Single-Atom Ru Alloyed with Ni Nanoparticles Boosts CO2 Methanation

被引:14
作者
Zhang, Tengfei [1 ,2 ]
Zheng, Peng [3 ]
Gao, Jiajian [4 ]
Han, Zhennan [3 ]
Gu, Fangna [5 ]
Xu, Wenqing [1 ]
Li, Lina [6 ]
Zhu, Tingyu [1 ]
Zhong, Ziyi [7 ,8 ]
Xu, Guangwen [3 ,9 ]
Su, Fabing [1 ,9 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
[3] Shenyang Univ Chem Technol, Key Lab Resources Chem & Mat, Minist Educ, Shenyang 110142, Peoples R China
[4] ASTAR, Inst Sustainabil Chem Energy & Environm ISCE2, 1 Pesek Rd, Singapore 627833, Singapore
[5] Beijing Inst Petrochem Technol, Coll New Mat & Chem Engn, Beijing Key Lab Enze Biomass Fine Chem, Beijing 102617, Peoples R China
[6] Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
[7] Guangdong Technion Israel Inst Technol GTIIT, Dept Chem Engn, 241 Daxue Rd, Shantou 515063, Peoples R China
[8] Guangdong Prov Key Lab Mat & Technol Energy Conver, 241 Daxue Rd, Shantou 515063, Peoples R China
[9] Shenyang Univ Chem Technol, Inst Ind Chem & Energy Technol, Shenyang 110142, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; methanation; mechanisms; Ni nanoparticles; Ru single atoms; single-atom alloy; SUPPORTED NICKEL; CATALYSTS; HYDROGENATION; METAL; PLATINUM; STRATEGY; PARTICLE; ROLES; CH4;
D O I
10.1002/smll.202308193
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 x 10(-3) s(-1)), much higher than those of Ni/SiO2 (TOF value: 4.40 x 10(-3) s(-1)) and most reported Ni-based catalysts (TOF value: 1.03 x 10(-3)-11.00 x 10(-3) s(-1)). Experimental studies verify that Ru single atoms are anchored onto the Ni NPs surface via the Ru-1-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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页数:10
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