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Identifying Heteroatomic and Defective Sites in Carbon with Dual-Ion Adsorption Capability for High Energy and Power Zinc Ion Capacitor
Aqueous zinc-based batteries (AZBs) attract tremendous attention due to the abundant and rechargeable zinc anode. Nonetheless, the requirement of high energy and power densities raises great challenge for the cathode development. Herein we construct an aqueous zinc ion capacitor possessing an unriva...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187496/ https://www.ncbi.nlm.nih.gov/pubmed/34138287 http://dx.doi.org/10.1007/s40820-021-00588-5 |
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author | Fan, Wenjie Ding, Jia Ding, Jingnan Zheng, Yulong Song, Wanqing Lin, Jiangfeng Xiao, Caixia Zhong, Cheng Wang, Huanlei Hu, Wenbin |
author_facet | Fan, Wenjie Ding, Jia Ding, Jingnan Zheng, Yulong Song, Wanqing Lin, Jiangfeng Xiao, Caixia Zhong, Cheng Wang, Huanlei Hu, Wenbin |
author_sort | Fan, Wenjie |
collection | PubMed |
description | Aqueous zinc-based batteries (AZBs) attract tremendous attention due to the abundant and rechargeable zinc anode. Nonetheless, the requirement of high energy and power densities raises great challenge for the cathode development. Herein we construct an aqueous zinc ion capacitor possessing an unrivaled combination of high energy and power characteristics by employing a unique dual-ion adsorption mechanism in the cathode side. Through a templating/activating co-assisted carbonization procedure, a routine protein-rich biomass transforms into defect-rich carbon with immense surface area of 3657.5 m(2) g(−1) and electrochemically active heteroatom content of 8.0 at%. Comprehensive characterization and DFT calculations reveal that the obtained carbon cathode exhibits capacitive charge adsorptions toward both the cations and anions, which regularly occur at the specific sites of heteroatom moieties and lattice defects upon different depths of discharge/charge. The dual-ion adsorption mechanism endows the assembled cells with maximum capacity of 257 mAh g(−1) and retention of 72 mAh g(−1) at ultrahigh current density of 100 A g(−1) (400 C), corresponding to the outstanding energy and power of 168 Wh kg(−1) and 61,700 W kg(−1). Furthermore, practical battery configurations of solid-state pouch and cable-type cells display excellent reliability in electrochemistry as flexible and knittable power sources. [Image: see text] SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s40820-021-00588-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-8187496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-81874962021-06-14 Identifying Heteroatomic and Defective Sites in Carbon with Dual-Ion Adsorption Capability for High Energy and Power Zinc Ion Capacitor Fan, Wenjie Ding, Jia Ding, Jingnan Zheng, Yulong Song, Wanqing Lin, Jiangfeng Xiao, Caixia Zhong, Cheng Wang, Huanlei Hu, Wenbin Nanomicro Lett Article Aqueous zinc-based batteries (AZBs) attract tremendous attention due to the abundant and rechargeable zinc anode. Nonetheless, the requirement of high energy and power densities raises great challenge for the cathode development. Herein we construct an aqueous zinc ion capacitor possessing an unrivaled combination of high energy and power characteristics by employing a unique dual-ion adsorption mechanism in the cathode side. Through a templating/activating co-assisted carbonization procedure, a routine protein-rich biomass transforms into defect-rich carbon with immense surface area of 3657.5 m(2) g(−1) and electrochemically active heteroatom content of 8.0 at%. Comprehensive characterization and DFT calculations reveal that the obtained carbon cathode exhibits capacitive charge adsorptions toward both the cations and anions, which regularly occur at the specific sites of heteroatom moieties and lattice defects upon different depths of discharge/charge. The dual-ion adsorption mechanism endows the assembled cells with maximum capacity of 257 mAh g(−1) and retention of 72 mAh g(−1) at ultrahigh current density of 100 A g(−1) (400 C), corresponding to the outstanding energy and power of 168 Wh kg(−1) and 61,700 W kg(−1). Furthermore, practical battery configurations of solid-state pouch and cable-type cells display excellent reliability in electrochemistry as flexible and knittable power sources. [Image: see text] SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s40820-021-00588-5) contains supplementary material, which is available to authorized users. Springer Nature Singapore 2021-01-21 /pmc/articles/PMC8187496/ /pubmed/34138287 http://dx.doi.org/10.1007/s40820-021-00588-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fan, Wenjie Ding, Jia Ding, Jingnan Zheng, Yulong Song, Wanqing Lin, Jiangfeng Xiao, Caixia Zhong, Cheng Wang, Huanlei Hu, Wenbin Identifying Heteroatomic and Defective Sites in Carbon with Dual-Ion Adsorption Capability for High Energy and Power Zinc Ion Capacitor |
title | Identifying Heteroatomic and Defective Sites in Carbon with Dual-Ion Adsorption Capability for High Energy and Power Zinc Ion Capacitor |
title_full | Identifying Heteroatomic and Defective Sites in Carbon with Dual-Ion Adsorption Capability for High Energy and Power Zinc Ion Capacitor |
title_fullStr | Identifying Heteroatomic and Defective Sites in Carbon with Dual-Ion Adsorption Capability for High Energy and Power Zinc Ion Capacitor |
title_full_unstemmed | Identifying Heteroatomic and Defective Sites in Carbon with Dual-Ion Adsorption Capability for High Energy and Power Zinc Ion Capacitor |
title_short | Identifying Heteroatomic and Defective Sites in Carbon with Dual-Ion Adsorption Capability for High Energy and Power Zinc Ion Capacitor |
title_sort | identifying heteroatomic and defective sites in carbon with dual-ion adsorption capability for high energy and power zinc ion capacitor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187496/ https://www.ncbi.nlm.nih.gov/pubmed/34138287 http://dx.doi.org/10.1007/s40820-021-00588-5 |
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