1.
Reaction Mechanisms of Fluoroethylene Carbonate Degradation, an Additive of Lithium-Ion Batteries, Unraveled by Radiation Chemistry Journal Article
In: Chemistry – A European Journal, vol. n/a, no. n/a, 2021.
@article{https://doi.org/10.1002/chem.202100562,
title = {Reaction Mechanisms of Fluoroethylene Carbonate Degradation, an Additive of Lithium-Ion Batteries, Unraveled by Radiation Chemistry},
author = {Marin Puget and Viacheslav Shcherbakov and Sergey Denisov and Philippe Moreau and Jean-Pierre Dognon and Mehran Mostafavi and Sophie {LE CAER}},
url = {https://elyse-platform.academy/2021/03/26/reaction-mechanisms-of-fluoroethylene-carbonate-degradation/},
doi = {https://doi.org/10.1002/chem.202100562},
year = {2021},
date = {2021-03-26},
journal = {Chemistry – A European Journal},
volume = {n/a},
number = {n/a},
abstract = {Numerous additives are used in electrolytes of lithium-ion batteries, especially for the formation of efficient solid electrolyte interphase at the surface of the electrodes. The understanding of the degradation processes of these compounds is thus important. They can be obtained through radiolysis. In the case of fluoroethylene carbonate (FEC), picosecond pulse radiolysis experiments evidenced the formation of FEC ●- . This radical is stabilized in neat FEC, whereas the ring opens to form more stable radical anions when FEC is a solute in other solvents, as confirmed by quantum chemistry calculations. In neat FEC, pre-solvated electrons primarily undergo attachment compared to solvation. At long timescales, produced gases (H 2 , CO, and CO 2 ) were quantified. A reaction scheme for both the oxidizing and reducing pathways at stake in irradiated FEC was proposed. This work evidences that the nature of the primary species formed in FEC depends on the amount of FEC in the solution.},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
Numerous additives are used in electrolytes of lithium-ion batteries, especially for the formation of efficient solid electrolyte interphase at the surface of the electrodes. The understanding of the degradation processes of these compounds is thus important. They can be obtained through radiolysis. In the case of fluoroethylene carbonate (FEC), picosecond pulse radiolysis experiments evidenced the formation of FEC ●- . This radical is stabilized in neat FEC, whereas the ring opens to form more stable radical anions when FEC is a solute in other solvents, as confirmed by quantum chemistry calculations. In neat FEC, pre-solvated electrons primarily undergo attachment compared to solvation. At long timescales, produced gases (H 2 , CO, and CO 2 ) were quantified. A reaction scheme for both the oxidizing and reducing pathways at stake in irradiated FEC was proposed. This work evidences that the nature of the primary species formed in FEC depends on the amount of FEC in the solution.
2.
Confined water radiolysis in aluminosilicate nanotubes: the importance of charge separation effects Journal Article
In: Nanoscale, vol. 13, pp. 3092-3105, 2021.
@article{Pignie2021,
title = {Confined water radiolysis in aluminosilicate nanotubes: the importance of charge separation effects},
author = {Marie-Claire Pignié and Viacheslav Shcherbakov and Thibault Charpentier and Mélanie Moskura and Cédric Carteret and Sergey Denisov and Mehran Mostafavi and Antoine Thill and Sophie Le Caër},
url = {https://elyse-platform.academy/2021/01/27/confined-water-radiolysis/},
doi = {10.1039/d0nr08948f},
year = {2021},
date = {2021-01-01},
journal = {Nanoscale},
volume = {13},
pages = {3092-3105},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
3.
Presolvated electron reactivity towards CO2, N2O in the water Journal Article
In: Phys. Chem. Chem. Phys., vol. 23, pp. 5804-5808, 2021.
