脱氢
甲酸
催化作用
机器学习
人工智能
电子效应
电子结构
化学
偏移量(计算机科学)
计算机科学
计算化学
电子系统
联轴节(管道)
纳米技术
优势(遗传学)
生物系统
材料科学
动能
从头算
人工神经网络
作者
Qiaoyi Zhang,Zhaojun Dong,Xinya Liu,Hongtan Cai,Xin Liu,Zeshuo Meng,Haoteng Sun,Meiyan Wang,Xiufeng Hao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-06-11
标识
DOI:10.1021/acs.nanolett.6c01270
摘要
Given the limited efficiency of geometric optimization in enhancing formic acid dehydrogenation (FAD), advancing Pd-based catalysts requires deeper insight into electronic structural regulation. Here, we developed a catalytic system confined within metal–nitrogen-doped carbon supports (Pd@MNC) and applied machine learning to innovatively establish a multiparameter correlation model integrating intrinsic kinetic barriers ( E ads ) with diverse descriptors. Unlike traditional single-factor analyses, our findings unravel the central role of electronic structure engineering (48% relative importance) over geometric tunability (12%) in regulating catalytic kinetics, with the d-band center offset ( ε d, 30%) and Pd(II) proportion ( ω Pd(II), 18%) accounting for the electronic contribution. Validated experimentally via Co and Cr doping, this theory-based machine learning framework offers a predictive paradigm for rational catalyst design and activity trend. Ultimately, this multidimensional electronic regulation strategy elevates FAD performance while providing broad applicability for accelerating other critical Pd-catalyzed processes, such as Suzuki coupling and CO 2 reduction reactions.
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