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Sub-nanosecond secondary geminate recombination in mercury halides HgX2 (X = I, Br) investigated by time-resolved x-ray scattering

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dc.contributor.authorDenis Leshchev-
dc.contributor.authorDmitry Khakhulin-
dc.contributor.authorGemma Newby-
dc.contributor.authorHosung Ki-
dc.contributor.authorHyotcherl Ihee-
dc.contributor.authorMichael Wulff-
dc.date.available2019-10-11T08:07:57Z-
dc.date.created2019-08-20-
dc.date.issued2019-08-
dc.identifier.issn0021-9606-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/6286-
dc.description.abstract© 2019 Author(s).In this work, we present a detailed investigation on the recombination dynamics of mercury halides HgX2 (X = I, Br) in acetonitrile solution after UV-induced photodissociation. The study is performed by combining time-resolved wide-angle x-ray scattering (TRWAXS) and optical transient absorption spectroscopy. Up to 68% of the UV (266 nm) photodissociated HgX and X radicals that escape the solvent cage surrounding parent HgX2 recombine within a nanosecond after photodissociation. In contrast to classical primary geminate recombination, occurring on much faster time scales, we interpret the sub-nanosecond recombination channel as secondary geminate recombination (SGR), also referred to as diffusion-limited geminate recombination. The family of triatomic mercury halides therefore represents an important class of molecules to study chemical mechanisms of solvent-dependent SGR by TRWAXS. The methodology described here allows for direct mapping of the time-dependent inter-radical distance distribution function, a critical parameter for the assessment of the SGR dynamics in solution phase and solvation in general-
dc.description.uri1-
dc.language영어-
dc.publisherAMER INST PHYSICS-
dc.titleSub-nanosecond secondary geminate recombination in mercury halides HgX2 (X = I, Br) investigated by time-resolved x-ray scattering-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000480258200004-
dc.identifier.scopusid2-s2.0-85070408755-
dc.identifier.rimsid69529-
dc.contributor.affiliatedAuthorHosung Ki-
dc.contributor.affiliatedAuthorHyotcherl Ihee-
dc.identifier.doi10.1063/1.5096422-
dc.identifier.bibliographicCitationJOURNAL OF CHEMICAL PHYSICS, v.151, no.5, pp.054310-
dc.citation.titleJOURNAL OF CHEMICAL PHYSICS-
dc.citation.volume151-
dc.citation.number5-
dc.citation.startPage054310-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusTRANSITION-STATE-
dc.subject.keywordPlusDYNAMICS-
dc.subject.keywordPlusPHOTODISSOCIATION-
dc.subject.keywordPlusPHOTOLYSIS-
dc.subject.keywordPlusMOLECULES-
dc.subject.keywordPlusRADICALS-
dc.subject.keywordPlusABSORPTION-
dc.subject.keywordPlusVIBRATION-
dc.subject.keywordPlusKINETICS-
Appears in Collections:
Center for Nanomaterials and Chemical Reactions(나노물질 및 화학반응 연구단) > 1. Journal Papers (저널논문)
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J. Chem. Phys. 151, 054310 (2019).pdfDownload

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