東華大學圖書館 |

Domain-Knowledge-Guided Machine Learning towards Accurate Materials Property Prediction and Materials Discovery.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Domain-Knowledge-Guided Machine Learning towards Accurate Materials Property Prediction and Materials Discovery./
作者:	Ye, Weike.
面頁冊數:	1 online resource (118 pages)
附註:	Source: Dissertations Abstracts International, Volume: 83-04, Section: B.
Contained By:	Dissertations Abstracts International83-04B.
標題:	Computational chemistry. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28644445click for full text (PQDT)
ISBN:	9798460451821

Domain-Knowledge-Guided Machine Learning towards Accurate Materials Property Prediction and Materials Discovery.
Ye, Weike.

Domain-Knowledge-Guided Machine Learning towards Accurate Materials Property Prediction and Materials Discovery. - 1 online resource (118 pages)

Source: Dissertations Abstracts International, Volume: 83-04, Section: B.

Thesis (Ph.D.)--University of California, San Diego, 2021.

Includes bibliographical references

In the past few decades, the first principles modeling algorithms, especially density functional theory (DFT), have been important complements to experiments in studying properties and materials design. Thanks to the success of DFT and the fast development of computational capabilities, we have witnessed the exploration of a huge amount of materials data. The logical next step is the introduction of tools capable of making use of the generated data. Machine learning (ML) techniques are such tools to extract knowledge from data and make predictions at a sub-second speed, which are currently steering materials science into a new data-driven paradigm.In this thesis, following the close guidance of domain knowledge in materials science, we strive to develop accurate, interpretable ML models that could potentially serve as the surrogate of DFT in property prediction and the design of new materials. A unifying theme that differentiates the models in this thesis from their counterparts in other existing ML works is the practice of the principle of parsimony, where we aspire to develop and explain the models with minimum features.The thesis is divided into three topics. In the first topic (Chapter 2), we aimed at predicting the phase stability of the inorganic crystals, which is often the first step in any materials discovery. Inspired by Pauling's rules, we show that deep neural networks utilizing just the Pauling electronegativity and ionic radii of the species of the symmetrically distinct sites can predict the DFT formation energies of garnets and perovskites within the low mean absolute errors (MAEs) of 7-34 meV atom-1. The models can be easily extended to mixed garnets and perovskites with little loss in accuracy by using a binary encoding scheme, extending the applicability of ML models to the infinite universe of mixed-species crystals.In the second topic (Chapter 3), we targeted predicting the bandgap. By machine learning on 1823 data, we show that the eXtreme gradient boosting(XGBoost) model reaches the state-of-the-art MAE of 0.13 eV at predicting the DFT bandgap (using generalized gradient approximation functional) of garnets. Interpreting the model's behavior reveals that the bandgap is affected mainly by the atomic number of the species occupying the tetrahedron sites in a garnet crystal. Integrating the models from both Chapter 2 and Chapter 3, we devised a high-throughput screening (HTS) workflow to screen for Eu2+-doped red emission phosphors in the garnet crystal family. Two candidates, Ca(Er,Tb)2Mg2Si3O12, were identified by rapidly transversing 5554 candidate compositions, which is computationally prohibitive for pure DFT-based HTS workflows due to the large cell size of the garnet structures.In the last topic (Chapter 4), we investigated the 2D defect, grain boundary (GB), in polycrystalline systems. We show that the energy of a grain boundary, normalized by the bulk cohesive energy, can be described purely by four geometric features. By machine learning on a large computed database of 369 low-Σ (Σ < 10) GBs of more than 50 metals, we developed a model that can predict the grain boundary energies to within 0.12 J m-2. This universal GB energy model can be extrapolated to the energies of higher sigma GBs with a modest increase in prediction error.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023

Mode of access: World Wide Web

ISBN: 9798460451821Subjects--Topical Terms:

3350019
Computational chemistry.
Subjects--Index Terms:

Machine learningIndex Terms--Genre/Form:

