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Updated: Jan 31, 2026

Setup of Capillary Electrophoresis-Inductively Coupled Plasma Mass Spectrometry CE-ICP-MS for Quantification of Iron Redox Species FeII, FeIII
Published on: May 4, 2020
Estabilización de especies bioactivas mediante la construcción de una interfaz Bi-O-Ce para mejorar la
Xinya Ren1, She Gong1, Zhenze Han1
1State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials Oriented Chemical Engineering, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, China. weiyu@dlut.edu.cn.
Abstract:
The electrocatalytic reduction of CO2 to formate is a key route for carbon resource recycling. Bismuth-based catalysts are widely studied for their high formate selectivity. However, at high current densities, rapid in situ over-reduction of Bi3+ often induces agglomeration of active species (Bi0), compromising structural stability, reducing active sites, and degrading catalytic performance. In this study, a CeO2@BOC catalyst featuring a Bi-O-Ce composite interface was designed by incorporating CeO2 into Bi2O2CO3 (BOC). This catalyst achieves a formate faradaic efficiency (FEformate) of 95.7% at -0.9 V vs. RHE in an H-cell. Moreover, in a flow cell, it maintains a current density of 225 mA cm-2 over 120 hours at the same potential, with FEformate consistently above 90%. Characterization results demonstrate that the high catalytic performance of the catalyst originates from the stabilization of active species by the Bi-O-Ce interface. This strategy of tuning the reduction behavior of bismuth species and inhibiting the aggregation of active species offers new insights for developing efficient and stable CO2 electroreduction to formate processes.
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