Structural Isomerization Effect on the Triplet Energy Consumption Process of Organic Room-Temperature Phosphorescence Molecules: A QM/MM Study

2021 ◽  
Author(s):  
Yuanyuan Xu ◽  
Kai Zhang ◽  
Jiancai Leng ◽  
Lili Lin ◽  
Chuan-Kui Wang ◽  
...  
Keyword(s):  
Energy Consumption ◽  
Room Temperature ◽  
Room Temperature Phosphorescence ◽  
Triplet Energy ◽  
Structural Isomerization

scholarly journals Guest-host doped strategy for constructing ultralong-lifetime near-infrared organic phosphorescence materials for bioimaging

2022 ◽  
Vol 13 (1) ◽  
Author(s):  
Fuming Xiao ◽  
Heqi Gao ◽  
Yunxiang Lei ◽  
Wenbo Dai ◽  
Miaochang Liu ◽  
...  
Keyword(s):  
Room Temperature ◽  
Near Infrared ◽  
Tumor Imaging ◽  
Energy Gap ◽  
Radiative Transition ◽  
Room Temperature Phosphorescence ◽  
Triplet Energy ◽  
Long Wavelength ◽  
Long Lifetime ◽  
First Time

AbstractOrganic near-infrared room temperature phosphorescence materials have unparalleled advantages in bioimaging due to their excellent penetrability. However, limited by the energy gap law, the near-infrared phosphorescence materials (>650 nm) are very rare, moreover, the phosphorescence lifetimes of these materials are very short. In this work, we have obtained organic room temperature phosphorescence materials with long wavelengths (600/657–681/732 nm) and long lifetimes (102–324 ms) for the first time through the guest-host doped strategy. The guest molecule has sufficient conjugation to reduce the lowest triplet energy level and the host assists the guest in exciton transfer and inhibits the non-radiative transition of guest excitons. These materials exhibit good tissue penetration in bioimaging. Thanks to the characteristic of long lifetime and long wavelength emissive phosphorescence materials, the tumor imaging in living mice with a signal to background ratio value as high as 43 is successfully realized. This work provides a practical solution for the construction of organic phosphorescence materials with both long wavelengths and long lifetimes.

Tuning the singlet–triplet energy gap of AIE luminogens: crystallization-induced room temperature phosphorescence and delay fluorescence, tunable temperature response, highly efficient non-doped organic light-emitting diodes

2015 ◽  
Vol 17 (2) ◽  
pp. 1134-1141 ◽  
Author(s):  
Jie Li ◽  
Yibin Jiang ◽  
Juan Cheng ◽  
Yilin Zhang ◽  
Huimin Su ◽  
...  
Keyword(s):  
Room Temperature ◽  
Light Emitting Diodes ◽  
Energy Gap ◽  
Temperature Response ◽  
Organic Light Emitting Diodes ◽  
Room Temperature Phosphorescence ◽  
Triplet Energy ◽  
Light Emitting ◽  
Organic Light ◽  
Delay Fluorescence

Tuning singlet–triplet energy gap of AIE luminogens: crystallization-induced phosphorescence, delay fluorescence and efficient non-doped OLEDs.

scholarly journals Wide-range lifetime-tunable and responsive ultralong organic phosphorescent multi-host/guest system

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Zongliang Xie ◽  
Xiayu Zhang ◽  
Hailan Wang ◽  
Cheng Huang ◽  
Haodong Sun ◽  
...  
Keyword(s):  
Room Temperature ◽  
Energy Levels ◽  
Room Temperature Phosphorescence ◽  
Triplet Energy ◽  
Time Resolved ◽  
Wide Range ◽  
Host Matrices ◽  
Tuning Strategy ◽  
Rigid Environment ◽  
Triplet Excitons

AbstractThe rational lifetime-tuning strategy of ultralong organic phosphorescence is extraordinarily important but seldom reported. Herein, a series of multi-host/guest ultralong organic phosphorescence materials with dynamic lifetime-tuning properties were reported. By doping a non-room-temperature phosphorescence emitter into various solid host matrices with continuously reduced triplet energy levels, a wide-range lifetime (from 3.9 ms gradually to 376.9 ms) phosphorescence with unchangeable afterglow colors were realized. Further studies revealed that the host matrices were employed to afford rigid environment and proper energy levels to generate and stabilize the long-live triplet excitons. Meanwhile, these multi-host/guest ultralong organic phosphorescence materials also exhibited excitation-dependent phosphorescence and temperature-controlled afterglow on/off switching properties, according to the virtue of various photophysical and thermal properties of the host matrices. This work provides a guiding strategy to realize lifetime-tuning ultralong organic phosphorescence with lifetime-order encoding characteristic towards widespread applications in time-resolved information displaying, higher-level security protection, and dynamic multi-dimensional anti-counterfeiting.

