Affiliation:
1. College of Biological Chemical Sciences and Engineering Jiaxing University Jiaxing Zhejiang 314001 China
2. College of Chemical Engineering Zhejiang University of Technology Hangzhou Zhejiang 310014 China
3. Peter the Great Saint‐Petersburg Polytechnic University Saint Petersburg 195251 Russia
4. Jiangsu Key Laboratory of Electrochemical Energy Storage Technologies College of Materials Science and Technology Nanjing University of Aeronautics and Astronautics Nanjing 210016 China
Abstract
AbstractIt is not enough to develop an ideal hydrogen evolution reaction (HER) electrocatalysts by single strategy. Here, the HER performances are significantly improved by the combined strategies of P and Se binary vacancies and heterostructure engineering, which is rarely explored and remain unclear. As a result, the overpotentials of MoP/MoSe2‐H heterostructures rich in P and Se binary vacancies are 47 and 110 mV at 10 mA cm−2 in 1 m KOH and 0.5 m H2SO4 electrolytes, respectively. Especially, in 1 m KOH, the overpotential of MoP/MoSe2‐H is very close to commercial Pt/C at the beginning and even better than Pt/C when current density is over 70 mA cm−2. The strong interactions between MoSe2 and MoP facilitate electrons transfer from P to Se. Thus, MoP/MoSe2‐H possesses more electrochemically active sites and faster charge transfer capability, which are all in favor of high HER activities. Additionally, Zn‐H2O battery with MoP/MoSe2‐H as cathode is fabricated for simultaneous generation of hydrogen and electricity, which displays the maximum power density of up to 28.1 mW cm−2 and stable discharging performance for 125 h. Overall, this work validates a vigorous strategy and provides guidance for the development of efficient HER electrocatalysts.
Funder
National Natural Science Foundation of China
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
29 articles.
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