Co2P2O7@MoO3/NF composite electrocatalysts by different phosphorus sources for efficient oxygen evolution reaction and overall water splitting

IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL
Tongtong Li, Wan Wan, Yali Cao, Jialing Xu, Hui Chai
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Abstract

Electrocatalysts comprising MoO3 coated by Co2P2O7 nanocrystals were grown on a nickel foam (NF) substrate. The applicability of the nanocomposite material (Co2P2O7@MoO3/NF) as an electrode for the oxygen evolution reaction (OER) and overall water splitting was verified. The as-synthesized product showed the overpotentials of 227 and 377 mV to drive the OER at current densities of 50 and 100 mA cm−2, respectively. Furthermore, the voltage of Co2P2O7@MoO3/NF as a bifunctional overall water splitting catalyst was 1.55 V at 10 mA cm−2. Co2P2O7@MoO3/NF@NF (+)//Co2P2O7@MoO3/NF (−) can maintain >80% of its initial current density after 30 h at 15 mA cm−2. The Co2P2O7@MoO3/NF electrode also showed a low hydrogen evolution reaction overpotential of 58.7 mV at 10 mA cm−2. The excellent oxygen evolution and electrochemical water decomposition stability of the catalyst have broad application prospects.

Abstract Image

Co2P2O7@MoO3/NF复合电催化剂采用不同磷源进行高效析氧反应和整体水分解
在泡沫镍(NF)基底上生长包含由Co2P2O7纳米晶体涂覆的MoO3的电催化剂。纳米复合材料的适用性(Co2P2O7@MoO3/NF)作为析氧反应(OER)的电极和总的水分解得到验证。合成的产物在50和100 mA cm−2的电流密度下分别显示出227和377 mV的超电势来驱动OER。此外Co2P2O7@MoO3/NF作为一种双功能整体水分解催化剂,在10mA cm−2下为1.55V。Co2P2O7@MoO3/NF@NF(+)//Co2P2O7@MoO3/NF(−)可以维持>;在15 mA cm−2下30小时后其初始电流密度的80%。这个Co2P2O7@MoO3/NF电极在10 mA cm−2时也显示出58.7 mV的低析氢反应过电位。该催化剂具有优异的析氧性和电化学水分解稳定性,具有广阔的应用前景。
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来源期刊
Colloid and Interface Science Communications
Colloid and Interface Science Communications Materials Science-Materials Chemistry
CiteScore
9.40
自引率
6.70%
发文量
125
审稿时长
43 days
期刊介绍: Colloid and Interface Science Communications provides a forum for the highest visibility and rapid publication of short initial reports on new fundamental concepts, research findings, and topical applications at the forefront of the increasingly interdisciplinary area of colloid and interface science.
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