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Fast hydrogenolytic debenzylation enabled by hierarchically ordered porosity and accessibly rich Pd(0) sites
Zhe Li, Gui-Long Wang, Xin Feng, Jia-Hui Guo, Lu Bai, Jie Chen*, Ming-Shui Yao* Submit a Manuscript
Tuning the d-band center of amorphous NiCo alloy via P doping for enhanced urea electrolysis

Wenjie Jiang, Jiali Lu, Jia Wu, Boyao Feng, Zhixiang Zhai, Huan Wen, Shibin Yin*

Chin. J. Struct. Chem., 2026, 45(5), 100865. DOI: 10.1016/j.cjsc.2026.100865

May 1, 2026

Phosphorus doping; Amorphous NiCo alloy; Reactant adsorption; Urea oxidation reaction; Hydrogen evolution reaction

ABSTRACT

Nickel-cobalt (NiCo) alloys with bimetallic electronic modulation are considered promising candidates for urea electrolysis. However, their highly occupied d-band states limit the adsorption of reaction intermediates, resulting in insufficient activity toward urea oxidation reaction (UOR) and hydrogen evolution reaction (HER). Herein, a phosphorus-doped amorphous NiCo alloy is synthesized, in which P incorporation modulates the electronic structure and upshifts the d-band center of NiCo alloy, thus optimizing the adsorption of OH and urea molecules. The sample with optimal P content exhibits low potentials for UOR (E10/1000 = 1.28/1.65 VRHE) and HER (E−10/−1000 = −67/−206 mVRHE). Furthermore, it achieves an industrial-level current density of 500 mA cm−2 at a cell voltage of 1.72 V in the membrane electrode assembly, while maintaining stable activity for 150 h. Therefore, this work provides a new strategy to optimize reactant adsorption and ultimately enhance the electrocatalytic activity by modulating the d-band center.


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