Operator-induced structural variable selection for identifying materials genes

TL;DR

This paper introduces a novel variable selection method leveraging operator-induced structure to efficiently identify meaningful materials descriptors, improving accuracy and speed over existing techniques, with applications in catalysis research.

Contribution

The paper proposes a new operator-induced structure-based variable selection method that enables fast, accurate dimension reduction in high-dimensional materials informatics problems.

Findings

Method outperforms existing techniques in speed and accuracy.

Robust performance in high-dimensional settings.

Identifies physical descriptors explaining catalytic binding energy.

Abstract

In the emerging field of materials informatics, a fundamental task is to identify physicochemically meaningful descriptors, or materials genes, which are engineered from primary features and a set of elementary algebraic operators through compositions. Standard practice directly analyzes the high-dimensional candidate predictor space in a linear model; statistical analyses are then substantially hampered by the daunting challenge posed by the astronomically large number of correlated predictors with limited sample size. We formulate this problem as variable selection with operator-induced structure (OIS) and propose a new method to achieve unconventional dimension reduction by utilizing the geometry embedded in OIS. Although the model remains linear, we iterate nonparametric variable selection for effective dimension reduction. This enables variable selection based on ab initio primary features, leading to a method that is orders of magnitude faster than existing methods, with improved accuracy. To select the nonparametric module, we discuss a desired performance criterion that is uniquely induced by variable selection with OIS; in particular, we propose to employ a Bayesian Additive Regression Trees (BART)-based variable selection method. Numerical studies show superiority of the proposed method, which continues to exhibit robust performance when the input dimension is out of reach of existing methods. Our analysis of single-atom catalysis identifies physical descriptors that explain the binding energy of metal-support pairs with high explanatory power, leading to interpretable insights to guide the prevention of a notorious problem called sintering and aid catalysis design.