Dual Electronic Modulations on NiFeV Hydroxide@FeO Boost Electrochemical Overall Water Splitting.

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State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources, Key Laboratory of Advanced Functional Materials, Autonomous Region, Institute of Applied Chemistry, College of Chemistry, Xinjiang University, Urumqi, Xinjiang, 830046, P. R. China.

Published: September 2023

Nickel-iron based hydroxides have been proven to be excellent oxygen evolution reaction (OER) electrocatalysts, whereas they are inactive toward hydrogen evolution reaction (HER), which severely limits their large-scale applications in electrochemical water splitting. Herein, a heterostructure consisted of NiFeV hydroxide and iron oxide supported on iron foam (NiFeV@FeO /IF) has been designed as a highly efficient bifunctional (OER and HER) electrocatalyst. The V doping and intimate contact between NiFeV hydroxide and FeO not only improve the entire electrical conductivity of the catalyst but also afford more high-valence Ni which serves as active sites for OER. Meanwhile, the introduction of V and FeO reduces the electron density on lattice oxygen, which greatly facilitates desorption of H . All of these endow the NiFeV@FeO /IF with exceptionally low overpotentials of 218 and 105 mV to achieve a current density of 100 mA cm for OER and HER, respectively. More impressively, the electrolyzer requires an ultra-low cell voltage of 1.57 V to achieve 100 mA cm and displays superior electrochemical stability for 180 h, which outperforms commercial RuO ||Pt/C and most of the representative catalysts reported to date. This work provides a unique route for developing high-efficiency electrocatalyst for overall water splitting.

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Source
http://dx.doi.org/10.1002/smll.202301294DOI Listing

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