期刊文献+

Ultra-strong phosphorescence with 48% quantum yield from grinding treated thermal annealed carbon dots and boric acid composite 被引量:4

原文传递
导出
摘要 Metal-free room-temperature phosphorescence(RTP)materials are of great significance for many applications;however,they usually exhibit low efficiency and weak intensity.This article reports a new strategy for the preparation of a high-efficiency and strong RTP materials from crystalline thermal-annealed carbon dots(CDs)and boric acid(BA)composite(g-t-CD@BA)through grinding-induced amorphous to crystallization transition.Amorphous thermal-annealed CDs and BA composite(t-CD@BA)is prepared following a thermal melting and super-cooling route,where the CDs are fully dispersed in molten BA liquid and uniformly frozen in an amorphous thermal annealed BA matrix after super-cooling to room temperature.Upon grinding treatment,the fracture and fragmentation caused by grinding promote the transformation of the high-energy amorphous state to the lower energy crystalline counterparts.As a result,the CDs are uniformly in situ embedded in the BA crystal matrix.This method affords maximum uniform embedding of the CDs in the BA crystals,decreases nonradiative decay,and promotes intersystem crossing by restraining the free vibration of the CDs,thus producing strong RTP materials with the highest reported phosphorescence quantum yield(48%).Remarkably,RTP from g-t-CD@BA powder is strong enough to illuminate items with a delay time exceeding 9 s.
出处 《SmartMat》 2022年第2期260-268,共9页 智能材料(英文)
基金 the National Natural Science Foundation of China(No.52002152,62005106 and 61922091) the Natural Science Foundation of Jiangsu(BK20190864 and BK20190865) the Natural Science Foundation of the Jiangsu Higher Education Institutions(19KJB430014) the Science and Technology Development Fund of Macao SAR(0040/2019/A1,0128/2020/A3,0131.2020.A3 and 0073/2019/AMJ) Fund from the University of Macao(SRG2019‐00163‐IAPME) the High-Tech Research Key Laboratory of Zhenjiang(SS2018002).
  • 相关文献

参考文献2

二级参考文献8

共引文献18

同被引文献25

引证文献4

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部