Affiliation:
1. Beijing Municipal Key Laboratory of New Energy Materials and Technologies School of Materials Sciences and Engineering University of Science and Technology Beijing Beijing 100083 China
2. Department of Materials Science and Engineering City University of Hong Kong Kowloon Hong Kong SAR 999077 China
3. Institute of Information Photonics Technology School of Physics and Optoelectronic Engineering Beijing University of Technology Beijing 100124 China
Abstract
AbstractNIR‐II luminescent materials are the key enablers of smart spectroscopy‐based techniques, offering capabilities for nondestructive analysis and bio‐imaging. Here, a broadband NIR‐II luminescence with a recorded external quantum efficiency (EQE) of 76% in LiGa5O8 are demonstrated, using heavily doping Cr3+ ion (10%) as a light harvester and a controllable energy transfer (ET) from Cr3+ to Ni2+ (0.4%) ions. Even though the Cr3+ ion produces substantially weak luminescence due to concentration quenching, the introduction of Ni2+ ions effectively extract the excitation energy to generate NIR‐II luminescence. Complementary investigations using synchrotron‐based EXAFS fittings and structural refinement disclose a significant structural distortion in the LiGa5O8 compound, which facilitates the relaxation of the parity‐selection rules for Cr3+ and Ni2+ ions. Additionally, DFT calculations identify specific site occupations, which favor unidirectional ET from Cr3+ to Ni2+ ions. As a result, the significant absorption of excitation light by heavy‐doping Cr3+ ions and high radiative transition probability in Ni2+ ions synergistically result in a record high EQE. These findings provide pioneering insight into rational NIR‐II light generation by deliberated control of ET pathway in heavily doped systems, thereby with promising implications for NIR spectroscopy applications.
Funder
Fundamental Research Funds for the Central Universities
Beijing Municipal Natural Science Foundation
National Natural Science Foundation of China