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Transparent, flexible MAPbI3 perovskite microwire array passivated with ultra-hydrophobic supramolecular assembly for stable and high-performance photodetectors
摘要： The emergence of organic-inorganic hybrid perovskites (OHPs) has revolutionised the potential performance of optoelectronic devices, most perovskites are opaque and hence incompatible with transparent optoelectronics, and sensitive to environmental degradation. Here, a single-step fabrication of ultra-long MAPbI3 perovskite microwire array over a large-area using stencil lithography based on a sequential vacuum sublimation. The environmental stability of MAPbI3 is empowered a newly designed and synthesized transparent supramolecular self-assembly, based on a mixture of two tripodal L-Phe-C11H23/C7F15 molecules, which showed a contact angle of 105° and served as ultra-hydrophobic passivation layer for more than 45 days in ambient atmosphere. The MAPbI3 microwire array passivated with supramolecular self-assembly demonstrate for the first time both excellent transparency of ~89% at 550 nm and remarkable photoresponse with photo-switching ratio of ~104, responsivity of 789 A/W, detectivity of 1014 Jones, linear dynamic range of ~ 122 dB, and rise time of 432 μs. Furthermore, the photodetector fabricated on flexible PET substrate demonstrated robust mechanical flexibility even beyond 1200 bending cycles. Therefore, the scalable stencil lithography and supramolecular passivation approaches have the potential to deliver next-generation transparent, flexible, and stable optoelectronics.
关键词： transparency,stencil lithography,photodetectors,MAPbI3,supramolecular self-assembly,flexibility,organic-inorganic hybrid perovskites,environmental stability
更新于2025-09-23 15:21:01
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Enhanced Ordering and Efficient Photoalignment of Nanostructures in Block Copolymers Enabled by Halogen Bond
摘要： Fabrication and manipulation of macroscopically ordered nanostructures in polymer ?lms via supramolecular self-organization are fascinating from the viewpoints of science and technology. Here, a halogen bond (XB) was introduced into a block copolymer to facilitate its microphase separation process upon XB-driven supramolecular self-assembly. To the best of our knowledge, this is an extremely rare example to elegantly maneuver nanostructures of polymers by the emerging supramolecular interaction, XB. The nonmesogenic block copolymer composed of poly(ethylene oxide) and azopyridine-containing polymethacrylate was transformed into a supramolecular liquid-crystalline polymer through the halogen-bonded interaction between 1,2-diiodo-3,4,5,6-tetra?uorobenzene and the azopyridine group with the optimal molar ratio of 1:1. For comparison, one hydrogen-bonded liquid-crystalline polymer was also fabricated but no such ordering enhancement was acquired, indicating that both the high directionality of XB and the resulting supramolecular mesogenic ordering played key roles in the enhanced ordering of nanostructures in polymer ?lms. In addition, e?cient photoalignment and photoreorientation of nanostructures coinciding with the oriented direction of the supramolecular mesogens were also obtained by manipulating photoirradiation of linearly polarized light for the present XB-involved liquid-crystalline block copolymer, which is promising for the development of a novel generation of advanced composite liquid crystal (LC) materials.
关键词： halogen bond,supramolecular self-assembly,photoalignment,block copolymer,nanostructures
更新于2025-09-23 15:19:57
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Physicala??Chemical Properties of Self-Assembled Structures in Solution of Zinc Phthalocyanine and Bis-3-pentyl-PTCDI Derivative
摘要： For the first time, in this work, we succeed in synthesizing in solution a novel supramolecular self-assembled zinc phthalocyanine (ZnPc) and N,N′-bis(3-pentyl)-perylene-3,4,9,10-bis(dicarboximide) (bis-3-pentyl-PTCDI) system with improved light absorption and phosphorescence lifetime of the charge separated states up to 2.5 ms. Moreover, the structural and optical properties of undoped and doped with iodine ZnPc thin films were investigated by X-ray diffraction, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Raman analysis, and UV?vis spectroscopy. Analysis of ZnPc:I2:bis-3-pentyl-PTCDI blend in a 2:1 ratio shows that sandwich complexes between them result in improved bulk properties as compared to those of the single-component systems.
关键词： light absorption,Fourier transform infrared spectroscopy,UV?vis spectroscopy,bis-3-pentyl-PTCDI,X-ray diffraction,supramolecular self-assembly,X-ray photoelectron spectroscopy,zinc phthalocyanine,phosphorescence lifetime,Raman analysis
更新于2025-09-23 15:19:57