@article{D1CP00373A,
title = {Presolvated electron reactivity towards CO_{2}, N_{2}O in the water},
author = {Sergey A. Denisov and Mehran Mostafavi},
url = {https://elyse-platform.academy/2021/02/11/presolvated-electron-reactivity-towards-co2-n2o-in-the-water/},
doi = {10.1039/D1CP00373A},
year = {2021},
date = {2021-01-01},
journal = {Phys. Chem. Chem. Phys.},
volume = {23},
pages = {5804-5808},
publisher = {The Royal Society of Chemistry},
abstract = {The reactivity of presolvated electrons with CO_{2} and N_{2}O was studied in the gas pressure range from 1 to 52 bar. To measure this reactivity, the home-made spectroscopic cell with liquid circulation was developed working up to 70 bar of gas pressure. The efficiency of presolvated electron scavenging was determined from the decrease of solvated electrons yield after the 5ps electron pulse. In addition, the reaction rate between these molecules and solvated electrons was directly determined at gas pressures below the critical point, which is in agreement with those presented in the literature measured at gas pressures below <1atm.},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
The reactivity of presolvated electrons with CO2 and N2O was studied in the gas pressure range from 1 to 52 bar. To measure this reactivity, the home-made spectroscopic cell with liquid circulation was developed working up to 70 bar of gas pressure. The efficiency of presolvated electron scavenging was determined from the decrease of solvated electrons yield after the 5ps electron pulse. In addition, the reaction rate between these molecules and solvated electrons was directly determined at gas pressures below the critical point, which is in agreement with those presented in the literature measured at gas pressures below <1atm.
4.
Selective Oxidation of Transient Organic Radicals in the Presence of Gold Nanoparticles Journal Article
In: Nanomaterials, vol. 11, pp. 727, 2021.
@article{nano11030727,
title = {Selective Oxidation of Transient Organic Radicals in the Presence of Gold Nanoparticles},
author = {Viacheslav Shcherbakov and Sergey A Denisov and Mehran Mostafavi},
doi = {10.3390/nano11030727},
year = {2021},
date = {2021-01-01},
journal = {Nanomaterials},
volume = {11},
pages = {727},
abstract = {The ability of gold nanoparticles (AuNPs) to catalyze reactions involving radicals is poorly studied. However, AuNPs are used in applications where chemical reactions involving transient radicals occur. Herein, we investigate AuNPs’ catalytic effect on 2-propanol oxidation and acetanilide hydroxylation in aqueous solutions under ionizing radiation at room temperature. In both cases, the presence of AuNPs led to selective oxidation of organic radicals, significantly changing the products’ composition and ratio. Based on these observations, we stress how AuNPs’ catalytic activity can affect the correctness of reactive oxygen species concentration determination utilizing organic dyes. We also provide a discussion on the role of AuNPs’ catalytic activity in the radiosensitization effect actively studied for radiotherapy.},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
The ability of gold nanoparticles (AuNPs) to catalyze reactions involving radicals is poorly studied. However, AuNPs are used in applications where chemical reactions involving transient radicals occur. Herein, we investigate AuNPs’ catalytic effect on 2-propanol oxidation and acetanilide hydroxylation in aqueous solutions under ionizing radiation at room temperature. In both cases, the presence of AuNPs led to selective oxidation of organic radicals, significantly changing the products’ composition and ratio. Based on these observations, we stress how AuNPs’ catalytic activity can affect the correctness of reactive oxygen species concentration determination utilizing organic dyes. We also provide a discussion on the role of AuNPs’ catalytic activity in the radiosensitization effect actively studied for radiotherapy.
5.
Real-Time Observation of Solvation Dynamics of Electron in Actinide Extraction Binary Solutions of Water and n-Tributyl Phosphate Journal Article
In: The Journal of Physical Chemistry B, vol. 125, no. 15, pp. 3843-3849, 2021.
@article{Bahry2021,
title = {Real-Time Observation of Solvation Dynamics of Electron in Actinide Extraction Binary Solutions of Water and n-Tributyl Phosphate},
author = {Teseer Bahry and Sergey A Denisov and Philippe Moisy and Jun Ma and Mehran Mostafavi},
doi = {10.1021/acs.jpcb.0c10831},
year = {2021},
date = {2021-01-01},
journal = {The Journal of Physical Chemistry B},
volume = {125},
number = {15},
pages = {3843-3849},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
6.
Anisotropic Time-Resolved Dynamics of Crystal Growth Induced by a Single Laser Pulse Nucleation Journal Article
In: Crystal Growth & Design, vol. 21, pp. 799-808, 2021.
