N, P-co-doped carbon coupled with CoP as superior electrocatalysts for hydrogen evolution reaction and overall water splitting

被引:32
作者
Chen, Zequn [1 ]
Jia, Hongfu [1 ]
Yuan, Jingrun [1 ]
Liu, Xi [2 ]
Fang, Chaohe [3 ]
Fan, Yunying [4 ]
Cao, Chuanbao [1 ]
Chen, Zhuo [1 ]
机构
[1] Beijing Inst Technol, Sch Mat Sci & Engn, Dept Mat Phys & Chem, Beijing 100081, Peoples R China
[2] Synfuels China Technol Co Ltd, SynCat Beijing, Beijing 101407, Peoples R China
[3] PetroChina Res Inst Petr Explorat & Dev, Langfang 065007, Hebei, Peoples R China
[4] Kunming Univ Sci & Technol, Fac Mat Sci & Engn, Kunming 650093, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
CoP; N; P-co-doped carbon; Electrocatalyst; Hydrogen evolution reaction; Water splitting; EFFICIENT HYDROGEN; OXYGEN EVOLUTION; EMBEDDED N; PHOSPHIDE; CATALYSTS; GRAPHENE; NANOSHEETS; NANOWIRE; CATHODE; CLOTH;
D O I
10.1016/j.ijhydene.2019.07.185
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
To achieve high activity and stability for both hydrogen and oxygen evolution reactions through the non-precious-metal based electrocatalysts is still facing the great challenge. Herein, we demonstrate a facile strategy to prepare CoP nanoparticles (NPs) loaded on N, P dual-doped carbon (NPC) electrocatalysts with high concentration N and P dopants through a pyrolysis-deposition-phosphidation process. The great bifunctional electrocatalytic activity for both HER (the overpotential of 98 mV and 86 mV at 10 mA cm(-2) in both 0.5 M H2SO4 and 1 M KOH electrolytes, respectively) and OER (the overpotential of 300 mV at 10 mA cm(-2) in 1 M KOH electrolyte) were achieved. When CoP@NPC hybrid was used as two electrodes in the 1 M KOH electrolyte system for overall water splitting, the needed cell potential for achieving the current density of 10 mA cm(-2) is 1.6 V, and it also showed superior stability for HER and OER after 10 h' test with almost negligible decay. Experimental results revealed that the P atoms in CoP were the active sites for HER and the CoP@NPC hybrid showed excellent bifunctional electrocatalytic properties due to the synergistic effects between the high catalytic activity of CoP NPs and NPC, in which the doping of N and P in carbon led to a stronger polarization between Co and P in CoP, promoting the charge transfer from Co to P in CoP, enhancing the catalytic activity of P sites and Co sites in CoP for HER and OER, respectively. Specifically, the improvements could result from the changed charge state, the increased active specific surface area, and the facilitated reaction kinetics by N, P co-doping and admixture. This work provides a high-efficient, low-cost and stable electrocatalyst for overall water splitting, and throws light on rational designing high performance electrocatalysts. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:24342 / 24352
页数:11
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