A Composite Catalyst Based on Perovskites for Overall Water Splitting in Alkaline Conditions

被引:47
作者
Bu, Yunfei [1 ]
Kim, Seona [2 ]
Kwon, Ohhun [2 ]
Zhong, Qin [3 ]
Kim, Guntae [2 ]
机构
[1] NUIST, Sch Environm Sci & Engn, Jiangsu Collaborat Innovat Ctr Atmospher Environm, Nanjing 210044, Jiangsu, Peoples R China
[2] UNIST, Dept Energy Engn, Ulsan 44919, South Korea
[3] Nanjing Univ Sci & Technol, Sch Chem & Engn, Nanjing 210094, Jiangsu, Peoples R China
基金
新加坡国家研究基金会; 中国国家自然科学基金;
关键词
perovskite oxides; electrocatalysts; overall water splitting; composites; sulfuration; N-DOPED GRAPHENE; OXYGEN REDUCTION; ANODE MATERIAL; BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT; OXIDE; PERFORMANCE; CARBON; NANOPARTICLES; STABILITY;
D O I
10.1002/celc.201801775
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical water splitting is considered a sustainable way to produce H-2. However, it is still a challenge to develop efficient and stable electrocatalysts. Here, a bifunctional composite catalyst for the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) was constructed by using a facile insitu growth route, which combines the carbonization on exsolved alloy nanoparticles and sulfurization in one continues step. This composite catalyst contains Ruddlesden-Popper-type S-adsorbed (Nd0.6Sr0.4)(3)((Co,Fe)(0.85)Nb-0.15)(2)O-7, metal sulfides, and hollow S-doped carbon fibers. Compared to the untreated catalyst, Nd0.6Sr0.4Co0.6Fe0.3Nb0.1O3-delta, the composite catalyst leads to significantly enhanced OER and HER activities as well as excellent stability (more than 400 h without inactivation) during overall water splitting. Our research offers a new route to fabricate hetero-architecture materials with S-doped hollow carbon fibers on alloy nanoparticles of perovskite oxides.
引用
收藏
页码:1520 / 1524
页数:5
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