Intensified Kirkendall effect assisted construction of double-shell hollow Cu-doped CoP nanoparticles anchored by carbon arrays for water splitting

被引:69
|
作者
Wang, Xian [1 ,3 ]
Huang, Haigen [2 ]
Qian, Jinjie [3 ]
Li, Yingwei [1 ]
Shen, Kui [1 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, State Key Lab Pulp & Paper Engn, Guangzhou 510640, Peoples R China
[2] Jinggangshan Univ, Coll Chem & Chem Engn, Jian 343000, Peoples R China
[3] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325000, Peoples R China
基金
中国国家自然科学基金;
关键词
Double-shell hollow nanoparticles; Metal-organic framework; Kirkendall effect; Transition metal phosphide; Water splitting; OXYGEN; PHOSPHIDE; EXCHANGE;
D O I
10.1016/j.apcatb.2022.122295
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
Precisely engineering the architectures of nanoparticles (NPs) to optimize their physicochemical properties and thus electrocatalytic performances are challenging for scientists. Here, we report the controllable construction of solid, hollow, and double-shell hollow metal phosphide NPs anchored by carbon nanosheet arrays on carbon cloth. We demonstrate that Cu doping can intensify the nanoscale Kirkendall effect, which promotes the transformation from solid CuCo to double-shell hollow CoP NPs. Benefiting from its high dispersity, large electrochemical specific surface area, fast mass diffusion and good conductivity, the optimal double-shell hollow Cu-CoP-based electrocatalyst exhibits excellent activities for OER (eta 10 =176 mV) and water splitting (1.494 V @ 10 mA) in 1.0 M KOH with favorable stability. DFT calculations further confirm the optimized OH* adsorption energy of Cu-CoOOH/Cu-CoP due to Cu doping and interfacial synergy for boosting OER. This work provides new perspectives for engineering the nanoarchitecture of multilevel hollow NPs through the Kirkendall effect for electrocatalysis.
引用
收藏
页数:13
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