@article{sarah2021,
title = {Anisotropic Time-Resolved Dynamics of Crystal Growth Induced by a Single Laser Pulse Nucleation},
author = {Sarah Al Gharib and Abdel Karim El Omar and Adnan Naja and Ariane Deniset-Besseau and Sergey A Denisov and Pascal Pernot and Mehran Mostafavi and Jacqueline Belloni},
doi = {10.1021/acs.cgd.0c01016},
year = {2021},
date = {2021-01-01},
journal = {Crystal Growth & Design},
volume = {21},
pages = {799-808},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
7.
Quasi-Free Electron-Mediated Radiation Sensitization by C5-Halopyrimidines Journal Article
In: The Journal of Physical Chemistry A, vol. 125, no. 36, pp. 7967-7975, 2021, (PMID: 34470211).
@article{doi:10.1021/acs.jpca.1c05974,
title = {Quasi-Free Electron-Mediated Radiation Sensitization by C5-Halopyrimidines},
author = {Jun Ma and Teseer Bahry and Sergey A. Denisov and Amitava Adhikary and Mehran Mostafavi},
url = {https://doi.org/10.1021/acs.jpca.1c05974},
doi = {10.1021/acs.jpca.1c05974},
year = {2021},
date = {2021-01-01},
journal = {The Journal of Physical Chemistry A},
volume = {125},
number = {36},
pages = {7967-7975},
note = {PMID: 34470211},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
8.
Real-Time Observation of Solvation Dynamics of Electron in Actinide Extraction Binary Solutions of Water and n-Tributyl Phosphate Journal Article
In: The Journal of Physical Chemistry B, vol. 125, no. 15, pp. 3843-3849, 2021, (PMID: 33650867).
@article{doi:10.1021/acs.jpcb.0c10831,
title = {Real-Time Observation of Solvation Dynamics of Electron in Actinide Extraction Binary Solutions of Water and n-Tributyl Phosphate},
author = {Teseer Bahry and Sergey A. Denisov and Philippe Moisy and Jun Ma and Mehran Mostafavi},
url = {https://doi.org/10.1021/acs.jpcb.0c10831},
doi = {10.1021/acs.jpcb.0c10831},
year = {2021},
date = {2021-01-01},
journal = {The Journal of Physical Chemistry B},
volume = {125},
number = {15},
pages = {3843-3849},
note = {PMID: 33650867},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
9.
Selective Oxidation of Transient Organic Radicals in the Presence of Gold Nanoparticles Journal Article
In: Nanomaterials, vol. 11, no. 3, 2021, ISSN: 2079-4991.
@article{nano11030727b,
title = {Selective Oxidation of Transient Organic Radicals in the Presence of Gold Nanoparticles},
author = {Viacheslav Shcherbakov and Sergey A. Denisov and Mehran Mostafavi},
url = {https://www.mdpi.com/2079-4991/11/3/727},
doi = {10.3390/nano11030727},
issn = {2079-4991},
year = {2021},
date = {2021-01-01},
journal = {Nanomaterials},
volume = {11},
number = {3},
abstract = {The ability of gold nanoparticles (AuNPs) to catalyze reactions involving radicals is poorly studied. However, AuNPs are used in applications where chemical reactions involving transient radicals occur. Herein, we investigate AuNPs’ catalytic effect on 2-propanol oxidation and acetanilide hydroxylation in aqueous solutions under ionizing radiation at room temperature. In both cases, the presence of AuNPs led to selective oxidation of organic radicals, significantly changing the products’ composition and ratio. Based on these observations, we stress how AuNPs’ catalytic activity can affect the correctness of reactive oxygen species concentration determination utilizing organic dyes. We also provide a discussion on the role of AuNPs’ catalytic activity in the radiosensitization effect actively studied for radiotherapy.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
The ability of gold nanoparticles (AuNPs) to catalyze reactions involving radicals is poorly studied. However, AuNPs are used in applications where chemical reactions involving transient radicals occur. Herein, we investigate AuNPs’ catalytic effect on 2-propanol oxidation and acetanilide hydroxylation in aqueous solutions under ionizing radiation at room temperature. In both cases, the presence of AuNPs led to selective oxidation of organic radicals, significantly changing the products’ composition and ratio. Based on these observations, we stress how AuNPs’ catalytic activity can affect the correctness of reactive oxygen species concentration determination utilizing organic dyes. We also provide a discussion on the role of AuNPs’ catalytic activity in the radiosensitization effect actively studied for radiotherapy.
