Spin-on Spintronics: Ultrafast Electron Spin Dynamics in ZnO and Zn1-xCoxO Sol-Gel Films

被引:42
作者
Whitaker, Kelly M. [1 ,2 ,3 ]
Raskin, Maxim [2 ,3 ]
Kiliani, Gillian [2 ,3 ]
Beha, Katja [2 ,3 ]
Ochsenbein, Stefan T. [1 ]
Janssen, Nils [1 ,2 ,3 ]
Fonin, Mikhail [2 ,3 ]
Ruediger, Ulrich [2 ,3 ]
Leitenstorfer, Alfred [2 ,3 ]
Gamelin, Daniel R. [1 ]
Bratschitsch, Rudolf [2 ,3 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[2] Univ Konstanz, Dept Phys, D-78464 Constance, Germany
[3] Univ Konstanz, Ctr Appl Photon, D-78464 Constance, Germany
基金
美国国家科学基金会;
关键词
ZnCoO; sol-gel; spin dynamics; hole trapping; exchange energy; time-resolved Faraday rotation; QUANTUM DOTS; EXCHANGE; SEMICONDUCTORS; FERROMAGNETISM; EXCITONS;
D O I
10.1021/nl201736p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We use time-resolved Faraday rotation spectroscopy to probe the electron spin dynamics in ZnO and magnetically doped Zn1-xCoxO sol gel thin films. In undoped ZnO, we observe an anomalous temperature dependence of the ensemble spin dephasing time T-2*, i.e., longer coherence times at higher temperatures, reaching T-2* similar to 1.2 ns at room temperature. Time-resolved transmission measurements suggest that this effect arises from hole trapping at grain surfaces. Deliberate addition of Co2+ to ZnO increases the effective electron Lande g factor, providing the first direct determination of the mean-field electron-Co2+ exchange energy in Zn1-xCoxO (N-0 alpha = +0.25 +/- 0.02 eV). In Zn1-xCoxO, T-2* also increases with increasing temperature, allowing spin precession to be observed even at room temperature.
引用
收藏
页码:3355 / 3360
页数:6
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