Introducing Mo <sub>2</sub> C To Construct Multi-interfaces and Heterojunctions of NiFe Layered Double Hydroxide Realizes Electrocatalytic Overall Water Splitting in an Alkaline Medium
Developing cost-effective, high-performance, and stable electrocatalysts for the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) remains a key challenge for the utilization of hydrogen energy. Herein, the heterostructure catalyst composed of NiFe-LDH coupled with Mo<sub>2</sub>C materials and carbon nanospheres (NiFe/MC/C) is synthesized via a two-step integrated strategy. Benefiting from the tunable electronic structure of NiFe-LDH and the suitable hydrogen binding energy of MC materials, the synergistic effect between multi-interfaces and heterojunctions significantly enhances the water splitting performance of NiFe-LDH. The optimized catalyst affords low overpotentials of 232 mV for the OER and 151 mV for the HER at a current density of 10 mA cm<sup>-2</sup> in 1 M KOH. The cell voltage required for the 1.0NiFe/MC/C electrolytic cell is only 1.68 V at a current density of 50 mA cm<sup>-2</sup>. The enhanced water splitting performance stems from the interfacial active sites, abundant channels, and significantly improved electrical conductivity. DFT calculations show that the rate-determining step energy barrier of NiFe-LDH/Mo<sub>2</sub>C (1.66 eV) is significantly lower than that of NiFe-LDH (1.90 eV), thereby enhancing its OER performance. This research presents a facile and effective strategy for constructing multicomponent and high-performance electrocatalysts for overall water splitting.
Authors
- Guoli Liu (ORCID: https://orcid.org/0000-0003-3786-1608)
- Shaoyang Zhang (ORCID: https://orcid.org/0000-0002-9221-7332)
- Jianping Du
- Zizai Ma
- Lu Liu
- Yuxuan Du
Institutions
- Shanxi University (CN)
- Taiyuan University of Technology (CN)
Publication Details
- Journal
- Langmuir
- Published
- 2026-02-24
- DOI
- https://doi.org/10.1021/acs.langmuir.5c06747
- Primary Topic
- Electrocatalysts for Energy Conversion
- Type
- article
- Field-Weighted Citation Impact
- 0.00