Hyperfine Coupling in Colloidal n-Type ZnO Quantum Dots: Effects on Electron Spin Relaxation
dc.contributor.author | Whitaker, Kelly M. | |
dc.contributor.author | Ochsenbein, Stefan T. | |
dc.contributor.author | Smith, Alyssa L. | |
dc.contributor.author | Echodu, Dorothy C. | |
dc.contributor.author | Robinson, Bruce H. | |
dc.contributor.author | Gamelin, Daniel R. | |
dc.date.accessioned | 2022-11-20T08:40:16Z | |
dc.date.available | 2022-11-20T08:40:16Z | |
dc.date.issued | 2010 | |
dc.description.abstract | Colloidal semiconductor nanocrystals are excellent systems for exploring the fundamental properties of quantum-confined charge carriers. Tremendous progress has already been made in understanding the properties of electron-hole pairs (excitons) confined in colloidal quantum dots (QDs) using optical spectroscopic techniques.1-6 In contrast with charge carriers in QD electronic excited states, the properties of QDs containing excess carriers in their ground states have received substantially less attention.7-19 To date, the primary experimental probe of such charged QDs has been electronic absorption spectroscopy, in which low-energy intraband excitations can be used to define the carrier wave function. | en_US |
dc.identifier.citation | Whitaker, K. M., Ochsenbein, S. T., Smith, A. L., Echodu, D. C., Robinson, B. H., & Gamelin, D. R. (2010). Hyperfine coupling in colloidal n-type ZnO quantum dots: effects on electron spin relaxation. The Journal of Physical Chemistry C, 114(34), 14467-14472. Doi: 10.1021/jp106356y | en_US |
dc.identifier.other | 10.1021/jp106356y | |
dc.identifier.uri | https://nru.uncst.go.ug/handle/123456789/5344 | |
dc.language.iso | en | en_US |
dc.publisher | The Journal of Physical Chemistry | en_US |
dc.subject | Hyperfine Coupling | en_US |
dc.subject | Colloidal n-Type ZnO Quantum Dots | en_US |
dc.subject | Electron Spin Relaxation | en_US |
dc.title | Hyperfine Coupling in Colloidal n-Type ZnO Quantum Dots: Effects on Electron Spin Relaxation | en_US |
dc.type | Article | en_US |
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