A novel computational methodology for large-scale screening of MOFs is applied to gas storage with the use of machine learning technologies. This approach is a promising trade-off between the accuracy of ab initio methods and the speed of classical approaches, strategically combined with chemical intuition. The results demonstrate that the chemical properties of MOFs are indeed predictable (stochastically, not deterministically) using machine learning methods and automated analysis protocols, with the accuracy of predictions increasing with sample size. Our initial results indicate that this methodology is promising to apply not only to gas storage in MOFs but in many other material science projects.
Metal–organic frameworks (MOFs) or porous coordination polymers are a rapidly growing family of hybrid inorganic–organic nanoporous materials, which belong to the category of coordination polymers.1,2,3 These relatively new materials consist of a three-dimensional periodic network, constructed from molecular building blocks, such as metal clusters and organic linkers (Fig. 1). The possible combinations of these numerous building blocks under different topologies result is an almost unlimited number of potential MOFs!
Since their discovery4 MOFs have attracted significant scientific attention due to their extraordinary properties. As “skeleton” materials, they pose very large pores and outstanding apparent surface area. If we were able to unwrap the surface of only one gram of these “very empty” materials, we could cover the area of a football court! These unique characteristics of the MOFs made them excellent candidates for catalysis and gas storage applications.
MOFs have shown exceptional performance in gas storage and separation. Both useful and harmful gases can be absorbed in their pores in very large amounts. The storage of hydrogen,5 methane,6,7 carbon dioxide,8,9 ammonia,10,11 hydrogen sulfide,11,12 etc. have been intensively investigated in MOFs and many new MOFs have been designed for that purpose.13 Some MOFs pose today the world record value for the storage of several gases.14,15
The two most studied gases in MOFs are H2 and CO2. The reasons are obvious: the 1st could solve the energy transferring problem, while the 2nd is responsible for global warming. There are several review papers presenting collections of MOFs and their youngest brothers—covalent organic frameworks,16,17 zeolitic imidazolate frameworks18,19 etc., with very high performance in gas storage.
Together with the experimental work, there is also a substantial theoretical support in the field. Theory undoubtedly plays a significant role in the development of the field, mainly in two ways: by explaining the experimental results20 and by leading the experiments.21 In the literature, there are several methodologies investigating the gas storage problem in MOFs. There are accurate ab initio quantum chemical approaches,22 computational light and fast classical Monte Carlo and molecular dynamics techniques23 and “multi-scale” methods that try to combine both.22 All of them address specific MOFs, either synthesized earlier, or designed for a specific application following chemical intuition.
Lately, a completely different computational approach appeared based on a large-scale screening of hypothetical MOFs.24,25 This new approach firstly generates all conceivable MOFs from a given chemical library of building blocks ending up in thousands of combinations. Then, a low computational cost screening is taking place using Monte Carlo classical techniques, ending up in the most promising candidates for a specific application.
Both general approaches have advantages and disadvantages in investigating existing MOFs and designing novel architectures. The 1st, that uses ab initio techniques and based in quantum theory is very accurate and the results are in most cases unquestionable. But unfortunately, since the computational cost is very high (approximately a week/MOF in a typical computer) it can be applied in very limited systems.
On the other hand, the large-scale screening with cost effective computational methods can monitor rapidly any MOF (approximately a minute/MOF in a typical computer) and thus thousands can be evaluated in the same period of time. But, as the authors state, “chemical intuition is absence and low-level computations can lead to unreal results or miss important species in the screening” .24
The ultimate computational technique should have the accuracy of the ab initio methods and the speed of the classical approaches, strategically combined with the chemical intuition of the researcher. But is this possible? “Can the computer learn chemistry?”
In this communication, we go one step further and we introduce “machine learning” for predicting gas adsorption in MOFs. Machine Learning is not new in the scientific community. Machine learning is the subfield of artificial intelligence that studies methods that can automatically learn interesting patterns from data. It overlaps with statistics in scope. The latter is a sub-branch of mathematics and so it traditionally favors problems with mathematical analytic solutions and arguably focuses less on automation and computation. The fields of statistics, machine learning, pattern recognition, and data mining are gradually merging into the emerging field of data science. Machine learning techniques have been successfully applied in a variety of domains. Examples of such applications include: recommender systems,26 automatic speech recognition,27 real-time face detection,28 identification of protein-protein interactions in yeast,29 peptide identification from tandem mass spectra,30 prediction of brain maturity from fMRI data,31 prediction of diffuse large B-cell lymphoma32 and hepatocellular carcinoma33 from gene expression data.
