{"title":"时变薛定谔方程解的稀疏自适应基集方法","authors":"Keiran C. Thompson, Todd J. Martinez","doi":"10.1080/00268976.2023.2268221","DOIUrl":null,"url":null,"abstract":"AbstractScalable numerical solutions to the time dependent Schrodinger equation remain an outstanding goal in theoretical chemistry. Here we present a method which utilises recent breakthroughs in signal processing to consistently adapt a dictionary of basis functions to the dynamics of the system. We show that for two low-dimensional model problems the size of the basis set does not grow quickly with time and appears only weakly dependent on dimensionality. The generality of this finding remains to be seen. The method primarily uses energies and gradients of the potential, opening the possibility for its use in on-the-fly ab initio quantum wavepacket dynamics.KEYWORDS: Wavepacket propagationtime-dependent Schrodinger equationcompressed sensing AcknowledgementsThis material is based upon work supported by the U.S. Department of Energy Office of Science National Quantum Information Science Research Centers as part of the Q-NEXT centre. Partial support was also provided by the AMOS programme of the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division.Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThis work was supported by Basic Energy Sciences [Q-Next Centre and AMOS Programme].","PeriodicalId":18817,"journal":{"name":"Molecular Physics","volume":"2 1","pages":"0"},"PeriodicalIF":1.6000,"publicationDate":"2023-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sparse adaptive basis set methods for solution of the time dependent Schrodinger equation\",\"authors\":\"Keiran C. Thompson, Todd J. Martinez\",\"doi\":\"10.1080/00268976.2023.2268221\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"AbstractScalable numerical solutions to the time dependent Schrodinger equation remain an outstanding goal in theoretical chemistry. Here we present a method which utilises recent breakthroughs in signal processing to consistently adapt a dictionary of basis functions to the dynamics of the system. We show that for two low-dimensional model problems the size of the basis set does not grow quickly with time and appears only weakly dependent on dimensionality. The generality of this finding remains to be seen. The method primarily uses energies and gradients of the potential, opening the possibility for its use in on-the-fly ab initio quantum wavepacket dynamics.KEYWORDS: Wavepacket propagationtime-dependent Schrodinger equationcompressed sensing AcknowledgementsThis material is based upon work supported by the U.S. Department of Energy Office of Science National Quantum Information Science Research Centers as part of the Q-NEXT centre. Partial support was also provided by the AMOS programme of the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division.Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThis work was supported by Basic Energy Sciences [Q-Next Centre and AMOS Programme].\",\"PeriodicalId\":18817,\"journal\":{\"name\":\"Molecular Physics\",\"volume\":\"2 1\",\"pages\":\"0\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2023-10-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Physics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/00268976.2023.2268221\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Physics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/00268976.2023.2268221","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Sparse adaptive basis set methods for solution of the time dependent Schrodinger equation
AbstractScalable numerical solutions to the time dependent Schrodinger equation remain an outstanding goal in theoretical chemistry. Here we present a method which utilises recent breakthroughs in signal processing to consistently adapt a dictionary of basis functions to the dynamics of the system. We show that for two low-dimensional model problems the size of the basis set does not grow quickly with time and appears only weakly dependent on dimensionality. The generality of this finding remains to be seen. The method primarily uses energies and gradients of the potential, opening the possibility for its use in on-the-fly ab initio quantum wavepacket dynamics.KEYWORDS: Wavepacket propagationtime-dependent Schrodinger equationcompressed sensing AcknowledgementsThis material is based upon work supported by the U.S. Department of Energy Office of Science National Quantum Information Science Research Centers as part of the Q-NEXT centre. Partial support was also provided by the AMOS programme of the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division.Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThis work was supported by Basic Energy Sciences [Q-Next Centre and AMOS Programme].
期刊介绍:
Molecular Physics is a well-established international journal publishing original high quality papers in chemical physics and physical chemistry. The journal covers all experimental and theoretical aspects of molecular science, from electronic structure, molecular dynamics, spectroscopy and reaction kinetics to condensed matter, surface science, and statistical mechanics of simple and complex fluids. Contributions include full papers, preliminary communications, research notes and invited topical review articles.