10 research outputs found
Visible light communication with efficient far-red/near-infrared polymer light-emitting diodes
Visible light communication (VLC) is a wireless technology that relies on optical intensity modulation and is potentially a game changer for internet-of-things (IoT) connectivity. However, VLC is hindered by the low penetration depth of visible light in non-transparent media. One solution is to extend operation into the “nearly (in)visible” near-infrared (NIR, 700–1000 nm) region, thus also enabling VLC in photonic bio-applications, considering the biological tissue NIR semitransparency, while conveniently retaining vestigial red emission to help check the link operativity by simple eye inspection. Here, we report new far-red/NIR organic light-emitting diodes (OLEDs) with a 650–800 nm emission range and external quantum efficiencies among the highest reported in this spectral range (>2.7%, with maximum radiance and luminance of 3.5 mW/cm2 and 260 cd/m2, respectively). With these OLEDs, we then demonstrate a “real-time” VLC setup achieving a data rate of 2.2 Mb/s, which satisfies the requirements for IoT and biosensing applications. These are the highest rates ever reported for an online unequalised VLC link based on solution-processed OLEDs
Amplified two-photon absorption in trans-A2B2-porphyrins bearing nitrophenylethynyl substituents.
We show that peripheral nitro groups enhance the maximum two-photon absorption cross-section of trans-A(2)B(2)-porphyrins bearing two phenylethynyl substituents by more than one order of magnitude. Maximum values as high as 1000 GM result from realization of suitable conditions for effective resonance enhancement along with a lowering of the energy and intensification of the two-photon allowed transitions in the Soret region
Two-photon absorption in butadiyne-linked porphyrin dimers: torsional and substituent effects
Dyes exhibiting efficient two-photon absorption (2PA) are in demand for a wide range of applications, and meso-meso butadiyne-linked porphyrin dimers (bis-porphyrins) are promising chromophores in this area. As part of an investigation of the structure-property relationships controlling the performance of these dyes, we present the synthesis of eight π-extended dimers, with substituents providing diverse push and pull electronic effects, and high solubility. We show that the peak 2PA cross sections can be increased from 3000 GM to 20000 GM by attaching terminal electron-withdrawing or -donating groups, and by converting the free-base dimers to zinc complexes. The two-photon excited fluorescence spectra of porphyrin dimers in viscous media, under conditions such that excited states do not planarize prior to emission, reveal that dimers in planar conformations dominate the two-photon absorption. This journal is © the Partner Organisations 2014
Synthesis and linear and nonlinear optical properties of low-melting pi-extended porphyrins
A large and diverse library of trans-A2B2 and A 2BC-porphyrins possessing two arylethynyl substituents at the meso positions has been efficiently synthesized and tested for their two-photon absorption (2PA) behavior. All compounds fall into three general types A-π-A, D-π-D or D-π-A, where A is an electron-acceptor and D is an electron-donor moiety. These porphyrins contain two polyalkoxyaryl substituents, resulting in very low melting points (typically 110-125 °C) and superb solubility in non-polar solvents. Some of these porphyrins exhibit two different crystal phases in addition to an isotropic liquid state. Their linear and nonlinear optical properties were thoroughly elucidated and analyzed. π-Extended porphyrins emit light in the NIR and have moderate triplet state lifetimes. The increase of 2PA cross-section in the Soret region for porphyrins bearing strong electron-donating groups has been attributed to resonance enhancement (caused by intensification, redshift and broadening of the lowest Q-band) of gerade-gerade transition. The combination of high two-photon absorption cross-sections (>500 GM) and low melting points makes them perfect candidates for nonlinear optical materials in the 600-900 nm range. © 2013 The Royal Society of Chemistry