• 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

Tuneable paramagnetic susceptibility and exciton g-factor in Mn-doped PbS colloidal nanocrystals.

作者信息

Turyanska L, Hill R J A, Makarovsky O, Moro F, Knott A N, Larkin O J, Patanè A, Meaney A, Christianen P C M, Fay M W, Curry R J

机构信息

School of Physics and Astronomy, The University of Nottingham, Nottingham NG7 2RD, UK.

出版信息

Nanoscale. 2014 Aug 7;6(15):8919-25. doi: 10.1039/c4nr02336f.

DOI:10.1039/c4nr02336f
PMID:24966016
Abstract

We report on PbS colloidal nanocrystals that combine within one structure solubility in physiological solvents with near-infrared photoluminescence, and magnetic and optical properties tuneable by the controlled incorporation of magnetic impurities (Mn). We use high magnetic fields (B up to 30 T) to measure the magnetization of the nanocrystals in liquid and the strength of the sp-d exchange interaction between the exciton and the Mn-ions. With increasing Mn-content from 0.1% to 7%, the mass magnetic susceptibility increases at a rate of ∼ 10(-7) m(3) kg(-1) per Mn percentage; correspondingly, the exciton g-factor decreases from 0.47 to 0.10. The controlled modification of the paramagnetism, fluorescence and exciton g-factor of the nanocrystals is relevant to the implementation of these paramagnetic semiconductor nanocrystals in quantum technologies ranging from quantum information to magnetic resonance imaging.

摘要

相似文献

1
Tuneable paramagnetic susceptibility and exciton g-factor in Mn-doped PbS colloidal nanocrystals.
Nanoscale. 2014 Aug 7;6(15):8919-25. doi: 10.1039/c4nr02336f.
2
Electrochemically controlled auger quenching of Mn²+ photoluminescence in doped semiconductor nanocrystals.掺杂半导体纳米晶体中 Mn2+光致发光的电化学控制俄歇猝灭。
ACS Nano. 2011 May 24;5(5):4158-68. doi: 10.1021/nn200889q. Epub 2011 Apr 11.
3
Radial-position-controlled doping of CdS/ZnS core/shell nanocrystals: surface effects and position-dependent properties.CdS/ZnS核壳纳米晶体的径向位置控制掺杂:表面效应和位置依赖性性质
Chemistry. 2009;15(13):3186-97. doi: 10.1002/chem.200802295.
4
Spin-polarized Mn2+ emission from Mn-doped colloidal nanocrystals.Mn 掺杂胶体纳米晶的自旋极化 Mn2+ 发射。
Phys Rev Lett. 2011 Aug 5;107(6):067402. doi: 10.1103/PhysRevLett.107.067402. Epub 2011 Aug 3.
5
Picosecond Dynamics of Excitonic Magnetic Polarons in Colloidal Diffusion-Doped Cd(1-x)Mn(x)Se Quantum Dots.胶态扩散掺杂 Cd(1-x)Mn(x)Se 量子点中激子磁极化子的皮秒动力学。
ACS Nano. 2015 Nov 24;9(11):11177-91. doi: 10.1021/acsnano.5b04719. Epub 2015 Oct 12.
6
Exciton-to-Dopant Energy Transfer in Mn-Doped Cesium Lead Halide Perovskite Nanocrystals.锰掺杂卤化铯钙钛矿纳米晶中的激子-掺杂剂能量转移。
Nano Lett. 2016 Dec 14;16(12):7376-7380. doi: 10.1021/acs.nanolett.6b02772. Epub 2016 Nov 2.
7
Mn(2+)-Doped CdSe/CdS Core/Multishell Colloidal Quantum Wells Enabling Tunable Carrier-Dopant Exchange Interactions.锰(2+)掺杂的 CdSe/CdS 核/多壳层胶体量子阱,实现可调载流子-掺杂剂交换相互作用。
ACS Nano. 2015 Dec 22;9(12):12473-9. doi: 10.1021/acsnano.5b05903. Epub 2015 Nov 26.
8
Exposure of the hidden anti-ferromagnetism in paramagnetic CdSe:Mn nanocrystals.暴露在顺磁 CdSe:Mn 纳米晶体中的隐藏反铁磁性。
ACS Nano. 2015 Jan 27;9(1):503-11. doi: 10.1021/nn5056892. Epub 2015 Jan 12.
9
Direct Measurements of Magnetic Polarons in CdMnSe Nanocrystals from Resonant Photoluminescence.CdMnSe 纳米晶体中磁极化子的共振光致发光直接测量。
Nano Lett. 2017 May 10;17(5):3068-3075. doi: 10.1021/acs.nanolett.7b00421. Epub 2017 Apr 13.
10
Tunable magnetic exchange interactions in manganese-doped inverted core-shell ZnSe-CdSe nanocrystals.锰掺杂的倒置核壳结构ZnSe-CdSe纳米晶体中的可调谐磁交换相互作用
Nat Mater. 2009 Jan;8(1):35-40. doi: 10.1038/nmat2342. Epub 2008 Dec 14.

引用本文的文献

1
Magnetic hard gap due to bound magnetic polarons in the localized regime.由于局域化中的束缚磁极化子而产生的磁硬隙。
Sci Rep. 2017 Feb 8;7:42224. doi: 10.1038/srep42224.