Issue 15, 2021

Nb-doped layered FeNi phosphide nanosheets for highly efficient overall water splitting under high current densities

Abstract

Nanostructured trimetallic phosphide electrocatalysts are promising for H2 and O2 evolution reactions (HER/OER) that are actively pursued nowadays to achieve commercial hydrogen production. Herein, a dual-functional Nb-doped NiFe phosphide nanosheet catalyst with a low cost and high stability was successfully prepared on nickel foam (NF) pretreated with dielectric barrier discharge (DBD) plasmas (PNF) operated under ambient conditions. The resulting Ni12P5–Fe2P–NbP layered nanosheets on the PNF show exceptional catalytic performances, evidenced by their low overpotentials for delivering current densities of 100 and 400 mA cm−2 (j100/j400) of only 178 and 265 mV for the HER, and 280 and 330 mV for the OER, as well as the small Tafel slope values of 52 (HER) and 59 (OER) mV dec−1, respectively. The catalyst also exhibits a good electrocatalytic durability and stability during 100 h continuous HER and OER tests at j300. Moreover, the current densities of 10 and 100 mA cm−2 are achieved at low cell voltages of 1.51 and 1.65 V, thus outperforming most of the reported electrocatalysts in two-electrode alkaline water electrolyzers. Numerical simulation analysis shows that the Ni and Nb atoms in the Ni12P5–Fe2P–NbP nanostructures are the key factors responsible for the achieved excellent performance in water electrolysis.

Graphical abstract: Nb-doped layered FeNi phosphide nanosheets for highly efficient overall water splitting under high current densities

Supplementary files

Article information

Article type
Paper
Submitted
14 Jan 2021
Accepted
22 Mar 2021
First published
22 Mar 2021

J. Mater. Chem. A, 2021,9, 9918-9926

Nb-doped layered FeNi phosphide nanosheets for highly efficient overall water splitting under high current densities

S. Wen, G. Chen, W. Chen, M. Li, B. Ouyang, X. Wang, D. Chen, T. Gong, X. Zhang, J. Huang and K. (. Ostrikov, J. Mater. Chem. A, 2021, 9, 9918 DOI: 10.1039/D1TA00372K

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