Bifunctional catalyst MoSx@H-Beta for highly selective conversion of CO2 to C2–6 hydrocarbons-Reference-Cited by-同舟云学术

Bifunctional catalyst MoS_x@H-Beta for highly selective conversion of CO₂ to C_2–6 hydrocarbons

Published:2024 Issue:8 Volume:14 Page:2166-2177
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Zhao Taotao¹,Shen Chenyang¹,Liu Yuchi¹,Liu Gui¹,Qian Xiaofeng¹,He Qiang¹,Mei Feifei¹,He Yu¹,Guo Xiangke¹,Xue Nianhua¹,Liu Xi²^ORCID,Ding Weiping¹^ORCID

Affiliation:

1. Key Lab of Mesoscopic Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China

2. School of Chemistry and Chemical, In-situ Centre for Physical Sciences, Frontiers Science Centre for Transformative Molecules, Shanghai Jiao Tong University, Shanghai, 200240, P. R. China

Abstract

MoSx clusters encapsulated in channels of H-Beta zeolite constitute a bifunctional catalyst and show excellent catalytic performance for CO2 hydrogenation: CO2 conversion >13%, C2–6 hydrocarbons selectivity >74% and stability >200 h on stream.

Funder

National Science and Technology Major Project

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CY/D3CY01741A

Reference47 articles.

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3. Catalyst Development for CO2Hydrogenation to Fuels

4. CO 2 capture from humid flue gases and humid atmosphere using a microporous coppersilicate

5. Global challenges and strategies for control, conversion and utilization of CO2 for sustainable development involving energy, catalysis, adsorption and chemical processing

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