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Antisintering Pd-1 Catalyst for Propane Direct Dehydrogenation with In Situ Active Sites Regeneration Ability
Peng, Mi4,5,6; Jia, Zhimin7,8; Gao, Zirui4,5,6; Xu, Ming4,5,6; Cheng, Danyang4,5,6; Wang, Meng4,5,6; Li, Chengyu4,5,6; Wang, Linlin7,8; Cai, Xiangbin2,9; Jiang, Zheng3
刊名ACS CATALYSIS
2022-02-18
卷号12期号:4页码:2244-2252
关键词propane dehydrogenation nanodiamond palladium catalyst catalyst deactivation single-atom catalyst
ISSN号2155-5435
DOI10.1021/acscatal.1c05590
通讯作者Jiang, Hong(h.jiang@pku.edu.cn) ; Liu, Hongyang(liuhy@imr.ac.cn) ; Ma, Ding(dma@pku.edu.cn)
英文摘要Atomically dispersed Pd (Pd-1) catalysts supported on annealed nanodiamond were prepared through a deposition-precipitation method toward propane direct dehydrogenation (PDDH). The Pd-1 catalyst is superior to Pd cluster/particle catalysts in activity and stability. Combining experimental characterizations and DFT calculations revealed that atomically dispersed Pd species have strong interactions with the hybrid nanodiamond/graphene support, leading to better resistance to coke formation. More importantly, Pd sintering is inevitable in the cluster/particle catalysts, while the high dispersion of Pd species in Pd-1 catalyst is well-preserved during the reaction, which is caused in part by the redistribution or migration of Pd single atoms onto the carbonaceous compound (coke). As a result, the Pd-1 catalyst shows significantly better activity and stability in high-reaction temperatures than Pd cluster/particle catalysts. This work reveals deeper insights on designing highly dispersed metal catalysts with the ability of in situ regeneration of active sites in high-temperature catalytic reactions.
资助项目National Key R&D Program of China[2017YFB0602200] ; National Key R&D Program of China[2017YFB0307303] ; National Key R&D Program of China[2016YFA0204100] ; National Natural Science Foundation of China[21725301] ; National Natural Science Foundation of China[21821004] ; National Natural Science Foundation of China[91645115] ; National Natural Science Foundation of China[21473003] ; National Natural Science Foundation of China[21878008] ; National Natural Science Foundation of China[91845201] ; National Natural Science Foundation of China[21961160722] ; National Natural Science Foundation of China[22072162] ; National Natural Science Foundation of China[22005007] ; Liaoning Revitalization Talents Program[XLYC1907055] ; Sinopec China
WOS研究方向Chemistry
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000766237100013
资助机构National Key R&D Program of China ; National Natural Science Foundation of China ; Liaoning Revitalization Talents Program ; Sinopec China
内容类型期刊论文
源URL[http://ir.imr.ac.cn/handle/321006/173119]  
专题金属研究所_中国科学院金属研究所
通讯作者Jiang, Hong; Liu, Hongyang; Ma, Ding
作者单位1.Univ New Haven, Dept Chem & Chem & Biomed Engn, Ctr Integrar Mat Discovery, West Haven, CT 06516 USA
2.Hong Kong Univ Sci & Technol, Ctr Quantum Mat, Kowloon, Hong Kong 999077, Peoples R China
3.Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201204, Peoples R China
4.Peking Univ, Beijing Natl Lab Mol Sci, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
5.Peking Univ, Coll Engn, Beijing 100871, Peoples R China
6.Peking Univ, BIC ESAT, Beijing 100871, Peoples R China
7.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
8.Univ Sci & Technol China, Sch Mat Sci & Engn, Hefei 230026, Peoples R China
9.Hong Kong Univ Sci & Technol, Dept Phys, Kowloon, Hong Kong 999077, Peoples R China
推荐引用方式
GB/T 7714
Peng, Mi,Jia, Zhimin,Gao, Zirui,et al. Antisintering Pd-1 Catalyst for Propane Direct Dehydrogenation with In Situ Active Sites Regeneration Ability[J]. ACS CATALYSIS,2022,12(4):2244-2252.
APA Peng, Mi.,Jia, Zhimin.,Gao, Zirui.,Xu, Ming.,Cheng, Danyang.,...&Ma, Ding.(2022).Antisintering Pd-1 Catalyst for Propane Direct Dehydrogenation with In Situ Active Sites Regeneration Ability.ACS CATALYSIS,12(4),2244-2252.
MLA Peng, Mi,et al."Antisintering Pd-1 Catalyst for Propane Direct Dehydrogenation with In Situ Active Sites Regeneration Ability".ACS CATALYSIS 12.4(2022):2244-2252.
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