dc.contributor.author |
Sharma, S.K. |
|
dc.contributor.author |
Bessiere, A. |
|
dc.contributor.author |
Gourier, D. |
|
dc.contributor.author |
Binet, L. |
|
dc.contributor.author |
Viana, B. |
|
dc.contributor.author |
Basavaraju, N. |
|
dc.contributor.author |
Priolkar, K.R. |
|
dc.contributor.author |
Maldiney, T. |
|
dc.contributor.author |
Scherman, D. |
|
dc.contributor.author |
Richard, C. |
|
dc.date.accessioned |
2015-06-04T05:10:50Z |
|
dc.date.available |
2015-06-04T05:10:50Z |
|
dc.date.issued |
2014 |
|
dc.identifier.citation |
Proc. SPIE 8982, Optical Components and Materials. 2014; 898215-. |
en_US |
dc.identifier.uri |
http://dx.doi.org/10.1117/12.2041838 |
|
dc.identifier.uri |
http://irgu.unigoa.ac.in/drs/handle/unigoa/3176 |
|
dc.description.abstract |
ZnGa2O4 (ZGO) is a normal spinel. When doped with Cr3+ ions, ZGO:Cr becomes a high brightness persistent luminescence material with an emission spectrum perfectly matching the transparency window of living tissues. It allows in vivo mouse imaging with a better signal to background ratio than classical fluorescent NIR probes. The most interesting characteristic of ZGO:Cr lies in the fact that its LLP can be excited with red light, well below its band gap energy and in the transparency window of living tissues. A mechanism based on the trapping of carriers localized around a special type of Cr3+ ions namely CrN2 can explain this singularity. The antisite defects of the structure are the main responsible traps in the persistent luminescence mechanism. When located around Cr3+ ions, they allow, via Cr3+ absorption, the storage of not only UV light but also all visible light from the excitation source. |
en_US |
dc.subject |
Physics |
en_US |
dc.title |
Persistent luminescence in ZnGa2O4:Cr: An outstanding biomarker for in-vivo imaging |
en_US |
dc.type |
Conference article |
en_US |