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Updated: Jan 28, 2026

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules
Published on: April 28, 2014
Facile synthesis, characterization and DFT studies of a nanostructured nickel-molybdenum-phosphorous planar electrode
Wenjuan Zhang1, Jian Zheng, Xundi Gu
1Laboratory of Advanced Materials and Energy Electrochemistry, Research Institute of Surface Engineering, Taiyuan University of Technology, Taiyuan, 030024, China. wangxiaog1982@163.com wangxiaoguang@tyut.edu.cn.
Abstract:
In this paper, we combined experimental and theoretical routes to develop a novel nanostructured nickel-molybdenum-phosphorous planar electrode as an efficient catalyst toward the hydrogen evolution reaction (HER). The HER activities of various Ni-based electrodes (Ni4Mo and Ni12P5) were evaluated not only experimentally but also by density functional theory. Meanwhile, the electrocatalytic performance of Ni-Mo-P prepared at different temperatures (500 °C, 600 °C, 700 °C, and 800 °C) was also explored. The results indicated that the sample prepared at 700 °C exhibited the best catalytic activity. The as-fabricated Ni-Mo-P electrode possessed lower overpotential, higher current density and a smaller Tafel slope than pristine modified Ni@Ni-Mo in 1.0 M KOH and also showed long-term stability. An overpotential as low as 276 mV could be achieved at 100 mA cm-2 H2 evolving current density, which was superior to those of most previously reported samples. After phosphorization treatment, the as-formed Ni12P5 played a crucial role in the activity enhancement. Density functional theory calculations revealed that Ni12P5 has a smaller |ΔGH*| value than Ni4Mo, further confirming that Ni12P5 shows better catalytic performance than Ni4Mo.
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