In our study, we carefully collected from the literature 100 MOFs that have been synthesized in different laboratories around the world and their CO2 and H2 storage properties were accurately measured in specific thermodynamic conditions. For the H2 we gather data from different MOFs measured at 1 bar, 77 K. For the CO2 a small pressure and temperature range (0.99–1.20 bar in 293–313 K) was unavoidable since the 100 selected experiments were not in identical thermodynamic conditions. Nevertheless, we believe this small deviation will not affect the findings of our investigation, which is the testing of a new methodology based in machine learning.
With those we construct a small database (also called “dataset”) containing their key structural parameters like organic linker, metal cluster and functional groups. Across all selected MOFs, 62 organic linkers, 18 metal clusters and 12 functional groups were identified. Each such structural property can be encoded as a binary parameter (also called variable or feature), indicating its presence or absence in a specific MOF. A matrix representation was used to represent each dataset, with one row for each MOF (100 in total) and one column for each structural feature (92 in total). The datasets are provided as Supplementary Material.
A Machine Learning algorithm then learns a function (also called “model”) f that approximates the storage properties of MOFs given their structural parameters (Fig. 2). The hope is that the model f can generalize and accurately predict an approximate value for a new material, never seen before, represented with the values of its structural parameters. If the predicted property for the new material is not in the desired level, there is no point in synthesizing the material and vice-versa. Thus, an accurate predictive model can guide the synthesis of new materials and experimentation.
For our computational experiments, we used a customized version of the Just Add Data v0.6 tool (JAD Bio; Gnosis Data Analysis; www.gnosisda.gr). JAD has also been recently successfully applied to the prediction of proteins to periplasmic or cytoplasmic given their mature amino acid sequence.34 Though, a totally different problem, the application shows the ability of the automated pipeline to learn patterns from data that generalize to new data. JAD employs a fully-automated machine learning pipeline for producing a model from a dataset and an estimate of its predictive performance on new, unseen MOFs. The latter is especially important, as the main goal is to create a model that is able to perform well on new data, rather than the data used for producing it.
We performed a computational experiment to validate the predictive performance estimation of the model provided by JAD on new MOFs. For each original dataset, sub-samples (i.e., subsets of MOFs) were randomly selected (without replacement) of size 40, 50, …, 100%, and a model was learned using JAD from each such sub-dataset. In other words, we simulate the scenario where only a portion of the original data is available, the tool is run to learn a predictive model on them, and subsequently more data is collected prospectively upon which the predictive performance of the model is estimated. JAD outputs a predictive performance estimation derived from its input dataset. This is compared against the remaining data held out to obtain a second performance estimation, simulating the application of the predictive models on new MOFs. The above was repeated 100 times for each sub-sample size. This experiment is used only as a verification of the whole procedure and the estimation of its variance.
It can be clearly seen in Fig. 3 that the error decreases with increased sample size. For both datasets, the mean absolute error on the test set is lower than that estimated on the training set, suggesting that the data analysis pipeline used by JAD does not provide optimistic estimations; on the contrary, it provides slightly conservative performance estimates. This allows us to have confidence in the performance estimation provided by the tool of the final models trained on the full dataset. Note that, even when 100% of the MOFs are used by JAD there is still some variance on the estimated error, which is the reason why all experiments were repeated 100 times. The (conservative) estimated mean absolute error of the models (when 100% of the available sample is used for training) is 4.07 g _CO2/g_MOF and 0.47 g_H2/g_MOF.
Internally, in order to provide with a conservative predictive performance estimate JAD also (repeatedly) holds out some of the input data and evaluates predictions of the model learnt on the remaining data on the held out set. These are called “out-of-sample” predictions. JAD also outputs the out-of-sample predictions on the input MOFs (see “Methods” for a detailed description). Figure 4 shows the average predicted values over 100 repeated executions of JAD on the complete set of MOFs. There is a clear positive relationship between the predicted and actual values (Pearson correlation of 0.68 and 0.61 for CO2 and H2, respectively), although the ones on the lower and upper ranges are overestimated and underestimated respectively. It is expected that predictions would further improve if more MOFs were used for training the models.
To gauge the practical significance of the results we check the accuracy of the model in filtering in practically useful and promising-to-synthesize MOFs. Specifically, we use the model to select the MOFs that are above a given threshold t, which is deemed of practical significance. We then measure how many predictions are indeed above the threshold. We used all predictions of JAD using the complete datasets and across all 100 repetitions. The results are shown in Table 1. The thresholds have been pre-selected and not optimized for performance through repeated trials. For example, for threshold 16 (gr_CO2/gr_MOF) for a researcher employing the model to synthesize a MOF with predicted CO2 above the threshold would expect 86% chance that the MOF actually exhibits a CO2 retention above 16 (gr_CO2/gr_MOF). In contrast, if the model is not employed for predictions, random guessing has a chance of about 21% to synthesize high retention MOFs.
