The electrochemical reduction of CO2 (CO2RR) to produce valuable synthetic fuel like CH3OH not only mitigates the accumulated greenhouse gas from the environment but is also a promising direction toward attenuating our continuous reliance on fossil fuels. However, CO2RR to yield CH3OH suffers because of large overpotential, competitive H2 evolution reaction (HER), and poor product selectivity. In this regard, intermetallic alloy catalysts open up a wide possibility of fine-tuning the electronic property and attain appropriate structures that facilitate selective CO2RR. Here, we report for the first time the CO2RR over carbon-supported PtZn nano-alloys and probed the crucial role of structures and interfaces as active sites. PtZn/C, Pt3Zn/C, and PtxZn/C (1 < x < 3) synthesized from the metal-organic framework material were characterized structurally and morphologically. The catalysts demonstrated structure dependency toward CH3OH selectivity, as the mixed-phase PtxZn/C outperformed the phase-pure PtZn/C and Pt3Zn/C. The structure-dependent reaction mechanism and the kinetics were elucidated over the synthesized catalysts with the help of detail experiments and associated density functional theory calculations. Results showed that in spite of low electrochemically active surface area, PtxZn could not only have facilitated the single electron transfer to adsorbed CO2 but also showed better binding of the intermediate CO2 •- over its surface. Moreover, the lower bond energy between the mixed-phase surface and -OCH3 compared to the phase-pure catalysts has enabled higher CH3OH selectivity over PtxZn. This work opens a wide possibility of studying the role of interfaces between phase-pure nano-alloys toward CO2RR. © 2020 American Chemical Society

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