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可扩展合成自组装双金属磷化物/N掺杂石墨烯纳米片作为用于全水分裂的高效电催化剂。

Scalable synthesis of self-assembled bimetallic phosphide/N-doped graphene nanoflakes as an efficient electrocatalyst for overall water splitting.

作者信息

Yang Dongxu, Hou Wenqiang, Lu Yingjiong, Zhang Wanli, Chen Yuanfu

机构信息

School of Electronic Science and Engineering, and State Key Laboratory of Electronic Thin Films and Integrated Devices, University of Electronic Science and Technology of China, Chengdu 610054, PR China.

出版信息

Nanoscale. 2019 Jul 21;11(27):12837-12845. doi: 10.1039/c9nr03614h. Epub 2019 Jun 19.

Abstract

In order to achieve clean hydrogen energy through overall water splitting, it is vitally important but still challenging to develop highly efficient and low-cost electrocatalysts to replace the noble metal-based electrocatalysts (e.g. Pt- and Ru-based catalysts). To address this issue, herein, we present a facile and scalable spray drying and subsequent phosphorization approach to synthesize iron-cobalt bimetallic nanoflakes encapsulated in N-doped graphene (FCP@NG). The optimized FCP@NG exhibits excellent performance in the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and overall water splitting. It demonstrates remarkable performance in the HER and superior activity in the OER, even outperforming the state-of-the-art RuO catalyst. Being employed as both the cathode and anode on nickel foams, this FCP@NG hybrid demonstrates promising performance in overall water splitting with a very low potential of 1.63 V to deliver a current density of 10 mA cm, which is superior among most of the recently reported transition-metal-based catalysts and comparable to the commercial Pt/RuO cell. The outstanding electrocatalytic performance of FCP@NG is attributed to a synergistic effect of its bi-metallization, unique nanoflake structure and conductive N-doped graphene encapsulation. This work provides a scalable and low-cost strategy to synthesize nonprecious and bi-functional transition-metal-based catalysts with unique nanoarchitecture and outstanding catalytic performance for overall water splitting.

摘要

为了通过全水解实现清洁氢能,开发高效且低成本的电催化剂以替代基于贵金属的电催化剂(如基于Pt和Ru的催化剂)至关重要但仍具有挑战性。为了解决这个问题,在此我们提出一种简便且可扩展的喷雾干燥及后续磷化方法来合成包裹在N掺杂石墨烯中的铁钴双金属纳米片(FCP@NG)。优化后的FCP@NG在析氢反应(HER)、析氧反应(OER)和全水解中表现出优异的性能。它在HER中表现出卓越性能,在OER中具有出色活性,甚至优于目前最先进的RuO催化剂。将这种FCP@NG用作泡沫镍上的阴极和阳极,该复合材料在全水解中展现出有前景的性能,在极低的1.63 V电位下即可达到10 mA cm的电流密度,这在大多数最近报道的基于过渡金属的催化剂中表现优异,且与商业Pt/RuO电池相当。FCP@NG出色的电催化性能归因于其双金属化、独特的纳米片结构和导电的N掺杂石墨烯封装的协同效应。这项工作提供了一种可扩展且低成本的策略,用于合成具有独特纳米结构和出色全水解催化性能的非贵金属双功能过渡金属基催化剂。

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