Sub-nanosecond secondary geminate recombination in mercury halides HgX2 (X = I, Br) investigated by time-resolved x-ray scattering
DC Field | Value | Language |
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dc.contributor.author | Denis Leshchev | - |
dc.contributor.author | Dmitry Khakhulin | - |
dc.contributor.author | Gemma Newby | - |
dc.contributor.author | Hosung Ki | - |
dc.contributor.author | Hyotcherl Ihee | - |
dc.contributor.author | Michael Wulff | - |
dc.date.available | 2019-10-11T08:07:57Z | - |
dc.date.created | 2019-08-20 | - |
dc.date.issued | 2019-08 | - |
dc.identifier.issn | 0021-9606 | - |
dc.identifier.uri | https://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.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | AMER INST PHYSICS | - |
dc.title | Sub-nanosecond secondary geminate recombination in mercury halides HgX2 (X = I, Br) investigated by time-resolved x-ray scattering | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000480258200004 | - |
dc.identifier.scopusid | 2-s2.0-85070408755 | - |
dc.identifier.rimsid | 69529 | - |
dc.contributor.affiliatedAuthor | Hosung Ki | - |
dc.contributor.affiliatedAuthor | Hyotcherl Ihee | - |
dc.identifier.doi | 10.1063/1.5096422 | - |
dc.identifier.bibliographicCitation | JOURNAL OF CHEMICAL PHYSICS, v.151, no.5, pp.054310 | - |
dc.citation.title | JOURNAL OF CHEMICAL PHYSICS | - |
dc.citation.volume | 151 | - |
dc.citation.number | 5 | - |
dc.citation.startPage | 054310 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | TRANSITION-STATE | - |
dc.subject.keywordPlus | DYNAMICS | - |
dc.subject.keywordPlus | PHOTODISSOCIATION | - |
dc.subject.keywordPlus | PHOTOLYSIS | - |
dc.subject.keywordPlus | MOLECULES | - |
dc.subject.keywordPlus | RADICALS | - |
dc.subject.keywordPlus | ABSORPTION | - |
dc.subject.keywordPlus | VIBRATION | - |
dc.subject.keywordPlus | KINETICS | - |