Effect of the solvation state of electron in dissociative electron attachment reaction in aqueous solutions. Issue 34 (17th August 2017)
- Record Type:
- Journal Article
- Title:
- Effect of the solvation state of electron in dissociative electron attachment reaction in aqueous solutions. Issue 34 (17th August 2017)
- Main Title:
- Effect of the solvation state of electron in dissociative electron attachment reaction in aqueous solutions
- Authors:
- Wang, Furong
Archirel, Pierre
Muroya, Yusa
Yamashita, Shinichi
Pernot, Pascal
Yin, Chengying
El Omar, Abdel Karim
Schmidhammer, Uli
Teuler, Jean-Marie
Mostafavi, Mehran - Abstract:
- Abstract : Dissociative electron attachment induced by prehydrated electron is observed by using multichannel transient absorption measurements at the picosecond range. Abstract : It is generally considered that the pre-solvated electron and the solvated electron reacting with a solute yield the same product. Silver cyanide complex, Ag(CN)2 −, is used as a simple probe to demonstrate unambiguously the existence of a different reduction mechanism for pre-hydrated electrons. Using systematic multichannel transient absorption measurements at different solute concentrations from millimolar to decimolar, global data analysis and theoretical calculations, we present the dissociative electron attachment on Ag(CN)2 − . The short-lived silver complex, Ag 0 (CN)2 2−, formed by hydrated electron with nanosecond pulse radiolysis, can be observed at room temperature. However, at higher temperatures only the free silver atom, Ag 0, is detected, suggesting that Ag 0 (CN)2 2− dissociation is fast. Surprisingly, pulse radiolysis measurements on Ag(CN)2 − reduction, performed by a 7 ps electron pulse at room temperature, show clearly that a new reduced form of silver complex, AgCN −, is produced within the pulse. This species, absorbing at 560 nm, is not formed by the hydrated electron but exclusively by its precursor. DFT calculations show that the different reactivity of the hydrated and pre-hydrated electrons can be due to the formation of different electronic states of Ag 0 (CN)2 2− : theAbstract : Dissociative electron attachment induced by prehydrated electron is observed by using multichannel transient absorption measurements at the picosecond range. Abstract : It is generally considered that the pre-solvated electron and the solvated electron reacting with a solute yield the same product. Silver cyanide complex, Ag(CN)2 −, is used as a simple probe to demonstrate unambiguously the existence of a different reduction mechanism for pre-hydrated electrons. Using systematic multichannel transient absorption measurements at different solute concentrations from millimolar to decimolar, global data analysis and theoretical calculations, we present the dissociative electron attachment on Ag(CN)2 − . The short-lived silver complex, Ag 0 (CN)2 2−, formed by hydrated electron with nanosecond pulse radiolysis, can be observed at room temperature. However, at higher temperatures only the free silver atom, Ag 0, is detected, suggesting that Ag 0 (CN)2 2− dissociation is fast. Surprisingly, pulse radiolysis measurements on Ag(CN)2 − reduction, performed by a 7 ps electron pulse at room temperature, show clearly that a new reduced form of silver complex, AgCN −, is produced within the pulse. This species, absorbing at 560 nm, is not formed by the hydrated electron but exclusively by its precursor. DFT calculations show that the different reactivity of the hydrated and pre-hydrated electrons can be due to the formation of different electronic states of Ag 0 (CN)2 2− : the prehydrated electron can form an excited state of this complex, which mainly dissociates into Ag 0 CN − + CN − . … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 19:Issue 34(2017)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 19:Issue 34(2017)
- Issue Display:
- Volume 19, Issue 34 (2017)
- Year:
- 2017
- Volume:
- 19
- Issue:
- 34
- Issue Sort Value:
- 2017-0019-0034-0000
- Page Start:
- 23068
- Page End:
- 23077
- Publication Date:
- 2017-08-17
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7cp03997b ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4559.xml