“…In particular the diphenylquinoxaline unit has shown a great potential in anti-aggregation and broadening spectra response. 141 The recent developments of quinoxaline derivatives for photovoltaic have been recently reviewed [142][143][144] and structures presented in these reviews will not be discussed here.…”
Extensive research on the synthesis and application of benzazine derivatives for electronic devices, luminescent elements, photoelectric conversion elements, and image sensors has been published recently. In the frames of this review article data obtained within the period 2012−2018 on the synthesis and optical properties of functionalized quinolines, quinoxalines and quinazolines are considered. Arylvinyl-, arylethynyl-and (het)arylderivatives of these benzazines, their photoluminescence and photoisomerisation are discussed. Examples of photosensitive annelated, oligo-and polymeric benzazines and also coordination compounds with benzazine ligands are reviewed.
“…In particular the diphenylquinoxaline unit has shown a great potential in anti-aggregation and broadening spectra response. 141 The recent developments of quinoxaline derivatives for photovoltaic have been recently reviewed [142][143][144] and structures presented in these reviews will not be discussed here.…”
Extensive research on the synthesis and application of benzazine derivatives for electronic devices, luminescent elements, photoelectric conversion elements, and image sensors has been published recently. In the frames of this review article data obtained within the period 2012−2018 on the synthesis and optical properties of functionalized quinolines, quinoxalines and quinazolines are considered. Arylvinyl-, arylethynyl-and (het)arylderivatives of these benzazines, their photoluminescence and photoisomerisation are discussed. Examples of photosensitive annelated, oligo-and polymeric benzazines and also coordination compounds with benzazine ligands are reviewed.
“…A literature search revealed that quinoxaline derivatives have been employed for various applications such as organic photovoltaics, organic light emitting diodes (OLEDs) and dye sensitized solar cells, etc. [ 24 , 25 , 26 , 27 ].…”
Quinoxaline-based novel acid-responsive probe Q1 was designed on the basis of a conjugated donor-acceptor (D-A) subunit. Q1 shows colorimetric and fluorometric changes through protonation and deprotonation in dichloromethane. With the addition of the trifluoroacetic acid (TFA), UV-vis absorption spectral changes in peak intensity of Q1 was observed. Moreover, the appearance of a new peaks at 284 nm 434 nm in absorption spectra with the addition of TFA indicating protonation of quinoxaline nitrogen and form Q1.H+ and Q1.2H+. The emission spectra display appearance of new emission peak at 515 nm. The optical property variations were supported by time resolved fluorescence studies. The energy band gap was calculated by employing cyclic voltammetry and density functional calculations. Upon addition of triethylamine (TEA) the fluorescence emission spectral changes of Q1 are found to be reversible. Q1 shows color changes from blue to green in basic and acidic medium, respectively. The paper strip test was developed for making Q1 a colorimetric and fluorometric indicator.
“…Ongoing efforts to optimize solar energy conversion are frequently inspired by Nature, which uses finely tuned assemblies of chromophores to harness sunlight. , In photosynthetic organisms, light-harvesting complexes of chlorophyll and bacteriochlorophyll derivatives are optimized to collect and funnel solar energy to reaction centers where charge separation takes place. TiO 2 -based dye-sensitized solar cells (DSSCs), on the other hand, depend on adsorbed dyes which perform both the light-harvesting and interfacial charge-separation steps. − Although self-assembly of dyes on the metal oxide surface is prevalent owing to their high surface density, , aggregation of dyes on TiO 2 is frequently reported to lower the rate and yield of electron injection, resulting in lower photocurrents. − Consequently, high-performing DSSCs often employ spacer molecules, − competitively binding molecules such as organophosphates, functionalized dyes with steric hindrance, − or surface treatments to prevent dye aggregation. The reduced photocurrents that result from sensitizer aggregation are variously attributed to decreased excited-state lifetime, self-quenching, attenuation of light by a thicker dye layer, and weak electronic coupling of dyes to TiO 2 as a result of greater distance from the surface.…”
Enhanced
light-harvesting and photoconversion efficiency of nanocrystalline
TiO2 sensitized with the plant pigment betanin is observed
in the presence of spectral signatures which reveal self-assembly
of betanin on the surface. Though aggregation of sensitizing chromophores
is generally considered detrimental to dye-sensitized solar energy
conversion, solar cells constructed with aggregated betanin show a
2.5-fold increase in power conversion efficiency compared to those
using mostly monomeric betanin. Dye aggregation results in a broadened
absorbance spectrum with extended light harvesting at blue and red
wavelengths. Variation in solution conditions and soaking times for
film sensitization enable control of the relative amounts of adsorbed
monomer and aggregate. Self-consistent modeling of the absorption
spectra of betanin-sensitized TiO2 films as a function
of dye loading suggests the templated formation of a betanin dimer
on the TiO2 surface and associated splitting of the excited
state. We show that dye aggregation increases the light-harvesting
efficiency as well as the incident photon-to-current conversion efficiency
(IPCE). Measurement of the absorbed photon-to-current conversion efficiency
(APCE) reveals that electron injection and collection of the putative
betanin dimer is more efficient than that of the monomer. Not only
is this the first report of a dye-sensitized solar cell performance
increase upon dye aggregation, but it also constitutes a record power
conversion efficiency for a natural dye-based solar cell of 3.0%.
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