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用于高效析氧反应的硒化物基三维折叠多金属纳米片

Selenide-based 3D folded polymetallic nanosheets for a highly efficient oxygen evolution reaction.

作者信息

Zhou Tianning, Bai Jie, Gao Yihao, Zhao Linxiu, Jing Xiaofei, Gong Yaqiong

机构信息

School of Chemical Engineering and Technology, North University of China, Taiyuan, 030051, PR China.

Northeast Normal University, Key Lab Polyoxometalate Sci, Minist Educ, Changchun, 130024, PR China.

出版信息

J Colloid Interface Sci. 2022 Jun;615:256-264. doi: 10.1016/j.jcis.2022.01.139. Epub 2022 Jan 25.

Abstract

Electrochemical water splitting, which is considered to be one of the fruitful strategies to achieve efficient and pollution-free hydrogen production, has been deemed as a key technology to achieve renewable energy conversion. Oxygen evolution reaction (OER) is a decisive step in water splitting. Slow kinetics seriously limits the effective utilization of energy thus it is extremely urgent to develop electrocatalysts that can effectively reduce the reaction energy barrier thus accelerate OER kinetics. Here, Mn-CoSe/NiSe/NF nanosheets with 3D folded structure was assembled on Ni foam by electrodeposition and vapor-deposition method. Mn-CoSe/NiSe/NF can achieve a current density of 10 mA cm with only 175 mV overpotential in an alkaline environment of 1 M KOH, which is much lower than other reported catalysts. In addition, catalyst Mn-CoSe/NiSe/NF also performed well in long-term stability tests. Through the synergy of polymetallic, the improvement of catalyst surface energy together with the tuning of electronic structure and the optimization of conductivity can be realized. This work may provide a feasible strategy for the design of efficient selenide-based oxygen evolution reaction catalysts.

摘要

电化学水分解被认为是实现高效无污染制氢的有效策略之一,已被视为实现可再生能源转换的关键技术。析氧反应(OER)是水分解中的决定性步骤。缓慢的动力学严重限制了能量的有效利用,因此开发能够有效降低反应能垒从而加速OER动力学的电催化剂迫在眉睫。在此,通过电沉积和气相沉积法在泡沫镍上组装了具有三维折叠结构的Mn-CoSe/NiSe/NF纳米片。Mn-CoSe/NiSe/NF在1 M KOH碱性环境中仅需175 mV过电位就能实现10 mA cm的电流密度,这远低于其他已报道的催化剂。此外,催化剂Mn-CoSe/NiSe/NF在长期稳定性测试中也表现良好。通过多金属的协同作用,可以实现催化剂表面能的提高、电子结构的调整以及导电性的优化。这项工作可能为设计高效的硒化物基析氧反应催化剂提供一种可行的策略。

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