Photocatalysis: Research and Potential Open Access

ISSN: 2958-8782 (Online)

2958-8774 (Print)

Photocatalysis: Research and Potential is an open access and international journal covering both fundamental and application-oriented aspects of photocatalysis. The journal establishes a platform for multidisciplinary discussions to promote the understanding of materials science, chemical engineering and physical chemistry of photocatalysis, as well as the potential across the field of environment and energy.

Editor-in-Chief

Articles (29) All articles

Article

01 April 2025

B, Gd Co-Doped TiO2 Nanotube Arrays for Efficient Degradation of Gaseous Toluene under Visible Light Irradiation

Although photocatalytic degradation of VOCs has attracted widespread attention, the efficient visible-light-driven photocatalytic degradation performance remains a challenge. This work presents the visible-light-driven photocatalytic degradation of gaseous toluene over B, Gd co-doped TiO2 nanotube arrays prepared via a controllable electrochemistry method. It was found that B and Gd co-doping strategy not only enhances the visible light responsiveness of TiO2 nanotube arrays but also introduces moderate oxygen vacancies on the surface of TiO2, which is beneficial to the formation of free hydroxyl radicals and their attack on toluene molecules. The doping order also affects the photocatalytic performance. The optimized sample achieves an enhanced degradation efficiency for toluene under visible light irradiation and exhibits considerable stability. This work may provide an efficient TiO2-based photocatalyst for the removal of volatile organic compounds for air purification and give an understanding of the mechanism of photocatalytic degradation of toluene over co-doping TiO2.

Perspective

01 April 2025

Perspectives on the Development in the Selective Oxidation of Glycerol to Value-Added Chemicals via Photoelectrocatalysis Coupled with Hydrogen Evolution

Harvesting sunlight to produce clean hydrogen fuel remains one of the main challenges for solving the energy crisis and ameliorating global warming. Photoelectrochemical (PEC) water splitting is considered to be a promising method for H2 production in the future. However, the efficiency still remains challenging due to the sluggish reaction dynamics for water oxidation. Recently, the thermodynamically favorable oxidation of glycerol in PEC systems has gained significant attention for its ability to produce value-added chemicals while simultaneously generating hydrogen. This process not only enhances the yield of high-value products but also minimizes energy consumption and reduces CO2 emissions. Valuable products from glycerol oxidation include 1,3-dihydroxyacetone (DHA), glyceraldehyde (GLD), tartronic acid (TA), formic acid (FA), and glyceric acid (GA). Thus, it is important to improve selectivity and productivity. In this work, we mainly summarize the recent research progress in improving the selectivity and productivity of glycerol upgrading products on the different photoanodes.

Research Highlight

31 March 2025

Linear Semiconducting Polymers as Photoanodes for Oxidation Reactions

Photoelectrochemical (PEC) water splitting has attracted significant attention in the general field of photocatalysis. However, the high cost of constructing PEC systems limits their practical application. Recently, an innovative approach was proposed to synthesize linear semiconducting polymer-based films. The polymer structure was optimized for oxidation reactions. Furthermore, the active site of the optimal linear polymer was investigated through in-situ characterizations. This work has the potential to address the challenges of high material costs and polymer film development in PEC technology.

Review

14 March 2025

Mechanistic Insights into Photocatalytic WO3 for Hydrogen Generation

Growing environmental concerns and the limitations of fossil fuel resources have recently led to increased focus on clean and renewable energy sources. Hydrogen (H2) has gained importance as an alternative clean fuel with its potential to become the primary chemical energy carrier. Photocatalytic hydrogen generation offers a capable solution to the energy crisis and has gained significant attention as a renewable energy solution, offering independence from fossil fuels and zero carbon dioxide emissions. Tungsten oxide (WO3) offers to be a promising photocatalyst for Hydrogen Evolution Reaction (HER) with its ability to tune the band gap, robust absorption in the visible spectrum range, steadiness in harsh reaction conditions, low cost, and reduced toxicity. Various synthetic methods can be employed to fabricate photocatalysts with diverse morphologies, sizes, and structures, all of which significantly influence their catalytic performance to varying extents. This review goals to explicitly highlight and discourse the main properties of WO3 and its modifications for photocatalytic HER via different synthesis methods. Modification in WO3 to its corresponding composites, heterojunctions are explicitly explained in this review.

