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Solution to fnb/n = 0 yields a maximum emission at frequency nmax = 3kT/h, corresponding to lmax = hc/3kT.
A 900 mW blue light-emitting diode (M455L3, Thorlabs, USA), with a maximum emission at 455 nm was used for OCPO → OCPR photoconversion of the samples.
Solid-state 1 and 2 have expected photoluminescence with maximum emission at 484 and 505 nm, respectively.
KP has a maximum emission at 462.3 nm which is in the blue region of visible light, whereas CN, has emissions at 501.5 nm and 512.2 nm which is deep within the green.
Due to the unilateral recognition process for cyanide the ICT orientation of PMI was redirected thus exhibited fluorescence enhancement with maximum emission at 630 nm.
Additionally, as-formed PDBTO was found to be a typical blue-light-emitter with maximum emission at 458 nm and concurrently exhibited good electroactivity and thermal stability.
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P1 showed strong emission upon excited at 378 nm with a maximum emission peak at 450 nm.
In the former case, the maximum emission intensity at 160 K is enhanced by 40% in comparison to that at low temperature.
The ECL spectrum was measured, showing maximum emission peaks at 544 nm, 434 nm and 404 nm.
The photoluminescence (PL) of (dmppy)2Ir tmd) and (dmppy)2Ir acac) produced orange emissions with maximum emission peaks at 577 and 570 nm, respectively.
These compounds possess good thermal stability with decomposition temperatures of 264 340 °C and exhibit intense blue fluorescence with maximum emission peaked at 457 470 nm.
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