Bi2WO6 and FeWO4 Nanocatalysts for the Electrochemical Water Oxidation Process

Rani, Balasubramanian Jansi; Ravi, Ganesan; Yuvakkumar, Rathinam; Praveenkumar, M.; Ravichandran, Subbiah; Mareeswaran, Paulpandian Muthu; Hong, Sun Ig

Abstract

Polyvinylpyrrolidone (PVP)-assisted nanocatalyst preparation was succeeded by employing a controlled solvothermal route to produce efficient electrodes for electrochemical water-splitting applications. Bi2WO6 and FeWO4 nanocatalysts have been confirmed through the strong signature of (113) and (111) crystal planes, respectively. The binding natures of Bi-W-O and Fe-W-O have been thoroughly discussed by employing X-ray photoelectron spectroscopy which confirmed the formation of Bi2WO6 and FeWO4. The freestanding nanoplate array morphology of Bi2WO6 and the fine nanosphere particle morphology of FeWO4 nanocatalysts were revealed by scanning electron microscopy images. With these confirmations, the fabrication of durable, long-term electrodes for electrochemical water splitting has been subjected to efficient oxidation of water, confirmed by obtaining 2.79 and 1.96 mA/g for 0.5 g PVP-assisted Bi2WO6 and FeWO4 nanocatalysts, respectively. The water oxidation mechanism of both nanocatalysts has been revealed with the support of 24 h stability test over continuous water oxidation and faster charge transfer achieved by the smaller Tafel slope values of 75 and 78 mV/dec, respectively. Generally, these nanocatalysts are utilized for photocatalytic applications. The present study revealed the PVP-assisted synthesis to produce electrocatalytically active nanocatalysts and their electrochemical water-splitting mechanism which will offer a pathway for research interests with regard to the production of multifunctional nanocatalysts for both electro- and photocatalytic applications in the near future.

Más información

Título según WOS: ID WOS:000462921900078 Not found in local WOS DB
Título de la Revista: ACS OMEGA
Volumen: 4
Número: 3
Editorial: AMER CHEMICAL SOC
Fecha de publicación: 2019
Página de inicio: 5241
Página final: 5253
DOI:

10.1021/acsomega.8b03003

Notas: ISI