• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

磷酸银钒(Ag(2)VO(2)PO(4))的电化学还原:导电金属银纳米颗粒的形成

Electrochemical reduction of silver vanadium phosphorous oxide, Ag(2)VO(2)PO(4): the formation of electrically conductive metallic silver nanoparticles.

作者信息

Takeuchi Esther S, Marschilok Amy C, Tanzil Kevin, Kozarsky Eric S, Zhu Shali, Takeuchi Kenneth J

机构信息

Department of Chemical and Biological Engineering, University at Buffalo (SUNY), Buffalo, NY 14260.

出版信息

Chem Mater. 2009 Oct 27;21(20):4934-4939. doi: 10.1021/cm902102k.

DOI:10.1021/cm902102k
PMID:20161435
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2788945/
Abstract

As a cathode material, silver vanadium phosphorous oxide (Ag(2)VO(2)PO(4)) displays several notable electrochemical properties: large capacity, high current capability, and an effective delivery of high current pulses. These cell performance characteristics can be attributed to the presence of silver nanoparticles formed in-situ during the electrochemical reduction of Ag(2)VO(2)PO(4). Specifically, changes in the composition and structure of Ag(2)VO(2)PO(4) with reduction, especially the formation of silver nanoparticles, are detailed to rationalize a 15,000 fold increase in conductivity with initial discharge, which can be related to the power characteristics associated with Ag(2)VO(2)PO(4) cathodes in primary lithium batteries.

摘要

作为一种阴极材料,磷酸银钒(Ag(2)VO(2)PO(4))展现出几种显著的电化学性质:大容量、高电流能力以及高电流脉冲的有效传递。这些电池性能特征可归因于在Ag(2)VO(2)PO(4)的电化学还原过程中原位形成的银纳米颗粒。具体而言,详细阐述了Ag(2)VO(2)PO(4)随着还原过程在组成和结构上的变化,尤其是银纳米颗粒的形成,以解释初始放电时电导率增加15000倍的现象,这可能与一次锂电池中Ag(2)VO(2)PO(4)阴极的功率特性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/ff10db09b12c/nihms149291f12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/7132c9b91f92/nihms149291f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/7193cb4b93fc/nihms149291f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/30c69b9453d8/nihms149291f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/7e8bfe31df13/nihms149291f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/2ce0fdc7c395/nihms149291f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/9e14b0d62ff0/nihms149291f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/35e9b82d28ab/nihms149291f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/9de450a9769c/nihms149291f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/1566fa158619/nihms149291f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/918488474714/nihms149291f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/5e45f20faadb/nihms149291f11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/ff10db09b12c/nihms149291f12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/7132c9b91f92/nihms149291f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/7193cb4b93fc/nihms149291f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/30c69b9453d8/nihms149291f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/7e8bfe31df13/nihms149291f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/2ce0fdc7c395/nihms149291f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/9e14b0d62ff0/nihms149291f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/35e9b82d28ab/nihms149291f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/9de450a9769c/nihms149291f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/1566fa158619/nihms149291f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/918488474714/nihms149291f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/5e45f20faadb/nihms149291f11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcae/2788945/ff10db09b12c/nihms149291f12.jpg

