{"title":"Enhanced Oxygen Evolution Reaction Performance of ZnO Nanorods on Activated Carbon Cloth","authors":"Chandra Prakash, Ula Suliman, Sadegh Pour-Ali, Ambesh Dixit*, Jing Liu* and Shiva Mohajernia*, ","doi":"10.1021/acs.energyfuels.4c0618410.1021/acs.energyfuels.4c06184","DOIUrl":null,"url":null,"abstract":"<p >The employment of an abundant and cost-effective electrocatalyst for water splitting gained significant attention, as there is a need for a substitute for precious metals in the production of affordable H<sub>2</sub> as a promising energy carrier. This study addresses the need for cost-effective, high-activity, and binder-free oxygen evolution reaction (OER) electrocatalysts by investigating ZnO nanorods (ZnO NRs) integrated with electrochemically activated carbon cloth (ECAT@CC). Various characterization techniques, including XRD, XPS, and FE-SEM, confirmed the formation of ZnO NRs on ECAT@CC during conventional hydrothermal synthesis in an aqueous solution containing (CH<sub>3</sub>COO)<sub>2</sub>Zn·2H<sub>2</sub>O and C<sub>6</sub>H<sub>12</sub>N<sub>4</sub> at 95 °C. The electrochemical performance was evaluated using linear sweep voltammetry, chronopotentiometry, and electrochemical impedance spectroscopy in alkaline conditions. The ZnO NRs/ECAT@CC annealed for 3 h at 450 °C exhibited superior OER activity, with an overpotential of 1.58 V vs RHE at a current density of 10 mA/cm<sup>2</sup>, and improved charge transfer resistance of 65.89 Ω·cm<sup>2</sup>, significantly lower than that of pristine and ECAT@CC samples. During the stability test, the robustness of the ZnO NRs/ECAT@CC-3h sample was demonstrated over the prolonged operation. This research highlights ZnO NRs/ECAT@CC-3h as a promising, binder-free, and self-supported OER electrocatalyst, which can contribute to more efficient and sustainable processes in electrochemical water splitting.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 12","pages":"5897–5906 5897–5906"},"PeriodicalIF":5.2000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.4c06184","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
Abstract
The employment of an abundant and cost-effective electrocatalyst for water splitting gained significant attention, as there is a need for a substitute for precious metals in the production of affordable H2 as a promising energy carrier. This study addresses the need for cost-effective, high-activity, and binder-free oxygen evolution reaction (OER) electrocatalysts by investigating ZnO nanorods (ZnO NRs) integrated with electrochemically activated carbon cloth (ECAT@CC). Various characterization techniques, including XRD, XPS, and FE-SEM, confirmed the formation of ZnO NRs on ECAT@CC during conventional hydrothermal synthesis in an aqueous solution containing (CH3COO)2Zn·2H2O and C6H12N4 at 95 °C. The electrochemical performance was evaluated using linear sweep voltammetry, chronopotentiometry, and electrochemical impedance spectroscopy in alkaline conditions. The ZnO NRs/ECAT@CC annealed for 3 h at 450 °C exhibited superior OER activity, with an overpotential of 1.58 V vs RHE at a current density of 10 mA/cm2, and improved charge transfer resistance of 65.89 Ω·cm2, significantly lower than that of pristine and ECAT@CC samples. During the stability test, the robustness of the ZnO NRs/ECAT@CC-3h sample was demonstrated over the prolonged operation. This research highlights ZnO NRs/ECAT@CC-3h as a promising, binder-free, and self-supported OER electrocatalyst, which can contribute to more efficient and sustainable processes in electrochemical water splitting.
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.