Pd Co Catalysts Research Articles

CsPbX3 Nanocrystal Incorporating Transition Metal Cocatalyst for Photocatalytic Organic Transformation by Single Electron Transfer

ABSTRACTThe construction of composite photocatalysts is a promising strategy for improving the overall catalytic efficiency in organic photochemical transformation. In this study, we synthesize a series of inorganic metal perovskite CsPbX3 (X = Cl, Br, I) nanocrystals (NCs) with excellent chemical stability and wide‐range visible‐light absorption. The Pd cocatalyst is then induced to the surfaces of CsPbX3 fabricating Pd/CsPbX3 composites via visible‐light reduction method. Photoelectrochemical measurements show the introduction of Pd cocatalyst promotes efficiently the charge separation and transfer of CsPbX3. The prepared Pd/CsPbX3 composites exhibit remarkable photocatalytic efficiency in visible‐light‐induced C–C cross‐coupling reaction. The reaction is characterized by mild reaction conditions, good recyclability, and high yield from a broad variety of substrates. Mechanism investigations show the reaction relies on the synergy of CsPbX3 photocatalysis and Pd catalysis. The valence band of CsPbX3 oxidizes the phenylboronic acid into active radical species via single electron transfer. On another hand, Pd(0) as active sites occurs oxidative addition with aryl halides for achieving the C–C cross‐coupling reaction. This study displays a feasible approach for the introduction of Pd catalyst in CsPbX3 to achieve the photocatalytic organic transformation via photoinduced electron transfer.

Optimizing H-adsorption affinity on electron-enriched Pdδ- active sites for efficient photocatalytic H2 evolution

Noble metal Pd is a promising H2-evolution cocatalyst and has attracted expansive attention in photocatalytic water splitting. However, the present H2-production rate of Pd cocatalysts is still limited due to its strong hydrogen adsorption on Pd active sites, resulting in poor hydrogen evolution kinetics. In this work, an electron-enriched Pdδ- modulation strategy is developed to weaken the hydrogen adsorption on Pd active sites by producing PdAu alloy, resulting in an increased H2-production rate. In this case, the PdAu homogeneous alloy with a particle size of 9–20 nm is uniformly deposited on the TiO2 surface to produce PdAu-modified TiO2 photocatalysts (TiO2/PdAu). It is found that the prepared TiO2/Pd79Au21 sample achieves the maximal photocatalytic H2-production performance of 31.98 mmol g-1 h−1, which is 1.53 times higher than that of TiO2/Pd photocatalyst. Experimental and theoretical studies show that in addition to the promoted transfer of photogenerated carriers, the PdAu alloy can spontaneously induce the electron transfer from Au to Pd to form electron-enriched Pdδ- sites, which prominently weakens the Pd-Hads bonds and thus improve the H2-production efficiency. This study provides further insight into the rational optimization of active sites to facilitate the design of efficient photocatalysts.

Synergistic engineering of palladium-cobalt nanoalloys on graphite sheet for efficient and sustainable hydrogen evolution reaction

The electrochemical hydrogen evolution reaction (HER)—a carbon-free route for hydrogen (H2) production—is of the utmost importance for H2-economy. Currently, HER performance is mainly restricted by the lack of promising alternatives to Pt-based electrocatalysts. In this study, we developed bimetallic PdCo alloy thin films with outstanding catalytic properties for the HER under acidic conditions. A simple aerosol-assisted chemical vapor deposition technique designed in-house was used to produce bimetallic alloy thin films on graphite sheets. The thin-film morphological patterns were significantly changed by varying the deposition time from 30 to 90 min. The optimized PdCo catalyst deposited for 30 min had a unique nanostructure with numerous active sites and exhibited faster HER kinetics than its analogs and pure Pd. As-prepared PdCo-30 electrode produced current densities of 10 and 1000 mA cm−2 at overpotentials of 41 and 161 mV, respectively, along with a Tafel slope of 42 mV/dec, high conductivity (0.28 Ω), and catalytic stability of ∼24 h in 0.5 M H2SO4. The excellent HER activity of the PdCo alloy was attributed to the synergy between the noble transition metal and the thin nanostructured layer of the bimetallic catalyst, which promoted formation of extensive electroactive sites on the conductive graphite surface. Density functional theory calculations confirmed the experimental findings. The Gibbs free energy (ΔGH*) of the PdCo alloy (−0.43 eV) was significantly lower than that of pure Pd (−0.57 eV), confirming the enhancement in HER activity due to the introduction of Co into the Pd lattice.

