Thermochromic Phosphors Based on One‐Dimensional Ionic Copper‐Iodine Chains Showing Solid‐State Photoluminescence Efficiency Exceeding 99
Thermochromic phosphors are intriguing materials for realizing thermochromic behaviors of light‐emitting diodes. Here a highly luminescent and stable thermochromic phosphor based on one‐dimensional Cu4I6(4‐dimethylamino‐1‐ethylpyridinium)2 is reported. This unique ionic copper‐iodine chain‐based hyb...
Saved in:
Published in | Angewandte Chemie Vol. 134; no. 38 |
---|---|
Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
Wiley Subscription Services, Inc
19.09.2022
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Thermochromic phosphors are intriguing materials for realizing thermochromic behaviors of light‐emitting diodes. Here a highly luminescent and stable thermochromic phosphor based on one‐dimensional Cu4I6(4‐dimethylamino‐1‐ethylpyridinium)2 is reported. This unique ionic copper‐iodine chain‐based hybrid exhibits near‐unity photoluminescence efficiency owing to the through‐space charge‐transfer character of relevant electronic transitions. More importantly, an alternative mechanism of thermochromic phosphorescence was unraveled, supported by a first principles simulation of concerted copper atom migration in the copper‐iodine chain. Furthermore, we successfully fabricate a bright thermochromic light‐emitting diode using this Cu4I6(4‐dimethylamino‐1‐ethylpyridinium)2 thermochromic phosphor. Our reported flexible ionic copper‐iodine chain‐based thermochromic luminescent material represents a new type of cost‐effective functional phosphor.
A novel thermochromic 1D‐Cu4I6(4‐dimethylamino‐1‐ ethylpyridinium)2 hybrid phosphor with near‐unity photoluminescence efficiency is reported involving a mechanism of reversible single‐crystal‐to‐single‐crystal transformation induced bytemperature‐responsive concerted Cu atom migration in ionic copper‐iodine chains . |
---|---|
ISSN: | 0044-8249 1521-3757 |
DOI: | 10.1002/ange.202208960 |