期刊
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 48, 期 100, 页码 39900-39909出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2023.09.063
关键词
Electrocatalyst; Bifunctional; Flower-shaped structure; Water splitting; Metallic nitride
Developing efficient bifunctional transition metal-based electrocatalysts is crucial for reducing the practical costs of water splitting. In this study, a flower-shaped disorderly nickel-iron nitride nanosheets bifunctional electrocatalyst (NiFeNx/NF) was synthesized and demonstrated exceptional performance and stability in the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), making it a promising candidate for cost-effective and environmentally friendly water splitting catalysts.
Developing highly efficient bifunctional transition metal-based electrocatalysts is important for reducing the practical costs of water splitting. Herein, we present a flower-shaped disorderly nickel-iron nitride nanosheets bifunctional electrocatalysts (NiFeNx/NF), which was prepared in situ on a nickel foam substrate using a hydrothermal and thermal ammonia-reduction method. The unique structure of the flower-shaped disorderly nano-sheets increases the amount of electrocatalytic active sites and promotes efficiency of both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) by facilitating charge and mass transfer. The bifunctional catalyst demonstrated exceptional perfor-mance with overpotentials of only 78 mV for HER and 280 mV for OER at current densities of 10 mA cm-2 and 100 mA cm-2, respectively. Additionally, the NiFeNx/NF exhibited outstanding stability, achieving a cell voltage of only 1.53 V for overall water splitting at 10 mA cm-2 in 1.0 M KOH, and continuously operated for 90 h at 20 mA cm-2 without significant voltage increase. These findings contribute to the development of high-performance, cost-effective, and environmentally friendly bifunctional catalysts based on transition metals for water splitting.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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