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Updated: Oct 18, 2025

Probing and Mapping Electrode Surfaces in Solid Oxide Fuel Cells
Published on: September 20, 2012
Nickel phosphide on Ni foam as anode and peroxymonosulfate as the chemical oxidizer for effective direct urea fuel
Jingwei Hao1, Shen Zhao2, Ran Mao2
1Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Abstract:
The direct urea fuel cell (DUFC) is a low cost and competitive approach for contemporaneous urine or urea-contaminated wastewater treatment and electricity generation. However, the lack of efficient urea oxidation reaction (UOR) electrocatalysts and suitable electron acceptors remains a challenge for practical applications. Here, we developed a DUFC system using Ni2P@Ni foam as the anode and peroxymonosulfate (PMS) as the chemical oxidizers. The Ni2P@Ni foam anode showed a high oxidation activity for UOR with an onset potential of 0.30 V vs. Ag/AgCl and Tafel slope of 34.4 mV/dec. PMS with high theoretical potential improved the cell voltage to 1.43 V. A power density of DUFC up to 4.91 mW/cm2 was achieved using PMS at room temperature, which was approximately twice as high as using H2O2 (2.38 mW/cm2). NiII/NiIII was the redox active species on the Ni2P anode in the DUFC process, and NiII was electrochemically oxidized to NiIII, which reverted to NiII by urea reduction. When real human urine was used as the fuel, a power density of 4.46 mW/cm2 can be achieved at room temperature. This DUFC with high cell performance showed potential application in urea wastewater treatment.