542853
Electronic books.

Domain-Knowledge-Guided Machine Learning towards Accurate Materials Property Prediction and Materials Discovery.
LDR:04719nmm a2200373K 4500 001 2355468
005 20230512095940.5
006 m o d
007 cr mn ---uuuuu
008 241011s2021 xx obm 000 0 eng d
020 $a 9798460451821
035 $a (MiAaPQ)AAI28644445
035 $a AAI28644445
040 $a MiAaPQ $b eng $c MiAaPQ $d NTU
100 1 $a Ye, Weike. $3 3695894
245 1 0 $a Domain-Knowledge-Guided Machine Learning towards Accurate Materials Property Prediction and Materials Discovery.
264 0 $c 2021
300 $a 1 online resource (118 pages)
336 $a text $b txt $2 rdacontent
337 $a computer $b c $2 rdamedia
338 $a online resource $b cr $2 rdacarrier
500 $a Source: Dissertations Abstracts International, Volume: 83-04, Section: B.
500 $a Advisor: Ong, Shyue Ping ; Paesani, Francesco.
502 $a Thesis (Ph.D.)--University of California, San Diego, 2021.
504 $a Includes bibliographical references
520 $a In the past few decades, the first principles modeling algorithms, especially density functional theory (DFT), have been important complements to experiments in studying properties and materials design. Thanks to the success of DFT and the fast development of computational capabilities, we have witnessed the exploration of a huge amount of materials data. The logical next step is the introduction of tools capable of making use of the generated data. Machine learning (ML) techniques are such tools to extract knowledge from data and make predictions at a sub-second speed, which are currently steering materials science into a new data-driven paradigm.In this thesis, following the close guidance of domain knowledge in materials science, we strive to develop accurate, interpretable ML models that could potentially serve as the surrogate of DFT in property prediction and the design of new materials. A unifying theme that differentiates the models in this thesis from their counterparts in other existing ML works is the practice of the principle of parsimony, where we aspire to develop and explain the models with minimum features.The thesis is divided into three topics. In the first topic (Chapter 2), we aimed at predicting the phase stability of the inorganic crystals, which is often the first step in any materials discovery. Inspired by Pauling's rules, we show that deep neural networks utilizing just the Pauling electronegativity and ionic radii of the species of the symmetrically distinct sites can predict the DFT formation energies of garnets and perovskites within the low mean absolute errors (MAEs) of 7-34 meV atom-1. The models can be easily extended to mixed garnets and perovskites with little loss in accuracy by using a binary encoding scheme, extending the applicability of ML models to the infinite universe of mixed-species crystals.In the second topic (Chapter 3), we targeted predicting the bandgap. By machine learning on 1823 data, we show that the eXtreme gradient boosting(XGBoost) model reaches the state-of-the-art MAE of 0.13 eV at predicting the DFT bandgap (using generalized gradient approximation functional) of garnets. Interpreting the model's behavior reveals that the bandgap is affected mainly by the atomic number of the species occupying the tetrahedron sites in a garnet crystal. Integrating the models from both Chapter 2 and Chapter 3, we devised a high-throughput screening (HTS) workflow to screen for Eu2+-doped red emission phosphors in the garnet crystal family. Two candidates, Ca(Er,Tb)2Mg2Si3O12, were identified by rapidly transversing 5554 candidate compositions, which is computationally prohibitive for pure DFT-based HTS workflows due to the large cell size of the garnet structures.In the last topic (Chapter 4), we investigated the 2D defect, grain boundary (GB), in polycrystalline systems. We show that the energy of a grain boundary, normalized by the bulk cohesive energy, can be described purely by four geometric features. By machine learning on a large computed database of 369 low-Σ (Σ < 10) GBs of more than 50 metals, we developed a model that can predict the grain boundary energies to within 0.12 J m-2. This universal GB energy model can be extrapolated to the energies of higher sigma GBs with a modest increase in prediction error.
533 $a Electronic reproduction. $b Ann Arbor, Mich. : $c ProQuest, $d 2023
538 $a Mode of access: World Wide Web
650 4 $a Computational chemistry. $3 3350019
650 4 $a Materials science. $3 543314
653 $a Machine learning
653 $a Materials discovery
653 $a Materials science
653 $a Property prediction
655 7 $a Electronic books. $2 lcsh $3 542853
690 $a 0794
690 $a 0219
710 2 $a ProQuest Information and Learning Co. $3 783688
710 2 $a University of California, San Diego. $b Chemistry and Biochemistry. $3 3430884
773 0 $t Dissertations Abstracts International $g 83-04B.
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28644445 $z click for full text (PQDT)