通过重构 M(OH)x/Fe3O4 催化剂促进氧气进化反应

IF 6.4 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Frontiers Pub Date : 2024-08-06 DOI:10.1039/D4QI01574F
Xiaoqu Wang, Limin Wang, Yongchun Liu, Rajkumar Devasenathipathy, Li Liu, Qiulan Huang, Dujuan Huang, Youjun Fan, Du-Hong Chen and Wei Chen
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引用次数: 0

摘要

在水的电催化大规模制氢过程中,通常使用镍基和/或铁基催化剂,但这些催化剂在高电流密度(500 mA cm-2)下具有超高过电位和稳定性差的缺点。在此,我们制备了重构的 M(OH)x/Fe3O4(M = Ni、Fe)阵列,用于促进氧进化反应(OER)。所制备的 M(OH)x/Fe3O4 长在泡沫铁上(M(OH)x/Fe3O4/IF)催化剂在 50 mA cm-2 和 500 mA cm-2 的电流密度下,OER 的过电位分别为 214 mV 和 311 mV。原位拉曼光谱显示,M(OH)x/Fe3O4/IF 的重构提高了 OER 的活性。理论计算显示,在 OER 过程中,M(OH)x/Fe3O4/IF 的 Ni 位点有利于吸收 O2。这项工作强调了重构结构明确的催化剂对提高 OER 催化活性和大规模水电催化的作用。
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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Boosting the oxygen evolution reaction via the reconstruction of an M(OH)x/Fe3O4 catalyst†

For large-scale hydrogen production from electrocatalysis of water, Ni- and/or Fe-based catalysts were commonly used but were limited by the ultrahigh overpotential and poor stability at a high current density (>500 mA cm−2). Here, the reconstruction of M(OH)x/Fe3O4 (M = Ni, Fe) arrays has been performed for boosting the oxygen evolution reaction (OER). The prepared M(OH)x/Fe3O4 grown on iron foam (M(OH)x/Fe3O4/IF) catalysts exhibited low overpotentials of 214 and 311 mV for the OER at current densities of 50 and 500 mA cm−2, respectively. In addition, an excellent stability up to 70 h of operation was achieved at a current density of 10 mA cm−2 in 1 M KOH. The in situ Raman spectra revealed that the reconstruction of M(OH)x/Fe3O4/IF boosted the OER activity. Theoretical calculations revealed favorable absorption of O2 at the Ni site of M(OH)x/Fe3O4/IF during the OER. This work highlights the reconstruction of structurally definite catalysts for promoting the catalytic activity toward the OER and the large-scale electrocatalysis of water.

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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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