Journal:Nat. Commun.
Abstract:Seawater electrolysis using renewable electricity offers an attractive route to sustainable hydrogen production, but the sluggish electrode kinetics and poor durability are two major challenges. We report a molybdenum nitride (Mo2N) catalyst for the hydrogen evolution reaction with activity comparable to commercial platinum on carbon (Pt/C) catalyst in natural seawater. The catalyst operates more than 1000 hours of continuous testing at 100 mA cm−2 without egradation, whereas massive precipitate (mainly magnesium hydroxide) forms on the Pt/C counterpart after 36 hours of operation at 10 mA cm−2. Our investigation reveals that ammonium groups generate in situ at the catalyst surface, which not only improve the connectivity of hydrogenbond networks but also suppress the local pH increase, enabling the enhanced performances. Moreover, a zero-gap membrane flow electrolyser assembled by this catalyst exhibits a current density of 1 A cm−2 at 1.87 V and 60 oC in simulated seawater and runs steadily over 900 hours.
Note:Xiao-Long Zhang†, Peng-Cheng Yu†, Shu-Ping Sun†, Lei Shi, Peng-Peng Yang, Zhi-Zheng Wu, Li-Ping Chi, Ya-Rong Zheng,* , and Min-Rui Gao*
Indexed by:Journal paper
Volume:15
Page Number:9462
Translation or Not:no
Date of Publication:2024-11-01
Links to published journals:https://www.nature.com/articles/s41467-024-53724-1
Researcher
Supervisor of Doctorate Candidates
Supervisor of Master's Candidates
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School/Department:Department of Chemistry
Administrative Position:化学系系主任
Education Level:Postgraduate (Doctoral)
Business Address:Shenghua Building Room 301
Gender:Male
Degree:Doctoral degree
Status:Employed
Alma Mater:University of Science and Technology
Discipline:Inorganic Chemistry
Physical Chemistry
Material Science
Applied Chemistry
Honors and Titles:
安徽省高层次人才青年项目
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