In Situ Formation of CoP/Co3O4 Heterojunction for Efficient Overall Water Splitting

Author:

Tian Guoliang1ORCID,Liu Xiaolei1,Song Shuhong1,Zhang Qianqian1,Wang Zeyan1,Liu Yuanyuan1,Zheng Zhaoke1,Cheng Hefeng1,Dai Ying2,Huang Baibiao1,Wang Peng1ORCID

Affiliation:

1. State Key Laboratory of Crystal Materials Shandong University Jinan 250100 P. R. China

2. School of Physics Shandong University Jinan 250100 P. R. China

Abstract

AbstractElectrochemical water splitting is an environmentally friendly and effective energy storage method. However, it is still a huge challenge to prepare non‐noble metal based electrocatalysts that possess high activity and long‐term durability to realize efficient water splitting. Here, we present a novel method of low‐temperature phosphating for preparing CoP/Co3O4 heterojunction nanowires catalyst on titanium mesh (TM) substrate that can be used for oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and overall water splitting. CoP/Co3O4@TM heterojunction showed an excellent catalytic performance and long‐term durability in 1.0 M KOH electrolyte. The overpotential of CoP/Co3O4@TM heterojunction was only 257 mV at 20 mA cm−2 during the OER process, and it could work stably more than 40 h at 1.52 V versus reversible hydrogen electrode (vs. RHE). During the HER process, the overpotential of CoP/Co3O4@TM heterojunction was only 98 mV at −10 mA cm−2. More importantly, when used as anodic and cathodic electrocatalyst, they achieved 10 mA cm−2 at 1.59 V. The Faradaic efficiencies of OER and HER were 98.4 % and 99.4 %, respectively, outperforming Ru/Ir‐based noble metal electrocatalysts and other non‐noble metal electrocatalysts for overall water splitting.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

National Key Research and Development Program of China

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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