可解释性
化学空间
工作流程
材料科学
机器学习
电负性
计算机科学
电池(电)
纳米技术
过电位
人工智能
Boosting(机器学习)
虚拟筛选
催化作用
鉴定(生物学)
可持续能源
储能
工作(物理)
电化学能量转换
能量(信号处理)
钥匙(锁)
高效能源利用
集合(抽象数据类型)
生化工程
作者
Peng Zhang,Yixin Yan,Dominik Legut,Yuanjian Li,Zhihao Li,Chao Lin,Xiang Feng,Hao Wang,Y. C. Xu,Shenqi Wang,Ruifeng Zhang,Zhi Wei Seh,Qiang Zhang
标识
DOI:10.1002/adfm.202532003
摘要
ABSTRACT The performance of lithium–oxygen (Li─O 2 ) batteries is limited by sluggish reaction kinetics, leading to issues such as poor reversibility and severe parasitic reactions. This necessitates advanced catalysts like MXenes, but their vast compositional diversity and complex structure‐activity relationships hinder traditional discovery approaches. Herein, we employ an integrated high‐throughput workflow (HTW) and machine learning (ML) framework for Li batteries for the first time to systematically investigate 2D transition metal carbides/nitrides MXenes‐based catalysts. We defined a virtual compositional space of ∼2 million MXene candidates. Guided by a combinatorial enumeration and subsequent rule‐based screening, we down‐selected this space to an HTW design set of 4896 unique MXene configurations for computation. Our developed Light Gradient Boosting Machine model achieved superior accuracy (MAE = 0.32 eV) in predicting reaction free energy change across four key steps, enabling the identification of exceptional catalysts including Mo 3 C 2 Cl 2 which exhibits an ultra‐low overpotential of 0.01 V. Our interpretability analysis reveals the intricate mechanisms by which different electronegativity terminals modulate the electronic structure and reaction mechanisms of MXenes. This work establishes an efficient computational reference for accelerating the discovery of advanced energy materials and provides fundamental insights into structure‐activity relationships in electrocatalysis.
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