Recent advances on surface metal hydrides studied by solidstate nuclear magnetic resonance spectroscopy

被引:5
|
作者
Gao, Pan [1 ]
Hou, Guangjin [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Collaborat Innovat Ctr Chem Energy Mat 2011, State Key Lab Catalysis,Dalian Natl Lab Clean Ener, 457 Zhongshan Rd, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal hydrides; Surface chemistry; Intermediate; Solid-state NMR; Heterogeneous catalysis; INTEGER QUADRUPOLAR NUCLEI; CHEMICAL-SHIFT CORRELATION; QUANTUM NMR-SPECTROSCOPY; C-H BOND; STATE NMR; HETEROLYTIC DISSOCIATION; ORGANOMETALLIC CHEMISTRY; HETEROGENEOUS CATALYSIS; METHANE ACTIVATION; ALUMINUM-HYDRIDE;
D O I
10.1016/j.mrl.2022.09.001
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
Metal hydrides (M -H) on solid surfaces, i.e., surface M -H, are ubiquitous but critical species in heterogeneous catalysis, and their intermediate roles have been proposed in numerous reactions such as (de)hydrogenation and alkanes activation, etc., however, the detailed spectroscopic characterizations remain challenging. Solid-state nuclear magnetic resonance (ssNMR) spectroscopy has become a powerful tool in surface studies, as it provides access to local structural characterizations at atomic level from multiple views, with comprehensive information on chemical bonding and spatial structures. In this review, we summarized and discussed the latest research developments on the successful application of ssNMR to characterize surface M -H species on solid catalysts including supported single -site heterogeneous catalysts, bulk metal oxides and metalmodified zeolites. We also discussed the opportunities and challenges in this field, as well as the potential application/development of state-of-the-art ssNMR technologies to enable further exploration of metal hydrides in heterogeneous catalysis. (c) 2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. This is an open access article under the CC BY -NC -ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:31 / 42
页数:12
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