Virtual high throughput screening (VHTS) and machine learning (ML) have greatly accelerated the design of single-site transition-metal catalysts. VHTS of catalysts, however, is often accompanied with high calculation failure rate and wasted computational resources due to the difficulty of simultaneously converging all mechanistically relevant reactive intermediates to expected geometries and electronic states. We demonstrate a dynamic classifier approach, i.e., a convolutional neural network that monitors geometry optimization on the fly, and exploit its good performance and transferability for catalyst design. We show that the dynamic classifier performs well on all reactive intermediates in the representative catalytic cycle of the radical rebound mechanism for methane-to-methanol despite being trained on only one reactive intermediate. The dynamic classifier also generalizes to chemically distinct intermediates and metal centers absent from the training data without loss of accuracy or model confidence. We rationalize this superior model transferability to the use of on-the-fly electronic structure and geometric information generated from density functional theory calculations and the convolutional layer in the dynamic classifier. Combined with model uncertainty quantification, the dynamic classifier saves more than half of the computational resources that would have been wasted on unsuccessful calculations for all reactive intermediates being considered.
翻译:虚拟高排量筛选(VHTS)和机器学习(ML)大大加快了单站点过渡金属催化剂的设计。但是,催化剂的VHTS往往伴随着高计算失败率和浪费的计算资源,因为很难同时将所有机械上相关的被动反应中间体与预期的地形和电子状态相融合。我们展示了一种动态分类方法,即监测飞行上几何优化并利用其良好性能和可转移性用于催化剂设计的良好性能和可转移性的连动神经神经网络。我们表明,动态分类器在甲烷至甲醇激进反弹机制具有代表性的催化循环中的所有反应中间体上表现良好,尽管只受过一个反应性中间体的培训。动态分类器还笼统地将培训数据中缺少的化学特性不同的中间体和金属中心归纳为不丧失准确性或模型信心。我们把这种高级模型的可移植性转移到使用现场电子结构和从密度功能理论计算中生成的几何信息合理化。动态分类器和动态分类器中继层中生成的几何等信息。结合了模型不确定性的定量定量定量计算,动态分类将使得中间反应性计算结果的计算结果比半为浪费。