10.
Confined water radiolysis in aluminosilicate nanotubes: the importance of charge separation effects Journal Article
In: Nanoscale, vol. 13, pp. 3092-3105, 2021.
@article{D0NR08948F,
title = {Confined water radiolysis in aluminosilicate nanotubes: the importance of charge separation effects},
author = {Marie-Claire Pignié and Viacheslav Shcherbakov and Thibault Charpentier and Mélanie Moskura and Cédric Carteret and Sergey Denisov and Mehran Mostafavi and Antoine Thill and Sophie Le Caër},
url = {http://dx.doi.org/10.1039/D0NR08948F},
doi = {10.1039/D0NR08948F},
year = {2021},
date = {2021-01-01},
journal = {Nanoscale},
volume = {13},
pages = {3092-3105},
publisher = {The Royal Society of Chemistry},
abstract = {Imogolite nanotubes are potentially promising co-photocatalysts because they are predicted to have curvature-induced, efficient electron–hole pair separation. This prediction has however not yet been experimentally proven. Here, we investigated the behavior upon irradiation of these inorganic nanotubes as a function of their water content to understand the fate of the generated electrons and holes. Two types of aluminosilicate nanotubes were studied: one was hydrophilic on its external and internal surfaces (IMO-OH) and the other had a hydrophobic internal cavity due to Si–CH3 bonds (IMO-CH3), with the external surface remaining hydrophilic. Picosecond pulse radiolysis experiments demonstrated that the electrons are efficiently driven outward. For imogolite samples with very few external water molecules (around 1% of the total mass), quasi-free electrons were formed. They were able to attach to a water molecule, generating a water radical anion, which ultimately led to dihydrogen. When more external water molecules were present, solvated electrons, precursors of dihydrogen, were formed. In contrast, holes moved towards the internal surface of the tubes. They mainly led to the formation of dihydrogen and of methane in irradiated IMO-CH3. The attachment of the quasi-free electron to water was a very efficient process and accounted for the high dihydrogen production at low relative humidity values. When the water content increased, electron solvation dominated over attachment to water molecules. Electron solvation led to dihydrogen production, albeit to a lesser extent than quasi-free electrons. Our experiments demonstrated the spontaneous curvature-induced charge separation in these inorganic nanotubes, making them very interesting potential co-photocatalysts.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Imogolite nanotubes are potentially promising co-photocatalysts because they are predicted to have curvature-induced, efficient electron–hole pair separation. This prediction has however not yet been experimentally proven. Here, we investigated the behavior upon irradiation of these inorganic nanotubes as a function of their water content to understand the fate of the generated electrons and holes. Two types of aluminosilicate nanotubes were studied: one was hydrophilic on its external and internal surfaces (IMO-OH) and the other had a hydrophobic internal cavity due to Si–CH3 bonds (IMO-CH3), with the external surface remaining hydrophilic. Picosecond pulse radiolysis experiments demonstrated that the electrons are efficiently driven outward. For imogolite samples with very few external water molecules (around 1% of the total mass), quasi-free electrons were formed. They were able to attach to a water molecule, generating a water radical anion, which ultimately led to dihydrogen. When more external water molecules were present, solvated electrons, precursors of dihydrogen, were formed. In contrast, holes moved towards the internal surface of the tubes. They mainly led to the formation of dihydrogen and of methane in irradiated IMO-CH3. The attachment of the quasi-free electron to water was a very efficient process and accounted for the high dihydrogen production at low relative humidity values. When the water content increased, electron solvation dominated over attachment to water molecules. Electron solvation led to dihydrogen production, albeit to a lesser extent than quasi-free electrons. Our experiments demonstrated the spontaneous curvature-induced charge separation in these inorganic nanotubes, making them very interesting potential co-photocatalysts.
11.
On the Primary Water Radicals’ Production in the Presence of Gold Nanoparticles: Electron Pulse Radiolysis Study Journal Article
In: Nanomaterials, vol. 10, pp. 2478, 2020.
