用于具有超高倍率能力的水性碱性电池的氧化铋阳极的突破性扩散系数限制

IF 6.4 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Fengming Zhou, Xiaodong Wang, Shiyu Gu, Mingjie Li, Ranqiang Xia, Xinyu Li, Zhenjiang Li, Qi Zhang, Zhenyu Xiao and Lei Wang
{"title":"用于具有超高倍率能力的水性碱性电池的氧化铋阳极的突破性扩散系数限制","authors":"Fengming Zhou, Xiaodong Wang, Shiyu Gu, Mingjie Li, Ranqiang Xia, Xinyu Li, Zhenjiang Li, Qi Zhang, Zhenyu Xiao and Lei Wang","doi":"10.1039/D4QI01011F","DOIUrl":null,"url":null,"abstract":"<p >Owing to the limitation of the diffusion rate of electrolyte ions, the two key parameters of energy density and power density of energy storage devices seem contradictory, and the construction of “double-high” electrode materials is the key challenge in the electrochemical energy storage field. To achieve outstanding capacity retention at high charging/discharging current density, a hierarchical porous amorphous bismuth oxide anode (<em>A</em>-Bi<small><sub>2</sub></small>O<small><sub>3</sub></small>) was constructed <em>via</em> an ion-exchange strategy using a Bi-based metal–organic framework as the precursor. Under a suitable alkaline solution, organic anions will be gradually substituted by OH<small><sup>−</sup></small> anions to form rich mesoporous channels, and the residual ligand can fix or functionalize the as-formed BiO<small><sub><em>x</em></sub></small> crystallites to form amorphous configuration, which provides tree vein-like channels for fast and deep electrolyte ion feeding. Therefore, the optimized <em>A</em>-Bi<small><sub>2</sub></small>O<small><sub>3</sub></small> cathode presents a high capacity of 319.6 mA h g<small><sup>−1</sup></small> at 1 A g<small><sup>−1</sup></small> and excellent retention rate of 83.7% when the current density was increased to 30 A g<small><sup>−1</sup></small>. Furthermore, the fabricated <em>H</em>-Ni(OH)<small><sub>2</sub></small>//<em>A</em>-Bi<small><sub>2</sub></small>O<small><sub>3</sub></small> aqueous alkaline battery (AAB) shows a high energy density of 104.58 W h kg<small><sup>−1</sup></small> at 0.24 kW kg<small><sup>−1</sup></small> and can make an electronic thermometer work for 30 min with a charging of several seconds.</p>","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":" 19","pages":" 6638-6648"},"PeriodicalIF":6.4000,"publicationDate":"2024-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Breaking the diffusion coefficient limitation of bismuth oxide anodes for aqueous alkaline batteries with ultra-high rate capability†\",\"authors\":\"Fengming Zhou, Xiaodong Wang, Shiyu Gu, Mingjie Li, Ranqiang Xia, Xinyu Li, Zhenjiang Li, Qi Zhang, Zhenyu Xiao and Lei Wang\",\"doi\":\"10.1039/D4QI01011F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Owing to the limitation of the diffusion rate of electrolyte ions, the two key parameters of energy density and power density of energy storage devices seem contradictory, and the construction of “double-high” electrode materials is the key challenge in the electrochemical energy storage field. To achieve outstanding capacity retention at high charging/discharging current density, a hierarchical porous amorphous bismuth oxide anode (<em>A</em>-Bi<small><sub>2</sub></small>O<small><sub>3</sub></small>) was constructed <em>via</em> an ion-exchange strategy using a Bi-based metal–organic framework as the precursor. Under a suitable alkaline solution, organic anions will be gradually substituted by OH<small><sup>−</sup></small> anions to form rich mesoporous channels, and the residual ligand can fix or functionalize the as-formed BiO<small><sub><em>x</em></sub></small> crystallites to form amorphous configuration, which provides tree vein-like channels for fast and deep electrolyte ion feeding. Therefore, the optimized <em>A</em>-Bi<small><sub>2</sub></small>O<small><sub>3</sub></small> cathode presents a high capacity of 319.6 mA h g<small><sup>−1</sup></small> at 1 A g<small><sup>−1</sup></small> and excellent retention rate of 83.7% when the current density was increased to 30 A g<small><sup>−1</sup></small>. Furthermore, the fabricated <em>H</em>-Ni(OH)<small><sub>2</sub></small>//<em>A</em>-Bi<small><sub>2</sub></small>O<small><sub>3</sub></small> aqueous alkaline battery (AAB) shows a high energy density of 104.58 W h kg<small><sup>−1</sup></small> at 0.24 kW kg<small><sup>−1</sup></small> and can make an electronic thermometer work for 30 min with a charging of several seconds.</p>\",\"PeriodicalId\":79,\"journal\":{\"name\":\"Inorganic Chemistry Frontiers\",\"volume\":\" 19\",\"pages\":\" 6638-6648\"},\"PeriodicalIF\":6.4000,\"publicationDate\":\"2024-08-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/qi/d4qi01011f\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/qi/d4qi01011f","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

摘要

由于电解质离子扩散速率的限制,能量密度和功率密度这两个储能装置的关键参数似乎是相互矛盾的,因此构建 "双高 "电极材料是电化学储能领域的关键挑战。为了在高充放电电流密度下实现出色的容量保持,研究人员以铋基金属有机框架为前驱体,通过离子交换策略构建了分层多孔非晶氧化铋阳极(A-Bi2O3)。在适当的碱性溶液中,有机阴离子会逐渐被 OH- 阴离子取代,形成丰富的介孔通道,而残留配体可以固定或官能化所形成的 BiOx 晶体,使其形成非晶态构型,从而为电解质离子的快速和深度馈入提供树脉状通道。因此,优化后的 A-Bi2O3 阴极在 1 A g-1 电流密度下具有 319.6 mAh g-1 的高容量,当电流密度增加到 30 A g-1 时,其优良率保持在 83.7%。此外,制备的 H-Ni(OH)2//A-Bi2O3 碱性水电池(AAB)在 0.24 kW kg-1 的条件下具有 104.58 Wh kg-1 的高能量密度,可使电子温度计在充电数秒后工作 30 分钟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Breaking the diffusion coefficient limitation of bismuth oxide anodes for aqueous alkaline batteries with ultra-high rate capability†

Breaking the diffusion coefficient limitation of bismuth oxide anodes for aqueous alkaline batteries with ultra-high rate capability†

Owing to the limitation of the diffusion rate of electrolyte ions, the two key parameters of energy density and power density of energy storage devices seem contradictory, and the construction of “double-high” electrode materials is the key challenge in the electrochemical energy storage field. To achieve outstanding capacity retention at high charging/discharging current density, a hierarchical porous amorphous bismuth oxide anode (A-Bi2O3) was constructed via an ion-exchange strategy using a Bi-based metal–organic framework as the precursor. Under a suitable alkaline solution, organic anions will be gradually substituted by OH anions to form rich mesoporous channels, and the residual ligand can fix or functionalize the as-formed BiOx crystallites to form amorphous configuration, which provides tree vein-like channels for fast and deep electrolyte ion feeding. Therefore, the optimized A-Bi2O3 cathode presents a high capacity of 319.6 mA h g−1 at 1 A g−1 and excellent retention rate of 83.7% when the current density was increased to 30 A g−1. Furthermore, the fabricated H-Ni(OH)2//A-Bi2O3 aqueous alkaline battery (AAB) shows a high energy density of 104.58 W h kg−1 at 0.24 kW kg−1 and can make an electronic thermometer work for 30 min with a charging of several seconds.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信