中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly Efficient Hydrosilylation of Ethyne over Pt/ZrO2 Catalysts with Size-Dependent Metal-Support Interactions

文献类型:期刊论文

作者Zhang, Tengfei1,2; Li, Mingyan1,3; Zheng, Peng3,4; Li, Jing5; Gao, Jiajian6; He, Hongyan7; Gu, Fangna1; Chen, Wenxing10; Ji, Yongjun11; Zhong, Ziyi8,9
刊名INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
出版日期2022-12-16
页码9
ISSN号0888-5885
DOI10.1021/acs.iecr.2c03553
英文摘要Replacing homogeneous noble-metal catalysts with supported catalysts in hydrosilylation reactions can overcome the difficulties of catalyst recovery and regeneration. Here, we report the scalable synthesis of heterogeneous Pt/ZrO2 catalysts with 1-5 wt % Pt supported on commercial ZrO2 nanocrystals. Pt/ZrO2 can effectively catalyze the hydrosilylation of triethoxysilane (TES) with ethyne to high-value triethoxyvinylsilane, even superior to the common homogeneous catalyst (H2PtCl6). Intensive characterizations indicate that the coating of ZrOx on Pt greatly depends on the size of Pt, with more ZrOx overlayers on smaller Pt metal particles. Among all the catalysts, 2Pt/ZrO2 exhibits the highest activity, optimal selectivity, and reusability toward hydrosilylation of TES with ethyne. The unusual catalytic properties of 2Pt/ZrO2 can be attributed to its more abundant surface PtOx species and the electron transfer between Pt and ZrO2. This change in local electronic properties promotes catalytic activity, which is also supported by the corresponding theoretical calculation. This work advances the understanding of metal-support interactions and provides a powerful approach to designing environmentally friendly heterogeneous catalysts for the industrially important hydrosilylation process.
WOS关键词TOTAL-ENERGY CALCULATIONS ; SINGLE-ATOM ; ALLYL CHLORIDE ; HIGH-DENSITY ; PLATINUM ; OXYGEN ; NANOPARTICLES ; ZRO2 ; SELECTIVITY ; ACTIVATION
资助项目Research Foundation for Advanced Talents of Beijing Technology and Business University ; Guangdong Key Discipline fund ; Youth Innovation Promotion Association of CAS ; [19008020159] ; [Y2021022]
WOS研究方向Engineering
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000901609500001
资助机构Research Foundation for Advanced Talents of Beijing Technology and Business University ; Guangdong Key Discipline fund ; Youth Innovation Promotion Association of CAS
源URL[http://ir.ipe.ac.cn/handle/122111/56218]  
专题中国科学院过程工程研究所
通讯作者Gu, Fangna; Chen, Wenxing; Ji, Yongjun; Su, Fabing
作者单位1.Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
3.Shenyang Univ Chem Technol, Minist Educ, Key Lab Resources Chem & Mat, Shenyang 110142, Peoples R China
4.Shenyang Univ Chem Technol, Inst Ind Chem & Energy Technol, Shenyang 110142, Peoples R China
5.China Three Gorges Corp, Inst Sci & Technol, Beijing 100049, Peoples R China
6.ASTAR, Inst Sustainabil Chem Energy & Environm, Jurong Isl 627833, Singapore
7.Chinese Acad Sci, Inst Proc Engn, Beijing Key Lab Ion Liquids Clean Proc, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
8.Guangdong Technion Israel Inst Technol GTIIT, Dept Chem Engn, Shantou 515063, Peoples R China
9.Technion Israel Inst Technol IIT, IL-32000 Haifa, Israel
10.Beijing Inst Technol, Energy & Catalysis Ctr, Sch Mat Sci & Engn, Beijing 100081, Peoples R China
推荐引用方式
GB/T 7714
Zhang, Tengfei,Li, Mingyan,Zheng, Peng,et al. Highly Efficient Hydrosilylation of Ethyne over Pt/ZrO2 Catalysts with Size-Dependent Metal-Support Interactions[J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,2022:9.
APA Zhang, Tengfei.,Li, Mingyan.,Zheng, Peng.,Li, Jing.,Gao, Jiajian.,...&Su, Fabing.(2022).Highly Efficient Hydrosilylation of Ethyne over Pt/ZrO2 Catalysts with Size-Dependent Metal-Support Interactions.INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,9.
MLA Zhang, Tengfei,et al."Highly Efficient Hydrosilylation of Ethyne over Pt/ZrO2 Catalysts with Size-Dependent Metal-Support Interactions".INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH (2022):9.

入库方式: OAI收割

来源:过程工程研究所

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