相似文献

1
Electrochemical reduction of silver vanadium phosphorous oxide, Ag(2)VO(2)PO(4): the formation of electrically conductive metallic silver nanoparticles.磷酸银钒(Ag(2)VO(2)PO(4))的电化学还原:导电金属银纳米颗粒的形成
Chem Mater. 2009 Oct 27;21(20):4934-4939. doi: 10.1021/cm902102k.
2
Electrochemical Reduction of Silver Vanadium Phosphorous Oxide, Ag(2)VO(2)PO(4): Silver Metal Deposition and Associated Increase in Electrical Conductivity.银钒磷氧化物Ag(2)VO(2)PO(4)的电化学还原:银金属沉积及电导率的相关增加
J Power Sources. 2010 Oct 1;195(19):6839-6846. doi: 10.1016/j.jpowsour.2010.04.033.
3
Ag(x)VOPO(4): A Demonstration of the Dependence of Battery-Related Electrochemical Properties of Silver Vanadium Phosphorous Oxides on Ag / V Ratios.Ag(x)VOPO(4):银钒磷氧化物的电池相关电化学性质对银/钒比例的依赖性证明
J Power Sources. 2011 Mar 15;196(6):3325-3330. doi: 10.1016/j.jpowsour.2010.11.144.
4
Silver Vanadium Phosphorous Oxide, Ag(2)VO(2)PO(4): Chimie Douce Preparation and Resulting Lithium Cell Electrochemistry.氧化银钒磷,Ag(2)VO(2)PO(4):温和化学合成法及其在锂电池中的电化学性能
J Power Sources. 2011 Aug 15;196(16):6781-6787. doi: 10.1016/j.jpowsour.2010.10.054.
5
Silver Vanadium Diphosphate AgVPO: Electrochemistry and Characterization of Reduced Material providing Mechanistic Insights.磷酸银钒(AgVPO):还原材料的电化学性质及表征,提供机理见解
J Solid State Chem. 2013 Apr;200:232-240. doi: 10.1016/j.jssc.2013.01.020.
6
The structural conversion from α-AgVO to β-AgVO: Ag nanoparticle decorated nanowires with application as cathode materials for Li-ion batteries.从α-AgVO 到 β-AgVO 的结构转化:Ag 纳米粒子修饰的纳米线作为锂离子电池的阴极材料。
Nanoscale. 2016 Sep 15;8(36):16266-16275. doi: 10.1039/c6nr04825k.
7
Vanadium Oxide-Poly(3,4-ethylenedioxythiophene) Nanocomposite as High-Performance Cathode for Aqueous Zn-Ion Batteries: The Structural and Electrochemical Characterization.氧化钒-聚(3,4-乙撑二氧噻吩)纳米复合材料作为水系锌离子电池的高性能阴极:结构与电化学表征
Nanomaterials (Basel). 2022 Nov 4;12(21):3896. doi: 10.3390/nano12213896.
8
Synthesis and characterization of self-bridged silver vanadium oxide/CNTs composite and its enhanced lithium storage performance.自桥连银钒氧化物/CNTs 复合材料的合成与表征及其增强的锂存储性能。
Nanoscale. 2013 Feb 7;5(3):1026-33. doi: 10.1039/c2nr33091a. Epub 2012 Dec 19.
9
Lithium/silver vanadium oxide batteries for implantable defibrillators.用于植入式除颤器的锂/银钒氧化物电池。
Pacing Clin Electrophysiol. 1988 Nov;11(11 Pt 2):2035-9. doi: 10.1111/j.1540-8159.1988.tb06346.x.
10
Structural and silver/vanadium ratio effects on silver vanadium phosphorous oxide solution formation kinetics: impact on battery electrochemistry.结构和银/钒比例对氧化银钒磷溶液形成动力学的影响:对电池电化学的影响。
Phys Chem Chem Phys. 2015 Jan 21;17(3):2034-42. doi: 10.1039/c4cp04819a. Epub 2014 Dec 5.

引用本文的文献

1
Reduction of silver ions in molybdates: elucidation of framework acidity as the factor controlling charge balance mechanisms in aqueous zinc-ion electrolyte.钼酸盐中银离子的还原:阐明框架酸度作为控制水系锌离子电解质中电荷平衡机制的因素。
RSC Adv. 2021 Dec 13;11(62):39523-39533. doi: 10.1039/d1ra07765a. eCollection 2021 Dec 6.
2
Secondary Battery Science: At the Confluence of Electrochemistry and Materials Engineering.二次电池科学:电化学与材料工程的交汇点
Electrochemistry (Tokyo). 2012 Oct;80(10):700-705. doi: 10.5796/electrochemistry.80.700.
3
Energy dispersive X-ray diffraction (EDXRD) for operando materials characterization within batteries.

