{"title":"基于广义价键波函数的量子模拟酉块相关耦合簇Ansatz","authors":"Jiaqi Hu, Qingchun Wang* and Shuhua Li*, ","doi":"10.1021/acs.jctc.5c0023910.1021/acs.jctc.5c00239","DOIUrl":null,"url":null,"abstract":"<p >Strongly correlated (SC) systems present significant challenges for classical quantum chemistry methods. Quantum computing, particularly the variational quantum eigensolver (VQE), offers a promising framework to address these challenges by inherently supporting exponentially large configuration spaces. However, its application to SC systems remains limited due to the single-reference nature of the widely used ansatzes such as unitary coupled cluster (UCC). To address this challenge, we propose the generalized valence bond-based unitary block correlated coupled cluster (GVB-UBCCC) method. This novel ansatz incorporates the multiconfigurational nature of generalized valence bond (GVB) and the accuracy of block correlated coupled cluster (BCCC) methods, making it well-suited for SC systems. We have implemented the GVB-UBCCC method with up to two-block correlation (GVB-UBCCC2) and applied it to investigate ground-state energies for several SC systems, including H<sub>4</sub>, the water dimer, N<sub>2</sub>H<sub>2</sub>, and S<sub>6</sub>, at most described by 24 qubits. Our approach demonstrates that for these systems, GVB-UBCCC2 can achieve more accurate ground-state energies than UCCSD in most cases while requiring only <i>O</i>(<i>N</i><sup>2</sup>) quantum gates and parameters, as opposed to the <i>O</i>(<i>N</i><sup>4</sup>) scaling of UCCSD. The results highlight the effectiveness and potential advantages of GVB-UBCCC in SC systems.</p>","PeriodicalId":45,"journal":{"name":"Journal of Chemical Theory and Computation","volume":"21 9","pages":"4579–4590 4579–4590"},"PeriodicalIF":5.5000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unitary Block-Correlated Coupled Cluster Ansatz Based on the Generalized Valence Bond Wave Function for Quantum Simulation\",\"authors\":\"Jiaqi Hu, Qingchun Wang* and Shuhua Li*, \",\"doi\":\"10.1021/acs.jctc.5c0023910.1021/acs.jctc.5c00239\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Strongly correlated (SC) systems present significant challenges for classical quantum chemistry methods. Quantum computing, particularly the variational quantum eigensolver (VQE), offers a promising framework to address these challenges by inherently supporting exponentially large configuration spaces. However, its application to SC systems remains limited due to the single-reference nature of the widely used ansatzes such as unitary coupled cluster (UCC). To address this challenge, we propose the generalized valence bond-based unitary block correlated coupled cluster (GVB-UBCCC) method. This novel ansatz incorporates the multiconfigurational nature of generalized valence bond (GVB) and the accuracy of block correlated coupled cluster (BCCC) methods, making it well-suited for SC systems. We have implemented the GVB-UBCCC method with up to two-block correlation (GVB-UBCCC2) and applied it to investigate ground-state energies for several SC systems, including H<sub>4</sub>, the water dimer, N<sub>2</sub>H<sub>2</sub>, and S<sub>6</sub>, at most described by 24 qubits. Our approach demonstrates that for these systems, GVB-UBCCC2 can achieve more accurate ground-state energies than UCCSD in most cases while requiring only <i>O</i>(<i>N</i><sup>2</sup>) quantum gates and parameters, as opposed to the <i>O</i>(<i>N</i><sup>4</sup>) scaling of UCCSD. The results highlight the effectiveness and potential advantages of GVB-UBCCC in SC systems.</p>\",\"PeriodicalId\":45,\"journal\":{\"name\":\"Journal of Chemical Theory and Computation\",\"volume\":\"21 9\",\"pages\":\"4579–4590 4579–4590\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2025-04-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Theory and Computation\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jctc.5c00239\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Theory and Computation","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jctc.5c00239","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Unitary Block-Correlated Coupled Cluster Ansatz Based on the Generalized Valence Bond Wave Function for Quantum Simulation
Strongly correlated (SC) systems present significant challenges for classical quantum chemistry methods. Quantum computing, particularly the variational quantum eigensolver (VQE), offers a promising framework to address these challenges by inherently supporting exponentially large configuration spaces. However, its application to SC systems remains limited due to the single-reference nature of the widely used ansatzes such as unitary coupled cluster (UCC). To address this challenge, we propose the generalized valence bond-based unitary block correlated coupled cluster (GVB-UBCCC) method. This novel ansatz incorporates the multiconfigurational nature of generalized valence bond (GVB) and the accuracy of block correlated coupled cluster (BCCC) methods, making it well-suited for SC systems. We have implemented the GVB-UBCCC method with up to two-block correlation (GVB-UBCCC2) and applied it to investigate ground-state energies for several SC systems, including H4, the water dimer, N2H2, and S6, at most described by 24 qubits. Our approach demonstrates that for these systems, GVB-UBCCC2 can achieve more accurate ground-state energies than UCCSD in most cases while requiring only O(N2) quantum gates and parameters, as opposed to the O(N4) scaling of UCCSD. The results highlight the effectiveness and potential advantages of GVB-UBCCC in SC systems.
期刊介绍:
The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.