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Catalytic H 2 Evolution with CoO, Co(OH) 2 and CoO(OH) Nanoparticles Generated from a Molecular Polynuclear Co Complex
Author(s) -
GilSepulcre Marcos,
GimbertSuriñach Carolina,
Aguilà David,
Velasco Verónica,
GarcíaAntón Jordi,
Llobet Antoni,
Aromí Guillem,
Bofill Roger,
Sala Xavier
Publication year - 2018
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201800033
Subject(s) - chemistry , overpotential , dichloromethane , catalysis , nanoparticle , electrochemistry , solvent , inorganic chemistry , x ray photoelectron spectroscopy , transition metal , electrocatalyst , context (archaeology) , nuclear chemistry , organic chemistry , chemical engineering , paleontology , electrode , engineering , biology
Electrochemical water reduction by employing first‐row transition‐metal nanoparticles (NPs) constitutes a sustainable way for the generation of H 2 . We have synthesized Co‐based NPs from a molecular Co II /Co III precursor after its reductive decomposition at –1.86 V versus NHE in different organic solvents. These NPs are able to electrochemically reduce water at pH 14. SEM, EDX and XPS analyses have allowed the determination of the chemical nature of the as‐deposited NPs: CoO when using MeCN as the solvent and CoO(OH) when employing either dichloromethane (DCM) or MeOH. After 2 h of constant polarization at 10 mA cm –2 , the electrocatalytic activity of the NPs obtained in MeCN and DCM decreases, whereas it increases for those obtained in MeOH. In this solvent, the overpotential is reduced by 215–220 mV and the specific current density is tripled. Interestingly, during this activation process in MeOH, the precursor CoO(OH) NPs are converted into Co(OH) 2 . The implications of these results in the context of the current research in the field are also discussed.