Amorphous Ir atomic clusters anchored on crystalline IrO2 nanoneedles for proton exchange membrane water oxidation

被引:36
作者
Lim, Jinkyu [1 ]
Kang, Gihun [1 ]
Jeon, Hyeseong [1 ]
Lee, Hyunjoo [1 ]
Lee, Jae Won [1 ]
Jeon, Sun Seo [1 ]
Kang, Phil Woong [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
Ir minimization; Nanoneedles; Atomic clusters; OER; PEMWE; OXYGEN EVOLUTION REACTION; ELECTROCATALYTIC OXYGEN; IRIDIUM; STABILITY; EFFICIENT; CATALYSTS; NANOPARTICLES; DURABILITY; MECHANISMS; OXIDES;
D O I
10.1016/j.jpowsour.2022.231069
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Proton exchange membrane water electrolysis (PEMWE) is a promising way to produce green hydrogen utilizing intermittent renewable energy. While Ir is the only catalyst with good activity and durability for PEMWE, Ir is the rarest material on earth. Ir minimization is crucial to expand the application of PEMWE. Previously, we reported ultrathin IrO2 nanoneedles (NN) for oxygen evolution reaction (OER) in PEMWE. Although IrO2 NN showed good electrical conductivity, its activity should be improved. Here, the OER activity of the NNs is further improved by depositing amorphous Ir atomic clusters (AC) on the one-dimensional NNs. The amorphous Ir ACs are highly active for the OER and the crystalline NN backbone aids facile electron transfers to the surface ACs. The het-erostructure of the Ir AC/NN catalysts decouple a trade-off relation between the OER activity and durability. PEMWE with the Ir AC/NN catalysts achieves a current density of 3 A cm(-2) at only 1.82 V and operates stably for more than 90 h, whereas pristine IrO2 NN and IrO2 particles synthesized by Adams-fusion method require higher potentials of 1.92 V and 1.97 V, respectively, at 3 A cm(-2).
引用
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页数:7
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