Abstract
Original language | English |
---|---|
Journal | Journal of Materials Chemistry C |
Volume | 7 |
Issue number | 32 |
Pages (from-to) | 9865-9877 |
Number of pages | 13 |
ISSN | 2050-7526 |
DOIs | |
Publication status | Published - 2019 |
Cite this
}
Tuning the Bi3+-photoemission color over the entire visible region by manipulating secondary cations modulation in the ScVxP1-xO4:Bi3+ (0 ≤ x ≤ 1) solid solution. / Kang, Fengwen; Sun, Guohuan; Boutinaud, Philippe; Gao, Fei; Wang, Zhenhu; Lu, Jian; Li, Yang Yang; Xiao, Sanshui .
In: Journal of Materials Chemistry C, Vol. 7, No. 32, 2019, p. 9865-9877.Research output: Contribution to journal › Journal article › Research › peer-review
TY - JOUR
T1 - Tuning the Bi3+-photoemission color over the entire visible region by manipulating secondary cations modulation in the ScVxP1-xO4:Bi3+ (0 ≤ x ≤ 1) solid solution
AU - Kang, Fengwen
AU - Sun, Guohuan
AU - Boutinaud, Philippe
AU - Gao, Fei
AU - Wang, Zhenhu
AU - Lu, Jian
AU - Li, Yang Yang
AU - Xiao, Sanshui
PY - 2019
Y1 - 2019
N2 - Unlike rare earth (RE) (e.g., Eu2+) and non-RE (e.g., Mn2+) doped tunable solid solutions that frequently suffer from the visible re-absorption issue, the Bi3+ ion features the remarkable advantages of a strong UV excitation intensity and an excitation tail of less than 430 nm, giving Bi3+ a strong potential to solve the re-absorption issue for future lighting technology. Herein, we report a type of zircon-type ScVxP1-xO4:Bi3+ (0 ≤ x ≤ 1) emission-tunable solid solution that has a strong UV excitation intensity yet no significant light absorption. We reveal that gradual substitution of larger V ions for smaller P ions, which means expansion of the lattice cell, can shift the excitation edge from 295 to 385 nm, the excitation tail from 340 to 425 nm and emission position from 455 to 641 nm, without causing a large change to the Stokes shift. This spectral shifting is found to be a consequence of the complex dependence of the intra-ion and charge-transfer related transitions of Bi3+ with the crystal structure. Owing to the remarkable excitation-triggered multi-emission properties, we then discover that the ScVxP1-xO4:Bi3+ solid solution can serve as a type of potential material for anti-counterfeiting and information protection applications. This work can provide design insights into discovering more RE and non-RE doped tunable solid solutions in the future, through modulation of the secondary cations in the isostructural crystals.
AB - Unlike rare earth (RE) (e.g., Eu2+) and non-RE (e.g., Mn2+) doped tunable solid solutions that frequently suffer from the visible re-absorption issue, the Bi3+ ion features the remarkable advantages of a strong UV excitation intensity and an excitation tail of less than 430 nm, giving Bi3+ a strong potential to solve the re-absorption issue for future lighting technology. Herein, we report a type of zircon-type ScVxP1-xO4:Bi3+ (0 ≤ x ≤ 1) emission-tunable solid solution that has a strong UV excitation intensity yet no significant light absorption. We reveal that gradual substitution of larger V ions for smaller P ions, which means expansion of the lattice cell, can shift the excitation edge from 295 to 385 nm, the excitation tail from 340 to 425 nm and emission position from 455 to 641 nm, without causing a large change to the Stokes shift. This spectral shifting is found to be a consequence of the complex dependence of the intra-ion and charge-transfer related transitions of Bi3+ with the crystal structure. Owing to the remarkable excitation-triggered multi-emission properties, we then discover that the ScVxP1-xO4:Bi3+ solid solution can serve as a type of potential material for anti-counterfeiting and information protection applications. This work can provide design insights into discovering more RE and non-RE doped tunable solid solutions in the future, through modulation of the secondary cations in the isostructural crystals.
U2 - 10.1039/c9tc01385g
DO - 10.1039/c9tc01385g
M3 - Journal article
VL - 7
SP - 9865
EP - 9877
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
SN - 2050-7526
IS - 32
ER -