@article{Shcherbakov2020,
title = {On the Primary Water Radicals’ Production in the Presence of Gold Nanoparticles: Electron Pulse Radiolysis Study},
author = {Viacheslav Shcherbakov and Sergey A. Denisov and Mehran Mostafavi},
url = {https://elyse-platform.academy/2020/12/05/on-the-primary-water-radicals/},
doi = {10.3390/nano10122478},
year = {2020},
date = {2020-01-01},
journal = {Nanomaterials},
volume = {10},
pages = {2478},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
12.
One Way Traffic: Base-to-Backbone Hole Transfer in Nucleoside Phosphorodithioate Journal Article
In: Chemistry—A European Journal, vol. 26, no. 43, pp. 9495–9505, 2020.
@article{Kaczmarek2020,
title = {One Way Traffic: Base-to-Backbone Hole Transfer in Nucleoside Phosphorodithioate},
author = {Renata Kaczmarek and Samuel Ward and Dipra Debnath and Taisiya Jacobs and Alexander D Stark and Dariusz Korczynski and Anil Kumar and Michael D Sevilla and Sergey A Denisov and Viacheslav Shcherbakov and Pascal Pernot and Mehran Mostafavi and Roman Dembinski and Amitava Adhikary},
url = {https://elyse-platform.academy/2020/06/22/one-way-traffic/},
doi = {10.1002/chem.202000247},
year = {2020},
date = {2020-01-01},
journal = {Chemistry—A European Journal},
volume = {26},
number = {43},
pages = {9495--9505},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
13.
Hot-Electron Photodynamics in Silver-Containing BEA-Type Nanozeolite Studied by Femtosecond Transient Absorption Spectroscopy Journal Article
In: ChemPhysChem, vol. 21, no. 24, pp. 2634–2643, 2020.
@article{Kawtharani_2020,
title = {Hot-Electron Photodynamics in Silver-Containing BEA-Type Nanozeolite Studied by Femtosecond Transient Absorption Spectroscopy},
author = {Farah Kawtharani and Svetlana Mintova and Richard Retoux and Mehran Mostafavi and Guy Buntinx and Vincent De Waele},
url = {https://elyse-platform.academy/2020/10/20/hotelectron-photodynamics-in-silver/},
doi = {10.1002/cphc.202000822},
year = {2020},
date = {2020-01-01},
journal = {ChemPhysChem},
volume = {21},
number = {24},
pages = {2634--2643},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
14.
Mechanisms of metal nanoparticles nucleation and growth studied by radiolysis Journal Article
In: Radiation Physics and Chemistry, vol. 169, pp. 107952, 2020.
@article{Belloni_2020,
title = {Mechanisms of metal nanoparticles nucleation and growth studied by radiolysis},
author = { Jacqueline Belloni and Jean-Louis Marignier and Mehran Mostafavi},
url = {https://elyse-platform.academy/2020/04/01/mechanisms-of-metal-nanoparticles/},
doi = {10.1016/j.radphyschem.2018.08.001},
year = {2020},
date = {2020-01-01},
journal = {Radiation Physics and Chemistry},
volume = {169},
pages = {107952},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
15.
In: Physical Chemistry Chemical Physics, vol. 22, pp. 5188–5197, 2020.
@article{Musat_2020,
title = {Pulse radiolysis study on the reactivity of NO_{3}^{•} radical toward uranous(IV), hydrazinium nitrate and hydroxyl ammonium nitrate at room temperature and at 45 °C},
author = {Raluca Musat and Jean-Louis Marignier and Claire Le Naour and Sergey A. Denisov and L Venault and Philippe Moisy and Mehran Mostafavi},
url = {https://elyse-platform.academy/2020/02/13/pulse-radiolysis-no3-radical/},
doi = {10.1039/c9cp07034f},
year = {2020},
date = {2020-01-01},
journal = {Physical Chemistry Chemical Physics},
volume = {22},
pages = {5188--5197},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
16.
Key Role of the Oxidized Citrate-Free Radical in the Nucleation Mechanism of the Metal Nanoparticle Turkevich Synthesis Journal Article
In: The Journal of Physical Chemistry C, vol. 123, no. 36, pp. 22624–22633, 2019.
