TY - JOUR
T1 - Hetero-site cobalt catalysts for higher alcohols synthesis by CO2hydrogenation
T2 - A review
AU - Liu, Shuilian
AU - He, Yiming
AU - Fu, Weijie
AU - Chen, Jian
AU - Ren, Jie
AU - Liao, Longfei
AU - Sun, Ruiyan
AU - Tang, Zhenchen
AU - Mebrahtu, Chalachew
AU - Zeng, Feng
N1 - Publisher Copyright:
© 2022 The Authors.
PY - 2023/1
Y1 - 2023/1
N2 - Synthesis of higher alcohols by CO2 hydrogenation is a promising way to mitigate CO2 emissions, meanwhile producing value-added fuels and chemicals. However, CO2 hydrogenation to higher alcohols is kinetically hindered and due to the absence of highly efficient catalysts, its industrial implementation is still limited. Among the catalysts designed for this reaction, Co-based catalysts are widely investigated due to earth-abundance and economic, possessing also relatively high activity and selectivity for this reaction. Considering the nature of the active site, the hetero sites of Co-based catalysts such as Co0-CoO, Co0-Coδ+, and Co2C-NaCo2C are critical for higher alcohol synthesis by CO2 hydrogenation. Thus, in this review, we first introduce the roles of Co0, CoO, Coδ+, and Co2C, as well as strategies to tailor their structure which influences the performance in CO2 hydrogenation. Then, we discuss the strategies to create highly efficient hetero-site Co-based catalysts. Finally, emerging methodologies yet to be explored and future directions to achieve highly efficient hetero-site Co catalysts for CO2 hydrogenation to higher alcohols are discussed.
AB - Synthesis of higher alcohols by CO2 hydrogenation is a promising way to mitigate CO2 emissions, meanwhile producing value-added fuels and chemicals. However, CO2 hydrogenation to higher alcohols is kinetically hindered and due to the absence of highly efficient catalysts, its industrial implementation is still limited. Among the catalysts designed for this reaction, Co-based catalysts are widely investigated due to earth-abundance and economic, possessing also relatively high activity and selectivity for this reaction. Considering the nature of the active site, the hetero sites of Co-based catalysts such as Co0-CoO, Co0-Coδ+, and Co2C-NaCo2C are critical for higher alcohol synthesis by CO2 hydrogenation. Thus, in this review, we first introduce the roles of Co0, CoO, Coδ+, and Co2C, as well as strategies to tailor their structure which influences the performance in CO2 hydrogenation. Then, we discuss the strategies to create highly efficient hetero-site Co-based catalysts. Finally, emerging methodologies yet to be explored and future directions to achieve highly efficient hetero-site Co catalysts for CO2 hydrogenation to higher alcohols are discussed.
KW - COhydrogenation
KW - Cobalt
KW - Hetero-site
KW - Higher alcohol
KW - Synergy
UR - http://www.scopus.com/inward/record.url?scp=85143893860&partnerID=8YFLogxK
U2 - 10.1016/j.jcou.2022.102322
DO - 10.1016/j.jcou.2022.102322
M3 - 文献综述
AN - SCOPUS:85143893860
SN - 2212-9820
VL - 67
JO - Journal of CO2 Utilization
JF - Journal of CO2 Utilization
M1 - 102322
ER -