NiFeCe nanosheet arrays by N and P doping as efficient electrocatalysts for oxygen evolution reaction

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Chao Xu, Dan Wu, Qiangqiang Wang, Xuan Kuang, Xu Sun, Xiang Ren, Qin Wei
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引用次数: 0

Abstract

The oxygen evolution reaction (OER) is commonly considered to be the major bottleneck in electrochemical water splitting, characterized by high overpotential requirement, so the fabrication of low cost and high-performing OER catalyst is of great significance for the process of electrocatalytic water splitting. Here, the nanocomposite material (denoted as N-Ni 0.75 Fe 0.15 Ce 0.10 P/NF) was obtained by simultaneously nitriding and phosphating the nanoneedle-like array (denoted as Ni 0.75 Fe 0.15 Ce 0.10 O x /NF) grown on nickel foam(NF). N-Ni 0.75 Fe 0.15 Ce 0.10 P/NF has an overpotential of only 244 mV at a current density of 50 mA cm -2 . In addition, the Tafel slope is remarkably low at 73.8 mV dec -1 . The material can work stably at a current density of 50 mA cm -2 for at least 48 h, indicating good stability. This investigation introduces innovative design methodologies for OER catalysts, offering significant contributions to sustainable energy research.
氮磷掺杂NiFeCe纳米片阵列作为析氧反应的高效电催化剂
析氧反应(OER)具有过电位要求高的特点,被普遍认为是电化学水分解的主要瓶颈,因此制备低成本、高性能的析氧反应催化剂对电催化水分解工艺具有重要意义。在泡沫镍(NF)上生长纳米针状阵列(Ni 0.75 Fe 0.15 Ce 0.10 O x /NF),通过同时氮化和磷化得到纳米复合材料(N-Ni 0.75 Fe 0.15 Ce 0.10 P/NF)。N-Ni 0.75 Fe 0.15 Ce 0.10 P/NF在电流密度为50 mA cm -2时过电位仅为244 mV。此外,在73.8 mV dec -1处,Tafel斜率非常低。该材料可在50 mA cm -2的电流密度下稳定工作至少48小时,具有良好的稳定性。本研究介绍了OER催化剂的创新设计方法,为可持续能源研究提供了重要贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
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