Key Role of the Oxidized Citrate Free Radical in the Nucleation Mechanism of the Metal Nanoparticles Turkevich Synthesis - CEA - Commissariat à l’énergie atomique et aux énergies alternatives Accéder directement au contenu
Article Dans Une Revue Journal of Physical Chemistry C Année : 2019

Key Role of the Oxidized Citrate Free Radical in the Nucleation Mechanism of the Metal Nanoparticles Turkevich Synthesis

Résumé

The step-by-step mechanism of the citrate oxidation, of the silver ion reduction into atoms, and of the nucleation of nanoparticles by the Turkevich method are deduced from the gamma- and pulse radiolysis yields of dicarboxy acetone (DCA), H2 and CO2 and of silver ion reduction. Our results demonstrate that the stronger reductant is not citrate (Cit) but the oxidized radical Cit(-H)•. The formation yields of DCA and CO2 confirm the decarboxylation process during the Cit(-H)• oxidation. In pulse radioly- sis of solutions of sodium citrate and silver perchlorate, the transient spectra and the kinetics are observed from 20 ps to 800 ms. In particular, the successive H abstraction from citrate by OH• radicals, then the one-electron transfer from the citrate radicals Cit(-H)• to silver ions initiating the simultaneous nucleation and growth of the reduced silver oligomers are observed. The knowledge of the nuclearity-dependent kinetics and thermodynamics of silver atoms, oligomers and nanoparticles in solution is used to bracket the standard reduction potentials of the first (≥ 0.4 VNHE) and the second one-electron transfers from citrate (≤ - 1.2 VNHE). During the Turkevich synthesis, the Cit(-H)• radical was shown to be released in the bulk solution from the citrate oxidation by Ag+ adsorbed on the walls, or directly by the trivalent AuIII ions present in the bulk, respectively. Then the strong Cit(-H)• reductant alone is able, as in radiolysis, to overcome the thermodynamic barrier of the very negative potential for the reduction of the free monovalent ions into atoms that is required to initiate the nucleation and growth. The reduction potentials values of citrate and Cit(-H)• also explain part of the antioxidant properties of citrate.
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Dates et versions

cea-02266279 , version 1 (13-08-2019)

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Sarah Al Gharib, Jean-Louis Marignier, Abdel Karim El Omar, Adnan Naja, Sophie Le Caer, et al.. Key Role of the Oxidized Citrate Free Radical in the Nucleation Mechanism of the Metal Nanoparticles Turkevich Synthesis. Journal of Physical Chemistry C, 2019, 123, pp.22624-22633. ⟨10.1021/acs.jpcc.9b06090⟩. ⟨cea-02266279⟩
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