Affiliation:
1. Hunan Provincial Key Laboratory of Chemical Power Sources College of Chemistry and Chemical Engineering Central South University Changsha 410083 P. R. China
2. Country College of Energy and Chemical Engineering Xinjiang Institute of Technology Aksu Prefecture Xinjiang Uygur Autonomous Region 843100 P. R. China
3. School of Chemistry and Chemical Engineering Henan Normal University Xinxiang 453007 P. R. China
Abstract
AbstractAqueous zinc‐ion batteries are promising for next‐generation energy storage systems. However, the zinc dendrite growth, corrosion, and hydrogen evolution reaction at the electrochemical interface severely impede their further development. Herein, a Zn2+‐rich and H2O‐poor Helmholtz plane is constructed to regulate the electrochemical interface between the zinc anode and the electrolyte. Electrochemical and in situ spectroscopy characterizations reveal that the designed electric double layer with abundant Zn2+ coordination sites and less H2O content can facilitate rapid electron transfer, homogenize Zn2+ deposition, and alleviate the side reactions induced by active H2O. Benefiting from the high reversibility and stability of zinc anode, the Zn||Zn symmetric cell can be cycled over 1000 h at 1 mA cm−2 and the Zn||NH4V4O10 full cell can maintain a capacity of 85.23% for 1000 cycles at 3 A g−1. This work aims at Helmholtz plane reconfiguration and provides a realizable strategy in interface construction for other similar systems.
Funder
National Natural Science Foundation of China
Science and Technology Planning Project of Shenzen Municipality
Natural Science Foundation of Hunan Province
Cited by
6 articles.
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