外推法
计算机科学
规范化(社会学)
人工智能
催化作用
机器学习
产量(工程)
航程(航空)
集合(抽象数据类型)
财产(哲学)
刮擦
特征(语言学)
帕累托原理
多目标优化
训练集
生化工程
协同催化
材料科学
稳健性(进化)
数学优化
反应条件
工艺工程
帕累托最优
作者
Zhenfeng Tan,Yuanming Zhu,Bin Shao,Feng Qian,Jun Hu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2026-01-02
卷期号:16 (2): 1312-1324
被引量:1
标识
DOI:10.1021/acscatal.5c07191
摘要
Machine learning (ML) holds great promise for discovering catalysts; however, simultaneously possessing high interpretability, prediction accuracy, and catalyst discovery efficiency remains a substantial challenge. Here, an ML framework with thermodynamic guidelines from scratch is constructed to explore superior multimetallic catalysts for the representative reverse water–gas shift (RWGS) reaction. A normalization approach is employed to redefine the elemental physicochemical properties, leveraging the advantages of the elemental and property features of active metals. This not only enables accurate predictions but also derives the value range of each feature through deep insights into the catalytic mechanisms. More importantly, a genetic algorithm (GA)-based multiobjective optimizer is developed for reverse engineering the compositions of multimetallic catalysts. Specifically, by enforcing explicit thermodynamic constraints and self-correcting by experimentally validated results into the ML models, both rigorous discovery of catalysts within the training data set and extrapolation are successfully achieved. After two rounds of self-corrections, optimal ternary-metallic catalysts are experimentally validated with a superior CO yield close to the equilibrium limitation. Therefore, this ML framework is a promising paradigm for catalyst research, as highlighted by intrinsic theoretical guidance and experimental validation.
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