A deeply rechargeable zinc anode with pomegranate-inspired nanostructure for high-energy aqueous batteries

Peng Chen, Yutong Wu, Yamin Zhang, Tzu Ho Wu, Yao Ma, Chloe Pelkowski, Haochen Yang, Yi Zhang, Xianwei Hu, Nian Liu

Research output: Contribution to journalArticlepeer-review

74 Scopus citations

Abstract

Rechargeable, Zn-based aqueous batteries because of their advantages of inflammability, high energy density, and low material cost are an attractive alternative to lithium-ion and lead-acid batteries for transportation and grid-scale applications. Historically, zinc anodes have shown low utilization and rechargeability in alkaline electrolytes due to the problems of ZnO passivation and Zn(OH)4 2− dissolution. Herein, we report a nanoscale, pomegranate-structured Zn anode (Zn-pome) fabricated via a bottom-up microemulsion approach to overcome these problems. In the Zn-pome, primary ZnO nanoparticles (ZnO NPs) assemble into secondary clusters after which they are individually encapsulated by a conductive, microporous carbon framework. The small size of ZnO NPs overcomes the issue of passivation, whereas the secondary structure and ion-sieving carbon shell mitigate the dissolution problem. Inductively coupled plasma (ICP) analysis confirms that Zn dissolution from the Zn-pome anode is effectively suppressed, leading to a considerably prolonged cycle life compared to that of a conventional ZnO anode in an alkaline aqueous electrolyte. The Zn-pome anode even maintains the capacity after long resting. This performance is achieved in harsh yet practical conditions: a limited amount of electrolyte, sealed coin cells, and 100% depth of discharge (DOD). This study represents an important step towards producing aqueous, rechargeable, high-energy batteries. In addition, the design principles reported here can be applied to other battery systems involving passivation or dissolution intermediates.

Original languageEnglish
Pages (from-to)21933-21940
Number of pages8
JournalJournal of Materials Chemistry A
Volume6
Issue number44
DOIs
StatePublished - 2018

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