Single‐Atom Ru Alloyed with Ni Nanoparticles Boosts CO2 Methanation

Author:

Zhang Tengfei12,Zheng Peng3,Gao Jiajian4,Han Zhennan3,Gu Fangna5,Xu Wenqing1,Li Lina6,Zhu Tingyu1,Zhong Ziyi7,Xu Guangwen38,Su Fabing18ORCID

Affiliation:

1. Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 P. R. China

2. School of Chemical Engineering University of Chinese Academy of Sciences Beijing 100049 P. R. China

3. Key Laboratory on Resources Chemicals and Materials of Ministry of Education Shenyang University of Chemical Technology Shenyang 110142 P. R. China

4. 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

5. 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

6. Shanghai Synchrotron Radiation Facility Shanghai Advanced Research Institute Chinese Academy of Sciences Shanghai 201204 P. R. China

7. 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

8. Institute of Industrial Chemistry and Energy Technology Shenyang University of Chemical Technology Shenyang 110142 P. R. China

Abstract

AbstractDesigning 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.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3