Metal-metal interactions in correlated single-atom catalysts

被引:174
|
作者
Shan, Jieqiong [1 ]
Ye, Chao [1 ]
Jiang, Yunling [1 ]
Jaroniec, Mietek [2 ,3 ]
Zheng, Yao [1 ]
Qiao, Shi-Zhang [1 ]
机构
[1] Univ Adelaide, Sch Chem Engn & Adv Mat, Adelaide, SA 5005, Australia
[2] Kent State Univ, Dept Chem & Biochem, Kent, OH 44242 USA
[3] Kent State Univ, Adv Mat & Liquid Crystal Inst, Kent, OH 44242 USA
基金
澳大利亚研究理事会;
关键词
ACTIVE-SITES; OXYGEN REDUCTION; NANOPARTICLE CATALYSTS; COORDINATION STRUCTURE; PERFORMANCE; PLATINUM; DIMERS; ELECTROCATALYST; CLUSTERS; DESIGN;
D O I
10.1126/sciadv.abo0762
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single-atom catalysts (SACs) include a promising family of electrocatalysts with unique geometric structures. Beyond conventional ones with fully isolated metal sites, an emerging class of catalysts with the adjacent metal single atoms exhibiting intersite metal-metal interactions appear in recent years and can be denoted as correlated SACs (C-SACs). This type of catalysts provides more opportunities to achieve substantial structural modification and performance enhancement toward a wider range of electrocatalytic applications. On the basis of a clear identification of metal-metal interactions, this review critically examines the recent research progress in C-SACs. It shows that the control of metal-metal interactions enables regulation of atomic structure, local coordination, and electronic properties of metal single atoms, which facilitate the modulation of electrocatalytic behavior of C-SACs. Last, we outline directions for future work in the design and development of C-SACs, which is indispensable for creating high-performing new SAC architectures.
引用
收藏
页数:14
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