DNA Inspirited Rational Construction of Nonconventional Luminophores with Efficient and Color-Tunable Afterglow

2020 ◽  
Author(s):  
Yunzhong Wang ◽  
Saixing Tang ◽  
Yating Wen ◽  
Shuyuan Zheng ◽  
Bing Yang ◽  
...  
Keyword(s):  
Rational Design ◽  
Room Temperature ◽  
Double Helix ◽  
Mechanical Grinding ◽  
Room Temperature Phosphorescence ◽  
Color Tunable ◽  
Potential Applications ◽  
Rational Construction ◽  
Double Helix Structure ◽  
Made In

<div>Persistent room-temperature phosphorescence (p-RTP) from pure organics is attractive </div><div>due to its fundamental importance and potential applications in molecular imaging, </div><div>sensing, encryption, anticounterfeiting, etc.1-4 Recently, efforts have been also made in </div><div>obtaining color-tunable p-RTP in aromatic phosphors5 and nonconjugated polymers6,7. </div><div>The origin of color-tunable p-RTP and the rational design of such luminogens, </div><div>particularly those with explicit structure and molecular packing, remain challenging. </div><div>Noteworthily, nonconventional luminophores without significant conjugations generally </div><div>possess excitation-dependent photoluminescence (PL) because of the coexistence of </div><div>diverse clustered chromophores6,8, which strongly implicates the possibility to achieve </div><div>color-tunable p-RTP from their molecular crystals assisted by effective intermolecular </div><div>interactions. Here, inspirited by the highly stable double-helix structure and multiple </div><div>hydrogen bonds in DNA, we reported a series of nonconventional luminophores based on </div><div>hydantoin (HA), which demonstrate excitation-dependent PL and color-tunable p-RTP </div><div>from sky-blue to yellowish-green, accompanying unprecedentedly high PL and p-RTP </div><div>efficiencies of up to 87.5% and 21.8%, respectively. Meanwhile, the p-RTP emissions are </div><div>resistant to vigorous mechanical grinding, with lifetimes of up to 1.74 s. Such robust, </div><div>color-tunable and highly efficient p-RTP render the luminophores promising for varying </div><div>applications. These findings provide mechanism insights into the origin of color-tunable </div><div>p-RTP, and surely advance the exploitation of efficient nonconventional luminophores.</div>

Clustering-Triggered Efficient Room Temperature Phosphorescence from Nonconventional Luminophores

2019 ◽  
Author(s):  
Shuyuan Zheng ◽  
Taiping Hu ◽  
Xin Bin ◽  
Yunzhong Wang ◽  
Yuanping Yi ◽  
...  
Keyword(s):  
Room Temperature ◽  
High Efficiency ◽  
Spin Orbit Coupling ◽  
Design Rationale ◽  
Emission Mechanism ◽  
Room Temperature Phosphorescence ◽  
Electronic Interactions ◽  
Energy Gaps ◽  
Theoretical Results

Pure organic room temperature phosphorescence (RTP) and luminescence from nonconventional luminophores have gained increasing attention. However, it remains challenging to achieve efficient RTP from unorthodox luminophores, on account of the unsophisticated understanding of the emission mechanism. Here we propose a strategy to realize efficient RTP in nonconventional luminophores through incorporation of lone pairs together with clustering and effective electronic interactions. The former promotes spin-orbit coupling and boost the consequent intersystem crossing, whereas the latter narrows energy gaps and stabilizes the triplets, thus synergistically affording remarkable RTP. Experimental and theoretical results of urea and its derivatives verify the design rationale. Remarkably, RTP from thiourea solids with unprecedentedly high efficiency of up to 24.5% is obtained. Further control experiments testify the crucial role of through-space delocalization on the emission. These results would spur the future fabrication of nonconventional phosphors, and moreover should advance understanding of the underlying emission mechanism.<br>

scholarly journals Tipping the Balance with the Aid of Stoichiometry: Room Temperature Phosphorescence versus Fluorescence in Organic Cocrystals

2015 ◽  
Vol 15 (4) ◽  
pp. 2039-2045 ◽  
Author(s):  
Simone d’Agostino ◽  
Fabrizia Grepioni ◽  
Dario Braga ◽  
Barbara Ventura
Keyword(s):  
Room Temperature ◽  
Room Temperature Phosphorescence

Boron nitride dots In-situ embedded in a B2O3 matrix with the long lifetime Room-Temperature phosphorescence in dry and wet states

2021 ◽  
Vol 417 ◽  
pp. 129175
Author(s):  
Shenghui Han ◽  
Gang Lian ◽  
Xu Zhang ◽  
Zhaozhen Cao ◽  
Qilong Wang ◽  
...  
Keyword(s):  
Boron Nitride ◽  
Room Temperature ◽  
Room Temperature Phosphorescence ◽  
Long Lifetime
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