Accelerating photoelectrochemical CO2RR selectively of C2+ products by integrating Ag/Pd cocatalysts on Cu/Cu2O/CuO heterojunction nanorods

The Cu-based photoelectrochemical CO2 reduction reaction (PEC–CO2RR) represents a convenient approach for producing value-added C2+ products, aiming to achieve carbon neutrality by reducing greenhouse gas emissions. However, these reactions typically suffer from limited selectivity. In this work, we fabricate Cu/Cu2O/CuO nanorod (CuR)-based heterojunction architectures integrated with Ag and Pd cocatalysts to boost the selectivity of C2+ products. The proposed Cu/Cu2O/CuO/Ag-Pd (CuR/Ag-Pd) photoelectrodes are used as photocathodes to generate a maximum Faradaic efficiency (FE) of C2+ products exceeding 53% by suppressing the hydrogen evolution reaction (HER). The FE improvement is approximately 22-fold (n-propanol), 12-fold (ethanol), 13-fold (acetaldehyde), and 6-fold (acetate) compared with CuR photoelectrodes operating at a negative applied potential of −1.8 V (vs. reversible hydrogen electrode, RHE). Conversely, the CuR photoelectrodes exhibit a maximum HER rate of ∼86% at −1.8 V (vs. RHE), higher than those of the CuR/Ag (54%) and CuR/Ag-Pd (35%) photoelectrodes. The superior PEC–CO2RR performance of CuR/Ag-Pd photoelectrodes is attributable to the higher electrochemical active surface area (6.7 mF/cm2) and faster charge transfer rate at the electrode/electrolyte interface owing to the presence of cocatalysts. In addition, the CuR/Ag-Pd photoelectrodes exhibit remarkable long-term stability retaining 70% of the initial performance even after a relatively more negative applied potential at −1.2 V. A comprehensive investigation into the changes in surface morphology, crystal structure, and elemental composition after PEC–CO2RR confirms the higher stability of CuR/Ag-Pd photoelectrodes. Thus, this work provides novel perceptions into the development of Cu-based heterojunction photoelectrodes integrated with Ag/Pd cocatalysts for improving the selectivity of C2+ products.

Design of efficient supported Pd-Co catalysts for selective hydrogenation of acetylene

The research is devoted to the study of active component formation in the novel Pd-Co catalysts supported on carbon material Sibunit. It was shown that 0.5 %Pd–0.5 %Co/C samples exhibit high ethylene yield in the acetylene hydrogenation process due to the presence of fcc PdxCo(1-x) particles. According to in situ XRD-TPR analysis, solid solution formation begins during the reduction of samples in H2 at T ≥ 500 °C. Using the EXAFS, XRD and EDX it was established that H2-treatment at 500 °C leads to the formation of ∼Pd0.6Co0.4 particles and an increase in the reduction temperature to 600 and 700 °C is accompanied by the enrichment of the Pd-Co-phase with cobalt to ∼Pd0.5Co0.5 and ∼Pd0.45Co0.55 compositions, respectively. The ethylene yield on Pd-Co/C catalysts reduced at 500, 600 and 700 °C is 56, 66 and 68 %, respectively, which significantly exceeds the ethylene quantity obtained on monometallic Pd/C samples (∼52 %). It is assumed that the excellent selectivity of Pd-Co/C samples treated in H2 at 600 and 700 °C is due to an increase in the amount of palladium atoms surrounded by cobalt and a change in the palladium electronic state (XPS).

Selective photocatalytic semihydrogenation of alkynols to alkenols on Pd–C3N4 nanosheets under ambient conditions

