Ultralong Phosphorescence from Organic Ionic Crystals under Ambient Conditions

被引:211
作者
Cheng, Zhichao [1 ,2 ]
Shi, Huifang [1 ,2 ]
Ma, Huili [1 ,2 ]
Bian, Lifang [1 ,2 ]
Wu, Qi [1 ,2 ]
Gu, Long [1 ,2 ]
Cai, Suzhi [1 ,2 ]
Wang, Xuan [1 ,2 ]
Xiong, Wei-wei [1 ,2 ]
An, Zhongfu [1 ,2 ]
Huang, Wei [1 ,2 ,3 ]
机构
[1] Nanjing Tech Univ NanjingTech, Key Lab Flexible Elect KLOFE, 30 South Puzhu Rd, Nanjing 211800, Jiangsu, Peoples R China
[2] Nanjing Tech Univ NanjingTech, IAM, 30 South Puzhu Rd, Nanjing 211800, Jiangsu, Peoples R China
[3] NPU, SIFE, 127 West Youyi Rd, Xian 710072, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
crystal engineering; gas sensing; organic ionic crystals; ultralong phosphorescence; ROOM-TEMPERATURE PHOSPHORESCENCE; PERSISTENT LUMINESCENCE; ACHIEVING PERSISTENT; DUAL-EMISSION; MOLECULES; NANOPARTICLES; ENVIRONMENTS; AGGREGATION; MECHANISM; ESTERS;
D O I
10.1002/anie.201710017
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new type of materials, organic salts in the crystal state, have ultralong organic phosphorescence (UOP) under ambient conditions. The change of cations (NH4+, Na+, or K+) in these phosphors gives access to tunable UOP colors ranging from sky blue to yellow green, along with ultralong emission lifetimes of over 504ms. Single-crystal analysis reveals that unique ionic bonding can promote an ordered arrangement of organic salts in crystal state, which then can facilitate molecular aggregation for UOP generation. Additionally, reversible ultralong phosphorescence can be realized through the alternative employment of fuming gases (ammonia and hydrogen chloride), demonstrating its potential as a candidate for visual ammonic or hydrogen chloride gas sensing. The results provide an environmental responsible and practicable synthetic approach to expanding the scope of ultralong organic phosphorescent materials as well as their applications.
引用
收藏
页码:678 / 682
页数:5
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