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Single-Atom Ru Alloyed with Ni Nanoparticles Boosts CO2 Methanation.
Zhang, Tengfei; Zheng, Peng; Gao, Jiajian; Han, Zhennan; Gu, Fangna; Xu, Wenqing; Li, Lina; Zhu, Tingyu; Zhong, Ziyi; Xu, Guangwen; Su, Fabing.
Afiliação
  • Zhang T; Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, P. R. China.
  • Zheng P; School of Chemical Engineering, University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.
  • Gao J; Key Laboratory on Resources Chemicals and Materials of Ministry of Education, Shenyang University of Chemical Technology, Shenyang, 110142, P. R. China.
  • Han Z; Institute of Sustainability for Chemicals, Energy and Environment (ISCE2), Agency for Science, Technology, and Research (A*STAR), 1 Pesek Road, Jurong Island, Singapore, 627833, Republic of Singapore.
  • Gu F; Key Laboratory on Resources Chemicals and Materials of Ministry of Education, Shenyang University of Chemical Technology, Shenyang, 110142, P. R. China.
  • Xu W; Beijing Key Laboratory of Enze Biomass Fine Chemicals, College of New Materials and Chemical Engineering, Beijing Institute of Petrochemical Technology, Beijing, 102617, P. R. China.
  • Li L; Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, P. R. China.
  • Zhu T; Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, 201204, P. R. China.
  • Zhong Z; Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, P. R. China.
  • Xu G; Department of Chemical Engineering, Guangdong Technion Israel Institute of Technology (GTIIT), and Guangdong Provincial Key Laboratory of Materials and Technologies for Energy Conversion (MATEC), 241 Daxue Road, Shantou, 515063, P. R. China.
  • Su F; Key Laboratory on Resources Chemicals and Materials of Ministry of Education, Shenyang University of Chemical Technology, Shenyang, 110142, P. R. China.
Small ; 20(12): e2308193, 2024 Mar.
Article em En | MEDLINE | ID: mdl-37953460
Designing catalysts to proceed with catalytic reactions along the desired reaction pathways, e.g., CO2 methanation, has received much attention but remains a huge challenge. This work reports one Ru1Ni single-atom alloy (SAA) catalyst (Ru1Ni/SiO2) prepared via a galvanic replacement reaction between RuCl3 and Ni nanoparticles (NPs) derived from the reduction of Ni phyllosilicate (Ni-ph). Ru1Ni/SiO2 achieved much improved selectivity toward hydrogenation of CO2 to CH4 and catalytic activity (Turnover frequency (TOF) value: 40.00 × 10-3 s-1), much higher than those of Ni/SiO2 (TOF value: 4.40 × 10-3 s-1) and most reported Ni-based catalysts (TOF value: 1.03 × 10-3-11.00 × 10-3 s-1). Experimental studies verify that Ru single atoms are anchored onto the Ni NPs surface via the Ru1-Ni coordination accompanied by electron transfer from Ru1 to Ni. Both in situ experiments and theoretical calculations confirm that the interface sites of Ru1Ni-SAA are the intrinsic active sites, which promote the direct dissociation of CO2 and lower the energy barrier for the hydrogenation of CO* intermediate, thereby directing and enhancing the CO2 hydrogenation to CH4.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article