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A corrosion-resistant RuMoNi catalyst for efficient and long-lasting seawater oxidation and anion exchange membrane electrolyzer

文献类型：期刊论文

作者Kang, Xin2,6; Yang, Fengning2,3,6; Zhang, Zhiyuan2,6; Liu, Heming2,6; Ge, Shiyu2,6; Hu, Shuqi2,6; Li, Shaohai2,6; Luo, Yuting2,4,6; Yu, Qiangmin2,6; Liu, Zhibo5
刊名NATURE COMMUNICATIONS
出版日期2023-06-17
卷号14期号:1页码:10
DOI10.1038/s41467-023-39386-5
通讯作者Yu, Qiangmin(yu.qiangmin@sz.tsinghua.edu.cn) ; Liu, Bilu(bilu.liu@sz.tsinghua.edu.cn)
英文摘要Direct seawater electrolysis is promising for sustainable hydrogen production but suffers severe side reactions and corrosion. Here, the authors report a corrosion-resistant electrocatalyst with in situ-formed chloride-ion-repelling cation layer for efficient and long-lasting seawater oxidation. Direct seawater electrolysis is promising for sustainable hydrogen gas (H-2) production. However, the chloride ions in seawater lead to side reactions and corrosion, which result in a low efficiency and poor stability of the electrocatalyst and hinder the use of seawater electrolysis technology. Here we report a corrosion-resistant RuMoNi electrocatalyst, in which the in situ-formed molybdate ions on its surface repel chloride ions. The electrocatalyst works stably for over 3000 h at a high current density of 500 mA cm(-2) in alkaline seawater electrolytes. Using the RuMoNi catalyst in an anion exchange membrane electrolyzer, we report an energy conversion efficiency of 77.9% and a current density of 1000 mA cm(-2) at 1.72 V. The calculated price per gallon of gasoline equivalent (GGE) of the H-2 produced is $ 0.85, which is lower than the 2026 technical target of $ 2.0/GGE set by the United Stated Department of Energy, thus, suggesting practicability of the technology.
资助项目National Science Fund for Distinguished Young Scholars[52125309] ; National Natural Science Foundation of China[52188101] ; Guangdong Basic and Applied Basic Research Foundation[2021A1515110829] ; Guangdong Basic and Applied Basic Research Foundation[2022B1515120004] ; Guangdong Innovative and Entrepreneurial Research Team Program[2017ZT07C341] ; Shenzhen Basic Research Project[JCYJ20200109144620815] ; Shenzhen Basic Research Project[WDZC20220812141108001]
WOS研究方向Science & Technology - Other Topics
语种英语
WOS记录号WOS:001009499200009
出版者NATURE PORTFOLIO
资助机构National Science Fund for Distinguished Young Scholars ; National Natural Science Foundation of China ; Guangdong Basic and Applied Basic Research Foundation ; Guangdong Innovative and Entrepreneurial Research Team Program ; Shenzhen Basic Research Project
源URL[http://ir.imr.ac.cn/handle/321006/178438]  
专题金属研究所_中国科学院金属研究所
通讯作者Yu, Qiangmin; Liu, Bilu
作者单位1.Univ Surrey, Adv Technol Inst, Guildford GU2 7XH, England
2.Tsinghua Univ, Inst Mat Res, Tsinghua Shenzhen Int Grad Sch, Shenzhen 518055, Peoples R China
3.Univ Oxford, Dept Phys, Clarendon Lab, Parks Rd, Oxford OX1 3PU, England
4.Univ Toronto, Dept Elect & Comp Engn, 35 St George St, Toronto, ON M5S 1A4, Canada
5.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
6.Tsinghua Univ, Tsinghua Berkeley Shenzhen Inst, Shenzhen Geim Graphene Ctr, Shenzhen 518055, Peoples R China
7.Swinburne Univ Technol, Dept Chem & Biotechnol, Hawthorn, Vic 3122, Australia
8.Chinese Acad Sci, Inst Technol Carbon Neutral, Shenzhen Inst Adv Technol, Fac Mat Sci & Engn, Shenzhen 518055, Peoples R China
推荐引用方式
GB/T 7714		 Kang, Xin,Yang, Fengning,Zhang, Zhiyuan,et al. A corrosion-resistant RuMoNi catalyst for efficient and long-lasting seawater oxidation and anion exchange membrane electrolyzer[J]. NATURE COMMUNICATIONS,2023,14(1):10.
APA Kang, Xin.,Yang, Fengning.,Zhang, Zhiyuan.,Liu, Heming.,Ge, Shiyu.,...&Liu, Bilu.(2023).A corrosion-resistant RuMoNi catalyst for efficient and long-lasting seawater oxidation and anion exchange membrane electrolyzer.NATURE COMMUNICATIONS,14(1),10.
MLA Kang, Xin,et al."A corrosion-resistant RuMoNi catalyst for efficient and long-lasting seawater oxidation and anion exchange membrane electrolyzer".NATURE COMMUNICATIONS 14.1(2023):10.

入库方式： OAI收割

来源：金属研究所

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