Selective hydrogenation of alkynols to alkenols is an essential process for producing fine and intermediate chemicals. Currently, thermocatalytic alkynol hydrogenation faces several challenges, e.g., the safety of high-pressure hydrogen (H2) gas and the need for elevated temperature, and unavoidable side reactions, e.g., overhydrogenation. Here, a novel photocatalytic strategy is proposed for selectively reducing alkynols to alkenols with water as a hydrogen source under ambient temperature and pressure. Under the irradiation of simulated solar light, carbon nitride (C3N4) nanosheets with palladium (Pd) nanoparticles as cocatalysts (Pd–C3N4 NSs) exhibit a 2-methyl-3-butyn-2-ol (MBY) conversion of 98% and 2-methyl-3-buten-2-ol (MBE) selectivity of 95%, outperforming state-of-the-art thermocatalysts and electrocatalysts. After natural-sunlight irradiation (average light intensity of 25.13 mW cm−2) for 36 h, a MBY conversion of 98% and MBE selectivity of 92% was achieved in a large-scale photocatalytic system (2500 cm2). Experimental and theoretical investigations reveal that Pd cocatalysts on C3N4 facilitate the adsorption and hydrogenation of MBY as well as the formation of active hydrogen species, which promote the selective semihydrogenation of alkynols. Moreover, the proposed strategy is applicable to various water-soluble alkynols. This work paves the way for photocatalytic strategies to replace thermocatalytic hydrogenation processes using pressurized hydrogen.

Sun-light driven hydrogen generation by Pd/Rb2O cocatalysts: Escalate the utility of rutile TiO2 for photocatalytic water splitting

Rising consumption and cost of fossil fuels invite the researchers to discover the renewable energy sources. Herein, a novel approach to enhance the photocatalytic performances of rutile-TiO2 has been revealed. To boost the hydrogen generation reactions, Pd/Rb2O cocatalysts have been deposited over TiO2 via chemical reduction. The morphology and optical characteristics of catalysts were demonstrated by XRD, Raman, UV-Vis/DRS, SEM and TEM analysis. Surface properties, particle sizes, and chemical composition were examined via AFM and XPS techniques. The H2 production activities were monitored by GC-TCD (Shimadzu-2010/Japan). Comparatively, Pd1.8/RbO0.2@TiO2 was found most active catalysts that can deliver hydrogen 22.74 mmolg−1h−1. Higher H2 generation activities were attributed to the presence of Pd and Rb2O cocatalysts. Rb2O promoted electrons from TiO2 to Pd active sites by elevation in fermi energy levels to attain the equilibrium during photoreactions. The mechanistic approach for higher electron transportation and better charge separation has been demonstrated and discussed over here. On the basis of results, it can be concluded that the work reported here in is reliable for sustainable energy applications.

Role of Ag, Pd cocatalysts on layered SrBi2Ta2O9 in enhancing the activity and selectivity of photocatalytic CO2 reaction

Photocatalytic CO2 reduction in presence of H2O provides an ideal way to alleviate the greenhouse effect and obtain valuable chemicals. Constructing active sites on the surface of photocatalysts significantly affects the activity and selectivity of photocatalytic CO2 reduction, which involves a multi-electron reduction process. Herein, we anchor Ag and Pd particles on the surface of layered perovskite SrBi2Ta2O9 to build CO and CH4 evolution sites, respectively, via a photodeposition method. Ag and Pd not only attract and accumulate the photoinduced electrons originating from SrBi2Ta2O9 due to the formed Schottky junction between them, but also activate CO2 molecules, thereby resulting in higher CO2 reduction activity. On the surface of Ag, intermediate species CO* desorb and form CO directly, whereas, on the surface of Pd, intermediate species CO* is further hydrogenated to form CH4, thus resulting in different selectivity. This work offers a new avenue for developing photocatalysts with high activity and selectivity for CO2 reduction.

Selective Hydrogenation of Acetylene over Pd-Co/C Catalysts: The Modifying Effect of Cobalt

Novel bimetallic Pd-Co catalysts supported on the carbon material Sibunit were synthesized by an incipient wetness impregnation method and used for ethylene production by selective acetylene hydrogenation. It has been established that an increase in the Pd:Co molar ratio from 1:0 to 1:2 in 0.5%Pd-Co/C catalysts, treated in hydrogen at 500 °C, leads to an increase in the ethylene selectivity from 60 to 67% (T = 45 °C). The selectivity does not change with a further increase in the modifier concentration. The catalysts were investigated by TPR-H2, XRD, TEM HR, EDS, and XPS methods. It was shown that palladium and cobalt in the 0.5%Pd-Co/C samples form Pd(1−x)Cox phases of solid solutions with different compositions depending on the Pd:Co ratio. The cobalt concentration in the Pd-Co particles increases with an increase in the Pd:Co ratio up to 1:2 and then remains at a constant level. In addition, monometallic Co particles were present in the samples with the Pd:Co ratio higher then 1:2. The optimal combination of catalytic properties (the ethylene yield is 62–63%) is typical for catalysts with a Pd:Co molar ratio of 1:2–1:4. which is mainly due to the presence of bimetallic particles containing ~41–43% by at. of cobalt.

