TY - JOUR
T1 - Synthesis and Near-Infrared Emission of Yb-Doped Cs2AgInCl6 Double Perovskite Microcrystals and Nanocrystals
AU - Mahor, Yogesh
AU - Mir, Wasim J.
AU - Nag, Angshuman
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019
Y1 - 2019
N2 - Cs2AgInCl6 double perovskite (DP) is a direct band gap, stable, and environmentally benign material with a three-dimensional perovskite structure. However, the band gap (?3.3 eV) is too wide for optoelectronic applications in the near-infrared (NIR) region. To achieve optical functionality in the NIR window, we have doped Yb3+ in both microcrystals and colloidal nanocrystals of Cs2AgInCl6 DPs. Our Yb-doped Cs2AgInCl6 DP microcrystals and nanocrystals show NIR emission at ?994 nm (1.24 eV), whereas the band gap of the hosts is in the UV region. Therefore, the Yb-emission does not suffer from self-absorption. The microcrystals exhibit a single-exponential decay with 2.7 ms long lifetime corresponding to 2F5/2 → 2F7/2 transition of Yb3+ f electrons. The nanocrystals show biexponential decay (3 ms and 749 μs), probably because of the proximity of Yb to the surface of nanocrystals. Interestingly, NIR emission and perovskite structure of samples are stable for >3 months in ambient conditions for future optoelectronic applications.
AB - Cs2AgInCl6 double perovskite (DP) is a direct band gap, stable, and environmentally benign material with a three-dimensional perovskite structure. However, the band gap (?3.3 eV) is too wide for optoelectronic applications in the near-infrared (NIR) region. To achieve optical functionality in the NIR window, we have doped Yb3+ in both microcrystals and colloidal nanocrystals of Cs2AgInCl6 DPs. Our Yb-doped Cs2AgInCl6 DP microcrystals and nanocrystals show NIR emission at ?994 nm (1.24 eV), whereas the band gap of the hosts is in the UV region. Therefore, the Yb-emission does not suffer from self-absorption. The microcrystals exhibit a single-exponential decay with 2.7 ms long lifetime corresponding to 2F5/2 → 2F7/2 transition of Yb3+ f electrons. The nanocrystals show biexponential decay (3 ms and 749 μs), probably because of the proximity of Yb to the surface of nanocrystals. Interestingly, NIR emission and perovskite structure of samples are stable for >3 months in ambient conditions for future optoelectronic applications.
UR - http://www.scopus.com/inward/record.url?scp=85068191538&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.9b02456
DO - 10.1021/acs.jpcc.9b02456
M3 - Article
AN - SCOPUS:85068191538
SN - 1932-7447
JO - JOURNAL OF PHYSICAL CHEMISTRY C
JF - JOURNAL OF PHYSICAL CHEMISTRY C
ER -