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铁掺杂的CoP纳米立方体与CoP纳米片阵列的协同耦合用于增强和稳健的析氧电催化

Synergistically coupling of Fe-doped CoP nanocubes with CoP nanosheet arrays towards enhanced and robust oxygen evolution electrocatalysis.

作者信息

Jiang Deli, Xu Shengjie, Quan Biao, Liu Chenchen, Lu Yikai, Zhu Jianjun, Tian Dan, Li Di

机构信息

School of Chemistry and Chemical Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.

School of Chemistry and Chemical Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.

出版信息

J Colloid Interface Sci. 2021 Jun;591:67-75. doi: 10.1016/j.jcis.2021.01.084. Epub 2021 Feb 1.

Abstract

The rational design of high-performance and low-cost oxygen evolution reaction (OER) electrocatalysts for water splitting is of vital importance for development of renewable hydrogen energy. Herein, we demonstrate an interfacial engineering strategy to prepare Fe-doped CoP nanocubes/CoP nanosheet arrays heterostructure supported on carbon cloth (denoted as CoFeP/CoP/CC). The resultant CoFeP/CoP/CC heterostructure catalyst possesses abundant heterogeneous interfaces, which enables the exposure of reaction active sites and possibly modulation of electronic structure of the catalyst. Furthermore, this strong interfacial coupling of CoFeP and CoP as well as the integration structure on the carbon cloth guarantee high electronic conductivity and enhanced mechanical stability. Benefiting from these advantages, the CoFeP/CoP/CC-heterostructure exhibits high electrocatalytic OER performance with a low overpotential of 240 mV for reaching a current density of 10 mA cm, which outperforms the commercial noble metal RuO (255 mV) and many reported TMPs-based electrocatalysts. Moreover, this CoFeP/CoP/CC catalyst shows a remarkable OER catalytic stability over 100 h. This work provides an effective avenue for the design of the high-performance OER catalyst by interfacial engineering strategy.

摘要

设计高性能、低成本的析氧反应(OER)电催化剂用于水分解,对于可再生氢能的发展至关重要。在此,我们展示了一种界面工程策略,用于制备负载在碳布上的铁掺杂CoP纳米立方体/CoP纳米片阵列异质结构(记为CoFeP/CoP/CC)。所得的CoFeP/CoP/CC异质结构催化剂具有丰富的异质界面,这使得反应活性位点得以暴露,并可能调节催化剂的电子结构。此外,CoFeP和CoP之间这种强大的界面耦合以及碳布上的集成结构保证了高电子导电性和增强的机械稳定性。受益于这些优势,CoFeP/CoP/CC异质结构表现出高的电催化OER性能,在达到10 mA cm的电流密度时过电位低至240 mV,优于商业贵金属RuO(255 mV)和许多已报道的基于过渡金属磷化物(TMPs)的电催化剂。此外,这种CoFeP/CoP/CC催化剂在超过100小时的时间内表现出显著的OER催化稳定性。这项工作通过界面工程策略为高性能OER催化剂的设计提供了一条有效途径。

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