Article

07 March 2025

WO3 Photoanodes for Photoelectrochemical Applications

WO3 layers were prepared by spray pyrolysis of a peroxotungstic acid solution on FTO/glass substrates. Investigated parameters were layer thickness and influence of post-annealing in air. Films deposited at 250 °C were amorphous. Post-annealing at 550 °C for 2 h resulted in the formation of monoclinic crystalline structure. A comprehensive account of electrochemical efficiency in terms of IPCE for WO3 films as a function of the three parameters (wavelength, thickness and direction of light incidence) fully characterizing the photoelectrodes is presented here for the first time. The highest improvement in crystallinity and also the highest photocurrent response was found for WO3 layers deposited at 250 °C and post-annealed at 550 °C, namely 1.9 mA/cm2 (in 0.1 M HClO4 at 1.6 V vs. Ag/AgCl) under irradiation with a solar simulator (AM 1.5, 100 mW/cm2) and IPCE = 0.5 at 369 nm (front side irradiation), which is comparable with values obtained by other deposition techniques (e.g., hydrothermal or sol gel). Spray pyrolysis as a method of fabricating WO3 electrodes has the advantage of being able to produce large electrodes for use in practical applications.

Review

07 March 2025

Unravelling the Role of Hydrogen Evolution Reaction Co-Catalysts in Photocatalytic Water Splitting: Mechanistic Insights and Material Strategies

The reliance on fossil fuels has led to a substantial increase in greenhouse gas emissions, presenting a critical environmental challenge. Addressing this issue necessitates the adoption of alternative renewable energy sources, with green hydrogen emerging as a promising candidate due to its high gravimetric energy density and absence of harmful emissions. Among the various hydrogen production techniques, photocatalytic technology has garnered significant attention for its dual potential to produce green hydrogen and degrade pollutants, thereby addressing both energy and climate crises. Efforts to scale photocatalytic technology for industrial applications have identified cocatalyst integration as a pivotal strategy, as it enhances reaction kinetics by lowering the activation energy and mitigating charge carrier recombination. This review comprehensively examines the hydrogen economy, the underlying principles of photocatalysis, recent technological advancements, key factors influencing photocatalytic reactions, the role of catalysts in hydrogen evolution reaction (HER) surface mechanisms, strategies for cocatalyst optimization, and future directions for the field.

Review

26 February 2025

Recent Progress on Utilising Visible Light to Better Catalyst Stability for the Dry Reforming of Methane

Dry reforming of methane (DRM) is a promising strategy to closing the carbon loop. DRM valorises CO2 and CH4 by producing synthesis gas (H2 and CO), the precursor to various synthetic fuels. Key limitations of the DRM are the high-temperature requirements (600–1000 °C) and competing side reactions, many of which produce carbon that can deactivate the catalyst. Designing a stable, low-cost and active catalyst remains one of the greatest DRM challenges. One potential strategy to curtail the limitations that hinder DRM is to utilise visible light to access the localised surface plasmon resonance (LSPR) of metal catalysts. The current review discusses the recent developments in designing catalysts for LSPR-assisted thermocatalytic DRM. The thermodynamic and kinetic principles that underpin DRM are first introduced, followed by an overview of thermocatalyst design strategies. The mechanism behind LSPR is discussed, with recent developments and strategies for introducing LSPR to the DRM examined. The review offers a thorough overview of catalyst design for light-assisted DRM and may be used as a guide to developing stable and light-receptive catalysts for the reaction.

Article

21 February 2025

Porous Cu(Mn)-Doped ZnO-MgO Nanocomposites for Photocatalytic and Antibacterial Applications

Porous Cu(Mn):ZnO-MgO composites synthesized by polymeric sol-gel method were characterized. The crystal structure, morphology, spectral properties, the ability of the photogeneration of chemically active singlet oxygen under external visible irradiation, photocatalytic and antibacterial properties of porous composites were studied. Obtained composites consist of small ZnO and MgO crystals having size less than 20 nm. It was found that Cu2+ and Mn2+ ions are embedded into the lattices of ZnO and MgO crystals, altering their crystal cell parameters. The band gap values of obtained composites are 3.41 ÷ 3.42 eV which are slightly higher than the band gap of pure ZnO. Prepared materials demonstrate a high ability of photogeneration of chemically active singlet oxygen under blue light (λ = 405 nm) irradiation. It was found that dependencies of the intensity of singlet oxygen photogeneration from the power density of visible irradiation are linear. Photocatalytic decomposition of the diazo dye Chicago Sky Blue in solutions under UV and blue light irradiation proceeds rapidly in the presence of the prepared composites (constants rate of photocatalytic dye decomposition under UV irradiation are 0.024 min−1 and 0.025 min−1 for ZnO-MgO composites doped with Cu and Mn, correspondingly). Porous composites demonstrate superior antibacterial activity against gram-positive bacteria. These materials are promising for practical application in medicine and photocatalytic technologies of air and water cleaning.

