过渡金属
自旋(空气动力学)
自旋态
化学
凝聚态物理
化学物理
协调数
金属
材料科学
氢
电子结构
吉布斯自由能
活动站点
国家(计算机科学)
活动中心
航程(航空)
相关性
原子物理学
能量(信号处理)
物理
价值(数学)
作者
Yu Shyang Tan,Lei Li,Zixuan Yang,Tao Huang,Qiaoling Wang,Tao Zhang,Junhang Luo,Gui‐Fang Huang,Wangyu Hu,Wei‐Qing Huang
摘要
Spin states are pivotal in modulating the electrocatalytic activity of transition metal (TM)-based compounds, yet quantitatively evaluating the activity-spin state correlation remains a formidable challenge. Here, we propose an “activity index (η)” as a descriptor, to assess the activity of the spin states for the hydrogen evolution reaction (HER). η descriptor integrates three key electronic parameters: the proportion (P), broadening range (R), and center (εact) of the active spin state, which collectively account for the electronic structure modulation induced by both the intrinsic active site and its local coordination environment. Using 1T-phase ZrSe2-anchored TM atoms (TM = Sc to Ni) as prototypes, we reveal that the correlation between Gibbs free energy (ΔGH) and the η value follows a linear relation—ΔGH reduces as η decreases. Notably, ZrSe2-Mn exhibits the optimal η value (−0.56), corresponding to the best HER activity with a ΔGH of −0.04 eV—closer to the thermoneutral ideal value (0 eV) than even Pt (ΔGH = −0.09 eV). This relationship suggests that η is an effective descriptor of the active spin state for HER of TM-based catalysts. Our study establishes a quantitative correlation between HER activity and spin polarization, enabling performance prediction through spin-resolved physical descriptor.
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