Manipulating dehydrogenation kinetics through dual-doping Co3N electrode enables highly efficient hydrazine oxidation assisting self-powered H2 production
Yi Liu,
Jihua Zhang,
Yapeng Li,
Qizhu Qian,
Ziyun Li,
Yin Zhu and
Genqiang Zhang ()
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Yi Liu: University of Science and Technology of China
Jihua Zhang: Guizhou Education University
Yapeng Li: University of Science and Technology of China
Qizhu Qian: University of Science and Technology of China
Ziyun Li: University of Science and Technology of China
Yin Zhu: University of Science and Technology of China
Genqiang Zhang: University of Science and Technology of China
Nature Communications, 2020, vol. 11, issue 1, 1-13
Abstract:
Abstract Replacing sluggish oxygen evolution reaction (OER) with hydrazine oxidation reaction (HzOR) to produce hydrogen has been considered as a more energy-efficient strategy than water splitting. However, the relatively high cell voltage in two-electrode system and the required external electric power hinder its scalable applications, especially in mobile devices. Herein, we report a bifunctional P, W co-doped Co3N nanowire array electrode with remarkable catalytic activity towards both HzOR (−55 mV at 10 mA cm−2) and hydrogen evolution reaction (HER, −41 mV at 10 mA cm−2). Inspiringly, a record low cell voltage of 28 mV is required to achieve 10 mA cm−2 in two-electrode system. DFT calculations decipher that the doping optimized H* adsorption/desorption and dehydrogenation kinetics could be the underlying mechanism. Importantly, a self-powered H2 production system by integrating a direct hydrazine fuel cell with a hydrazine splitting electrolyzer can achieve a decent rate of 1.25 mmol h−1 at room temperature.
Date: 2020
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DOI: 10.1038/s41467-020-15563-8
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