Article

11 February 2025

Functionalization of 3D-Printed Plastics for the Photocatalytic Removal of Organic Pollutants in Air

The study explored the use of 3D-printed plastics as catalyst supports for gas-phase photocatalytic applications. Specifically, it compared three commonly used plastic materials: PLA, ABS, and PETG. The process involved 3D modeling, additive manufacturing through 3D printing, and functionalization via dip-coating with titanium dioxide (TiO2). The study evaluated the loading capacity of the materials, the adhesion of the films, and the optical properties of the photocatalytic plates. Finally, the three plastic samples were tested as support materials in a laboratory-scale flat-plate reactor for the photocatalytic oxidation of dichloromethane in air. Loading capacities of around 3 mg/cm2 for TiO2 were achieved, along with radiation absorption capacities close to 65%. A correlation between loading and absorption fraction was identified, leading to the proposal of a simple saturation model; in turn, it allowed the predictive model of pollutant conversion as a function of the absorbed fraction of radiation. By analyzing both qualitative and quantitative properties and results, in order to determine the most suitable plastic material to be used in a photocatalytic wall reactor, PLA emerged as the best choice among the materials tested. These results show promise for the effective utilization of these plastics in the design of air decontamination devices.

Article

08 February 2025

Degradation of Metformin Hydrochloride and Glibenclamide by Several Advanced Oxidation Processes

The degradation of metformin hydrochloride (MET) and glibenclamide (GLI), widely used anti-diabetics, was performed using an electrochemical advanced oxidation process, namely electro-Fenton, and several other Advanced Oxidation Processes (AOPs) of photocatalytic nature, like UV/H2O2, UV/persulfate, and UV/TiO2. The electrochemical behavior of the drugs was first characterized by cyclic and differential pulse voltammetry. The data implied that both drugs present quasi-reversible oxidation. The effect of the applied current and the airflow in the electrogeneration of hydrogen peroxide was studied. Degradations of 60% of the initial drug were obtained for aqueous solutions of 30 mg·L−1 of MET and 15 mg·L−1 of GLI by using photoelectron-Fenton conditions with 1.0 A of current and a Fe2+ concentration of 3.5 mg·L−1, although the removal of MET required 60 min of reaction while for GLI only 45 min were needed. The mineralization (organic carbon removal) percentages after 60 min of treatment were 20%and 30% for electro-Fenton and photo electro-Fenton processes, respectively. For UV/H2O2, UV/persulfate, and UV/TiO2 treatments of MET solutions, the order of observed degradations was UV/PS > UV/H2O2 > UV/TiO2 with maximum values of drug removal of 30% after 60 min of irradiation. This efficiency is lower than the removal observed with the electro-Fenton reaction. For GLI the order of degradation efficiency was UV/PS > UV/TiO2 > UV/H2O2, with maximum values of drug removals of 99.5% after only 10 min of irradiation. This performance is clearly better that in the case of electro-Fenton or photo-electro-Fenton. The removals of the two drugs when dissolved in chemical matrices that mimic real hospital wastewaters and seawater were also studied. They showed a clear dependency on the pharmaceutical of choice. While the degradation of MET was hampered by the presence of other chemicals in the two water matrices, GLI removal was remarkable, pointing towards a possible application in real wastewaters.

Review

12 October 2023

New Trends on Photoswitchable Antibiotics: From Syntheses to Applications

Antibiotics are excreted in the environment after being used to treat bacterial infections in human and animals. These residues are poorly eliminated by the actual wastewater treatment processes, affecting animal, human and environmental health. This has led to the emergence of antibiotic resistance in bacterial pathogens. To combat this problem, photopharmacology has emerged in the last decades. This approach, based on the coupling of a drug with a photochromic component, is a promising way to control antibiotic activity by light irradiation and consequently limit antibioresistance. Thus, this review summarizes the study on the effect of the irradiation light on the antimicrobial activity of coupling compounds.

