen evolution reaction starting.
advantages of the higher sensitivity in comparison with CV, this technique was tested in various working conditions related to modulation amplitude and the step potential. The detection results depended by the direction of the applied potential scanning. No reproducible results were achieved for anodic scanning, which suggest that this technique is not appropriate for the CCB detection based on its oxidation process. However, very good results were reached by potential scanning in a cathodic sense under a modulation amplitude of 0.2 V and step potential of 0.05 V (Figure 10). Cathodic peak characteristics to CCB reduction was found at the potential value of −1.02 V/SCE, which should be due to the oxidation-based activation of the electrode surface. The cathodic peak current increased linearly with CCB concentration for two concentration ranges below 2.5 µ M CCB and ranged from 2.5 µ M to 17 µ M CCB (see inset of Figure 10).  One of the most desired technique for electro-detection is chronoamperometry (CA) due to its simplicity and easy application, which was tested for the LaFeO3/BDD electrode in CCB detection. A very low signal was achieved (the results are not shown here), which led to testing three-levels potential based multiple-pulsed amperometry (MPA) as a variant of CA. The potential levels were selected based on the results of voltammetry techniques of both CV and DPV, considering the oxidation and reduction processes related to CCB. According to the literature [59], the oxidation steps of the CCB to 5"-deoxy-5-fluorocytudine and further to five fluorouracil and its reduction to dihydrofluorouracil should be considered based on the previous results of CV and DPV related to the potential range and scanning sense. Amperograms recorded by MPA are presented in Figure 11. The pulses were applied continuously using the following scheme: a) −1.  The electroanalytical parameters for CCB detection related to sensitivity, the lowest limit of detection, and the limit of quantification determined for each above-mentioned technique are gathered in Table 2.  The electroanalytical parameters for CCB detection related to sensitivity, the lowest limit of detection, and the limit of quantification determined for each above-mentioned technique are gathered in Table 2.
In comparison with reported results related to CCB electrochemical detection presented in Table 3, it can be noticed that the superiority of this electrode in relation with a very good limit of detection (LOD) and considering its availability for either CCB oxidation or CCB reduction with the mention that the literature reported only the detection procedure based on CCB reduction.

Conclusions
In the present work, LaFeO 3 powders were synthesized using a new method, based on the thermal decomposition of in situ obtained LaFe(C 2 O 4 ) 3 ·3H 2 O compound.
Single phase LaFeO 3 powders with orthorombic Pbnm perovskite structure were obtained after annealing at temperatures ranging between 550 and 800 • C. The crystallinity degree reflected in the values of the average crystallite size increases as the annealing temperature increased. Concurrently, a contraction of the unit cell volume is induced by the increase of the annealing temperature. Small particles, with sizes below 20 nm and with a high aggregation tendency, were obtained after annealing at 550 • C. Even if the increase of the annealing temperature at 800 • C induces a coarsening process, the size of the LaFeO 3 particles was kept in the nanometric range (~70 nm). However, a clear tendency to form partially-sintered blocks due to the coalescence of the small particles into larger, polyhedral grains with well-defined boundaries was noticed for the LaFeO 3 sample calcined at 800 • C.
The LaFeO 3 /BBD electrode exhibited the electrocatalytic activity toward the capecitabine (CCB) oxidation and reduction depending on the applied potential range and scanning direction that influenced the iron redox systems, considered as a basis for developing detection methods. Cyclic voltammetry (CV) and differential-pulsed voltammetry (DPV) techniques operated under specific working conditions allowed us to develop the CCB voltammetric detection method. The best analytical performance was reached using DPV based on the CCB reduction mechanism. Multiple-pulsed amperometry operated under three potential levels implied CCB oxidation and a reduction mechanism, which allows CCB detection in the same time at the two potential values of −1.1 V/SCE and −0.4 V/SCE corresponding to CCB reduction and respective oxidation. The results of electroanalytical performance for CCB detection and its flexibility for anodic and/or cathodic detection made the LaFeO 3 /BDD electrode have great potential for selective or simultaneous detection of CCB in aqueous matrix.