Molybdenum-Incorporated Mesoporous Silica: Surface Engineering toward Enhanced Metal-Support Interactions and Efficient Hydrogenation

被引:22
|
作者
Chen, Ting [1 ]
Shi, Zhangping [2 ,3 ]
Zhang, Guanghui [4 ]
Chan, Hang Cheong [1 ]
Shu, Yijin [1 ]
Gao, Qingsheng [1 ]
Tang, Yi [2 ,3 ]
机构
[1] Jinan Univ, Dept Chem, Coll Chem & Mat Sci, Guangzhou 510632, Guangdong, Peoples R China
[2] Fudan Univ, Adv Mat Lab, Shanghai Key Lab Mol Catalysis & Innovat Mat, Dept Chem, Shanghai 200433, Peoples R China
[3] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, Shanghai 200433, Peoples R China
[4] Purdue Univ, Davidson Sch Chem Engn, W Lafayette, IN 47907 USA
基金
中国国家自然科学基金;
关键词
metal-support interactions; mesoporous silica; surface engineering; iridium; hydrogenation; CHEMOSELECTIVE HYDROGENATION; CO OXIDATION; CATALYSTS; SBA-15; OXIDE; NANOPARTICLES; PERFORMANCES; REDUCTION; STRATEGY; NANORODS;
D O I
10.1021/acsami.8b16496
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In heterogeneous catalysis, strong metal-support interactions are highly desired to improve catalytic turnover on metal catalysts. Herein, molybdenum is uniformly incorporated into mesoporous silica (KIT-6) to accomplish strong interactions with iridium catalysts, and consequently, active and selective hydrogenation of carbonyl compounds. Mo-incorporated KIT-6 (Mo-KIT-6) affords electronic interactions to improve the proportion of metallic Ir-0 species, avoiding the easy surface oxidation of ultrafine metals in silica mesocavities. Owing to the effective H-2 activation and subsequent hydrogenation on metallic Ir-0 sites, optimal Ir/Mo-KIT-6 with a high Ir-0/Ir delta+ ratio delivers prominent performance in the hydrogenation of amides to amines and alpha,beta-unsaturated aldehydes to unsaturated alcohols. As for N-acetylmorpholine hydrogenation, the Ir/Mo-KIT-6 catalyst achieves efficient turnover toward N-ethylmorpholine with high selectivity (>99%) and exhibits activity that relies on the engineered chemical state of Ir sites. Such promotion is further proved to be universal in cinnamaldehyde hydrogenation. This work will provide new opportunities for catalyst design through surface/interface engineering.
引用
收藏
页码:42475 / 42483
页数:9
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