AmélieAubert
AntoineFayeulle
MurielVayssade
MurielBillamboz
EstelleLéonard

Article

05 July 2023

Photocatalytic Efficiency of Suspended and Immobilized TiO2 P25 for Removing Myclobutanil, Penconazole and Their Commercial Formulations

Fungicide application in viticulture is a major source of surface and groundwater contamination. It is therefore essential to find solutions to stop this environmental pollution. Heterogeneous photocatalysis is an advanced oxidation method for the degradation and mineralization of organic pollutants in water. TiO2 P25 photocatalyst in suspension has been used for removing the fungicides Myclobutanil and Penconazol, and their respective commercial formulations Systhane and Topas, in contaminated water. The apparent kinetic constants kapp of fungicides removal over 30 min batch treatment was higher for a mixture of pure molecules of Myclobutanil and Penconazol than for a mixture of their commercial formulations (17.5 × 10−3 by comparison with 10.3 × 10−3 min−1 for Myclobutanil, and 10.0 × 10−3 by comparison with 2.80 × 10−3 min−1 for Penconazol). TOC removal constants kTOC were similar for the two mixtures, due to the presence of mineral and organic additives in the commercial formulations. To easily recover the photocatalyst after fungicide removal, TiO2 P25 has been supported on β-SiC foam. Fungicides degradation was lower with supported photocatalysts than with the suspension of photocatalyst nanoparticles (NPs) because of a lower concentration of active sites on the supported photocatalyst than in the catalyst suspension. However, catalyst recovery and reuse after fungicide removal is obviously easier with TiO2/β-SiC material than with a suspension of TiO2 which requires long and expensive filtration operations.

Ignace ChristianM'Bra
NicolasKeller
AlbertTrokourey
DidierRobert

Article

11 October 2023

Fibrous SiC-based Mesoporous Solids for the Photocatalytic Degradation of Organic Pollutants under Artificial Light

SiC-based mesoporous solids with fibrous nanostructure were prepared by impregnation of a polycarbosilane precursor on annealed polyacrylonitrile (PAN) fibers and subsequent pyrolysis. The obtained material exhibits a mesoporous structure and has a specific surface area of ~20 m2/g. It has a semiconducting electronic character with a bandgap of 2.65 eV, i.e., in the visible range. Adsorption tests of methylene blue were performed on the material under dark conditions, which showed an adsorption amount of 78 wt%. The photocatalytic activity of the material was then evaluated for the degradation of the dye under artificial daylight irradiation over a period of 7 h. A degradation of 94 wt% was achieved. Regeneration and reuse of the material was also tested and resulted in 97 wt% degradation after reuse, indicating potential interest of the material as a contactor in environmental remediation devices.

KarlaB.Cervantes-Diaz
JulienCambedouzou

Article

07 February 2023

Plasmon Enhanced Nickel(II) Catalyst for Photocatalytic Lignin Model Cleavage

Photocatalytic-induced cleaving of the ether C–O bond in model lignin compounds was studied with a closely-coupled compo-site material consisting of Ni(OH)2 and gold nanoparticles (NPs) on a zirconia support (Au/ZrO2–Ni(OH)2). The three important ether bond types consisting of α-O-4, β-O-4, and 4-O-5 linkages can all be cleaved using this catalyst at reaction temperatures 40, 85 and 95 °C when under low-flux visible light irradiation. The Au NPs action as a light-harvesting antenna provided light-generated hot electrons that reduced Ni2+ to Ni0. The Ni0 was the active catalytic site where reductive cleavage of ether C–O bonds occurred while it was oxidized to Ni2+ to complete the catalysis cycle. The plasmonic antenna system with supported Ni(OH)2 exhibited better ability for the catalytic reductive ether cleavages under visible light irradiation compared to photocata-lysts of Au NPs and Ni2+ ions immobilized on alumina fibers.

YichaoJin
XiayanWu
SarinaSarina
YingpingHuang
EricR.Waclawik
HuaiyongZhu

Article

03 March 2023

SnS2 Quantum Dots Decorated MoS2 Nanosheets Enabling Efficient Photocatalytic H2 Evolution in CO2 Saturated Water

SnS2/MoS2 heterojunction nanocomposite was prepared by a one-step hydrothermal synthesis method. The nanocomposite exhibited much improved photocatalytic hydrogen evolution performance in CO2 saturated solution compared with pure MoS2 and SnS2 samples. The improved photocatalytic activity was attributed to the S-scheme heterojunction structure between SnS2 quantum dots and MoS2 nanosheets which facilitate electron-hole separation both in MoS2 and SnS2. In the S-scheme structure, the strong reduction ability of SnS2 quantum dots was well maintained for the improved H2 evolution. In situ DRIFT studies allowed us to suggest reaction pathways from CO2 and H2O to photocatalytic H2, CO, and CH4 generation.

