电解质
计算机科学
学习迁移
锂(药物)
人工智能
深度学习
概率逻辑
主动学习(机器学习)
水准点(测量)
材料科学
化学空间
生物系统
纳米技术
电池(电)
金属锂
钥匙(锁)
统计的
机器学习
锂电池
工作(物理)
作者
Xufeng Hong,Xizhe Wang,Stephen J. Harris,Hongbo Zhao,Jiashen Meng,Qingshan Jia,Qianchuan Zhao,Kang Xu,Quanquan Pang,Benben Jiang
标识
DOI:10.1038/s41467-026-70973-4
摘要
Abstract Designing electrolyte materials for high-energy lithium metal batteries requires navigating vast, discrete chemical spaces, where intricate interphasial and electrolyte chemistries render component interactions largely unclear. Traditional trial-and-error methods struggle with discontinuous electrolyte-performance relationships and inefficient adaptation to new molecular candidates, hindering discovery. Here, we propose a two-stage deep active learning framework with knowledge transfer for rapid electrolyte design. In stage one, deep active learning with deep kernel learning selects informative experiments and models discontinuous relationships between formulation and performance, improving sample efficiency and reducing experimental cost. In stage two, target statistic coding quantifies what was learned and transfers it to new design settings, such as expanded formulation spaces and newly introduced components, using only a small number of additional measurements. Using this framework, we found electrolytes that increase the average lifetime of lithium metal symmetric cells by threefold after three learning iterations, and we rapidly identified improved formulations for Li 0 | |LiNi 0.8 Co 0.1 Mn 0.1 O 2 full cells in expanded chemical spaces. This work provides an experiment-driven, sample-efficient route to explore complex electrolyte formulation spaces and quantify inter-component correlations, as well as a realistic, high-cost, small-data benchmark for probabilistic surrogate modeling and sequential decision-making in discrete chemical spaces.
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