Synergistic Effect of Pd Co-Catalyst and rGO–TiO2 Hybrid Support for Enhanced Photoreforming of Oxygenates

Photoreforming biomass-derived waste such as glycerol into hydrogen fuel is a renewable hydrogen generation technology that has the potential to become important due to unavoidable CO2 production during methane steam reforming. Despite tremendous efforts, the challenge of developing highly active photocatalysts at a low cost still remains elusive. Here, we developed a novel photocatalyst with a hybrid support comprising reduced graphene oxide (rGO) and TiO2 nanorods (TNR). rGO in the hybrid support not only performed as an excellent scavenger of electrons from the semiconductor conduction band due to its suitable electrochemical potential, but also acted as an electron transport highway to the metal co-catalyst, which otherwise is not possible by simply increasing metal loading due to the shadowing effect. A series of hybrid supports with different TNR and rGO ratios were prepared by the deposition method. Pd nanoparticles were deposited over hybrid support through the chemical reduction method. Pd/rGO-TNRs photocatalyst containing 4 wt.% rGO contents in the support and 1 wt.% nominal Pd loading demonstrated hydrogen production activity ~41 mmols h−1g−1, which is 4 and 40 times greater than benchmark Au/TiO2 and pristine P25. The findings of this works provide a new strategy in optimizing charge extraction from TiO2, which otherwise has remained impossible due to a fixed tradeoff between metal loading and the detrimental shadowing effect.

Creating and Stabilizing an Oxidized Pd Surface under Reductive Conditions for Photocatalytic Hydrogenation of Aromatic Carbonyls.

Photocatalysis provides an eco-friendly route for the hydrogenation of aromatic carbonyls to O-free aromatics, which is an important refining process in the chemical industry that is generally carried out under high pressure of hydrogen at elevated temperatures. However, aromatic carbonyls are often only partially hydrogenated to alcohols, which readily desorbs and are hardly further deoxygenated under ambient conditions. Here, we show that by constructing an oxide surface over the Pd cocatalyst supported on graphitic carbon nitride, an alternative hydrogenation path of aromatic carbonyls becomes available via a step-wise acetalization and hydrogenation, thus allowing efficient and selective production of O-free aromatics. The PdO surface allows for optimum adsorption of reactants and intermediates and rapid abstraction of hydrogen from the alcohol donor, favoring fast acetalization of the carbonyls and their consecutive hydrogenation to O-free hydrocarbons. The photocatalytic hydrogenation of benzaldehyde into toluene shows a high selectivity of >90% and a quantum efficiency of ∼10.2% under 410 nm irradiation. By adding trace amounts of HCl to the reaction solution, the PdO surface remains stable and active for long-term operation at high concentrations, offering perspective for practical applications.

2D photosensitive porphyrin-based MOFs integrated with a Pd cocatalyst with fast charge transfer for efficient photocatalytic hydrogen evolution

A series of 2D MOF nanosheets are prepared by a simple hydrothermal method for photocatalytic hydrogen production, in which PdTCPP integrates a photosensitive porphyrin with cocatalysts so as to realize fast charge carrier transport.

Construction of PdCo catalysts on Ni bowl-like micro/nano array films for efficient methanol and ethanol electrooxidation

Direct alcohol fuel cells (DAFCs) are renewable energy sources with the potential to replace fossil fuels. Investigating high-performance electrocatalysts that promote alcohol oxidation is critical. In this study, we demonstrate simple electrodeposition for the controlled synthesis of PdCo catalysts on Ni bowl-like micro/nano array films with the assistance of the monodisperse colloidal sphere template. The PdCo catalysts with the optimal properties was synthesized by optimizing the stirring rate of the electrolyte and the solution concentration. The Pd8Co1/Ni array film catalyst synthesized at a stirring speed of 200 Revolutions Per Minute (RPM) exhibited the highest electrochemical active surface area (ECSA, 95.65 cm2/mg) and specific and mass activities in methanol (173.2 mA/cm2 and 2032.9 mA/mgPd, respectively) and ethanol (240.1 mA/cm2 and 2846.1 mA/mgPd, respectively) oxidation in alkaline media. This was a considerable improvement compared to the electrocatalytic activities of single-phase Pd and a commercial Pd/C catalyst, and the superior performance of the Pd8Co1 micro/nano array film could be attributed to the bowl-like structure with a high ECSA and the synergistic effect of Pd and Co. Therefore, this study yields necessary insights into the development of high-performance electrocatalysts with potential applications in DAFCs.

