Ln3+ Induced Thermally Activated Delayed Fluorescence of Chiral Heterometallic Clusters Ln2Ag28

Author:

Wang Xue‐Tao1,He Sheng‐Rong1,Lv Fang‐Wen1,Wang Xue‐Ting1,Hong Mei‐Xin1,Cao Lingyun2,Zhuang Gui‐Lin3,Chen Cheng1,Zheng Jun1,Long La‐Sheng2,Zheng Xiu‐Ying1ORCID

Affiliation:

1. Institutes of Physical Science and Information Technology Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education Anhui University Hefei 230601 P. R. China

2. State Key Laboratory of Physical Chemistry of Solid Surfaces and Department of Chemistry College of Chemistry and Chemical Engineering Xiamen University Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM) Xiamen University Xiamen 361005 P. R. China

3. Key Laboratory of Functional Molecular Solids Ministry of Education College of Chemistry and Materials Science Anhui Normal University Wuhu 241002 P. R. China

Abstract

AbstractA series of TADF‐active compounds: 0D chiral Ln−Ag(I) clusters L‐/D‐Ln2Ag28‐0D (Ln=Eu/Gd) and 2D chiral Ln−Ag(I) cluster‐based frameworks L‐/D‐Ln2Ag28‐2D (Ln=Gd) has been synthesized. Atomic‐level structural analysis showed that the chiral Ag(I) cluster units {Ag14S12} in L‐/D‐Ln2Ag28‐0D and L‐/D‐Ln2Ag28‐2D exhibited similar configurations, linked by varying numbers of [Ln(H2O)x]3+ (x=6 for 0D, x=3 for 2D) to form the final target compounds. Temperature‐dependent emission spectra and decay lifetimes measurement demonstrated the presence of TADF in L‐Ln2Ag28‐0D (Ln=Eu/Gd) and L‐Gd2Ag28‐2D. Experimentally, the remarkable TADF properties primarily originated from {Ag14S12} moieties in these compounds. Notably, {Ag14S12} in L‐Eu2Ag28‐0D and L‐Gd2Ag28‐2D displayed higher promote fluorescence rate and shorter TADF decay times than L‐Gd2Ag28‐0D. Combined with theoretical calculations, it was determined that the TADF behaviors of {Ag14S12} cluster units were induced by 4 f perturbation of Ln3+ ions. Specially, while maintaining ΔE(S1–T1) small enough, it can significantly increase k(S1→S0) and reduce TADF decay time by adjusting the type or number of Ln3+ ions, thus achieving the purpose of improving TADF for cluster‐based luminescent materials.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

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