XuelianChen
XiLuo
LeiLiu
JingPing
SongmeiSun

Editorial

06 September 2022

Article

31 August 2023

Potential Role of Exciton in Photocatalysis

This article commemorates the outstanding Russian scientists E.F. Gross and A.N. Terenin. It revisits their successors’ efforts to develop Terenin’s idea of using excitons, discovered by Gross, for photocatalytic redox reactions on wide-gap semiconductors. Terenin proposed ZnO as the subject of study. To explore the possibility of replacing photogenerated electrons and holes in a redox reaction by an exciton being a quasi-neutral particle, the test reaction of the photoactivated oxygen isotope exchange (POIE) was studied. It was found that many years of initial unsuccessful attempts were due to the fact that the exciton energy is spent on luminescence. In our experiments, the excitons decayed non-radiatively, and the long-lived electron-donor F-type and hole V-type active centers were formed by creating the 2D surface nanostructure ZnO/ZnO1−x/O. These centers allowed to obtain the reaction efficiency 5–8 times higher than with the interband transitions. Thus, the developed 2D surface nanostructure ZnO/ZnO1−x/O resolved the problem of using an exciton in photocatalysis and demonstrated the perspective of this nanostructure as an efficient photocatalyst.

AndreyALisachenko
BorisVNovikov

Article

11 April 2024

Exploring Bi4V2O11 as Photoanode for Water Splitting with a Wide Range of Solar Light Capture and Suitable Band Potential

Bi4V2O11 possesses a bandgap of ~1.9 eV, and the band positions of minimum conduction band and maximum valence band straddle the redox potentials of H+/H2 and O2/H2O. In the current work, photoanode made of particulate Bi4V2O11 film displays a wide range of light adsorption. However, when the anode was fabricated by drop-casting and examined for photoelectrochemical water splitting, the photocurrent density of the pristine Bi4V2O11 was low. Improvement has then been carried out by Mo-doping. The Mo-doped Bi4V2O11 photoanode achieves a maximum photocurrent density of 0.3 mA/cm2 after a post deposition necking treatment to improve the connectivity of the drop-cast particles in the film. This material also shows a stability with maintaining 80% photocurrent after 2 h test. Discussion has been made on the displayed performance in PEC water splitting of the Bi4V2O11 materials. Potential solutions have been proposed for this type of promising photoanode material for water splitting.

XinZhao
NingsiZhang
Yang Yu
TaoFang
JunHu
JianyongFeng
ZhongChen

Article

05 January 2024

Benzene Bridged Carbon Nitride for Efficient Photocatalytic Hydrogen Evolution

Turing the electronic structure by inserting certain functional groups in graphitic carbon nitride (g-C3N4, CN for short) skeleton through molecular doping is an effective way to improve its photocatalytic performance. Herein, we prepare a benzene bridged carbon nitride (BCN) by calcining urea and 1,3,5-tribromobenzene at elevated temperature. The introduction of benzene ring in g-C3N4 layers improves the separation efficiency and lifetime of photogenerated carriers, inhibits the recombination rate of electron/hole pairs, thus the performance of photocatalytic hydrogen evolution improves. The optimal hydrogen evolution rate of 1.5BCN reaches 1800 µmol/h·g, which is nine times that of the pure g-C3N4. DFT calculation proved the benzene bridged CN increased the distance of charge transfer (DCT) and the push-pull electronic effect of intramolecular electrons. This work may provide a pathway for preparing molecular doped g-C3N4 with improved photocatalytic performance.

JunxiaChu
WenchengLi
ZhijunCao
XinBai
XiRao
ShaohuiZheng
YongpingZhang

Review

11 July 2024

Photocatalytic Aerobic Conversion of Methane

The direct conversion of methane into high-value chemicals has been a persistent research focus in the fields of chemical engineering and energy. Photocatalysis, as an innovative technology, not only circumvents the issues of catalyst sintering and carbon deposition associated with traditional thermal catalysis but also transcends thermodynamic limitations by providing new reaction pathways. Utilizing molecular oxygen as an oxidant generates various reactive oxygen species, offering unique thermodynamic advantages for methane conversion. This review summarizes the advancements in photocatalytic partial oxidation (PPOM) and oxidative coupling of methane (POCM) using oxygen as an oxidant. It discusses the activation mechanisms and reaction pathways of methane and oxygen in different systems, as well as the application of photochemical cycling strategies in methane conversion. Finally, it addresses the challenges in this field, proposes potential solutions, and offers perspectives on the future development of photocatalytic systems.

YuxiangKong
ChunxiangYang
YiyuCai
XiaoweiMu
LuLi

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