Temperature/Component‐Dependent Luminescence in Lead‐Free Hybrid Metal Halides for Temperature Sensor and Anti‐Counterfeiting

Author:

Zhou Guojun1ORCID,Wang Yanting1,Mao Yilin1,Guo Caihong1,Zhang Jian1,Molokeev Maxim S.23ORCID,Xia Zhiguo4ORCID,Zhang Xian‐Ming15ORCID

Affiliation:

1. Key Laboratory of Magnetic Molecules and Magnetic Information Materials (Ministry of Education) School of Chemistry and Material Science Shanxi Normal University Taiyuan 030031 P. R. China

2. Laboratory of Crystal Physics Kirensky Institute of Physics Federal Research Center KSC SB RAS Krasnoyarsk 660036 Russia

3. International Research Center of Spectroscopy and Quantum Chemistry‐IRC SQC Siberian Federal University Krasnoyarsk 660041 Russia

4. State Key Laboratory of Luminescent Materials and Devices Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques Guangdong Engineering Technology Research and Development Center of Special Optical Fiber Materials and Devices School of Physics and Optoelectronics South China University of Technology Guangzhou Guangdong 510641 P. R. China

5. College of Chemistry & Chemical Engineering Key Laboratory of Interface Science and Engineering in Advanced Material Ministry of Education Taiyuan University of Technology Taiyuan Shanxi 030024 P. R. China

Abstract

AbstractHybrid metal halides (HMHs) have emerged as a promising platform for optically functional crystalline materials, but it is extremely challenging to thoroughly elucidate the electron transition coupled to additional ligand emission. Herein, to discover sequences of lead‐free HMHs with distinct optically active metal cations are aimed, that is, Sb3+ (5s2) with the lone‐pair electron configuration and In3+ (4d10) with the fully‐filled electron configuration. (Me2NH2)4MCl6·Cl (Me = −CH3, M = Sb, In) exhibits the superior temperature/component‐dependent luminescence behaviors resulting from the competition transition between triplet‐states (Tn‐S0) self‐trapped excitons (STEs) of inorganic units and singlet‐state (S1‐S0) of organic cations, which is manipulated by the optical activity levels of [SbCl6]3− and [InCl6]3−. The bonding differences between Sb3+/In3+ and Cl in terms of electronic excitation and hybridization are emphasized, and the different electron‐transition mechanisms are established according to the PL spectra at the extreme temperature of 5 to 305 K and theoretical calculations. By fine‐tuning the B‐site Sb3+/In3+ alloying, the photoluminescence quantum yield (PLQY = 81.5%) and stability are optimized at 20% alloying of Sb3+. This research sheds light on the rules governing PL behaviors of HMHs, as well as exploring the optical‐functional application of aviation temperature sensors and access‐control systems.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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