Improvement of Visible-Light H2 Evolution Activity of Pb2 Ti2 O5.4 F1.2 Photocatalyst by Coloading of Rh and Pd Cocatalysts.

Pb2Ti2O5.4F1.2 modified with various metal cocatalysts was studied as a photocatalyst for visible‐light H2 evolution. Although unmodified Pb2Ti2O5.4F1.2 showed negligible activity, modification of its surface with Rh led to the best observed promotional effect among the Pb2Ti2O5.4F1.2 samples modified with a single metal cocatalyst. The H2 evolution activity was further enhanced by coloading with Pd; the Rh−Pd/Pb2Ti2O5.4F1.2 photocatalyst showed 3.2 times greater activity than the previously reported Pt/Pb2Ti2O5.4F1.2. X‐ray absorption fine‐structure spectroscopy, photoelectrochemical, and transient absorption spectroscopy measurements indicated that the coloaded Rh and Pd species, which were partially alloyed on the Pb2Ti2O5.4F1.2 surface, improved the electron‐capturing ability, thereby explaining the high activity of the coloaded Rh−Pd/Pb2Ti2O5.4F1.2 catalyst toward H2 evolution.

Optimizing Oxygen and Intermediate HOO* Adsorption of Cu–Pd Alloy Cocatalyst for Boosting Photocatalytic H2O2 Production of BiVO4

AbstractThe modification of Pd cocatalysts is considered to be an effective strategy to improve H2O2 production of photocatalysts because it can accelerate the reaction rate of O2 reduction. However, the strong adsorption between O2 molecules and Pd atoms is not conducive to the formation of intermediate HOO* and leads to the further reduction of H2O2 to H2O, thus limiting the improvement of H2O2 production. To solve the issue, in this work, Cu–Pd alloy cocatalysts are selectively modified on the electron‐rich facets of BiVO4 via facile photoinduced deposition and subsequent galvanic displacement. DFT calculations indicate that the incorporation of Cu atoms to Pd atoms weakens the oxygen adsorption energy and HOO* binding energy on Pd atom surfaces, thus increasing the activity and selectivity of O2 reduction to H2O2. Further experimental results show that the optimized Cu‐Pd/BiVO4(5:1) photocatalyst exhibits markedly boosted activity for H2O2 production (2189 µmol L‐1), which is 3.2‐fold higher than that of BiVO4 with modification of 0.3 wt% Pd cocatalyst (675 µmol L‐1). Additionally, the incorporation of metal Cu enables the economic utilization of Pd atoms and reduces the expense of the Pd cocatalyst.

Photocatalytic performance of alkali metal doped graphitic carbon nitrides and Pd-alkali metal doped graphitic carbon nitride composites

Although there are several reports about the beneficial performance of metal doped graphitic carbon nitrides (g-C3N4) in various photocatalytic reactions, the effect of different alkali metal dopants has not been studied systematically. Series of undoped, Li-, Na- and K-doped samples was synthetized and used for the preparation of novel type of photocatalysts, composed of palladium nanoparticles supported on alkali metals-doped graphitic carbon nitride. Palladium loading was achieved via citrate reduction of palladium precursor in the presence of the carbon nitride material. Several physicochemical characterization methods such as attenuated total reflection infrared-(ATR-IR), diffuse reflectance UV–visible spectroscopy, high-resolution transmission microscopy (HRTEM), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD), and thermogravimetric analysis (TGA) were used to get information about the morphology and composition of the novel composites. According to the optical characterization results, the band gap of g-C3N4 decreased upon Na- and K doping but increased after Li-doping. The palladium nanoparticles were distributed over the support and appeared in dispersed (undoped g-C3N4, Li-g-C3N4) or agglomerated (Na-g-C3N4, K-g-C3N4) form with individual particle size below 5 nm. The catalytic performance of these composite materials was tested in two processes: (i) photodegradation of methyl orange and (ii) hydrogen production from methanol. The Na- doping of graphitic carbon nitride was found to be a key issue to enhance hydrogen production. The carbon nitride matrix was found to be stable during the photocatalytic experiments, while the Pd component underwent certain changes during the photocatalytic reforming reaction of methanol. Our results indicated that the really acting metallic Pd cocatalyst was formed mainly in situ.

