Photochemistry of HI on argon and water nanoparticles: Hydronium radical generation in HI(H(2)O)(n)

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F11%3A43880127" target="_blank" >RIV/60461373:22340/11:43880127 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1039/c0cp01518k" target="_blank" >http://dx.doi.org/10.1039/c0cp01518k</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c0cp01518k" target="_blank" >10.1039/c0cp01518k</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Photochemistry of HI on argon and water nanoparticles: Hydronium radical generation in HI(H(2)O)(n)

Popis výsledku v původním jazyce

Photochemistry of HI molecules on large Ar(n) and (H(2)O)(n), (n) over bar similar to 100-500, clusters was investigated after excitation with 243 nm and 193 nm laser radiation. The measured H-fragment kinetic energy distributions pointed to a completelydifferent photodissociation mechanism of HI on water than on argon clusters. Distinct features corresponding to the fragment caging (slow fragments) and direct exit (fast fragments) were observed in the spectra from HI photodissociation on Ar(n) clusters. On the other hand, the fast fragments were entirely missing in the spectrum from HI center dot(H(2)O)(n) and the slow-fragment part of the spectrum had a different shape from HI center dot Ar(n). The HI center dot(H(2)O)(n) spectrum was interpreted interms of the acidic dissociation of HI on (H(2)O)(n) in the ground state, and hydronium radical H(3)O formation following the UV excitation of the ionically dissociated species into states of a charge-transfer-to-solvent character. The H

Název v anglickém jazyce

Photochemistry of HI on argon and water nanoparticles: Hydronium radical generation in HI(H(2)O)(n)

Popis výsledku anglicky

Photochemistry of HI molecules on large Ar(n) and (H(2)O)(n), (n) over bar similar to 100-500, clusters was investigated after excitation with 243 nm and 193 nm laser radiation. The measured H-fragment kinetic energy distributions pointed to a completelydifferent photodissociation mechanism of HI on water than on argon clusters. Distinct features corresponding to the fragment caging (slow fragments) and direct exit (fast fragments) were observed in the spectra from HI photodissociation on Ar(n) clusters. On the other hand, the fast fragments were entirely missing in the spectrum from HI center dot(H(2)O)(n) and the slow-fragment part of the spectrum had a different shape from HI center dot Ar(n). The HI center dot(H(2)O)(n) spectrum was interpreted interms of the acidic dissociation of HI on (H(2)O)(n) in the ground state, and hydronium radical H(3)O formation following the UV excitation of the ionically dissociated species into states of a charge-transfer-to-solvent character. The H

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CF - Fyzikální chemie a teoretická chemie

OECD FORD obor

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Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2011

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Physical Chemistry Chemical Physics

ISSN

1463-9076

e-ISSN

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Svazek periodika

13

Číslo periodika v rámci svazku

6

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

9

Strana od-do

2250-2258

Kód UT WoS článku

000286628200039

EID výsledku v databázi Scopus

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