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Updated: May 1, 2026

Synthesis of Core-shell Lanthanide-doped Upconversion Nanocrystals for Cellular Applications
Published on: November 10, 2017
Core-shell-like Y2O3:[(Tb3+-Yb3+), Li+]/CdZnS heterostructure synthesized by super-close-space sublimation for
Xiaojie Wu1, Zhenzhong Zhang, Fanzhi Meng
1State Key Laboratory of Rare Earth Resources Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, People's Republic of China. jmeng@ciac.jl.cn.
Abstract:
Combination with semiconductors is a promising approach to the realization of broadband excitation of light conversion materials based on rare earth compounds, to boost the energy efficiency of silicon solar cells. Cd(1-x)Zn(x)S is a wide bandgap semiconductor with large exciton binding energy. By changing its composition, the bandgap of Cd(1-x)Zn(x)S can be tuned to match the absorption of trivalent lanthanide (Ln) ions, which makes it a competent energy donor for the Ln(3+)-Yb(3+) couple. In this work, we designed a clean route to a broadband down-converter based on a core-shell-like Y2O3:[(Tb(3+)-Yb(3+)), Li(+)]/Cd0.81Zn0.19S (CdZnS) heterostructure. By hot-pressing and subsequent annealing of a Y2O3:[(Tb(3+)-Yb(3+)), Li(+)]/CdZnS mixture, highly pure CdZnS was sublimated and deposited on the Y2O3:[(Tb(3+)-Yb(3+)), Li(+)] grains while maintaining the original composition of the precursor. The CdZnS shell acted as a light absorber and energy donor for the Tb(3+)-Yb(3+) quantum cutting couple. Because the use of solvents was avoided during the formation of the heterostructures, few impurities were incorporated into the samples, and the non-radiative transition was therefore markedly suppressed. The Y2O3:[(Tb(3+)-Yb(3+)), Li(+)]/CdZnS heterostructures possess strong near-infrared (NIR) luminescence from Yb(3+). Broadband down-conversion to the Yb(3+) NIR emission was obtained in a wide range of 250-650 nm.

