富氧空位掺杂钕的 RuO2 用于高效酸性整体水分离

IF 4.1 3区 化学 Q1 CHEMISTRY, ANALYTICAL
Boyan Ai, Guoxiang Wang, Pengchao Liang, Jinxiu Bing, Majie Zhang, Qingwang Min, Xinxin Zhang
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引用次数: 0

摘要

开发高活性、酸性稳定的 Ru 基电催化剂对电解水具有重要意义,但由于 Ru 在酸性介质中受到严重腐蚀,因此开发 Ru 基电催化剂仍是一项巨大挑战。在此,我们通过水热法合成富含氧空位(OV)的掺钕 RuO2 纳米晶体,并随后进行退火处理,制备出高效的整体水分离催化剂。在 0.5 M H2SO4 电解质中,电流密度为 10 mA cm-2 时,该催化剂的 OER 过电位仅为 200 mV,HER 过电位为 44 mv。密度泛函理论进一步揭示,新构建的掺钕 RuO2 位点激活了难以反应的 *O 中间体,降低了 OER 中间体的吸附能,从而有效降低了反应速率决定步骤的吉布斯自由能(*O 至 *OOH),并调节了活性位点 d 带的中心。异价掺杂和空位工程的协同效应造就了掺钕 RuO2 卓越的电催化性能。这种性能控制策略可为开发有效且经济可行的催化剂铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oxygen vacancy-rich Nd-doped RuO2 for efficient acid overall water splitting
The development of highly active and acid-stable Ru-based electrocatalysts is of great significance for water electrolysis but remains a huge challenge due to serious Ru corrosion in an acid medium. Herein, we prepared oxygen vacancy (OV)-rich Nd-doped RuO2 nanocrystals by facile synthesis via hydrothermal and subsequent annealing for efficient overall water splitting. The catalyst exhibits an overpotential of only 200 mV for OER and 44 mv for HER at the current density of 10 mA cm−2 in 0.5 M H2SO4 electrolyte. Nd-doped RuO2 only demands a cell voltage of 1.52 V to drive the overall water splitting reaction and displays excellent stability for 100 h. Density functional theory further revealed that the newly constructed Nd-doped RuO2 sites activate the difficult to react *O intermediates, reducing the adsorption energy of the OER intermediates to effectively minimize the Gibbs free energy (*O to *OOH) of the reaction rate-determining step and regulate the center of the active site d-band. The synergistic effect of aliovalent doping and vacancy engineering contributes to the excellent electrocatalytic performance of Nd-doped RuO2. This performance control strategy can pave the way for the development of effective and economically viable catalysts.
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来源期刊
CiteScore
7.80
自引率
6.70%
发文量
912
审稿时长
2.4 months
期刊介绍: The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied. Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.
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