材料科学
催化作用
过电位
双金属片
析氧
化学工程
纳米颗粒
过渡金属
金属
碳纤维
纳米笼
无机化学
纳米技术
电极
化学
有机化学
复合材料
电化学
冶金
物理化学
工程类
复合数
作者
Lei Du,Langli Luo,Zhenxing Feng,Mark Engelhard,Xiaohong Xie,Binghong Han,Junming Sun,Jianghao Zhang,Geping Yin,Chongmin Wang,Yong Wang,Yuyan Shao
出处
期刊:Nano Energy
[Elsevier]
日期:2017-07-05
卷期号:39: 245-252
被引量:152
标识
DOI:10.1016/j.nanoen.2017.07.006
摘要
Abstract Oxygen evolution reaction (OER) plays a crucial role in various energy conversion devices such as water electrolyzers and metal–air batteries. Precious metal catalysts such as Ir, Ru and their oxides are usually used for enhancing reaction kinetics but are limited by their scarcity. The challenges associated with alternative non–precious metal catalysts such as transition metal oxides and (oxy)hydroxides are their low electronic conductivity and durability. The carbon encapsulating transition metal nanoparticles are expected to address these challenges. However, the relationship between precursor compositions and catalyst properties, and the intrinsic functions of each component has been rarely studied. Herein, we report a highly durable (no degradation after 20,000 cycles) and highly active (360 mV overpotential at 10 mA cm–2GEO) OER catalyst derived from bimetallic metal–organic frameworks (MOFs) precursors. This catalyst consists of NiFe nanoparticles encapsulated by nitrogen–doped graphitized carbon shells. The electron–donation/deviation from Fe and tuned lattice and electronic structures of metal cores by Ni are revealed to be primary contributors to the enhanced OER activity, whereas N concentration contributes negligibly. We further demonstrated that the structure and morphology of encapsulating carbon shells, which are the key factors influencing the durability, are facilely controlled by the chemical state of precursors.
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