A new Ru(II) dye, Ru(L1)(L2) (NCS)2, L1 = (4-(5-hexylthiophen-2-yl)-4'(4-carboxyl-phenyl 2,2'-bipyridine) and L2 = (4-4'-dicarboxy-2,2'-bipyridine), labelled MC112, based on a dissymmetric bipyridine ligand for improved interfacial and optical properties, was synthesized and used in DSCs, yielding photovoltaic efficiencies of 7.6% under standard AM 1.5 sunlight and an excellent device stability. Increased light harvesting and IPCE maximum were observed with MC112 compared to the prototypical homoleptic N719 dye, due to the functionalized bipyridyne ligand acting as an antenna. In addition, the mixed bipyridyne ligand allowed MC112 binding to TiO2 to occur via three anchoring carboxylic groups, thus exhibiting similar interfacial properties to those of the N719 dye. DFT/TDDFT calculations were performed on the new dye, both in solution and adsorbed on a TiO2 surface model, revealing that the peculiar photovoltaic properties of the MC112 dye are related to its anchoring mode. The new design rule thus allows us to engineer both light-harvesting and interfacial properties in the same dye.
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Sci Rep
October 2024
Department of Chemistry, Faculty of Science, Mansoura University, Mansoura, 35516, Egypt.
This study presents a significant advancement in tandem dye-sensitized solar cells (T-DSSCs) through the strategic synthesis of novel triazatruxene (TAT) sensitizers MS-1 and MS-2. These organic sensitizers demonstrate exceptional light-harvesting capacity and overall performance, pushing the boundaries of power conversion efficiency (PCE) in DSSCs. The MS-1-based DSSCs achieved an impressive PCE of 12.
View Article and Find Full Text PDFJ Am Soc Mass Spectrom
December 2024
UHasselt, Data Science Institute, Interuniversity Institute for Biostatistics and Statistical Bioinformatics, Center for Statistics, Agoralaan, 3590 Diepenbeek, Belgium.
In time-of-flight secondary ion mass spectrometry (ToF-SIMS), multivariate analysis (MVA) methods such as principal component analysis (PCA) are routinely employed to differentiate spectra. However, additional insights can often be gained by comparing processes, where each process is characterized by its own start and end spectra, such as when identical samples undergo slightly different treatments or when slightly different samples receive the same treatment. This study proposes a strategy to compare such processes by decomposing the loading vectors associated with them, which highlights differences in the relative behavior of the peaks.
View Article and Find Full Text PDFMikrochim Acta
August 2024
Physical Education Department, Shandong University of Traditional Chinese Medicine, Jinan, 250355, Shandong, China.
A novel photoelectrochemical (PEC) sensor for the detection of microcystic toxins (MC-LR) was developed on the basis of signal-sensitive change strategy. NiO nanoarray as a basic photoactive material was grown directly on the ITO glass electrode via calcination after hydrothermal reaction, while dye N719 was used to sensitize the electrode for enhancing visible light absorption, and the first signal-on stage was obtained. In the meantime, p-type CuO was applied as the signal probe attached to probe DNA (DNA) to improve the sensitivity, and the second "signal-on" stage appeared because of its synergistic effect with NiO nanoarrays.
View Article and Find Full Text PDFRSC Adv
August 2024
Department of Chemistry, Faculty of Science, Mansoura University El-Gomhoria Street Mansoura 35516 Egypt
Dye-sensitized solar cells (DSSCs) have emerged as a promising alternative for renewable energy conversion. The synthesis and characterization of the 2-acetonitrile-benzoxazole (BOA) sensitizer MSW-1-4 are presented along with their chemical structures. Four new organic dyes, MSW-1 through MSW-4, were synthesized using BOA as the main building block, with different additional donor groups.
View Article and Find Full Text PDFChem Asian J
October 2024
Department of Chemistry, Tunghai University, No.1727, Sec.4, Taiwan Boulevard, Xitun District, Taichung, 40704, Taiwan.
Novel D-A-A-π-A organic sensitizers (FZ-sensitizer), utilizing spiro [fluorene-9,9'-phenanthren]-10'-one and benzo [c][1,2,5]thiadiazole moiety as two auxiliary acceptors, are synthesized and applied in dye-sensitized solar cells (DSSCs) and hydrogen production. By incorporating a bulky spiro [fluorene-9,9'-phenanthrene]-10'-one (A) and benzo[c][1,2,5]thiadiazole (A) between the donor (D) and π-bridge moiety, structural modifications inhibit molecular aggregation, while the carbonyl group enhances the capture of Li ions, thereby delaying charge recombination. Furthermore, the extended π-conjugation broadens the light absorption range and enhances the power conversion efficiency (PCE) of FZ-2 under AM1.
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