Hollow Mo-doped CoP nanoarrays for efficient overall water splitting

被引:623
|
作者
Guan, Cao [1 ]
Xiao, Wen [1 ]
Wu, Haijun [1 ]
Liu, Ximeng [1 ]
Zang, Wenjie [1 ]
Zhang, Hong [1 ]
Ding, Jun [1 ]
Feng, Yuan Ping [2 ]
Pennycook, Stephen J. [1 ]
Wang, John [1 ]
机构
[1] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore 117574, Singapore
[2] Natl Univ Singapore, Dept Phys, Singapore 117542, Singapore
关键词
Hollow nanoarrays; Binder-free; Metal phosphide; Electrochemical electrocatalyst; 2D metal-organic framework; HYDROGEN EVOLUTION REACTION; GENERALIZED GRADIENT APPROXIMATION; HIGH CATALYTIC-ACTIVITY; OXYGEN EVOLUTION; BIFUNCTIONAL ELECTROCATALYSTS; HIGHLY EFFICIENT; NANOWIRE ARRAYS; SURFACE; NANOSHEETS; GENERATION;
D O I
10.1016/j.nanoen.2018.03.034
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Earth-abundant, efficient and durable electrocatalysts for water splitting are vitally important for a sustainable energy system. Here we report the rational design of hollow Mo-doped CoP (Mo-CoP) nanoarrays, which simultaneously combine electronic structure modification through doping with a high density of reaction sites through nanostructuring. With this strategy the Mo-CoP arrays give significantly improved hydrogen evolution reaction (HER) performance, and also, when in situ transformed into Mo-doped CoOOH (Mo-CoOOH) arrays, excellent activity towards the oxygen evolution reaction (OER) is obtained. The origin of the improvement is determined by atomic-resolution imaging combined with density functional theory (DFT). An electrolyzer using Mo-CoP and Mo-CoOOH can be powered by a single AA battery (similar to 1.5 V), and maintains a stable water-splitting current for 20 h, superior to most reported electrocatalysts in alkaline media, offering great promise for practical applications.
引用
收藏
页码:73 / 80
页数:8
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