Co3O4 nanoparticles in the spinel crystalline structure are among the most promising catalysts for the water oxidation reaction, displaying remarkable activity under electrochemical and light-assisted conditions. In the presence of Ru(bpy)(3)(2+) as a photosensitizer (bpy = 2,2-bipyridine) and Na2S2O8 as an electron acceptor, 5 +/- 1 nm size Co3O4 nanoparticles show a slow primary electron transfer (ET) to photogenerated Ru(iii), occurring in a timescale of tens of milliseconds. We demonstrate herein that (i) photo-oxidation of Co3O4 NPs by Ru(iii) involves transformation of surface Co(iii)-OH sites to formal Co(iv)?O, along a proton-coupled electron-transfer (PCET) pathway; (ii) the rate of the process depends on pH, and on the nature and concentration of the buffer; (iii) borate promotes general base catalysis of the PCET; and (iv) inhibition of the PCET is observed at high buffer concentration, due to H3BO3 poisoning of the surface Co sites, resulting in depletion of the O-2 evolution activity.

Proton coupled electron transfer from Co3O4 nanoparticles to photogenerated Ru(bpy)(3)(3+): base catalysis and buffer effect

Bonchio Marcella;
2018

Abstract

Co3O4 nanoparticles in the spinel crystalline structure are among the most promising catalysts for the water oxidation reaction, displaying remarkable activity under electrochemical and light-assisted conditions. In the presence of Ru(bpy)(3)(2+) as a photosensitizer (bpy = 2,2-bipyridine) and Na2S2O8 as an electron acceptor, 5 +/- 1 nm size Co3O4 nanoparticles show a slow primary electron transfer (ET) to photogenerated Ru(iii), occurring in a timescale of tens of milliseconds. We demonstrate herein that (i) photo-oxidation of Co3O4 NPs by Ru(iii) involves transformation of surface Co(iii)-OH sites to formal Co(iv)?O, along a proton-coupled electron-transfer (PCET) pathway; (ii) the rate of the process depends on pH, and on the nature and concentration of the buffer; (iii) borate promotes general base catalysis of the PCET; and (iv) inhibition of the PCET is observed at high buffer concentration, due to H3BO3 poisoning of the surface Co sites, resulting in depletion of the O-2 evolution activity.
2018
nanoparticles
photo-oxidation
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/345474
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