{"title":"客分子占位和电场对CO2水合物导热性能的影响。","authors":"Yuan Li, Kaibin Xiong, Yongxiao Qu, Xiaoyu Shi, Zhisen Zhang, Jianyang Wu","doi":"10.1063/5.0286293","DOIUrl":null,"url":null,"abstract":"<p><p>CO2 hydrate technology plays a pivotal role in carbon dioxide capture/storage, gas separation, and natural gas recovery from natural gas hydrates, while simultaneously serving as a cost-effective phase-change material for thermal energy storage. The thermal transport characteristics of CO2 hydrates are of particular importance in these promising applications. Here, the role of CO2 molecular occupancy and external electric fields on the thermal conductivity (κ) of sI-type CO2 hydrates is explored using equilibrium molecular dynamics simulations. Results reveal that increasing CO2 occupancy in large 51262 cages enhances κ by up to 27.2%, while small 512 cages contribute minimally (<1%). The water framework dominates heat transport (>90%), with CO2@51262 and CO2@512 cages contributing ∼17%-18% and <1%, respectively, mediated by synergistic host-guest interactions. External electric fields reduce κ by around 4%-5% due to enhanced low-frequency phonon localization in CO2 and intensified anharmonic scattering. Phonon analyses, including phonon density of states, phonon lifetime, phonon participation ratio, and spectral energy density, reveal that CO2 occupancy suppresses water lattice vibrations, while electric fields redistribute phonon modes, reducing delocalization. This work advances the fundamental understanding of thermal transport in hydrate systems.</p>","PeriodicalId":15313,"journal":{"name":"Journal of Chemical Physics","volume":"163 8","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of guest molecular occupancy and electric field on thermal conductivity of CO2 hydrates.\",\"authors\":\"Yuan Li, Kaibin Xiong, Yongxiao Qu, Xiaoyu Shi, Zhisen Zhang, Jianyang Wu\",\"doi\":\"10.1063/5.0286293\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>CO2 hydrate technology plays a pivotal role in carbon dioxide capture/storage, gas separation, and natural gas recovery from natural gas hydrates, while simultaneously serving as a cost-effective phase-change material for thermal energy storage. The thermal transport characteristics of CO2 hydrates are of particular importance in these promising applications. Here, the role of CO2 molecular occupancy and external electric fields on the thermal conductivity (κ) of sI-type CO2 hydrates is explored using equilibrium molecular dynamics simulations. Results reveal that increasing CO2 occupancy in large 51262 cages enhances κ by up to 27.2%, while small 512 cages contribute minimally (<1%). The water framework dominates heat transport (>90%), with CO2@51262 and CO2@512 cages contributing ∼17%-18% and <1%, respectively, mediated by synergistic host-guest interactions. External electric fields reduce κ by around 4%-5% due to enhanced low-frequency phonon localization in CO2 and intensified anharmonic scattering. Phonon analyses, including phonon density of states, phonon lifetime, phonon participation ratio, and spectral energy density, reveal that CO2 occupancy suppresses water lattice vibrations, while electric fields redistribute phonon modes, reducing delocalization. This work advances the fundamental understanding of thermal transport in hydrate systems.</p>\",\"PeriodicalId\":15313,\"journal\":{\"name\":\"Journal of Chemical Physics\",\"volume\":\"163 8\",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-08-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Physics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1063/5.0286293\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Physics","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1063/5.0286293","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Effects of guest molecular occupancy and electric field on thermal conductivity of CO2 hydrates.
CO2 hydrate technology plays a pivotal role in carbon dioxide capture/storage, gas separation, and natural gas recovery from natural gas hydrates, while simultaneously serving as a cost-effective phase-change material for thermal energy storage. The thermal transport characteristics of CO2 hydrates are of particular importance in these promising applications. Here, the role of CO2 molecular occupancy and external electric fields on the thermal conductivity (κ) of sI-type CO2 hydrates is explored using equilibrium molecular dynamics simulations. Results reveal that increasing CO2 occupancy in large 51262 cages enhances κ by up to 27.2%, while small 512 cages contribute minimally (<1%). The water framework dominates heat transport (>90%), with CO2@51262 and CO2@512 cages contributing ∼17%-18% and <1%, respectively, mediated by synergistic host-guest interactions. External electric fields reduce κ by around 4%-5% due to enhanced low-frequency phonon localization in CO2 and intensified anharmonic scattering. Phonon analyses, including phonon density of states, phonon lifetime, phonon participation ratio, and spectral energy density, reveal that CO2 occupancy suppresses water lattice vibrations, while electric fields redistribute phonon modes, reducing delocalization. This work advances the fundamental understanding of thermal transport in hydrate systems.
期刊介绍:
The Journal of Chemical Physics publishes quantitative and rigorous science of long-lasting value in methods and applications of chemical physics. The Journal also publishes brief Communications of significant new findings, Perspectives on the latest advances in the field, and Special Topic issues. The Journal focuses on innovative research in experimental and theoretical areas of chemical physics, including spectroscopy, dynamics, kinetics, statistical mechanics, and quantum mechanics. In addition, topical areas such as polymers, soft matter, materials, surfaces/interfaces, and systems of biological relevance are of increasing importance.
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