High-Power and Ultralong-Life Aqueous Zinc-Ion Hybrid Capacitors Based on Pseudocapacitive Charge Storage
Highlights This work starts the research of pseudocapacitive oxide materials for multivalent Zn 2+ storage. The constructed RuO 2 ·H 2 O||Zn systems exhibit outstanding electrochemical performance, including a high discharge capacity, ultrafast charge/discharge capability, and excellent cycling stab...
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Veröffentlicht in: | Nano-Micro Letters 2019-10, Vol.11 (1), p.94-9, Article 94 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Highlights
This work starts the research of pseudocapacitive oxide materials for multivalent Zn
2+
storage.
The constructed RuO
2
·H
2
O||Zn systems exhibit outstanding electrochemical performance, including a high discharge capacity, ultrafast charge/discharge capability, and excellent cycling stability.
The redox pseudocapacitive behavior of RuO
2
·H
2
O for Zn
2+
storage is revealed.
Rechargeable aqueous zinc-ion hybrid capacitors and zinc-ion batteries are promising safe energy storage systems. In this study, amorphous RuO
2
·H
2
O for the first time was employed to achieve fast and ultralong-life Zn
2+
storage based on a pseudocapacitive storage mechanism. In the RuO
2
·H
2
O||Zn zinc-ion hybrid capacitors with Zn(CF
3
SO
3
)
2
aqueous electrolyte, the RuO
2
·H
2
O cathode can reversibly store Zn
2+
in a voltage window of 0.4–1.6 V (vs. Zn/Zn
2+
), delivering a high discharge capacity of 122 mAh g
−1
. In particular, the zinc-ion hybrid capacitors can be rapidly charged/discharged within 36 s with a very high power density of 16.74 kW kg
−1
and a high energy density of 82 Wh kg
−1
. Besides, the zinc-ion hybrid capacitors demonstrate an ultralong cycle life (over 10,000 charge/discharge cycles). The kinetic analysis elucidates that the ultrafast Zn
2+
storage in the RuO
2
·H
2
O cathode originates from redox pseudocapacitive reactions. This work could greatly facilitate the development of high-power and safe electrochemical energy storage. |
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ISSN: | 2311-6706 2150-5551 |
DOI: | 10.1007/s40820-019-0328-3 |