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基于负载在还原氧化石墨烯上的 CoSe 修饰 FeSe 纳米粒子的纳米复合材料作为高性能析氧反应电催化剂。

Nanocomposites Based on CoSe-Decorated FeSe Nanoparticles Supported on Reduced Graphene Oxide as High-Performance Electrocatalysts toward Oxygen Evolution Reaction.

机构信息

School of Chemistry and Chemical Engineering , Jiangsu University , Zhenjiang 212013 , China.

School of Environmental and Chemical Engineering , Jiangsu University of Science and Technology , Zhenjiang 202018 , China.

出版信息

ACS Appl Mater Interfaces. 2018 Jun 6;10(22):19258-19270. doi: 10.1021/acsami.8b04024. Epub 2018 May 21.

DOI:10.1021/acsami.8b04024
PMID:29741088
Abstract

FeCo-based materials are promising candidates as efficient, affordable, and sustainable electrocatalysts for oxygen evolution reaction (OER). Herein, a composite based on FeSe@CoSe particles supported on reduced graphene oxide (rGO) was successfully prepared as an OER catalyst. In the catalyst, the CoSe phase was located on the FeSe surface, forming a large number of exposed heterointerfaces with acidic iron sites because of strong charge interaction between CoSe and FeSe. It is believed that the exposed heterointerfaces act as catalytic active sites for OER via a two-site mechanism, manifesting an overpotential as low as 260 mV to reach the current density of 10 mA cm in 1 M KOH and excellent stability for at least 6 h, which is superior to those of CoSe/rGO, FeSe/rGO, as well as most of the FeNi- and FeCo-based electrocatalysts reported in recent literatures. It was demonstrated that the most optimal composite electrocatalysts release more Fe species into the electrolyte during the OER process, whereas the releasing of Co species is negligible. When the FeSe@CoSe/rGO catalysts were loaded on a α-FeO photoanode, the photocurrent density was increased by three times. These results may open up a promising avenue into the design and engineering of highly active and durable catalysts for water oxidation.

摘要

基于 FeCo 的材料是一种很有前途的高效、经济、可持续的析氧反应 (OER) 电催化剂,本文成功制备了一种负载在还原氧化石墨烯 (rGO) 上的 FeSe@CoSe 颗粒复合材料作为 OER 催化剂。在该催化剂中,CoSe 相位于 FeSe 表面,由于 CoSe 和 FeSe 之间的强烈电荷相互作用,形成了大量具有酸性铁位的暴露异质界面。据信,暴露的异质界面通过双位点机制充当 OER 的催化活性位点,在 1 M KOH 中达到 10 mA cm 的电流密度仅需 260 mV 的过电势,并且具有至少 6 小时的出色稳定性,优于 CoSe/rGO、FeSe/rGO 以及大多数最近文献中报道的 FeNi-和 FeCo 基电催化剂。研究表明,最优化的复合电催化剂在 OER 过程中会将更多的 Fe 物质释放到电解质中,而 Co 物质的释放则可以忽略不计。当将 FeSe@CoSe/rGO 催化剂负载在 α-FeO 光阳极上时,光电流密度增加了三倍。这些结果可能为设计和工程高效、持久的水氧化催化剂开辟了一条有前途的途径。

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