The Fabrication of Pd Single Atoms/Clusters on COF Layers as Co-catalysts for Photocatalytic H2 Evolution.

The particle size of co-catalysts significantly affects the activity of semiconductors in photocatalysis. Herein, we report that the photocatalytic H2 evolution (PHE) activity of a visible light responsive covalent organic framework (COF) layer supported on SiO2 nanoparticles was greatly promoted from 47.7 to 85.5 μmol/h by decreasing the particle size of the Pd co-catalyst from 3.3 nm to single atoms/clusters. A PHE rate of 156 mmol gCOF-1 h-1 and apparent quantum efficiency up to 7.3% were achieved with the Pd SAs/Cs co-catalyst. The relationship between the activity of Pd in H2 dissociation, proton reduction, and PHE rate suggests that the promotion effect of Pd SAs/Cs is mainly attributed to their enhancement in charge separation of COF layers rather than proton reduction. Furthermore, a photoactive film was fabricated and steady production of H2 was achieved under visible light irradiation and static conditions. The optimization of the particle size of co-catalysts provides an efficient method for enhancing the photocatalytic activity of semiconductors.

Modulating the oxidative active species by regulating the valence of palladium cocatalyst in photocatalytic degradation of ciprofloxacin

Nano-structured metal cocatalysts are easy to be oxidized and form mixed valences and interfaces which would facilitate the catalytic performance in previous studies. Herein, as an example in photocatalysis, three kinds of Pd cocatalysts with various valence distributions (PdO70-Pd30/CN, PdO50-Pd50/CN and PdO30-Pd70/CN) were loaded on g-C3N4 nanosheets with the close loading amounts (~1 wt%) and uniform sizes (2–3 nm). Then, the results of the photocatalytic degradation of ciprofloxacin showed that the generated oxidative active species are highly related to the distribution of palladium valence. Pd2+ (PdO) benefits the production of·O2-, while Pd0 benefits the production of h+. The theoretical simulations revealed that surface states e.g., electron distribution and the adsorption ability of O2 on different Pd species determined the production of·O2- and h+. Besides, PdO50-Pd50/CN showed the best performance for degrading ciprofloxacin, due to the joint action of·O2- and h+ in the CIP degradation.

S-Scheme α-Fe2O3/TiO2 Photocatalyst with Pd Cocatalyst for Enhanced Photocatalytic H2 Production Activity and Stability

S-Scheme α-Fe2O3/TiO2 Photocatalyst with Pd Cocatalyst for Enhanced Photocatalytic H2 Production Activity and Stability

Effects of Reaction Temperature on the Photocatalytic Activity of TiO2 with Pd and Cu Cocatalysts

The aim of this study was to investigate the effects of reaction temperature on the photocatalytic activity of TiO2 with Pd and Cu cocatalysts. N2 sorption, transmission electron microscopy and high-resolution transmission electron microscopy were used to characterize the specific surface area, pore volume, pore size, morphology and metal distribution of the catalysts. The photocatalytic destruction of methylene blue under UV light irradiation was used to test its activity. The concentration of methylene blue in water was determined by UV-vis spectrophotometer. Pd/TiO2 catalyst was more active than Cu/TiO2 and TiO2. At 0–50 °C reaction temperature, the activity of TiO2 and Pd/TiO2 increased with an increase of reaction temperature. When the temperature was as high as 70 °C, the reaction rate of TiO2 drop slightly and Pd/TiO2 became less effective. In contrast, Cu/TiO2 was more active at room temperature than the other temperatures. The results indicate that the photocatalytic activity of the catalyst is influenced by the reaction temperature and the type of cocatalyst. When the reaction temperature is higher than 70 °C, the recombination of charge carriers will increase. The temperature range of 50–80 °C is regarded as the ideal temperature for effective photolysis of organic matter. The effects of reaction temperature mainly influence quantum effect, i.e., electron-hole separation and recombination.