Guoxiao Liu, Jörn Manz, Huihui Wang, Yonggang Yang
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Here we investigate the electronic chirality flips in oriented RbCs induced by all possible ( <math> <semantics><mrow><mo>+</mo> <mo>+</mo></mrow> <annotation>${ + + }$</annotation> </semantics> </math> , <math> <semantics><mrow><mo>-</mo> <mo>+</mo></mrow> <annotation>${ - + }$</annotation> </semantics> </math> , <math> <semantics><mrow><mo>+</mo> <mo>-</mo></mrow> <annotation>${ + - }$</annotation> </semantics> </math> , <math> <semantics><mrow><mo>-</mo> <mo>-</mo></mrow> <annotation>${ - - }$</annotation> </semantics> </math> ) combinations of circular polarizations of two coincident well-designed laser pulses. Accordingly, the <math> <semantics><mrow><mo>+</mo> <mo>+</mo></mrow> <annotation>${ + + }$</annotation> </semantics> </math> and <math> <semantics><mrow><mo>-</mo> <mo>-</mo></mrow> <annotation>${ - - }$</annotation> </semantics> </math> as well as the <math> <semantics><mrow><mo>+</mo> <mo>-</mo></mrow> <annotation>${ + - }$</annotation> </semantics> </math> and <math> <semantics><mrow><mo>-</mo> <mo>+</mo></mrow> <annotation>${ - + }$</annotation> </semantics> </math> combinations generate opposite electronic enantiomers, e. g. R<sub>a</sub> versus S<sub>a</sub>, followed by opposite periodic chirality flips, e. g. from R<sub>a</sub> to S<sub>a</sub> to R<sub>a</sub> to S<sub>a</sub> etc. versus from S<sub>a</sub> to R<sub>a</sub> to S<sub>a</sub> to R<sub>a</sub> etc, with periods in the fs and as time domains, respectively. The laser induced spatio-temporal symmetries are derived from first principles and illustrated by quantum dynamics simulations.</p>","PeriodicalId":9819,"journal":{"name":"Chemphyschem","volume":" ","pages":"e202400595"},"PeriodicalIF":2.3000,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Spatio-Temporal Symmetries of Electronic Chirality Flips in Oriented RbCs Induced by two Coincident Laser Pulses with Circular ++, +-, -+, -- Polarizations.\",\"authors\":\"Guoxiao Liu, Jörn Manz, Huihui Wang, Yonggang Yang\",\"doi\":\"10.1002/cphc.202400595\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Recently it has been shown that two coincident well designed laser pulses with two different combinations of circular polarizations ( <math> <semantics><mrow><mo>+</mo> <mo>+</mo></mrow> <annotation>${ + + }$</annotation> </semantics> </math> or <math> <semantics><mrow><mo>-</mo> <mo>+</mo></mrow> <annotation>${ - + }$</annotation> </semantics> </math> ) can create chiral electronic densities in an oriented heteronuclear diatomic molecule. Subsequently, the chirality flips from the electronic R<sub>a</sub> to S<sub>a</sub> to R<sub>a</sub> to S<sub>a</sub> etc. enantiomers, with periods in the femtosecond (fs) and attosecond (as) time domains. The results were obtained by means of quantum dynamics simulations for oriented NaK. Here we investigate the electronic chirality flips in oriented RbCs induced by all possible ( <math> <semantics><mrow><mo>+</mo> <mo>+</mo></mrow> <annotation>${ + + }$</annotation> </semantics> </math> , <math> <semantics><mrow><mo>-</mo> <mo>+</mo></mrow> <annotation>${ - + }$</annotation> </semantics> </math> , <math> <semantics><mrow><mo>+</mo> <mo>-</mo></mrow> <annotation>${ + - }$</annotation> </semantics> </math> , <math> <semantics><mrow><mo>-</mo> <mo>-</mo></mrow> <annotation>${ - - }$</annotation> </semantics> </math> ) combinations of circular polarizations of two coincident well-designed laser pulses. Accordingly, the <math> <semantics><mrow><mo>+</mo> <mo>+</mo></mrow> <annotation>${ + + }$</annotation> </semantics> </math> and <math> <semantics><mrow><mo>-</mo> <mo>-</mo></mrow> <annotation>${ - - }$</annotation> </semantics> </math> as well as the <math> <semantics><mrow><mo>+</mo> <mo>-</mo></mrow> <annotation>${ + - }$</annotation> </semantics> </math> and <math> <semantics><mrow><mo>-</mo> <mo>+</mo></mrow> <annotation>${ - + }$</annotation> </semantics> </math> combinations generate opposite electronic enantiomers, e. g. R<sub>a</sub> versus S<sub>a</sub>, followed by opposite periodic chirality flips, e. g. from R<sub>a</sub> to S<sub>a</sub> to R<sub>a</sub> to S<sub>a</sub> etc. versus from S<sub>a</sub> to R<sub>a</sub> to S<sub>a</sub> to R<sub>a</sub> etc, with periods in the fs and as time domains, respectively. The laser induced spatio-temporal symmetries are derived from first principles and illustrated by quantum dynamics simulations.</p>\",\"PeriodicalId\":9819,\"journal\":{\"name\":\"Chemphyschem\",\"volume\":\" \",\"pages\":\"e202400595\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-11-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemphyschem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/cphc.202400595\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/9/12 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemphyschem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cphc.202400595","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/12 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
最近的研究表明,两个设计良好的、具有两种不同圆偏振(++ 或 -+)组合的重合激光脉冲可以在定向异核二原子分子中产生手性电子密度。随后,手性从电子 Ra 对映体翻转到 Sa 对映体,再从 Ra 对映体翻转到 Sa 对映体等,翻转周期为飞秒(fs)和阿秒(as)时域。这些结果是通过量子动力学模拟定向 NaK 得到的。在此,我们研究了取向 RbCs 中所有可能的(++ , -+ , +- , -- )圆偏振组合诱导的电子手性翻转。因此,++ 和 -- 以及 +- 和 -+ 组合会产生相反的电子对映体,例如 Ra 对 Sa,随后会产生相反的周期性手性翻转,例如从 Ra 到 Sa 再到 Ra 到 Sa 等与从 Sa 到 Ra 再到 Sa 到 Ra 等,周期分别为 fs 和时间域。激光诱导的时空对称性源自第一原理,并通过量子动力学模拟加以说明。
Spatio-Temporal Symmetries of Electronic Chirality Flips in Oriented RbCs Induced by two Coincident Laser Pulses with Circular ++, +-, -+, -- Polarizations.
Recently it has been shown that two coincident well designed laser pulses with two different combinations of circular polarizations ( or ) can create chiral electronic densities in an oriented heteronuclear diatomic molecule. Subsequently, the chirality flips from the electronic Ra to Sa to Ra to Sa etc. enantiomers, with periods in the femtosecond (fs) and attosecond (as) time domains. The results were obtained by means of quantum dynamics simulations for oriented NaK. Here we investigate the electronic chirality flips in oriented RbCs induced by all possible ( , , , ) combinations of circular polarizations of two coincident well-designed laser pulses. Accordingly, the and as well as the and combinations generate opposite electronic enantiomers, e. g. Ra versus Sa, followed by opposite periodic chirality flips, e. g. from Ra to Sa to Ra to Sa etc. versus from Sa to Ra to Sa to Ra etc, with periods in the fs and as time domains, respectively. The laser induced spatio-temporal symmetries are derived from first principles and illustrated by quantum dynamics simulations.
期刊介绍:
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