Composition-regulated lattice strain of PdSn/C for boosting C1 pathway in ethanol electrooxidation

Yin Cai, Tao Yi, Jie Ding, Fuhua Li, Rongsheng Chen, Tao Ma, Feng Liang
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引用次数: 3

Abstract

The rational design of Pd-based catalysts to enhance their applications in ethanol oxidation reaction (EOR) presents both exciting opportunities and significant challenges. Herein, a series of carbon-supported PdSn nanoparticle catalysts (PdSn/C-X, X = 0.1, 0.5, 1, 2) with tunable lattice strains were synthesized using a facile method at room temperature and applied to the EOR. Our findings demonstrate that the activity and stability of EOR can be modulated by manipulating the lattice strain in Pd-based catalysts. Remarkably, PdSn/C-1 exhibits an excellent mass current density of 8,452.3 mA/mgPd, which is higher than that of most Pd-based catalysts, along with great stability, maintaining a mass activity of 573.9 mA/mgPd after 5,000 s. By combining structural analysis, in situ spectral characterization, and theoretical calculation, we elucidate that the optimal tensile strain adjusted by Sn composition in PdSn/C optimizes the free energy of the key intermediate (*CH2CO) during EOR, thereby favoring the C1 pathway and enhancing catalytic activity. This study demonstrates that by controlling the composition, the lattice strain can be altered to improve catalytic performance of Pd-based catalysts in EOR.
组成调控PdSn/C晶格应变对乙醇电氧化中C1通路的促进作用
合理设计钯基催化剂以提高其在乙醇氧化反应(EOR)中的应用提供了令人兴奋的机遇和重大的挑战。本文在室温条件下合成了一系列碳负载的PdSn纳米颗粒催化剂(PdSn/C-X, X = 0.1, 0.5, 1,2),其晶格应变可调,并应用于提高采收率。我们的研究结果表明,提高采收率的活性和稳定性可以通过控制钯基催化剂的晶格应变来调节。值得注意的是,PdSn/C-1表现出优异的质量电流密度,为8,452.3 mA/mgPd,高于大多数pd基催化剂的质量电流密度,并且具有良好的稳定性,在5000 s后保持573.9 mA/mgPd的质量活性。通过结构分析、原位光谱表征和理论计算相结合,我们阐明了由PdSn/C中Sn组成调整的最佳拉伸应变优化了EOR过程中关键中间体(*CH2CO)的自由能,从而有利于C1途径,提高了催化活性。研究表明,通过控制组成,可以改变钯基催化剂的晶格应变,从而提高其在提高采收率中的催化性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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