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https://hdl.handle.net/10356/156936
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DC Field | Value | Language |
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dc.contributor.author | Zeng, Yinxiang | en_US |
dc.contributor.author | Wang, Yan | en_US |
dc.contributor.author | Jin, Qi | en_US |
dc.contributor.author | Pei, Zhihao | en_US |
dc.contributor.author | Luan, Deyan | en_US |
dc.contributor.author | Zhang, Xitian | en_US |
dc.contributor.author | Lou, David Xiong Wen | en_US |
dc.date.accessioned | 2022-04-27T07:28:27Z | - |
dc.date.available | 2022-04-27T07:28:27Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Zeng, Y., Wang, Y., Jin, Q., Pei, Z., Luan, D., Zhang, X. & Lou, D. X. W. (2021). Rationally designed Mn₂O₃ -ZnMn₂ O₄ hollow heterostructures from metal-organic frameworks for stable Zn-ion storage. Angewandte Chemie International Edition, 60(49), 25793-25798. https://dx.doi.org/10.1002/anie.202113487 | en_US |
dc.identifier.issn | 1433-7851 | en_US |
dc.identifier.uri | https://hdl.handle.net/10356/156936 | - |
dc.description.abstract | Mn-based oxides have sparked extensive scientific interest for aqueous Zn-ion batteries due to the rich abundance, plentiful oxidation states, and high output voltage. However, the further development of Mn-based oxides is severely hindered by the rapid capacity decay during cycling. Herein, a two-step metal-organic framework (MOF)-engaged templating strategy has been developed to rationally synthesize heterostructured Mn2 O3 -ZnMn2 O4 hollow octahedrons (MO-ZMO HOs) for stable zinc ion storage. The distinctive composition and hollow heterostructure endow MO-ZMO HOs with abundant active sites, enhanced electric conductivity, and superior structural stability. By virtue of these advantages, the MO-ZMO HOs electrode shows high reversible capacity, impressive rate performance, and outstanding electrochemical stability. Furthermore, ex situ characterizations reveal that the charge storage of MO-ZMO HOs mainly originates from the highly reversible Zn2+ insertion/extraction reactions. | en_US |
dc.description.sponsorship | Ministry of Education (MOE) | en_US |
dc.language.iso | en | en_US |
dc.relation | RG3/20 | en_US |
dc.relation | MOE2017-T2-2–003 | en_US |
dc.relation.ispartof | Angewandte Chemie International Edition | en_US |
dc.rights | This is the peer reviewed version of the following article: Zeng, Y., Wang, Y., Jin, Q., Pei, Z., Luan, D., Zhang, X. & Lou, D. X. W. (2021). Rationally designed Mn₂O₃ -ZnMn₂ O₄ hollow heterostructures from metal-organic frameworks for stable Zn-ion storage. Angewandte Chemie International Edition, 60(49), 25793-25798, which has been published in final form at https://doi.org/10.1002/anie.202113487. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | en_US |
dc.subject | Engineering::Chemical engineering | en_US |
dc.title | Rationally designed Mn₂O₃ -ZnMn₂ O₄ hollow heterostructures from metal-organic frameworks for stable Zn-ion storage | en_US |
dc.type | Journal Article | en |
dc.contributor.school | School of Chemical and Biomedical Engineering | en_US |
dc.identifier.doi | 10.1002/anie.202113487 | - |
dc.description.version | Submitted/Accepted version | en_US |
dc.identifier.pmid | 34676649 | - |
dc.identifier.scopus | 2-s2.0-85118509500 | - |
dc.identifier.issue | 49 | en_US |
dc.identifier.volume | 60 | en_US |
dc.identifier.spage | 25793 | en_US |
dc.identifier.epage | 25798 | en_US |
dc.subject.keywords | Heterostructures | en_US |
dc.subject.keywords | Hollow Octahedrons | en_US |
dc.description.acknowledgement | X.W.L. acknowledges the funding support from the Ministry of Education of Singapore through the Academic Research Fund (AcRF)Tier-1 grant (RG3/20) and Tier-2 grant (MOE2017-T2-2–003). | en_US |
item.fulltext | With Fulltext | - |
item.grantfulltext | embargo_20221208 | - |
Appears in Collections: | SCBE Journal Articles |
Files in This Item:
File | Description | Size | Format | |
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Rationally Designed Mn2O3–ZnMn2O4 Hollow Heterostructures from Metal–Organic Frameworks for Stable Zn-Ion Storage.pdf Until 2022-12-08 | 1.01 MB | Adobe PDF | Under embargo until Dec 08, 2022 |
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