Issue 23, 2023

Selenium-transition metal supported on a mixture of reduced graphene oxide and silica template for water splitting

Abstract

Exploration of economical, highly efficient, and environment friendly non-noble-metal-based electrocatalysts is necessary for hydrogen and oxygen evolution reactions (HER and OER) but challenging for cost-effective water splitting. Herein, metal selenium nanoparticles (M = Ni, Co & Fe) are anchored on the surface of reduced graphene oxide and a silica template (rGO-ST) through a simple one-pot solvothermal method. The resulting electrocatalyst composite can enhance mass/charge transfer and promote interaction between water molecules and electrocatalyst reactive sites. NiSe2/rGO-ST shows a remarkable overpotential (52.5 mV) at 10 mA cm−2 for the HER compared to the benchmark Pt/C E-TEK (29 mV), while the overpotential values of CoSeO3/rGO-ST and FeSe2/rGO-ST are 246 and 347 mV, respectively. The FeSe2/rGO-ST/NF shows a low overpotential (297 mV) at 50 mA cm−2 for the OER compared to RuO2/NF (325 mV), while the overpotentials of CoSeO3-rGO-ST/NF and NiSe2-rGO-ST/NF are 400 and 475 mV, respectively. Furthermore, all catalysts indicate negligible deterioration, indicating better stability during the process of HER and OER after a stability test of 60 h. The water splitting system composed of NiSe2-rGO-ST/NF||FeSe2-rGO-ST/NF electrodes requires only ∼1.75 V at 10 mA cm−2. Its performance is nearly close to that of a noble metal-based Pt/C/NF||RuO2/NF water splitting system.

Graphical abstract: Selenium-transition metal supported on a mixture of reduced graphene oxide and silica template for water splitting

Supplementary files

Article information

Article type
Paper
Submitted
24 Mar 2023
Accepted
18 May 2023
First published
25 May 2023
This article is Open Access
Creative Commons BY license

RSC Adv., 2023,13, 15856-15871

Selenium-transition metal supported on a mixture of reduced graphene oxide and silica template for water splitting

R. S. Amin, A. E. Fetohi, D. Z. Khater, J. Lin, Y. Wang, C. Wang and K. M. El-Khatib, RSC Adv., 2023, 13, 15856 DOI: 10.1039/D3RA01945D

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