详细信息
Rh nanoclusters encaged in hollow mesoporous silica nanoreactors with enhanced catalytic performance for phenol selective hydrogenation ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Rh nanoclusters encaged in hollow mesoporous silica nanoreactors with enhanced catalytic performance for phenol selective hydrogenation
作者:Yan, Peijian;Tian, Pengfei;Li, Kaijie;Stuart, Martien A. Cohen;Wang, Junyou;Yu, Xinhai[1];Zhou, Shenghu[1]
机构:[1]East China Univ Sci & Technol, Sch Chem Engn, Shanghai Key Lab Multiphase Mat Chem Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China; East China Univ Sci & Technol, Sch Mech Engn, Key Lab Pressure Syst & Safety MOE, 130 Meilong Rd, Shanghai 200237, Peoples R China
年份:2020
卷号:397
外文期刊名:CHEMICAL ENGINEERING JOURNAL
收录:;EI(收录号:20202108701201);WOS:【SCI-EXPANDED(收录号:WOS:000552025300026)】;
基金:S. Zhou and X. Yu thank the National Natural Science Foundation of China for financial supports (Grant No. 21776090, 21476073 and 21176069), and this work is also partially supported by Natural Science Foundation of Shanghai (Grant No. 17ZR1440500).
语种:英文
外文关键词:Rhodium; Hydrogenation; Catalysis; Mesoporous; Hollow nanoreactors
摘要:Here, we report the synthesis of Rh nanoclusters (similar to 0.8 nm) encapsulated in hollow mesoporous silica nanoreactors (Rh@HMSNs) for phenol selective hydrogenation. Specifically, triple ligands were used to bind Rh3+ ions to form negatively charged coordination complex network, which further combines by electrostatic attraction with positively charged diblock copolymers to obtain Rh3+ ions bound polymer micelles. Following silica deposition onto micelles, calcination and H-2 reduction result in hollow mesoporous silica nanoreactors and residence of Rh nanoclusters close to their hollow cavities. Relative to the control silica supported Rh catalysts, the obtained Rh@HMSNs show significantly enhanced catalytic activity, cyclohexanol selectivity and stability for phenol hydrogenation. By DFT theoretic calculations and comparison of control experiments, the performance enhancement of Rh@HMSNs is ascribed to their unique nanostructures, where the small size of Rh nanoclusters increases the cyclohexanol selectivity by suppressing the formation of cyclohexanone, and the residence of Rh nanoclusters close to hollow cavities enhances their thermal and catalytic stability.
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