Favorable role of heterojunction in trimetallic Fe-Co-Cu phosphides on nitrogen-doped carbon materials for hydrogen evolution

被引:10
|
作者
Li, S. [1 ]
Zhang, Q. [2 ]
Sun, J. [1 ]
Guan, J. [2 ]
机构
[1] Changchun Univ Technol, Sch Chem & Life Sci, Changchun 130012, Jilin, Peoples R China
[2] Jilin Univ, Key Lab Surface & Interface Chem Jilin Prov, Coll Chem, Changchun 130021, Peoples R China
关键词
Cobalt phosphide; Copper phosphide; Graphene; Hydrogen evolution reaction; Iron phosphide; OXYGEN REDUCTION REACTION; BIMETALLIC PHOSPHIDES; ENERGY-STORAGE; EFFICIENT; CATALYSTS; FRAMEWORK; ALKALINE; ARRAY; NANOARRAYS; NANOSHEETS;
D O I
10.1016/j.mtener.2020.100464
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
Development of high-efficiency and cost-efficient electrocatalysts is vital for hydrogen generation by electrochemical water splitting. Here we report a facile two-step approach to fabricate trimetallic Fe/Co/Cu-based phosphides embedded onto nitrogen-doped carbon-graphene (FeCoCuP@NC). The FeCoCuP@NC exhibits excellent electrocatalytic hydrogen evolution reaction (HER) performance with low overpotential and durable long-term stability in both acidic and alkaline conditions. To reach a current density of 10 mA/cm(2), FeCoCuP@NC requires overpotential of 80 and 169 mV in 0.5 M H2SO4 and 1.0 M KOH, respectively. The superior HER performance of FeCoCuP@NC could be attributed to the formation of heterojunctions between different phosphides and the synergetic action between active phosphides and N-doped carbon-graphene matrix. This work affords a feasible strategy to fabricate trimetallic transition metal phosphides embedded onto carbonaceous materials using metal-organic frameworks as precursors for energy and environmental applications. (C) 2020 Elsevier Ltd. All rights reserved.
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页数:9
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