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Efficient charge injection/extraction from/to contact electrodes is essential to realize organic electronic and optoelectronic devices with optimum characteristics for many applications. Herein, we studied a versatile reductive interlayer based on sodium borohydride (NaBH) to control the contact properties of the staggered organic field-effect transistors (OFETs) either by doping and/or by regulating the contribution of charge carriers. The versatile functionalities of the NaBH layer are mainly determined by the alignment of frontier molecular orbitals of donor-acceptor (D-A) type copolymer semiconductors and the work function of the contact electrode. After incorporating the NaBH layer, the work function of the bottom-contact gold electrode can be decreased significantly by 1.0 eV, which makes it favorable to efficient electron injection. An Ohmic contact is achieved by the spontaneous injection of electrons to the n-type organic semiconductors with high electron affinity while converting the OFET operation mode to n-type characteristics by blocking the counter-charge carriers for the other types of ambipolar and p-type semiconductors. The solution-processed reducing agent can be a valuable approach to develop high-performance printed and flexible electronic devices through careful engineering to obtain proper contributions of charge carriers either as electrons or holes in various D-A copolymer semiconductors.
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http://dx.doi.org/10.1021/acsami.1c21864 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
Affiliated Hospital of Shandong Second Medical University, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.
Decades of antibiotic misuse have spurred an antimicrobial resistance crisis, creating an urgent demand for alternative treatment options. Although phototherapy has therapeutic potential, the efficacy of the most advanced photosensitizers (PS) is essentially limited by aggregation-induced quenching, which significantly reduces their therapeutic effect. To address these challenges, we developed a cationic metallocovalent organic framework (CRuP-COF) via a solvent-mediated dual-reaction synthesis strategy.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
School of Energy and Environment, Southeast University, Nanjing, 211189, China.
Two-dimensional covalent organic frameworks (2D COFs) have emerged as promising photocatalysts due to their high surface areas and precisely tunable physicochemical properties. However, it remains a significant challenge to precisely control over interlayer stacking configurations in 2D COFs, which critically influence charge carrier transport and consequently determine catalytic efficiency. In this study, we demonstrate a solvent-driven strategy to precisely regulate the interlayer stacking configurations of metal-incorporated 2D COFs, successfully achieving both AA eclipsed (COF-TD-AA) and ABC staggered (COF-TD-ABC) configurations.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2025
Nanotechnology Centre, School of Fashion and Textiles, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, PR China. Electronic address:
While the metal halide perovskite materials are emerging as potentially promising photocatalysts, they still suffer from the intrinsic instability, seriously hampering their further practical applications. In this study, a perovskite-based composite with a sandwich structure is first established to realize the encapsulation of individual octylamine-capped MAPbBr (OM-PE) quantum dots (QDs), and the Zeolitic Imidazolate Framework-67 (ZIF-67) isolates the individual OM-PE@PbBrOH QDs (2 nm) to preserve their unique optoelectronic properties while preventing degradation from environmental factors. The resulting sandwich composite was proved to be a staggered-gap heterostructure with a p-n junction, in which the PbBrOH layer acted as a water-resisting covering and ZIF-67 layer promoted the electron mobility.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2025
State Key Laboratory of Advanced Fiber Materials, Key Lab of Science and Technology of Eco-Textile, Ministry of Education, College of Chemistry and Chemical Engineering, Donghua University, Shanghai, 201620, China.
To achieve multi-state, visible-light-excited, long-wavelength thermally activated delayed fluorescence (TADF) with high emission efficiency within a single molecular dye system remains a significant challenge. Herein, we developed a series of V-shaped emitters comprising electron-deficient benzothiadiazole and electron-rich triphenylamine (TPA) or carbazole (Cz) units, featuring small singlet-triplet energy gaps. These molecules exhibit long-wavelength TADF emission and bright luminescence in both single-molecule and aggregate states.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemistry, University of Texas at Austin, Welch Hall 4.428, 105 E. 24th St. Stop A5300, Austin, Texas 78712-0165, United States.
A new triaryl arsine (ArAs)-based metal-organic framework (MOF) named AsCM-102 has been prepared by the reaction of As(CH-4-COH) with Co(BF) and 4,4'-bipyridine. AsCM-102 contains pairs of staggered As donors that function as chelators for the facile incorporation of organometallic Rh species via a single crystal-to-single crystal transformation. Coordination of Rh is achieved by soaking crystals in a solution of [Rh(CO)Cl] at 70 °C.
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