Thiamine Pyrophosphate-Enhanced NiFe Layered Double Hydroxide for Robust and Durable Seawater Oxidation Electrocatalysis

被引:0
|
作者
Li, Ran [1 ,4 ]
Zhang, Min [3 ]
Peng, Jiaoying [1 ]
Sun, Shengjun [3 ]
Zhang, Gang [1 ]
Cai, Zhengwei [3 ]
Wang, Xiaoyan [3 ]
Song, Jiayun [3 ]
He, Xun [2 ]
Yao, Yongchao [1 ,2 ]
Sun, Xuping [2 ,3 ]
Luo, Jianbin [4 ]
Hu, Wenchuang [1 ]
机构
[1] Sichuan Univ, West China Hosp, Precis Med Translat Res Ctr, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Ctr High Altitude Med, Chengdu 610041, Sichuan, Peoples R China
[3] Shandong Normal Univ, Coll Chem Chem Engn & Mat Sci, Jinan 250014, Shandong, Peoples R China
[4] Southwest Minzu Univ, Coll Chem & Environm, Chengdu 610041, Sichuan, Peoples R China
关键词
NiFe layered double hydroxide; seawater electrolysis; oxygen evolution reaction; thiamine pyrophosphate; chlorine-resistant; EFFICIENT; EVOLUTION;
D O I
10.1021/acsanm.4c06382
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Seawater electrolysis has garnered considerable interest as an environmentally sustainable method for hydrogen production. However, the abundance of chloride ions in seawater poses a challenge to electrocatalyst stability, underscoring the need for catalysts with exceptional durability and efficiency to facilitate effective seawater oxidation. In this study, thiamine pyrophosphate (TPP) was intercalated into a NiFe layered double hydroxide on nickel foam (NF/NiFe LDH), creating an advanced seawater oxidation electrocatalyst (NF/NiFe LDH@TPP) that effectively resists chloride-induced corrosion. Remarkably, the TPP-intercalated catalyst demonstrates superior kinetics and selectivity for the oxygen evolution reaction, reaching a current density of 1 A cm-2 with an overpotential as low as 385 mV, while sustaining stable seawater oxidation performance for over 500 h.
引用
收藏
页码:1332 / 1337
页数:6
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