Journal
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 48, Issue 74, Pages 28882-28890Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2023.04.057
Keywords
Galvanic reaction; Oxides; Copper and nickel; Electrocatalysts; Urine; Direct urea fuel cell
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The sluggish kinetics of urea oxidation reaction (UOR) in direct urea fuel cells (DUFC) can be improved by utilizing copper and nickel-based composite oxides as catalysts. Through meticulous control of galvanic reaction and high-temperature oxidation, the nano-architectures of the catalysts are optimized to achieve low potential and high performance. Moreover, DUFCs assembled with bio-urine without further purification show similar voltage, indicating the possibility of converting bio-waste into valuable energy sources.
The sluggish kinetics of urea oxidation reaction (UOR) critically restrict the prevalence of direct urea fuel cell (DUFC), utilizing electrolyte containing urea/urine. In this work, the copper and nickel-based composite oxides are prepared by meticulously controlling the galvanic reaction of copper ion to metallic nickel and the high-temperature oxidation process. Based on a systematic electrochemical characterization of the catalyst, the asfabricated nano-architectures are optimized toward UOR performance, showing a low potential of 1.39 V vs. RHE to drive 100 mA cm-2 in alkaline solution. The button-like DUFCs configuration of as-developed catalysts exhibits a maximum power density of 1.19 mW cm-2. Furthermore, the DUFCs assembled with bio-urine, including men, dogs, cats, and rats as electrolytes without further purification, show a similar voltage. These findings open up a direction to convert bio-waste into treasure.& COPY; 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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