@article{Al_Gharib_2019,
title = {Key Role of the Oxidized Citrate-Free Radical in the Nucleation Mechanism of the Metal Nanoparticle Turkevich Synthesis},
author = {Sarah Al Gharib and Jean-Louis Marignier and Abdel Karim El Omar and Adnan Naja and Sophie Le Caer and Mehran Mostafavi and Jacqueline Belloni},
url = {https://elyse-platform.academy/2019/08/08/oxidized-citrate-free-radical/},
doi = {10.1021/acs.jpcc.9b06090},
year = {2019},
date = {2019-01-01},
journal = {The Journal of Physical Chemistry C},
volume = {123},
number = {36},
pages = {22624--22633},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
17.
Mechanism of (SCN)2•- Formation and Decay in Neutral and Basic KSCN Solution under Irradiation from a Pico- to Microsecond Range Journal Article
In: The Journal of Physical Chemistry B, vol. 123, no. 30, pp. 6599–6608, 2019.
@article{Wang_2019,
title = {Mechanism of (SCN)_{2}^{•-} Formation and Decay in Neutral and Basic KSCN Solution under Irradiation from a Pico- to Microsecond Range},
author = {Furong Wang and Pascal Pernot and Jean-Louis Marignier and Pierre Archirel and Mehran Mostafavi},
url = {https://elyse-platform.academy/2019/07/11/mechanism-of-scnsub2/},
doi = {10.1021/acs.jpcb.9b05560},
year = {2019},
date = {2019-01-01},
journal = {The Journal of Physical Chemistry B},
volume = {123},
number = {30},
pages = {6599--6608},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
18.
Ultrafast Electron Attachment and Hole Transfer Following Ionizing Radiation of Aqueous Uridine Monophosphate Journal Article
In: The Journal of Physical Chemistry Letters, vol. 9, no. 17, pp. 5105–5109, 2018.
@article{Ma_2018,
title = {Ultrafast Electron Attachment and Hole Transfer Following Ionizing Radiation of Aqueous Uridine Monophosphate},
author = {Jun Ma and Sergey A Denisov and Jean-Louis Marignier and Pascal Pernot and Amitava Adhikary and Shu Seki and Mehran Mostafavi},
url = {https://elyse-platform.academy/2018/08/22/ump-ultrafast-radiolysis/},
doi = {10.1021/acs.jpclett.8b02170},
year = {2018},
date = {2018-01-01},
journal = {The Journal of Physical Chemistry Letters},
volume = {9},
number = {17},
pages = {5105--5109},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
19.
Picosecond Pulse Radiolysis Study on the Radiation-Induced Reactions in Neat Tributyl Phosphate Journal Article
In: The Journal of Physical Chemistry B, vol. 122, no. 28, pp. 7134–7142, 2018.
@article{Wang_2018_1,
title = {Picosecond Pulse Radiolysis Study on the Radiation-Induced Reactions in Neat Tributyl Phosphate},
author = {Furong Wang and Gregory P Horne and Pascal Pernot and Pierre Archirel and Mehran Mostafavi},
url = {https://elyse-platform.academy/2018/06/14/tbp-radiolysis/},
doi = {10.1021/acs.jpcb.8b03715},
year = {2018},
date = {2018-01-01},
journal = {The Journal of Physical Chemistry B},
volume = {122},
number = {28},
pages = {7134--7142},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}
20.
Time-dependent yield of the hydrated electron and the hydroxyl radical in D2O: a picosecond pulse radiolysis study Journal Article
In: Physical Chemistry Chemical Physics, vol. 20, no. 23, pp. 15671–15679, 2018.
@article{Wang_2018_2,
title = {Time-dependent yield of the hydrated electron and the hydroxyl radical in D_{2}O: a picosecond pulse radiolysis study},
author = {Furong Wang and Uli Schmidhammer and Jean-Philippe Larbre and Zizhao Zong and Jean-Louis Marignier and Mehran Mostafavi},
url = {https://elyse-platform.academy/2018/05/10/yield-solvated-electron/},
doi = {10.1039/c8cp02276c},
year = {2018},
date = {2018-01-01},
journal = {Physical Chemistry Chemical Physics},
volume = {20},
number = {23},
pages = {15671--15679},
keywords = {posted},
pubstate = {published},
tppubtype = {article}
}