Colloidal Ni2-: XCoxP nanocrystals for the hydrogen evolution reaction
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hdl:2117/119655
Tipus de documentArticle
Data publicació2018-05-11
EditorRoyal Society of Chemistry (RSC)
Condicions d'accésAccés obert
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Abstract
A cost-effective and scalable approach was developed to produce monodisperse Ni2-xCoxP nanocrystals (NCs) with composition tuned over the entire range (0 = x = 2). Ni2-xCoxP NCs were synthesized using low-cost, stable and low-toxicity triphenyl phosphite (TPP) as a phosphorus source, metal chlorides as metal precursors and hexadecylamine (HDA) as a ligand. The synthesis involved the nucleation of amorphous Ni–P and its posterior crystallization and simultaneous incorporation of Co. The composition, size and morphology of the Ni2-xCoxP NCs could be controlled simply by varying the ratio of Ni and Co precursors and the amounts of TPP and HDA. Ternary Ni2-xCoxP-based electrocatalysts exhibited enhanced electrocatalytic activity toward the hydrogen evolution reaction (HER) compared to binary phosphides. In particular, NiCoP electrocatalysts displayed the lowest overpotential of 97 mV at J = 10 mA cm-2 and an excellent long-term stability. DFT calculations of the Gibbs free energy for hydrogen adsorption at the surface of Ni2-xCoxP NCs showed NiCoP to have the most appropriate composition to optimize this parameter within the whole Ni2-xCoxP series. However, the hydrogen adsorption energy was demonstrated not to be the only parameter controlling the HER activity in Ni2-xCoxP.
CitacióLiu, J., Wang, Z., David, J., Llorca, J. Colloidal Ni2-: XCoxP nanocrystals for the hydrogen evolution reaction. "Journal of materials chemistry A", 11 Maig 2018, vol. 6, p. 11453-11462.
ISSN2050-7488
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