| Literature DB >> 33306263 |
Qizhu Qian1, Jihua Zhang2, Jianming Li3, Yapeng Li1, Xu Jin3, Yin Zhu1, Yi Liu1, Ziyun Li1, Ahmed El-Harairy1, Chong Xiao4,5, Genqiang Zhang1, Yi Xie4,5.
Abstract
Electrochemical water splitting for H2 production is limited by the sluggish anode oxygen evolution reaction (OER), thus using hydrazine oxidation reaction (HzOR) to replace OER has received great attention. Here we report the hierarchical porous nanosheet arrays with abundant Ni3 N-Co3 N heterointerfaces on Ni foam with superior hydrogen evolution reaction (HER) and HzOR activity, realizing working potentials of -43 and -88 mV for 10 mA cm-2 , respectively, and achieving an industry-level 1000 mA cm-2 at 200 mV for HzOR. The two-electrode overall hydrazine splitting (OHzS) electrolyzer requires the cell voltages of 0.071 and 0.76 V for 10 and 400 mA cm-2 , respectively. The H2 production powered by a direct hydrazine fuel cell (DHzFC) and a commercial solar cell are investigated to inspire future practical applications. DFT calculations decipher that heterointerfaces simultaneously optimize the hydrogen adsorption free energy (ΔGH* ) and promote the hydrazine dehydrogenation kinetics. This work provides a rationale for advanced bifunctional electrocatalysts, and propels the practical energy-saving H2 generation techniques.Entities:
Keywords: heterointerfaces; hydrazine electro-oxidation; hydrogen evolution; nickel; overall hydrazine splitting
Year: 2020 PMID: 33306263 DOI: 10.1002/anie.202014362
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336