2020
DOI: 10.1016/j.matt.2020.01.023
|View full text |Cite
|
Sign up to set email alerts
|

Near-Infrared Organic Single-Crystal Nanolaser Arrays Activated by Excited-State Intramolecular Proton Transfer

Abstract: Near-infrared lasing beyond 760 nm is achieved in the organic nanowire arrays made from the ESIPT-active organic molecule of (E)-3-(4-(dimethylamino)phenyl)-1-(1-hydroxynaphthalen-2-yl)prop-2-en-1-one, and the dynamic intramolecular proton transfer process within $2.5 ps is verified. The single-mode NIR lasing highquality factor Q of $2,340 can be achieved from a single nanowire with L = 10 mm, and the multi-mode NIR lasing with the lasing threshold of 2.2 mJ cm À2 can be achieved from a single nanowire with L… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
72
0

Year Published

2020
2020
2023
2023

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 70 publications
(74 citation statements)
references
References 42 publications
(45 reference statements)
2
72
0
Order By: Relevance
“…Restricting the dimensions of the same wires in the transversal direction can be an effective tool to design the resonant cavity geometry. This can be achieved for instance with capillary bridge lithography [ 123 , 137 ]. This method exploits de-wetting of a liquid film deposited on a substrate by placing the solution in contact with a template of periodically arranged ribs with their surface modified with heptadecafluorodecyltrimethoxysilane ( Figure 12 a–c).…”
Section: Organic Solid Lasersmentioning
confidence: 99%
“…Restricting the dimensions of the same wires in the transversal direction can be an effective tool to design the resonant cavity geometry. This can be achieved for instance with capillary bridge lithography [ 123 , 137 ]. This method exploits de-wetting of a liquid film deposited on a substrate by placing the solution in contact with a template of periodically arranged ribs with their surface modified with heptadecafluorodecyltrimethoxysilane ( Figure 12 a–c).…”
Section: Organic Solid Lasersmentioning
confidence: 99%
“…Also employing this method, our group recently prepared the NIR array and first achieved the nanolaser arrays over 760 nm. [ 29 ] Figure 6e was the PL microscopy image of ( E )‐3‐(4‐(dimethylamino)phenyl)‐1‐(1‐hydroxynaphthalen‐2‐yl)prop‐2‐en‐1‐one (DMHC) nanowires arrays with the length of 10 µm. The single DMHC nanowire was excited with a 532 nm laser (Figure 6c).…”
Section: Optical Generation Based On Organic Nanowiresmentioning
confidence: 99%
“…[ 13 ] Under excited with a certain power of a pulsed laser, nanowires show obvious stimulated emission behavior. [ 27–31 ] Nanowires of different lengths and diameters can form resonant cavities with different sizes, and single‐mode and multi‐mode lasing emission can be achieved, respectively. [ 32–34 ] In addition, by changing the doping ratios of the organic material, the ambient temperature, and the excitation energy of the pulsed laser, a wide‐spectrum tunable nanolaser based on OMNSs can be realized.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Additionally, nanolaser arrays offer distinct advantages for some of these applications such as higher sensitivity compared to Raman-based sensors as well as a label-free imaging method [59,61]. The use of such arrays can also be extended to telecommunications, lab-on-a-chip applications, spectroscopy, and parallel detection [62][63][64]. Finally, integration of up to 11,664 nanolasers has already been demonstrated in a photonic crystal uncoupled array, underlining the feasibility of achieving even higher onchip packing density in the future [65].…”
Section: Uncoupled Arraysmentioning
confidence: 99%