4.8 Review

Recent progress of Bi-based electrocatalysts for electrocatalytic CO2 reduction

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Summary: This review emphasizes the dynamic evolution of active sites in electrocatalytic CO2 reduction reaction (CO2RR) and its relationship with catalytic performance. The fundamental principles and operando techniques for studying dynamic evolution are first discussed, followed by the exploration of dynamic evolution behaviors and their correlations with catalytic properties on typical catalysts. Finally, the emerging technique for manipulating dynamic evolution and future opportunities are considered.

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Customizable CO2 Electroreduction to C1 or C2+ Products through Cuy/CeO2 Interface Engineering

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Summary: A highly challenging task to produce 3D electrodes with high activity, selectivity, and durability for CO2 mediated energy conversion was achieved by densely dispersing Bi dendrites on 3D carbon cloth and exposing specific facets of Bi nanoparticles. The resulting Bi NPs/CC electrode exhibited high current density, Faradaic efficiency, and durability, showcasing great potential for large-scale applications in CO2 conversion.

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Customizable CO2 Electroreduction to C-1 or C-2(+) Products through Cu-y/CeO2 Interface Engineering

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A general strategy for obtaining BiOX nanoplates derived Bi nanosheets as efficient CO2 reduction catalysts by enhancing CO2.- adsorption and electron transfer

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Selective Etching Quaternary MAX Phase toward Single Atom Copper Immobilized MXene (Ti3C2Clx) for Efficient CO2 Electroreduction to Methanol

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Facile synthesis of porous Cu-Sn alloy electrode with prior selectivity of formate in a wide potential range for CO2 electrochemical reduction

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Summary: The study prepared a porous Cu6.26Sn5 electrode, tuning the electronic structure of the catalyst by alloying Cu with Sn atoms to balance the adsorption and protonation of intermediates, resulting in increased CO2 concentration and selectivity, promising efficient CO2 electroreduction.

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High-selectivity electrochemical CO2 reduction to formate at low overpotential over Bi catalyst with hexagonal sheet structure

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Accessing Organonitrogen Compounds via C-N Coupling in Electrocatalytic CO2 Reduction

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Summary: This study demonstrates that enhancing CO2 reduction catalysts through noncovalent interactions can improve the selectivity and activity of SnO catalysts, leading to efficient formate production. Moreover, the introduction of hydroxyl groups can be a general strategy for CO2 hydrogenation on various metal oxides.

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Bi-Sn Oxides for Highly Selective CO2 Electroreduction to Formate in a Wide Potential Window

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