The importance of inversion disorder in the visible light induced persistent luminescence in Cr3+ doped AB2O4 (A = Zn or Mg and B = Ga or Al)Electronic supplementary information (ESI) available. See DOI: 10.1039/c4cp03866e

Cr 3+ doped spinel compounds AB 2 O 4 with A = Zn, Mg and B = Ga, Al exhibit a long, near infrared persistent luminescence when excited with UV or X-rays. In addition, the persistent luminescence of ZnGa 2 O 4 , and to a lesser extent MgGa 2 O 4 , can also be induced by visible light excitation via...

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Hauptverfasser: Basavaraju, Neelima, Priolkar, Kaustubh R, Gourier, Didier, Sharma, Suchinder K, Bessière, Aurélie, Viana, Bruno
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Priolkar, Kaustubh R
Gourier, Didier
Sharma, Suchinder K
Bessière, Aurélie
Viana, Bruno
description Cr 3+ doped spinel compounds AB 2 O 4 with A = Zn, Mg and B = Ga, Al exhibit a long, near infrared persistent luminescence when excited with UV or X-rays. In addition, the persistent luminescence of ZnGa 2 O 4 , and to a lesser extent MgGa 2 O 4 , can also be induced by visible light excitation via 4 A 2 → 4 T 2 transition of Cr 3+ , which makes these compounds suitable as biomarkers for in vivo optical imaging of small animals. We correlate this peculiar optical property with the presence of antisite defects, which are present in ZnGa 2 O 4 and MgGa 2 O 4 . By using X-ray absorption fine structure (XAFS) spectroscopy, associated with electron paramagnetic resonance (EPR) and optical emission spectroscopy, it is shown that an increase in antisite defects concentration results in a decrease in the Cr-O bond length and the octahedral crystal field energy. A part of the defects occurs in the close environment of Cr 3+ ions, as shown by the increasing strain broadening of EPR and XAFS peaks observed upon increasing antisite disorder. It appears that ZnAl 2 O 4 , which exhibits the largest crystal field splitting of Cr 3+ and the smallest antisite disorder, does not show considerable persistent luminescence upon visible light excitation as compared to ZnGa 2 O 4 and MgGa 2 O 4 . These results highlight the importance of Cr 3+ ions with neighboring antisite defects in the mechanism of persistent luminescence exhibited by Cr 3+ doped AB 2 O 4 spinel compounds. The visible light persistent luminescence seen in Cr 3+ doped AB 2 O 4 (A = Zn, Mg; B = Ga, Al) is mainly due to the site inversion present around Cr ions.
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See DOI: 10.1039/c4cp03866e</title><source>Royal Society Of Chemistry Journals</source><source>Alma/SFX Local Collection</source><creator>Basavaraju, Neelima ; Priolkar, Kaustubh R ; Gourier, Didier ; Sharma, Suchinder K ; Bessière, Aurélie ; Viana, Bruno</creator><creatorcontrib>Basavaraju, Neelima ; Priolkar, Kaustubh R ; Gourier, Didier ; Sharma, Suchinder K ; Bessière, Aurélie ; Viana, Bruno</creatorcontrib><description>Cr 3+ doped spinel compounds AB 2 O 4 with A = Zn, Mg and B = Ga, Al exhibit a long, near infrared persistent luminescence when excited with UV or X-rays. In addition, the persistent luminescence of ZnGa 2 O 4 , and to a lesser extent MgGa 2 O 4 , can also be induced by visible light excitation via 4 A 2 → 4 T 2 transition of Cr 3+ , which makes these compounds suitable as biomarkers for in vivo optical imaging of small animals. We correlate this peculiar optical property with the presence of antisite defects, which are present in ZnGa 2 O 4 and MgGa 2 O 4 . By using X-ray absorption fine structure (XAFS) spectroscopy, associated with electron paramagnetic resonance (EPR) and optical emission spectroscopy, it is shown that an increase in antisite defects concentration results in a decrease in the Cr-O bond length and the octahedral crystal field energy. A part of the defects occurs in the close environment of Cr 3+ ions, as shown by the increasing strain broadening of EPR and XAFS peaks observed upon increasing antisite disorder. It appears that ZnAl 2 O 4 , which exhibits the largest crystal field splitting of Cr 3+ and the smallest antisite disorder, does not show considerable persistent luminescence upon visible light excitation as compared to ZnGa 2 O 4 and MgGa 2 O 4 . These results highlight the importance of Cr 3+ ions with neighboring antisite defects in the mechanism of persistent luminescence exhibited by Cr 3+ doped AB 2 O 4 spinel compounds. 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A part of the defects occurs in the close environment of Cr 3+ ions, as shown by the increasing strain broadening of EPR and XAFS peaks observed upon increasing antisite disorder. It appears that ZnAl 2 O 4 , which exhibits the largest crystal field splitting of Cr 3+ and the smallest antisite disorder, does not show considerable persistent luminescence upon visible light excitation as compared to ZnGa 2 O 4 and MgGa 2 O 4 . These results highlight the importance of Cr 3+ ions with neighboring antisite defects in the mechanism of persistent luminescence exhibited by Cr 3+ doped AB 2 O 4 spinel compounds. 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By using X-ray absorption fine structure (XAFS) spectroscopy, associated with electron paramagnetic resonance (EPR) and optical emission spectroscopy, it is shown that an increase in antisite defects concentration results in a decrease in the Cr-O bond length and the octahedral crystal field energy. A part of the defects occurs in the close environment of Cr 3+ ions, as shown by the increasing strain broadening of EPR and XAFS peaks observed upon increasing antisite disorder. It appears that ZnAl 2 O 4 , which exhibits the largest crystal field splitting of Cr 3+ and the smallest antisite disorder, does not show considerable persistent luminescence upon visible light excitation as compared to ZnGa 2 O 4 and MgGa 2 O 4 . These results highlight the importance of Cr 3+ ions with neighboring antisite defects in the mechanism of persistent luminescence exhibited by Cr 3+ doped AB 2 O 4 spinel compounds. 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title The importance of inversion disorder in the visible light induced persistent luminescence in Cr3+ doped AB2O4 (A = Zn or Mg and B = Ga or Al)Electronic supplementary information (ESI) available. See DOI: 10.1039/c4cp03866e
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