双金属片
密度泛函理论
催化作用
铂金
材料科学
氢
纳米技术
计算机科学
计算化学
化学
化学工程
工程类
生物化学
有机化学
作者
Ismail Can Oğuz,Nabil Khossossi,Marco Brunacci,Haldun Bucak,Süleyman Er
标识
DOI:10.26434/chemrxiv-2025-0whpn
摘要
Despite platinum’s exceptional catalytic activity for the hydrogen evolution reaction (HER), its limited supply and steep cost hinder large-scale adoption. Earth-abundant bimetallic alloys thus emerge as attractive substitutes, though their vast compositional and structural diversity makes exhaustive density functional theory (DFT) screening unfeasible. Here, we introduce a machine learning (ML)–DFT workflow for the discov- ery and prioritization of bimetallic HER catalysts. By integrating EquiformerV2 into the AdsorbML surrogate-DFT pipeline, we efficiently predict hydrogen adsorption en- ergies on thousands of alloy surfaces. Sabatier-volcano filtering combined with targeted DFT validation yields a mean absolute error of 0.12 eV across the screened space. Two surface motifs stand out: (i) transition-metal dimers or isolated top sites embedded in Sn- or Sb-rich layers, and (ii) Cu-rich surfaces (Cu–Sn, Cu–Sb) featuring Cu–Cu bridge or hollow sites without direct Sn or Sb interaction. A multi-objective assess- ment of activity, stability, and cost highlights four synthesis-ready candidates—Fe2Sb4, Cu6Sb2, Cu6Sn2, and Ni2Sb2—which combine platinum-like performance with signifi- cantly lower material costs. This integrated ML–DFT strategy transforms an otherwise intractable chemical landscape into a concise, experimental roadmap for earth-abundant HER catalyst development.
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