TY - JOUR
T1 - Cr-doped ZnGa2O4
T2 - Simple synthesis of intense red-NIR emitting nanoparticles with enhanced quantum efficiency
AU - G., Sridhar
AU - Hebbar N., Deepak
AU - Menon, Samvit G.
AU - Lewis, Prinston Melroy
AU - Choudhari, K. S.
AU - Kroon, Robin E.
AU - Swart, Hendrik C.
AU - Kulkarni, Suresh D.
N1 - Funding Information:
We gratefully acknowledge financial support from – (1) SERB , DST , Govt. of India, through the projects SB/S2/CMP-017/2014 and SB/FT/CS-123/2013 ; (2) Joint Manipal Academy of Higher Education and DST-FIST (Govt. of India) Program via approval letter SR/FST/PSI-174/2012 (3) ICUP, the Indian Cluster for Ultrafast Photonics, Government of India, for providing the UV–VIS–NIR spectrophotometer.
Funding Information:
We gratefully acknowledge financial support from ? (1) SERB, DST, Govt. of India, through the projects SB/S2/CMP-017/2014 and SB/FT/CS-123/2013; (2) Joint Manipal Academy of Higher Education and DST-FIST (Govt. of India) Program via approval letter SR/FST/PSI-174/2012 (3) ICUP, the Indian Cluster for Ultrafast Photonics, Government of India, for providing the UV?VIS?NIR spectrophotometer.
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2022/1
Y1 - 2022/1
N2 - Red-NIR emitting ZnGa2-xCrxO4 nanoparticles were synthesized using simple co-precipitation, and the effect of annealing was studied (600–1200 °C). Upon annealing, crystallite size increased (12 nm–73 nm), and color tone turned pink beyond 1000 °C, inferring dopant diffusion. Blue, green absorption bands in diffuse-reflectance spectra revealed Cr3+ in octahedral crystal field. Photoluminescence excitation spectra showed characteristic Cr3+ bands (∼400 nm and ∼550 nm), and the asymmetric 400 nm band suggested splitting the 4T1g(F) state due to trigonal distortion. Emission spectra consisted of a zero-phonon line (∼688 nm), along with associated multi-phonon sidebands. ZnGa1.98Cr0.02O4 showed intense red emission with λexc = 420 nm, while the tri-exponential fitting of the excited-state lifetime implied multiple decay processes due to Cr3+ occupying different environments. The internal quantum efficiency of the 1200 °C annealed sample was impressive (48%). Both UV and visible light up to 600 nm could induce persistent-luminescence (λem = 688 nm) for longer durations. The smaller size, intense emission, higher quantum yield, and visible light activation suggest that the nanoparticles are suitable for bioimaging applications.
AB - Red-NIR emitting ZnGa2-xCrxO4 nanoparticles were synthesized using simple co-precipitation, and the effect of annealing was studied (600–1200 °C). Upon annealing, crystallite size increased (12 nm–73 nm), and color tone turned pink beyond 1000 °C, inferring dopant diffusion. Blue, green absorption bands in diffuse-reflectance spectra revealed Cr3+ in octahedral crystal field. Photoluminescence excitation spectra showed characteristic Cr3+ bands (∼400 nm and ∼550 nm), and the asymmetric 400 nm band suggested splitting the 4T1g(F) state due to trigonal distortion. Emission spectra consisted of a zero-phonon line (∼688 nm), along with associated multi-phonon sidebands. ZnGa1.98Cr0.02O4 showed intense red emission with λexc = 420 nm, while the tri-exponential fitting of the excited-state lifetime implied multiple decay processes due to Cr3+ occupying different environments. The internal quantum efficiency of the 1200 °C annealed sample was impressive (48%). Both UV and visible light up to 600 nm could induce persistent-luminescence (λem = 688 nm) for longer durations. The smaller size, intense emission, higher quantum yield, and visible light activation suggest that the nanoparticles are suitable for bioimaging applications.
UR - http://www.scopus.com/inward/record.url?scp=85121677246&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85121677246&partnerID=8YFLogxK
U2 - 10.1016/j.optmat.2021.111919
DO - 10.1016/j.optmat.2021.111919
M3 - Article
AN - SCOPUS:85121677246
SN - 0925-3467
VL - 123
JO - Optical Materials
JF - Optical Materials
M1 - 111919
ER -