析氧
材料科学
分解水
塔菲尔方程
催化作用
氧化物
阳极
化学工程
电催化剂
双金属
电子转移
退火(玻璃)
纳米技术
电化学
电极
冶金
物理化学
工程类
光催化
生物化学
化学
作者
Yangde Ma,Xiaoping Dai,Mengzhao Liu,Jiaxi Yong,Hongyan Qiao,Axiang Jin,Zhanzhao Li,Xingliang Huang,Hai Wang,Xin Zhang
标识
DOI:10.1021/acsami.6b11821
摘要
Hydrogen produced from electrocatalytic water splitting is a promising route due to the sustainable powers derived from the solar and wind energy. However, the sluggish kinetics at the anode for water splitting makes the highly effective and inexpensive electrocatalysts desirable in oxygen evolution reaction (OER) by structure and composition modulations. Metal–organic frameworks (MOFs) have been intensively used as the templates/precursors to synthesize complex hollow structures for various energy-related applications. Herein, an effective and facile template-engaged strategy originated from bimetal MOFs is developed to construct hollow microcubes assembled by interconnected nanopolyhedron, consisting of intimately dominant FeNi alloys coupled with a small NiFe2O4 oxide, which was confined within carbonitride outer shell (denoted as FeNi/NiFe2O4@NC) via one-step annealing treatment. The optimized FeNi/NiFe2O4@NC exhibits excellent electrocatalytic performances toward OER in alkaline media, showing 10 mA·cm–2 at η = 316 mV, lower Tafel slope (60 mV·dec–1), and excellent durability without decay after 5000 CV cycles, which also surpasses the IrO2 catalyst and most of non-noble catalysts in the OER, demonstrating a great perspective. The superior OER performance is ascribed to the hollow interior for fast mass transport, in situ formed strong coupling between FeNi alloys and NiFe2O4 for electron transfer, and the protection of carbonitride layers for long stability.
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