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Current-voltage characteristics of single molecule junctions are governed both by the energy level alignment of molecular orbitals with respect to the Fermi level of the electrodes and by the hybridization of electronic structures at the interface between the molecule and the electrodes. While there have been many studies on tuning the former, only a few works intended to control the latter. In the present study, we demonstrate that molecular junctions based on carbazole oligomers showed a current rectification behavior due to asymmetric-symmetric control of electronic hybridization between the molecule and electrodes at the both terminals. The carbazole oligomers originally showed an asymmetric molecular orbital and, hence, electronic hybridization with the electrodes because of the electric dipole moment. Symmetric electronic hybridization was achieved when the applied electric field between electrodes deformed molecular orbital to be symmetric. This is a novel way to control charge transport in single-molecule junctions.
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http://dx.doi.org/10.1039/c8nr06049e | DOI Listing |
Mar Pollut Bull
October 2025
Department of Earth, Environmental & Space Sciences, Chungnam National University, Daejeon 34134, Republic of Korea. Electronic address:
This study investigated 63 persistent toxic substances (PTSs) in surface sediments along the Yangtze River, analyzing contamination levels, spatial distribution, sources, and ecological risks. High PTS levels were observed in Nanjing due to organic pollution, with significant regional variations in styrene oligomers (SOs), alkylphenols (APs), and polyhalogenated carbazoles (PHCZs) in Nantong, Changzhou, and Shanghai, respectively. These patterns were linked to local anthropogenic activities, with higher contamination in more densely populated and industrialized areas.
View Article and Find Full Text PDFACS Chem Neurosci
June 2025
Organic and Medicinal Chemistry and Structural Biology and Bioinformatics Division, CSIR-Indian Institute of Chemical Biology, 4, Raja S. C. Mullick Road, Jadavpur, Kolkata , WB 700 032, India.
The amyloid-beta 42 (Aβ) peptide assembles into neurotoxic soluble oligomers and extracellular fibrillary aggregates during the progression of Alzheimer's disease (AD), which ultimately leads to amyloid plaque in the brain, causing major disruption of the neural circuit and leading to the severe loss of memory. Thus, perturbation or inhibition of this process through the development of advanced inhibitors is crucial for the treatment of AD. Here, we adopted an advanced strategy that showcases the design of a carbazole-based chemical inhibitor targeting the Aβ peptide.
View Article and Find Full Text PDFJ Chem Phys
April 2025
Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-Koen, Kasuga-shi, Fukuoka 816-8580, Japan.
Luminescent radicals are gathering much attention as a new class of luminescent material. We have synthesized a new carbazole oligomer (mono, di, tri, tetra) substituted luminescent tris (2,4,6-trichlorophenyl) methyl (TTM) radicals. The photoluminescence (PL) spectra showed emission stemmed from the excited state charge transfer character.
View Article and Find Full Text PDFJ Phys Chem B
April 2025
Department of Materials Science and Engineering, University of Ioannina, POB 1186, Ioannina GR45110, Greece.
Conjugated polymers are indispensable building blocks in a variety of organic electronics applications such as solar cells, light-emitting diodes, and field-effect transistors. Poly[-9'-heptadecanyl-2,7-carbazole--5,5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)] (PCDTBT) is a carbazole-benzothiadiazole-based copolymer with a donor-acceptor structure, consisting of electron-donating and electron-withdrawing subunits and featuring a low band gap. In this work, the General Amber Force Field is extended in two ways, specifically for modeling PCDTBT.
View Article and Find Full Text PDFLangmuir
October 2024
State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.
Immobilizing catalysts and photosensitizers on an electrode surface is crucial in interfacial energy conversion. However, their combination for optimizing catalytic performance is an unpredictable challenge. Herein, we report that catalyst and photosensitizer monomers are selectively grafted one-by-one addition onto the electrode surface by interfacial electrosynthesis to achieve composition and sequence-controlled oligomer photoelectrocatalytic monolayers.
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