Dual-metal hydroxide with ordering frustrated Lewis pairs for photoactivating CO2 to CO

被引:47
|
作者
Wang, Hailian [1 ,2 ]
Zhang, Weining [2 ,3 ]
Lu, Lei [2 ]
Liu, Depei [2 ,3 ]
Liu, Duanduan [2 ,3 ]
Li, Taozhu [2 ]
Yan, Shicheng [2 ]
Zhao, Siqin [1 ]
Zou, Zhigang [2 ,3 ]
机构
[1] Inner Mongolia Normal Univ, Chem & Environm Sci Coll, 81 Zhaowuda Rd, Hohhot 010022, Inner Mongolia, Peoples R China
[2] Nanjing Univ, Ecomat & Renewable Energy Res Ctr ERERC, Collaborat Innovat Ctr Adv Microstruct, Coll Engn & Appl Sci, 22 Hankou Rd, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Sch Phys, Natl Lab Solid State Microstruct, Jiangsu Key Lab Nano Technol, 22 Hankou Rd, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Frustrated lewis pairs; Hydroxides; Photocatalysis; CO2; reduction; Light-driven defects; INITIO MOLECULAR-DYNAMICS; SURFACE-CHEMISTRY; REDUCTION; PERFORMANCE; ADSORPTION;
D O I
10.1016/j.apcatb.2020.119639
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
To break challenges in creating frustrated Lewis pairs (FLPs) on highly stable inorganic materials, an ordering FLPs route is proposed by irradiation of dual-metal hydroxide with alternating light-stable and light-unstable terminal hydroxyls on dual-metal hydroxide. As a successful example, a single-crystal ZnSn(OH)(6) cube with a (100) surface of alternating Zn-OH and Sn-OH terminal hydroxyl groups is irradiated under 300 W Xe lamp to create oxygen vacancies (O-Vs, Lewis acid) via holes oxidizing light-unstable terminal hydroxyls at Sn sites. The FLPs are accordingly constructed between the photo-induced O-Vs and its proximal light-stable Zn-OH terminal hydroxyls (Lewis base), significantly contributing to the decreased barriers during capture, activation, and reduction of CO2 into CO with the assistance of H-2. The present findings are a big leap for designing highly stable FLPs-based inorganic solid catalysts.
引用
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页数:7
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