{"title":"Photoelectrochemical generation of H2O2 using hematite (α-Fe2O3) and gas diffusion electrode (GDE)","authors":"T. Imrich , T. Nakata , T. Ohno , J. Krýsa","doi":"10.1016/j.cattod.2025.115206","DOIUrl":null,"url":null,"abstract":"<div><div>In contrast to the industrial-scale production of H<sub>2</sub>O<sub>2</sub>, electrochemical or photoelectrochemical synthesis is an environmentally friendly alternative. In this study, the photoelectrochemical generation of H<sub>2</sub>O<sub>2</sub> was investigated using a hematite (α-Fe<sub>2</sub>O<sub>3</sub>/FTO/glass) photoanode in combination with a gas diffusion electrode (GDE) modified by the incorporation of tin(II) phthalocyanine (SnPc) in its hydrophilic layer. The experiments were conducted in a photoelectrochemical cell with two compartments separated by a proton exchange membrane, under an applied bias and AM1.5 irradiation (100 mW/cm<sup>2</sup>). The amount of H<sub>2</sub>O<sub>2</sub> generated was quantified through chemical analysis using visible light spectrophotometry of the electrolyte. To assess the process efficiency, the Faradaic efficiency (<em>FE</em>) was calculated. The optimal configuration employed air as the inlet gas for the GDE and phosphate buffer (pH 6.4) as the electrolyte in the cathodic compartment. The combination of the hematite photoanode and the GDE modified with SnPc was the most effective for H<sub>2</sub>O<sub>2</sub> photoelectrochemical generation. The highest <em>FE</em> values achieved were 52.4 % for the GDE (O<sub>2</sub> reduction to H<sub>2</sub>O<sub>2</sub>) and 0.4 % for the hematite photoanode (H<sub>2</sub>O oxidation to H<sub>2</sub>O<sub>2</sub>).</div></div>","PeriodicalId":264,"journal":{"name":"Catalysis Today","volume":"450 ","pages":"Article 115206"},"PeriodicalIF":5.2000,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Today","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920586125000240","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
In contrast to the industrial-scale production of H2O2, electrochemical or photoelectrochemical synthesis is an environmentally friendly alternative. In this study, the photoelectrochemical generation of H2O2 was investigated using a hematite (α-Fe2O3/FTO/glass) photoanode in combination with a gas diffusion electrode (GDE) modified by the incorporation of tin(II) phthalocyanine (SnPc) in its hydrophilic layer. The experiments were conducted in a photoelectrochemical cell with two compartments separated by a proton exchange membrane, under an applied bias and AM1.5 irradiation (100 mW/cm2). The amount of H2O2 generated was quantified through chemical analysis using visible light spectrophotometry of the electrolyte. To assess the process efficiency, the Faradaic efficiency (FE) was calculated. The optimal configuration employed air as the inlet gas for the GDE and phosphate buffer (pH 6.4) as the electrolyte in the cathodic compartment. The combination of the hematite photoanode and the GDE modified with SnPc was the most effective for H2O2 photoelectrochemical generation. The highest FE values achieved were 52.4 % for the GDE (O2 reduction to H2O2) and 0.4 % for the hematite photoanode (H2O oxidation to H2O2).
期刊介绍:
Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues.
Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.