材料科学
金属间化合物
电催化剂
吸附
催化作用
制作
合金
密度泛函理论
乙醇
化学工程
纳米技术
耐久性
表面工程
科技与社会
铂金
乙醇燃料
过程(计算)
曲面(拓扑)
壳体(结构)
过渡金属
劈理(地质)
键裂
燃料电池
作者
Wen Chen,Lei Xie,Yong Li,Shuiping Luo,Xinyi Cai,Tangting Li,Junhao Qiu,Zhichao Yang,Zhihan Yuan,Shao‐Qing Liu,Xian‐Zhu Fu,Jing‐Li Luo
标识
DOI:10.1002/adma.202519429
摘要
Single-atom alloys (SAAs) emerge as an intriguing model system for electrocatalysis by combining the advantages of single-atom catalysts and nanoalloys, yet it faces the challenge in engineering their surface structure at the atomic level. Herein, to fully utilize active Pt sites to boost ethanol oxidation electrocatalysis, single-Pt-atoms anchored onto the surface of intermetallic Pd5Bi3 core-ultrathin Pd shell octahedrons, namely a tensile-strained PdPt1 SAA skin, were rationally designed and engineered. This unique PdPt1 SAA skin achieves a record-high mass activity (553.58 A mgPt -1 or 34.73 A mgPt+Pd -1) and outstanding durability toward ethanol oxidation in alkaline electrolyte, outperforming the current high-performance electrocatalysts. Density functional theory (DFT) calculations reveal that the isolated-Pt-atoms effectively enhance the adsorption of ethanol, accelerate the C2 pathway, and enhance the C-C bond cleavage of the *CH2CO intermediate. The wet-chemical fabrication of SAA skin opens up a general strategy to construct model surface that completely exposes and stabilizes active atoms, facilitating the development of highly efficient electrocatalysts.
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