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Nanodefect-Stabilized Pd Nanoparticles on CuO Nanosheets Enable Efficient C2+ Production in Electrochemical CO2
Ziyan Lu1, Jiansen Wang2, Chen Qin1
1State Key Laboratory of Water Pollution Control and Green Resource Recycling, State Key Laboratory of Analytical Chemistry for Life Science, Frontiers Science Center for Critical Earth Material Cycling, School of the Environment, School of Chemistry, Nanjing University, Nanjing, P. R. China.
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Developing efficient electrocatalysts for selective CO2-to-C2+ conversion remains challenging due to the kinetic limitations of C-C coupling and catalyst stability issues. In this work, we report a nano-defect-stabilized approach where Pd nanoparticles are immobilized in electrochemically generated nanoscale pits on CuO nanosheets, forming a stable CuO-Pd interface. The optimized catalyst achieves 70.30% Faradaic efficiency for C2+ products at -1.5 V versus RHE, outperforming bare CuO by over two-fold, while maintaining stable performance over 17 h. In situ spectroscopic studies reveal that the Pd-enhanced interface promotes CO coverage and stabilizes C-C coupling intermediates (*COCO and *COCHO). Theoretical calculations validate that the Pd-Cu interaction facilitates CO adsorption and reduces the energy barrier for C-C coupling. This nano-defect-stabilized strategy, which utilizes in situ-formed nano-defects to stabilize active metal sites, provides a generalizable design strategy for developing robust bimetallic CO2 reduction electrocatalysts.
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