NiCoP nanoarchitectures: One-step controlled electrodeposition and their application as efficient electrocatalysts for boosting hydrogen evolution reaction

被引:0
|
作者
Mohammadi, Omid [1 ]
Bahari, Yaser [1 ]
Daryakenari, Ahmad Ahmadi [1 ]
Koldeh, Fatemeh Jalali [1 ]
Zhang, Xiaoran [2 ]
Tian, Zhi Qun [2 ]
Shen, Pei Kang [2 ]
机构
[1] Univ Guilan, Fac Engn, Nanotechnol Dept, Rasht, Iran
[2] Guangxi Univ, Collaborat Innovat Ctr Sustainable Energy Mat, Guangxi Key Lab Electrochem Energy Mat, State Key Lab Proc Nonferrous, Nanning 530004, Peoples R China
基金
美国国家科学基金会;
关键词
NiCoP; Hydrogen evolution reaction; Nanostructures; Electrodeposition; Electrocatalyst; NI-CO-P; HIGHLY EFFICIENT; METAL PHOSPHIDES; NANOWIRE ARRAY; CARBON CLOTH; COBALT; FOAM; FILM; NANOPARTICLES; CATHODE;
D O I
10.1016/j.ijhydene.2022.08.087
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
Designing non-precious and long-lasting electrocatalysts with enhanced catalytic properties for hydrogen evolution reaction (HER) is a fundamental approach to address the needs for hydrogen industry and overcome the current challenges in sustainable energy generation. Herein, we present ternary NiCoP nanostructures synthesized through a direct and controlled electrochemical deposition at room temperature as highly efficient electrocatalysts for HER. Different Ni/Co ratios in the alloy were investigated resulting in different nanoarchitectured morphologies, chemical compositions and HER performances, in turn. The NiCoP-I alloy exhibited a nanoparticulated morphology comprising well-defined nanoparticles of similar to 20-30 nm which evolved to nanoparticulated caps at prolonged electrodeposition times presenting a large electrochemical surface area of 526 cm(2). The NiCoP -I electrocatalyst demonstrated a small Tafel slope of 49 mV dec(-1) and an ultra-low overpotential of 68 mV vs. RHE at -10 mA cm(-2) in alkaline solution which well rivals to that of Pt foil and outmatches its binary alloy counterparts. (C) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:34943 / 34954
页数:12
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