Abstract
Rechargeable aqueous metal-ion (such as Li+, Na+, Mg2+, Al3+) batteries are of great importance to enrich safer, cheaper and sustainable electrochemical energy storage technologies. One of the major challenges in developing such batteries is that few electrode material systems are available to achieve prominent, reversible and stable redox reactions in aqueous electrolytes. Here we systematically report that a versatile Bi2O3 electrode material is able to electrochemically store charges in more than ten types of aqueous monovalent, divalent and trivalent metal ion electrolytes. A remarkably high specific capacity (∼357 mA h g-1 at 0.72C), outstanding rate capability (217C; 75000 mA g-1) and good cycle life (>200 cycles) are demonstrated in a neutral mixed Li+ electrolyte. A unique "quasi-conversion reaction" charge storage mechanism that differs from a conventional intercalation-type mechanism is further unveiled (Bi2O3 ↔ Bi0). By pairing with a Li+ intercalation electrode, an aqueous LiMn2O4//Bi2O3 full cell is fabricated, which exhibits stable cycling with a low self-discharge rate and delivers a high energy density of ∼78 W h kg-1, far superior to typical aqueous lithium ion batteries (≤50 W h kg-1). Moreover, even with a relatively high mass loading of 5 mg cm-2 by slurry casting, the Bi2O3 electrode still manifests excellent performance. We anticipate that our work will stimulate the development of diverse electrode materials for aqueous rechargeable batteries. © 2016 The Royal Society of Chemistry.
| Original language | English |
|---|---|
| Pages (from-to) | 2881-2891 |
| Journal | Energy and Environmental Science |
| Volume | 9 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - 1 Sept 2016 |
| Externally published | Yes |
Bibliographical note
Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].Funding
This work was supported by grants from the National Key Research Program of China (No. 2016YFA0202602), the National Natural Science Foundation of China (No. 51102105, 11104088), the Science Fund for Distinguished Young Scholars of Hubei Province (Grant No. 2013CFA023), the Youth Chenguang Project of Science and Technology of Wuhan City (Grant No. 2014070404010206), the Research Start-Up Fund from Wuhan University of Technology, and the Fundamental Research Funds for the Central Universities (WUT: 2016IVA083).
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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