Trifunctional Single-Atomic Ru Sites Enable Efficient Overall Water Splitting and Oxygen Reduction in Acidic Media

Cell Press Pub Date : 2020-01-14 DOI:10.2139/ssrn.3517557
Xianyun Peng, Yuying Mi, Shunzheng Zhao, Xijun Liu, Defeng Qi, Jiaqiang Sun, Yifan Liu, Haihong Bao, Di Qu, L. Zhuo, Junqiang Ren, Jun Luo, Xiaoming Sun
{"title":"Trifunctional Single-Atomic Ru Sites Enable Efficient Overall Water Splitting and Oxygen Reduction in Acidic Media","authors":"Xianyun Peng, Yuying Mi, Shunzheng Zhao, Xijun Liu, Defeng Qi, Jiaqiang Sun, Yifan Liu, Haihong Bao, Di Qu, L. Zhuo, Junqiang Ren, Jun Luo, Xiaoming Sun","doi":"10.2139/ssrn.3517557","DOIUrl":null,"url":null,"abstract":"Development of cost-effective, active trifunctional catalysts for acidic oxygen reduction (ORR) as well as hydrogen- and oxygen-evolution reactions (HER and OER, respectively) is highly desirable, albeit challenging. Herein, single-atomic Ru sites anchored onto Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> MXene nanosheets are first reported to serve as trifunctional electrocatalysts for simultaneously catalyzing acidic HER, OER, and ORR. A half-wave potential of 0.80 V for ORR and small overpotentials of 290 mV and 70 mV for OER and HER, respectively, at 10 mA cm<sup>−2</sup> are achieved. Hence, a low cell voltage of 1.56 V&nbsp;is required for the acidic overall water splitting. The maximum power density of an H<sub>2</sub>–O<sub>2</sub>&nbsp;fuel cell using the as-prepared catalyst can reach as high as 941 mW cm<sup>−2</sup>. Theoretical calculations revealed that isolated Ru–O<sub>2</sub> sites can effectively optimize the adsorption of reactants/intermediates and lower the energy barriers for the potential-determining steps, thereby accelerating the HER, ORR, and OER kinetics.","PeriodicalId":244417,"journal":{"name":"Cell Press","volume":"36 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Press","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2139/ssrn.3517557","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

Abstract

Development of cost-effective, active trifunctional catalysts for acidic oxygen reduction (ORR) as well as hydrogen- and oxygen-evolution reactions (HER and OER, respectively) is highly desirable, albeit challenging. Herein, single-atomic Ru sites anchored onto Ti3C2Tx MXene nanosheets are first reported to serve as trifunctional electrocatalysts for simultaneously catalyzing acidic HER, OER, and ORR. A half-wave potential of 0.80 V for ORR and small overpotentials of 290 mV and 70 mV for OER and HER, respectively, at 10 mA cm−2 are achieved. Hence, a low cell voltage of 1.56 V is required for the acidic overall water splitting. The maximum power density of an H2–O2 fuel cell using the as-prepared catalyst can reach as high as 941 mW cm−2. Theoretical calculations revealed that isolated Ru–O2 sites can effectively optimize the adsorption of reactants/intermediates and lower the energy barriers for the potential-determining steps, thereby accelerating the HER, ORR, and OER kinetics.
三功能的单原子Ru位点在酸性介质中实现了高效的整体水分解和氧还原
开发具有成本效益、活性的三功能催化剂用于酸性氧还原(ORR)以及析氢和析氧反应(分别为HER和OER)是非常需要的,尽管具有挑战性。本文首次报道了锚定在Ti3C2Tx MXene纳米片上的单原子Ru位点作为三功能电催化剂,同时催化酸性HER、OER和ORR。在10 mA cm−2下,ORR的半波电位为0.80 V, OER和HER的过电位分别为290 mV和70 mV。因此,需要1.56 v的低电池电压来进行酸性整体水分解。使用该催化剂制备的h2 - o2燃料电池的最大功率密度可达941 mW cm−2。理论计算表明,分离的Ru-O2位点可以有效地优化反应物/中间体的吸附,降低势决定步骤的能垒,从而加快HER、ORR和OER动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信