Kobayashi Shunsuke, Omori Yuki, Nakayama Kei, Ooe Kousuke, Huang Hsin-Hui, Kuwabara Akihide
Nanostructures Research Laboratory, Japan Fine Ceramics Center, Atsuta, Nagoya 456-8587, Japan.
ACS Nano. 2025 Jan 28;19(3):3510-3518. doi: 10.1021/acsnano.4c13291. Epub 2025 Jan 16.
Pt-based intermetallic alloy particles with a Pt skin layer have higher catalytic activity than solid-solution alloy particles and have attracted considerable attention for practical applications in polymer electrolyte fuel cells. However, the reason for the superior performance of intermetallic alloys is not yet fully understood. Because the catalytic reaction proceeds on the topmost surface of the particle, it is necessary to clarify the relationship between the periodic structure of the intermetallic alloy and the Pt atomic coordination on the surface. This study investigated the Pt-Pt interatomic distance of a Pt skin layer formed on intermetallic PtCo particles at atomic resolution through precise measurements using scanning transmission electron microscopy and theoretical calculations. The Pt atomic coordination on the surface shows good agreement between experimental observations and theoretical models, although the experimental image is a projection and thus provides indirect results. The theoretical calculation model revealed that structural relaxation at the Pt and PtCo interfaces led to two distinct Pt bonding states at the surface, including asymmetric atomic coordination. The asymmetric coordination of the Pt site deepens the d-band center, diversifies the oxygen adsorption energies, and enhances catalytic activity. Further exploration and control of the unique surface Pt coordination environments formed on the periodic structures of intermetallic alloys should reveal promising routes for the development of catalytic particles.
具有铂皮层的铂基金属间化合物合金颗粒比固溶体合金颗粒具有更高的催化活性,并且在聚合物电解质燃料电池的实际应用中引起了相当大的关注。然而,金属间化合物合金优异性能的原因尚未完全明了。由于催化反应在颗粒的最表面进行,因此有必要阐明金属间化合物合金的周期性结构与表面铂原子配位之间的关系。本研究通过使用扫描透射电子显微镜进行精确测量和理论计算,在原子分辨率下研究了在金属间化合物铂钴颗粒上形成的铂皮层的铂-铂原子间距。尽管实验图像是一个投影,因此提供的是间接结果,但表面的铂原子配位在实验观察和理论模型之间显示出良好的一致性。理论计算模型表明,铂与铂钴界面处的结构弛豫导致表面出现两种不同的铂键合状态,包括不对称原子配位。铂位点的不对称配位加深了d带中心,使氧吸附能多样化,并增强了催化活性。对在金属间化合物合金周期性结构上形成的独特表面铂配位环境进行进一步探索和控制,应该能够揭示出催化颗粒开发的有前景的途径。