TY - JOUR
T1 - Long-Term CO2 Hydrogenation into Liquid Fuels with a Record-High Single-Pass Yield of 31.7% over Interfacial Fe-Zn Sites
AU - Zhang, Lijun
AU - Zhao, Jiankang
AU - Li, Teng
AU - Gao, Weizhe
AU - Li, Hongliang
AU - Wu, Luyao
AU - Xia, Wei
AU - Wu, Wenlong
AU - Wang, Chengwei
AU - Wang, Fan
AU - Yasuda, Shuhei
AU - Guo, Xiaoyu
AU - He, Yingluo
AU - Yang, Guohui
AU - Liu, Guangbo
AU - Jin, Zhiliang
AU - Zeng, Jie
AU - Tsubaki, Noritatsu
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/3/26
Y1 - 2025/3/26
N2 - Despite extensive research efforts in CO2 hydrogenation, achieving a high yield of liquid fuels remains a significant challenge due to the limited conversion of CO2 and the considerable formation of undesired C1 byproducts. In this study, we report a record-high yield of liquid fuels from CO2 hydrogenation facilitated by an Fe-Zn catalyst enriched with interfacial sites. These interfacial sites effectively enhanced carbon chain growth through the synergistic interaction of the carbide pathway and CO insertion while simultaneously suppressing the formation of CO and CH4. Consequently, the selectivity for undesired C1 byproducts was minimized to 14.7%, while maintaining a high selectivity of 72.2% for liquid fuels. Under optimized reaction conditions including 360 °C, 4.0 MPa, 4,000 mL gcat-1 h-1, and CO2/H2 = 3, the liquid fuel yield reached 31.7% at a single-pass CO2 conversion of 48.2%.
AB - Despite extensive research efforts in CO2 hydrogenation, achieving a high yield of liquid fuels remains a significant challenge due to the limited conversion of CO2 and the considerable formation of undesired C1 byproducts. In this study, we report a record-high yield of liquid fuels from CO2 hydrogenation facilitated by an Fe-Zn catalyst enriched with interfacial sites. These interfacial sites effectively enhanced carbon chain growth through the synergistic interaction of the carbide pathway and CO insertion while simultaneously suppressing the formation of CO and CH4. Consequently, the selectivity for undesired C1 byproducts was minimized to 14.7%, while maintaining a high selectivity of 72.2% for liquid fuels. Under optimized reaction conditions including 360 °C, 4.0 MPa, 4,000 mL gcat-1 h-1, and CO2/H2 = 3, the liquid fuel yield reached 31.7% at a single-pass CO2 conversion of 48.2%.
KW - CO hydrogenation
KW - long-chain hydrocarbon
KW - modified Fischer−Tropsch synthesis
KW - molten-salt-assisted
KW - ZnFeO
UR - http://www.scopus.com/inward/record.url?scp=105001871263&partnerID=8YFLogxK
U2 - 10.1021/acs.nanolett.5c00150
DO - 10.1021/acs.nanolett.5c00150
M3 - 学術論文
C2 - 40094429
AN - SCOPUS:105001871263
SN - 1530-6984
VL - 25
SP - 4904
EP - 4912
JO - Nano Letters
JF - Nano Letters
IS - 12
ER -