d-sp orbital hybridization: a strategy for activity improvement of transition metal catalysts

被引:88
作者
Chen, Hui [1 ]
Wu, Qiannan [1 ]
Wang, Yanfei [2 ]
Zhao, Qinfeng [2 ]
Ai, Xuan [1 ]
Shen, Yucheng [1 ]
Zou, Xiaoxin [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, 2699 Qianjin St, Changchun 130012, Peoples R China
[2] Petrochina Petrochem Res Inst, Beijing 102206, Peoples R China
基金
中国国家自然科学基金;
关键词
SINGLE-ATOM CATALYSTS; ELECTRONIC-STRUCTURE; HYDROGEN EVOLUTION; REDUCTION REACTION; SUBSURFACE CARBON; CO2; REDUCTION; BORON; NANOPARTICLES; PERFORMANCE; SELECTIVITY;
D O I
10.1039/d2cc02299k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Orbital hybridization to regulate the electronic structures and surface chemisorption properties of transition metals has been extensively investigated for searching high-performance catalysts toward various reactions. Unlike conventional d-d hybridization, the d-sp hybridization interaction between transition metals and p-block elements could result in surprising electronic properties and catalytic activities. This feature article highlights the recent progress in the development of high-performance transition metal-based catalysts through the extraordinary d-sp hybridization strategy, particularly for energy-related electrocatalytic applications. We start by giving an introduction of fundamental concepts associated with electronic structures of transition metal catalysts, including the Sabatier principle, d-band theory, electronic descriptor, as well as the comparison of d-d hybridization and d-sp hybridization strategies. Then, we summarize the theoretical and experimental advances in d-sp hybridization catalysts, including p-block element-doped metal catalysts, intermetallic catalysts and supported metal catalysts, with emphasis on the important roles of d-sp hybridization in tuning catalytic performances. Finally, we present existing challenges and future development prospects for the rational design of advanced d-sp hybridization catalysts.
引用
收藏
页码:7730 / 7740
页数:11
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