维数之咒
钙钛矿(结构)
合理设计
密度泛函理论
理论(学习稳定性)
反向
结构稳定性
材料科学
表征(材料科学)
化学稳定性
计算化学
组分(热力学)
化学
钥匙(锁)
选择(遗传算法)
财产(哲学)
纳米技术
理性
多尺度建模
统计物理学
材料设计
分子动力学
化学物理
维数(图论)
计算机科学
生物系统
分子
复杂系统
电流(流体)
分子模型
热力学
作者
Weijie Wu,Yu Wang,Chen Xiaoting,Qingduan Li,Yue‐Peng Cai,Songyang Yuan,Shengjian Liu
标识
DOI:10.1021/acs.jpclett.5c02433
摘要
Organic spacer cations critically influence the dimensionality and stability of low-dimensional perovskites (LDPs), yet current A-site candidate selection remains largely empirical. Herein, we present a machine-learning-driven molecular generation framework based on a Long Short-Term Memory Network model guided by key molecular descriptors, incorporating a Double-Fit strategy to improve dimensional property alignment and structural rationality of LDPs. Our model inversely generates organic cations targeting specific structural dimensions. Subsequent density functional theory calculations identify candidates with favorable thermodynamic stability and configurational features. Experimental synthesis and structural characterization of the resulting perovskites confirm the model's predictive accuracy. This approach provides a rational design paradigm for A-site cations in LDPs and establishes a general platform to accelerate discovery of new organic-inorganic hybrid perovskite materials.
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