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原位生成双功能铁掺杂二硫化钼纳米冠用于高效电催化水分解

In Situ Generation of Bifunctional Fe-Doped MoS Nanocanopies for Efficient Electrocatalytic Water Splitting.

作者信息

Xue Jiang-Yan, Li Fei-Long, Zhao Zhong-Yin, Li Cong, Ni Chun-Yan, Gu Hong-Wei, Young David James, Lang Jian-Ping

机构信息

Suzhou Key Laboratory of Precise Transformation of Resource Molecules, College of Chemistry, Chemical Engineering and Materials Science , Soochow University , Suzhou 215123 , Jiangsu , People's Republic of China.

State Key Laboratory of Organometallic Chemistry , Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , Shanghai 200032 , People's Republic of China.

出版信息

Inorg Chem. 2019 Aug 19;58(16):11202-11209. doi: 10.1021/acs.inorgchem.9b01814. Epub 2019 Aug 6.

Abstract

Design and synthesis of non-noble metal electrocatalysts with high activity and durability for the electrolysis of water is of great significance for energy conversion and storage. In this work, we prepared a series of Fe-doped MoS nanomaterials by simple one-pot solvothermal reactions of (NH)MoS with FeCl·6HO. An optimized working electrode of Fe-MoS-5 displayed high hydrogen evolution reaction (HER) activity with a relatively small overpotential of 173 mV to achieve a current density of 10 mA cm in 0.5 M HSO, along with no significant change in catalytic performance even after 1000 cyclic voltammetry (CV) cycles. Fe-MoS nanoparticles on nickel foam (NF; denoted as Fe-MoS/NF) exhibited an overpotential of 230 mV at 20 mA cm for the oxygen evolution reaction (OER) and 153 mV at 10 mA cm for the HER in 1.0 M KOH electrolyte. Fe-MoS/NF was stable for more than 140 h under these conditions. Furthermore, the two electrode system of Fe-MoS/NF (anode)//Fe-MoS/NF (cathode) electrodes demonstrated excellent electrocatalytic activity toward overall water splitting with a low potential of 1.52 V at 10 mA cm in 1.0 M KOH electrolyte.

摘要

设计并合成具有高活性和耐久性的非贵金属电催化剂用于水电解,对于能量转换和存储具有重要意义。在这项工作中,我们通过(NH)MoS与FeCl·6HO的简单一锅溶剂热反应制备了一系列Fe掺杂的MoS纳米材料。优化后的Fe-MoS-5工作电极表现出高析氢反应(HER)活性,在0.5 M HSO中,过电位相对较小,为173 mV时可实现10 mA cm的电流密度,即使经过1000次循环伏安(CV)循环后催化性能也无显著变化。泡沫镍(NF)上的Fe-MoS纳米颗粒(记为Fe-MoS/NF)在1.0 M KOH电解液中,析氧反应(OER)在20 mA cm时过电位为230 mV,HER在10 mA cm时过电位为153 mV。在这些条件下,Fe-MoS/NF稳定超过140小时。此外,Fe-MoS/NF(阳极)//Fe-MoS/NF(阴极)电极的双电极体系在1.0 M KOH电解液中,对全水解表现出优异的电催化活性,在10 mA cm时低电位为1.52 V。

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