TY - JOUR
T1 - Metal-organic framework-derived BiSn bimetallic oxides for the electrocatalytic reduction of CO2 to formate
AU - Chen, Leibing
AU - Wang, Yali
AU - Mei, Jing
AU - Li, Guoying
AU - Yao, Han
AU - Lu, Jiaxing
AU - Wang, Huan
N1 - Publisher Copyright:
© 2026 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
PY - 2026/4/30
Y1 - 2026/4/30
N2 - AbstractTo address the issue of excessive atmospheric CO2 levels, electrochemical CO2 reduction reaction (eCO2RR) to fuels and chemicals has been extensively studied. Herein, we report a metal-organic framework-derived spherical catalyst Bi3Sn1Ox, consisting of stacked nanosheets, by combining hydrothermal and pyrolysis methods. Bi3Sn1Ox demonstrates outstanding performance in eCO2RR for HCOO− production, achieving over 94% FEHCOO− in H-cells across a potential range of −0.9 V to −1.4 V. It also exhibits considerable current density in flow cells, reaching up to 800 mA/cm2 with a FEHCOO− of 96.1%. Characterization tests demonstrate that Bi3Sn1Ox's unique porous structure confer superior CO2 adsorption capacity. Furthermore, the electron transfer between Bi and Sn in Bi3Sn1Ox creates a positive charge center at Sn sites, which inhibits nucleophilic reactions on CO2, favors the generation of the *OCHO intermediate and promotes HCOO− formation.
AB - AbstractTo address the issue of excessive atmospheric CO2 levels, electrochemical CO2 reduction reaction (eCO2RR) to fuels and chemicals has been extensively studied. Herein, we report a metal-organic framework-derived spherical catalyst Bi3Sn1Ox, consisting of stacked nanosheets, by combining hydrothermal and pyrolysis methods. Bi3Sn1Ox demonstrates outstanding performance in eCO2RR for HCOO− production, achieving over 94% FEHCOO− in H-cells across a potential range of −0.9 V to −1.4 V. It also exhibits considerable current density in flow cells, reaching up to 800 mA/cm2 with a FEHCOO− of 96.1%. Characterization tests demonstrate that Bi3Sn1Ox's unique porous structure confer superior CO2 adsorption capacity. Furthermore, the electron transfer between Bi and Sn in Bi3Sn1Ox creates a positive charge center at Sn sites, which inhibits nucleophilic reactions on CO2, favors the generation of the *OCHO intermediate and promotes HCOO− formation.
KW - BiSn bimetallic oxides
KW - COreduction
KW - Electrocatalysis
KW - HCOOH
KW - Metal-organic frameworks
UR - https://www.scopus.com/pages/publications/105034740527
U2 - 10.1016/j.ijhydene.2026.154803
DO - 10.1016/j.ijhydene.2026.154803
M3 - 文章
AN - SCOPUS:105034740527
SN - 0360-3199
VL - 230
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
M1 - 154803
ER -