Platinum-Tellurium Heterojunction Nanosheet Assemblies for Efficient Direct Formic Acid Electrooxidation Catalysis.

Dong, Chengyuan; Zhang, Biao; Song, Huijun; Zhou, Shiyuan; Ye, Jinyu; Liao, Hong-Gang; Dong, Lisha; Huang, Xiaoqing et al. · ACS Nano · 2024

basic_science · Level V

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Abstract

Two-dimensional (2D) heterojunction nanomaterials offer exceptional physicochemical and catalytic properties, thanks to their special spatial electronic structure. However, synthesizing morphologically uniform 2D platinum (Pt)-based metallic nanomaterials with diverse crystalline phases remains a formidable challenge. In this study, we have achieved the successful synthesis of advanced 2D platinum-tellurium heterojunction nanosheet assemblies (Pt<sub><i>x</i></sub>-PtTe<sub>2</sub> HJNSAs, <i>x</i> = 0, 1, 2), seamlessly integrating both trigonal PtTe<sub>2</sub> (<i>t</i>-PtTe<sub>2</sub>) and cubic Pt (<i>c</i>-Pt) phases. By enabling efficient electron transport and leveraging the specific electron density present at the heterojunction, the Pt<sub>2</sub>-PtTe<sub>2</sub> HJNSAs/C demonstrated exceptional formic acid oxidation reaction (FAOR) activity and stability. Specifically, the specific and mass activities reached 8.4 mA cm<sup>-2</sup> and 6.1 A mg<sub>Pt</sub><sup>-1</sup>, which are 46.7 and 50.8 times higher than those of commercial Pt/C, respectively. Impressively, aberration-corrected high-angle annular dark field scanning transmission electron microscopy (AC-HAADF-STEM) revealed a closely packed arrangement of atomic layers and a coherent intergrowth heterogeneous structure. Density functional theory (DFT) calculations further indicated that rearrangement of electronic structure occurred on the surface of Pt<sub>2</sub>-PtTe<sub>2</sub> HJNSAs resulting in a more favorable dehydrogenation pathway and excellent CO tolerance, beneficial for performance improvement. This work inspires the targeted exploration of Pt-based nanomaterials through 2D heterostructure design, leading to an important impact on fuel cell catalysis and beyond.