scholarly journals Near infrared-emitting tris-bidentate Os(ii) phosphors: control of excited state characteristics and fabrication of OLEDs

2015 ◽  
Vol 3 (19) ◽  
pp. 4910-4920 ◽  
Author(s):  
Jia-Ling Liao ◽  
Yun Chi ◽  
Chia-Chi Yeh ◽  
Hao-Che Kao ◽  
Chih-Hao Chang ◽  
...  

Os(ii) complexes bearing chromophoric 1,10-phenanthroline, diphosphine and bipyrazolate ancillaries display efficient NIR emission ranging from 717 nm to 779 nm in the solid state at RT.

2021 ◽  
Author(s):  
xiudi wu ◽  
shuang zhao ◽  
Liang Zhang ◽  
Langping Dong ◽  
Yonghui Xu ◽  
...  

Abstract:Gd2GaSbO7:Cr3+,Yb3+ phosphors with efficient broadband NIR emission were prepared by solid-state reaction. Under the excitation of 448 nm, Gd2GaSbO7:Cr3+ (GGS:Cr3+) phosphor exhibits a broadband NIR emission band centered at approximately...


ACS Omega ◽  
2018 ◽  
Vol 3 (10) ◽  
pp. 14341-14348 ◽  
Author(s):  
Abhishek Kumar Gupta ◽  
Ashwani Kumar ◽  
Ranjit Singh ◽  
Manisha Devi ◽  
Abhimanew Dhir ◽  
...  

2017 ◽  
Vol 95 (5) ◽  
pp. 547-552 ◽  
Author(s):  
Joe P. Harris ◽  
Christian Reber ◽  
Hannah E. Colmer ◽  
Timothy A. Jackson ◽  
Adam P. Forshaw ◽  
...  

The molecular bis-(tris(carbene)borate) manganese(IV) complex [{PhB(MeIm)3}2Mn](OTf)2 shows 2Eg → 4A2g luminescence at 828 nm in the solid state at 85 K; this wavelength is longer by approximately 100 nm than the wavelengths typically observed for manganese(IV) and chromium(III) doped solids and for molecular chromium(III) complexes. Weak luminescence is also observed from a LMCT excited state with an absorption maximum at 500 nm. This represents the first molecular manganese(IV) compound for which luminescence has been reported.


2014 ◽  
Vol 2 (35) ◽  
pp. 7385-7391 ◽  
Author(s):  
Xiao Cheng ◽  
Zhenyu Zhang ◽  
Houyu Zhang ◽  
Shenghua Han ◽  
Kaiqi Ye ◽  
...  

Crystalline-enhanced red/NIR emission of beryllium complexes can be switched between dark and bright states by different stimuli, providing the first example of reversible multiple-channel solid-state fluorescence “ON/OFF” switching.


2020 ◽  
Vol 4 (11) ◽  
pp. 3378-3383
Author(s):  
Yangyang Li ◽  
Xian Wang ◽  
Lei Zhang ◽  
Luqi Liu ◽  
Qiusheng Wang ◽  
...  

An AIEgen exhibits a fluorescence switch between the visible and the NIR region upon acid/base stimuli, and accessible solid-state NIR emission.


2018 ◽  
Author(s):  
Dinesh Mishra ◽  
Sisi Wang ◽  
Zhicheng Jin ◽  
Eric Lochner ◽  
Hedi Mattoussi

<p>We describe the growth and characterization of highly fluorescing, near-infrared-emitting nanoclusters made of bimetallic Au<sub>25-x</sub>Ag<sub>x</sub> cores, prepared using various monothiol-appended hydrophobic and hydrophilic ligands. The reaction uses well-defined triphenylphosphine-protected Au<sub>11</sub> clusters (as precursors), which are reacted with Ag(I)-thiolate complexes. The prepared nanoclusters are small (diameter < 2nm, as characterized by TEM) with emission peak at 760 nm and long lifetime (~12 µs). The quantum yield measured for these materials was 0.3 - 0.4 depending on the ligand. XPS measurements show the presence of both metal atoms in the core, with measured binding energies that agree with reported values for nanocluster materials. The NIR emission combined with high quantum yield, small size and ease of surface functionalization afforded by the coating, make these materials suitable to implement investigations that address fundamental questions and potentially useful for biological sensing and imaging applications.<br></p>


2019 ◽  
Author(s):  
Haoke Zhang ◽  
Lili Du ◽  
Lin Wang ◽  
Junkai Liu ◽  
Qing Wan ◽  
...  

<p>Building molecular machine has long been a dream of scientists as it is expected to revolutionize many aspects of technology and medicine. Implementing the solid-state molecular motion is the prerequisite for a practical molecular machine. However, few works on solid-state molecular motion have been reported and it is almost impossible to “see” the motion even if it happens. Here the light-driven molecular motion in solid state is discovered in two non-conjugated molecules <i>s</i>-DPE and <i>s</i>-DPE-TM, resulting in the formation of excited-state though-space complex (ESTSC). Meanwhile, the newly formed ESTSC generates an abnormal visible emission which is termed as clusteroluminescence. Notably, the original packing structure can recover from ESTSC when the light source is removed. These processes have been confirmed by time-resolved spectroscopy and quantum mechanics calculation. This work provides a new strategy to manipulate and “see” solid-state molecular motion and gains new insights into the mechanistic picture of clusteroluminescence.<br></p>


2021 ◽  
Author(s):  
Abhineet Verma ◽  
Sk Saddam Hossain ◽  
Sailaja S Sunkari ◽  
Joseph Reibenspies ◽  
Satyen Saha

Lanthanides (LnIII) are well known for their characteristic emission in the Near-Infrared Region (NIR). However, direct excitation of lanthanides is not feasible as described by Laporte’s parity selection rule. Here,...


Author(s):  
Fabrice Pointillart ◽  
Bertrand Lefeuvre ◽  
Carlo Andrea Mattei ◽  
Jessica Flores Gonzalez ◽  
Frédéric Gendron ◽  
...  

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