本文引用的文献

1
Synthesis, structural characterization, and electronic structure of single-crystalline Cu(x)V2O5 nanowires.单晶Cu(x)V2O5纳米线的合成、结构表征及电子结构
Inorg Chem. 2009 Apr 6;48(7):3145-52. doi: 10.1021/ic802408c.
2
Lithium deintercalation in LiFePO4 nanoparticles via a domino-cascade model.通过多米诺级联模型实现LiFePO₄纳米颗粒中的锂脱嵌
Nat Mater. 2008 Aug;7(8):665-71. doi: 10.1038/nmat2230. Epub 2008 Jul 20.
3
Alpha-CuV2O6 nanowires: hydrothermal synthesis and primary lithium battery application.α- CuV₂O₆纳米线:水热合成及在锂原电池中的应用
用于电池内部原位材料表征的能量色散X射线衍射(EDXRD)。
Phys Chem Chem Phys. 2020 Sep 30;22(37):20972-20989. doi: 10.1039/d0cp00778a.
4
A Kinetics and Equilibrium Study of Vanadium Dissolution from Vanadium Oxides and Phosphates in Battery Electrolytes: Possible Impacts on ICD Battery Performance.电池电解质中钒从钒氧化物和磷酸盐的溶解动力学与平衡研究:对植入式心律转复除颤器(ICD)电池性能的可能影响
J Power Sources. 2013 Jun 1;231:219-225. doi: 10.1016/j.jpowsour.2013.01.012.
5
Silver Vanadium Diphosphate AgVPO: Electrochemistry and Characterization of Reduced Material providing Mechanistic Insights.磷酸银钒(AgVPO):还原材料的电化学性质及表征,提供机理见解
J Solid State Chem. 2013 Apr;200:232-240. doi: 10.1016/j.jssc.2013.01.020.
6
Batteries used to Power Implantable Biomedical Devices.用于为可植入生物医学设备供电的电池。
Electrochim Acta. 2012 Dec 1;84. doi: 10.1016/j.electacta.2012.03.057.
7
Silver Vanadium Phosphorous Oxide, Ag(2)VO(2)PO(4): Chimie Douce Preparation and Resulting Lithium Cell Electrochemistry.氧化银钒磷,Ag(2)VO(2)PO(4):温和化学合成法及其在锂电池中的电化学性能
J Power Sources. 2011 Aug 15;196(16):6781-6787. doi: 10.1016/j.jpowsour.2010.10.054.
8
Ag(x)VOPO(4): A Demonstration of the Dependence of Battery-Related Electrochemical Properties of Silver Vanadium Phosphorous Oxides on Ag / V Ratios.Ag(x)VOPO(4):银钒磷氧化物的电池相关电化学性质对银/钒比例的依赖性证明
J Power Sources. 2011 Mar 15;196(6):3325-3330. doi: 10.1016/j.jpowsour.2010.11.144.
9
Electrochemical Reduction of Silver Vanadium Phosphorous Oxide, Ag(2)VO(2)PO(4): Silver Metal Deposition and Associated Increase in Electrical Conductivity.银钒磷氧化物Ag(2)VO(2)PO(4)的电化学还原:银金属沉积及电导率的相关增加
J Power Sources. 2010 Oct 1;195(19):6839-6846. doi: 10.1016/j.jpowsour.2010.04.033.
J Am Chem Soc. 2008 Apr 16;130(15):5361-7. doi: 10.1021/ja800109u.
4
Nanostructured materials for advanced energy conversion and storage devices.用于先进能量转换与存储设备的纳米结构材料。
Nat Mater. 2005 May;4(5):366-77. doi: 10.1038/nmat1368.
5
Various strategies to tune the ionic/electronic properties of electrode materials.
Dalton Trans. 2004 Oct 7(19):2988-94. doi: 10.1039/b408442j. Epub 2004 Jul 23.
6
A reversible copper extrusion-insertion electrode for rechargeable Li batteries.一种用于可充电锂电池的可逆铜挤压插入式电极。
Nat Mater. 2003 Nov;2(11):755-61. doi: 10.1038/nmat1002. Epub 2003 Oct 26.
7
Electronically conductive phospho-olivines as lithium storage electrodes.作为锂存储电极的导电磷橄榄石
Nat Mater. 2002 Oct;1(2):123-8. doi: 10.1038/nmat732.
8
Issues and challenges facing rechargeable lithium batteries.可充电锂电池面临的问题与挑战。
Nature. 2001 Nov 15;414(6861):359-67. doi: 10.1038/35104644.