Overall, the results demonstrate that:
(a) the chemical properties of MOFs are predictable (stochastically, not deterministically)
(b) the accuracy of predictions increases with sample size
(c) modern machine learning algorithms and automated predictive analytics pipelines can learn predictive models that generalize to unseen MOFs, and guide experiments in material discovery by predicting properties of new materials.
Despite the promising results, both the theory and the scope of the computational experiments have limitations that need to be considered. First, we note that the performance estimation is correct when employed on new MOFs coming from the same statistical distribution as the MOFs employed during training. The collection of MOFs used for training is a selection from a “universe” of possible MOFs. If new MOFs are selected for testing with a different probability, the performance of predictions may increase or decrease.
Another limitation of the approach is that the models cannot be expected to generalize to unseen linkers or metals. This is a restriction of the data representation, rather than machine learning in general. If for example, the representation of a MOF included not just the presence or absence of a linker or metal, but in a finer detail, chemical properties of the linker or metal, then potentially a model could learn to predict gas storage in new MOFs employing new linkers not seen in the training test.
The problem that we study, that is, to predict the gas adsorption properties of MOFs given their structural properties, is called “supervised” learning in the field of machine learning. In “supervised learning”, the computer learns from labeled historical examples where the outcome is known, to generalize and make predictions on future data where the outcome is unknown.
Just Add Data (JAD Bio; Gnosis Data Analysis PC; www.gnosisda.com) is an automated tool that produces a supervised machine learning model and an estimate of its predictive performance. For regression problems (i.e., when the outcome is a continuous value, like CO2 and H2 adsorption), JAD employs state-of-the-art machine learning algorithms, such as “random forest regression” (RF),35 “support vector regression” (SVR)36 using both polynomial and Gaussian kernels and “ridge linear regression”37 although the list is continuously being enriched. In the computational experiments, out of 100 repetitions on the full set of MOFs, RF and ridge regression were selected two times each and SVR 96 times for the H2 data, while for the CO2 data only SVR models were selected. This happens due to the random split of the data in the cross-validation procedure. Overall however, the results are fairly robust.
Recently it has been shown experimentally on a variety of problems that random forests and support vector machines outperform other algorithms on average,38 and thus these were deemed sufficient choices for the moment. We note however that the best algorithm depends on the problem (see the no free lunch theorem for machine learning,39 and thus there may be better suited algorithms for the problems considered in this work. A high-level overview of the pipeline used by JAD is shown in Fig. 5. A detailed description of the pipeline follows.
All those algorithms require the user to set a number of parameters (called “hyper-parameters” in this context) that determine their behavior, and whose optimal values are problem-dependent. Results can greatly vary depending on correctly tuning the values of the hyper-parameters. The hyper-parameters are depicted as sliders in Fig. 5. Their optimal values cannot be found analytically; their values must be found by trial-and-error. JAD uses the statistical properties of the input data (such as the number of training examples and number of features) to determine a set of hyper-parameter combinations (called “configuration” hereafter) to try. In order to find the best algorithm and hyper-parameter configuration and to learn a final model, JAD uses the “K-fold cross-validation protocol”,40 described next.
The K-fold cross-validation protocol splits the data into K non-overlapping approximately equal-sized sets (called “folds”) of MOFs. In this work, we used K = 5. Each of them is held-out for testing purposes and the rest are used for training. It proceeds by keeping each fold out once, training models using all configurations on the remaining K-1 folds, and estimating their performance on the held-out fold. The held-out test sets are used to simulate the application of the models on new MOFs. In the end, K performance estimates are computed for each configuration, and the one with the best average performance is selected as the best configuration. A final model is produced by applying the best configuration on the complete set of MOFs. Note that, the predictions obtained for each MOF when in the hold-out test set can also be returned, and can be used to get an idea of how the final model would perform on unseen MOFs; these are the predictions used for Fig. 4 and Table 1.
Unfortunately, the estimation of this best performing configuration is optimistically biased because numerous models have been tried.41 The optimistic estimation is equivalent to the problem of multiple testing in statistics, called “the multiple induction problem in Machine Learning”.42 The problem is created because the test sets (folds) are employed multiple times, once for each configuration tried. The optimism problem has been noted both theoretically as well as experimentally. JAD estimates the bias of the performance using a bootstrap method,43,44 and removes it to return the final performance estimate.
The 2 databases of the 100 MOFs (one for CO2 and one for H2 gases) used for this study are available as Supplementary Material.
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This research has been co-financed by the European Union (European Social Fund – ESF) and Greek national funds through the Operational Program “Education and Lifelong Learning” of the National Strategic Reference Framework (NSRF)—Research Funding Program: THALES. This research has been co-financed by AFOSR/EOARD under grant numberFA9550-15-1-0291.
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