Leveraging Pd(100)/SnO2 interfaces for highly efficient electrochemical formic acid oxidation†

Haiyan Huang, Tianyi Yang, Fang Sun, Zhaohui Liu, Qing Tang, Lingmei Liu, Yu Han, Jianfeng Huang

Research output: Contribution to journalArticlepeer-review

1 Scopus citations


The electrocatalytic formic acid oxidation (FAO) is the crucial anodic reaction of direct formic acid fuel cells (DFAFCs), but its activity remains to be largely improved in order to be practically viable. The rational development of enhanced catalysts requires thorough consideration of various contributing factors that are possibly integrated in composite systems. Here, we demonstrate that, Pd(100)/SnO2 interfaces, provided being efficiently exploited, can significantly boost FAO activity by a factor of ∼10, compared with pure Pd(100) facets, with the mass activity reaching a record of 14.55 A mgPd−1 at a 40 mV-lower peak potential. Unique Pd/SnO2 nanocomposites with a myriad of Pd(100)/SnO2 interfaces were obtained by a newly developed successive seeded growth strategy, wherein pre-formed SnO2 nanospheres are used as seeds for two-round overgrowth of multitudinous Pd nanocubes. Using electron microscopic, electrochemical, spectroscopic and computational analyses, we found that the Pd(100)/SnO2 interfaces induce lattice contraction and electron loss on Pd nanocubes, which optimize intermediate binding during FAO. Moreover, we showed that the good cubicity of the Pd nanocubes and the presence of SnO2 nearby further promote the activity by facilitating the potential-determining step and the elimination of the poisoning CO intermediate, respectively. As such, the combined high intrinsic activity and number density of Pd(100)/SnO2 interfaces enabled the superior activity of the Pd/SnO2 nanocomposites. The composite material presented here holds promise for application in DFAFCs, but equally importantly, the insights regarding the structure–performance relationship would be beneficial for designing efficient metal/oxide composite catalysts for diverse electro- and photo-catalytic reactions.
Original languageEnglish (US)
StatePublished - Jan 2 2023

Bibliographical note

KAUST Repository Item: Exported on 2023-01-26
Acknowledgements: This work was supported by the Fundamental Research Funds for the Central Universities (2020CDJQY-A072), the Thousand Talents Program for Distinguished Young Scholars, the Venture and Innovation Support Program for Chongqing Overseas Returnees (cx2020107) and Natural Science Foundation of Chongqing (cstc2021jcyj-msxmX0945). Mr Xiangnan Gong from the Analytical and Testing Center of Chongqing University is acknowledged for the assistance in the ATR-IR measurements.

ASJC Scopus subject areas

  • Materials Science(all)


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