High-Performing Atomic Electrocatalyst for Chlorine Evolution Reaction

被引:28
|
作者
Ha, Miran [1 ]
Thangavel, Pandiarajan [1 ]
Dang, Ngoc Kim [1 ]
Kim, Dong Yeon [1 ]
Sultan, Siraj [1 ]
Lee, Jae Sung [2 ]
Kim, Kwang S. [1 ]
机构
[1] Ulsan Natl Inst Sci & Technol UNIST, Ctr Superfunct Mat, Dept Chem, 50 UNIST Gil, Ulsan 44919, South Korea
[2] Ulsan Natl Inst Sci & Technol UNIST, Sch Energy & Chem Engn, 50 UNIST Gil, Ulsan 44919, South Korea
基金
新加坡国家研究基金会;
关键词
chlorine evolution reaction; electrocatalysts; metal single atom catalysts; N-doped graphene; Pt single atoms; CHLORALKALI PROCESS; ACTIVE-SITES; OXYGEN; SELECTIVITY; REDUCTION; EFFICIENT; PLATINUM; HISTORY;
D O I
10.1002/smll.202300240
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalysts facilitating chlorine evolution reaction (ClER) play a vital role in chlor-alkali industries. Owing to a huge amount of chlorine consumed worldwide, inexpensive high-performing catalysts for Cl-2 production are highly demanded. Here, a superb ClER catalyst fabricated through uniform dispersion of Pt single atoms (SAs) in -C2N2 moieties of N-doped graphene (denoted as Pt-1) is presented, which demonstrates near 100% exclusive ClER selectivity, long-term durability, extraordinary Cl-2 production rate (3500 mmol h(-1) g(Pt)(-1)), and >140 000-fold increased mass activity over industrial electrodes in acidic medium. Excitingly, at the typical chlor-alkali industries' operating temperature (80 degrees C), Pt-1 supported on carbon paper electrode requires a near thermoneutral ultralow overpotential of 5 mV at 1 mA cm(-2) current density to initiate the ClER, consistent with the predicted density functional theory (DFT) calculations. Altogether these results show the promising electrocatalyst of Pt-1 toward ClER.
引用
收藏
页数:8
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