Ruiyuan Sun, Qinglu Liu, Qitao Liu, Weilong Qin, Jiabo Le, Xiaopei Ren, Muhammad Bilal Akbar, Yang Zhou, Chonghan Xia, Licheng Sun, Yongbo Kuang
{"title":"Scalable Reduced Graphene Oxide Conductive Layer‐Based Particulate Photocathodes for Photoelectrochemical Water Splitting","authors":"Ruiyuan Sun, Qinglu Liu, Qitao Liu, Weilong Qin, Jiabo Le, Xiaopei Ren, Muhammad Bilal Akbar, Yang Zhou, Chonghan Xia, Licheng Sun, Yongbo Kuang","doi":"10.1002/admt.202400392","DOIUrl":null,"url":null,"abstract":"Particle transfer method photoelectrodes show superior photoelectrochemical performance compared to traditional powder‐based methods, making them a promising solution for solar water splitting in sustainable energy. This study introduces an innovative nonvacuum particle transfer method for fabricating photoelectrodes on a conductive carbon substrate, addressing the challenges associated with the high costs and vacuum deposition processes of traditional methods. Utilizing a p‐type CuFeO<jats:sub>2</jats:sub> powder semiconductor, a unique substrate is developed by applying a graphene oxide layer mixed with a small amount of silica binder on the particle layer's backside through ultrasonic atomization spraying. This layer is converted into multilayered reduced graphene oxide (ML‐rGO) via wet chemical reduction, resulting in a substrate boasting a high work function (4.8 eV), alongside remarkable chemical stability, mechanical strength, and conductivity. The fabricated CuFeO<jats:sub>2</jats:sub> photocathode demonstrated an onset potential of 0.97 V versus RHE and a photocurrent density of 1.5 mA cm<jats:sup>−2</jats:sup> at 0.6 V versus RHE for H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> reduction. Further enhancement is achieved by depositing Pt as a cocatalyst, which ensured stability for over 20 h in an alkaline medium for water splitting. This study sets a new benchmark for developing CuFeO<jats:sub>2</jats:sub>‐based photocathodes, paving the way for broader particle transfer method applications.","PeriodicalId":7200,"journal":{"name":"Advanced Materials & Technologies","volume":"7 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials & Technologies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/admt.202400392","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Particle transfer method photoelectrodes show superior photoelectrochemical performance compared to traditional powder‐based methods, making them a promising solution for solar water splitting in sustainable energy. This study introduces an innovative nonvacuum particle transfer method for fabricating photoelectrodes on a conductive carbon substrate, addressing the challenges associated with the high costs and vacuum deposition processes of traditional methods. Utilizing a p‐type CuFeO2 powder semiconductor, a unique substrate is developed by applying a graphene oxide layer mixed with a small amount of silica binder on the particle layer's backside through ultrasonic atomization spraying. This layer is converted into multilayered reduced graphene oxide (ML‐rGO) via wet chemical reduction, resulting in a substrate boasting a high work function (4.8 eV), alongside remarkable chemical stability, mechanical strength, and conductivity. The fabricated CuFeO2 photocathode demonstrated an onset potential of 0.97 V versus RHE and a photocurrent density of 1.5 mA cm−2 at 0.6 V versus RHE for H2O2 reduction. Further enhancement is achieved by depositing Pt as a cocatalyst, which ensured stability for over 20 h in an alkaline medium for water splitting. This study sets a new benchmark for developing CuFeO2‐based photocathodes, paving the way for broader particle transfer method applications.