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A new set of dyes was designed in an effort to increase its solar cell efficiency that was patterned after PSS with an additional donor moiety such as fluorene, cyclopentaindole, and pyrene attached asymmetrically at the triphenylamine ring.
Currently, most multi-color MPM relies on the absorbance at one intermediate wavelength of multiple dyes, which introduces problems such as decreased and unequal excitation efficiency across the set of dyes.
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The new model was found to correlate better for the set of dye compounds considered in this study than the most frequently used fourteen density based semi-empirical models in terms of percentage average absolute relative deviation (% AARD).
A set of dye-swap experiments was also carried out, giving a total of 6 replicate experiments.
In the present paper, using density functional theory (DFT) and time-dependent DFT, we have investigated two sets of dyes (CN11s and CN12s) with various anchoring groups, such as biscarbodithiolic acid, sulfonic acid, phosphonic acid, and hydroxamic acid.
Quantitative structure-property relationships (QSPR) are developed for a set of phenothiazine dyes used in dye sensitized solar cells (DSSCs).
The central acceptors were dicyanovinylidene and 1,3-diethylthiobarbituric acid derivatives of 2-indanone in the set of symmetrical dyes and dicyanovinylidene in unsymmetrical dyes.
The three dyes were selected among a set of different dyes on the basis of their chemical structure since azoic (MO and EB) and anthraquinoid (RBB) dyes are the most common chromophores utilized in the dying industry [ 39].
The replicate embryo pools were analyzed in two sets of dye-swaps making a total of four hybridizations.
Four technical replicates (2 sets of dye-swaps) were performed for each animal.
Two sets of dye-swapped experiments were performed to obtain a total of four replicate hybridizations per developmental stage.
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