Discovering Physically Interpretable Mathematical Expression for Predicting CO2 Adsorption in Metal-Organic Frameworks via Machine Learning-Symbolic Regression
This work presents a machine learning-symbolic regression strategy to develop a physically interpretable formula for predicting low pressure CO2 adsorption capacity in hypothetical metal-organic frameworks (hMOFs), and proposes a physics-guided expression that enables efficient prediction and provides clearer insight into adsorption mechanisms.
Abstract
This work presents a machine learning-symbolic regression (ML-SR) strategy to develop a physically interpretable formula for predicting low pressure CO2 adsorption capacity in hypothetical metal-organic frameworks (hMOFs). Four ML models were trained on a small dataset of 1,000 samples, and five key descriptors-largest cavity diameter, pore limiting diameter, void fraction, gravimetric surface area, and number of hydrogen atoms-were identified through SHAP and feature importance analyses. Symbolic regression was then employed to derive a concise adsorption formula, Q=aA, where a represents an adsorption baseline (mmol/g) and A is a dimensionless adsorption number incorporating four structural descriptors. We interpret A as the ratio between an adsorption binding force and a diffusion driving force, revealing how pore topology and surface chemistry jointly influence adsorption. Validation against a comprehensive dataset of 137,652 hMOFs demonstrates that this formula achieves over 70% prediction accuracy for 62,448 structures, confirming strong applicability within defined structural and operational ranges. Unlike conventional black box ML models, the proposed physics-guided expression enables efficient prediction and provides clearer insight into adsorption mechanisms.
Identifying descriptors associated with gaseous arsenic adsorption by metal oxides remains challenging because literature data are heterogeneous and incomplete. A database of 280 experimental records and 20 descriptors from 17 studies was compiled to predict adsorption capacity and interpret descriptor-performance rela...
Yanhong Zhu, Qi Liu, Shuang-Chun Wen et al.· Journal of Environmental Man...· 0 citations
Metal–organic frameworks (MOFs) are promising materials for adsorption and separation, but accurately predicting water adsorption remains a major challenge in molecular simulation. Classical force fields, such as UFF, often fail to capture the strong, directional hydrogen-bonding interactions between water and MOFs, wh...
Yu-Tao Li, Xiao-Qi Zhang, Xin Jin et al.· Journal of Chemical Theory a...· 0 citations
Despite the rapid adoption of machine learning (ML) in materials discovery, its application to water contaminant adsorption remains fundamentally constrained. In this study, we systematically evaluated whether current peer-reviewed literature on magnetite nanoparticle (MNPs) adsorbents contains sufficient descriptor...
A. I. Yunus, Jacob Song, Samuel Darko et al.· ACS ES&T Water· 0 citations
Hydrogen (H2) is expected to play a critical role in modern industry, particularly in ammonia synthesis, petroleum refining, and low-carbon transportation. The safe storage of H2 remains a major challenge due to its low volumetric density under ambient conditions. Metal–Organic Frameworks (MOFs), highly porous crystall...
R. Taylor, Shahin Alipour Bonab, M. Yazdani-Asrami· Algorithms· 0 citations
A realistic performance boundary is outlined for bulk-to-surface ML in this benchmark: O* can be very coarsely prioritized from bulk descriptors within a limited domain, whereas H* and OH* are unlikely to be quantitatively predicted from bulk descriptors alone and would benefit from surface-aware models.
Aggregation‐induced emission (AIE) has revolutionized the design of photoluminescent materials by enabling strong solid‐state emission from molecularly nonemissive compounds. However, rational prediction of AIE properties remains challenging because photophysical behavior depends not only on molecular structure but a...