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Flexible and Ultrasensitive Piezoelectric Composites Based on Highly (00l)‐Assembled BaTiO <sub/>3</sub> Microplatelets for Wearable Electronics Application
摘要： Piezoelectric wearable electronics with flexibility and high sensitivity have received increasing attention in the fields of health monitoring, flexible robots, and artificial intelligence. Here, a flexible organic–inorganic hybrid composite for wearable electronics application based on (00l)-aligned BaTiO3 (BT) single-crystal microplatelets is prepared by layer-by-layer self-assembly technology. For the polyvinylidene fluoride-trifluoroethylene (P(VDF-TrFE))/BT single-crystal microplatelets composite film, the sensitivity is nearly 20 times higher than that of its counterparts of P(VDF-TrFE)/BT microparticles composite film and pure P(VDF-TrFE) film. The orderly alignment of BT microplatelets also has been found advantageous to the strength of the composite film. The tensile strength is up to 204.3 MPa even at a high inorganic phase content of 53.8 wt% in P(VDF-TrFE)/BT single-crystal microplatelets composite film, which is four times that of pure P(VDF-TrFE) film. Moreover, the flexible piezoelectric wearable device based on P(VDF-TrFE)/BT single-crystal microplatelets film effectively provides detailed information for monitoring human activities such as pronunciation, frequency, and waveform of pulse beating, and motion states. This high sensitivity, high strength, and flexible piezoelectric composite provides much potential on the applications of wearable equipments and health monitoring devices.
关键词： organic–inorganic hybrids,wearable sensors,flexible piezoelectric composites,BaTiO3
更新于2025-11-21 11:01:37
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Laser-induced synthesis and photocatalytic properties of hybrid organic–inorganic composite layers
摘要： A laser-based method was developed for the synthesis and simultaneous deposition of multicomponent hybrid thin layers consisting of nanoentities, graphene oxide (GO) platelets, transition metal oxide nanoparticles, urea, and graphitic carbon nitride (g-C3N4) for environmental applications. The photocatalytic properties of the layers were tested through the degradation of methyl orange organic dye probing molecule. It was further demonstrated that the synthesized hybrid compounds are suitable for the photodegradation of chloramphenicol, a widely used broad-spectrum antibiotic, active against Gram-positive and Gram-negative bacteria. However, released in aquatic media represents a serious environmental hazard, especially owing to the formation of antibiotic-resistant bacteria. The obtained results revealed that organic, urea molecules can become an alternative to noble metals co-catalysts, promoting the separation and transfer of photoinduced charge carriers in catalytic composite systems. Laser radiation induces the reduction of GO platelets and the formation of graphene-like material. During the same synthesis process, g-C3N4 was produced, by laser pyrolysis of urea molecules, without any additional heat treatment. The layers exhibit high photocatalytic activity, being a promising material for photodegradation of organic pollutants in wastewater.
关键词： transition metal oxide nanoparticles,urea,photocatalytic properties,hybrid organic–inorganic composite layers,graphene oxide,graphitic carbon nitride,methyl orange,laser-based synthesis,chloramphenicol
更新于2025-11-14 17:04:02
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A molecular-based design of RGO/TiO2-PAM composite flocculant with photocatalytic self-degrading characteristics and the application of the oil sand tailings flocculant
摘要： Polymer flocculation technology has a very broad application in the flocculation industry of oil sand tailings at present. Nevertheless, the most commonly used commercial polyacrylamide flocculant has problems of low flocculation efficiency and secondary pollution. In this paper, we proposed an organic-inorganic composite flocculant with self-degrading properties for the flocculation treatment of oil sand tailings, which was prepared by photocatalytic surface initiation technique. Further, the functional groups of the materials before and after polymerization composites were characterized by infrared spectrum to explore the polymerization mechanism, the structure was observed by transmission electron microscope, and the molecular weight of polyacrylamide was measured by gel permeation chromatography. Then, the flocculation performance was characterized by the flocculation experiment (tested with simulated oil sand tailings). Subsequently, the flocculation mechanism was explored by testing the zeta potential of the organic-inorganic composites and analyzing images of sediment observed by transmission electron microscope and atomic force microscope. Finally, the test of self-degradation performance was carried out under illumination. Based on the above experiments, the following conclusions were obtained. First, the structural characterization results indicate the polymerization mechanism is that under the condition of light, the surface of the inorganic photocatalyst generates free radicals to initiate the radical polymerization of the monomers, so that the monomers successfully grow on the surface of the inorganic particles into comb structure. And then, the flocculation experiment shows that reduced graphene oxide/titanium dioxide-polyacrylamide(2:40) has the best flocculation effect, of which the supernatant transmittance is 21.4 higher and the sedimentation ratio is 8.9% higher than those of the commercial polyacrylamide. The reason for its excellent flocculation performance is that the zeta potential of the organic-inorganic composite increases, reducing repulsion of particles and flocculant molecules, simultaneously, the formed comb structure is beneficial to the expansion of the polymer chain and increases the contact area, thereby improving the flocculation effect. Ultimately, the degradation results indicates that the new organic-inorganic composite had good degradation effect, with the degradation rate up to 75.9% within 4 hours. Therefore, this work has made great contributions to solving the oil sand tailings pollution field.
关键词： Flocculant,Oil sand tailings,Photocatalytic Self-degrading,Organic-inorganic composite,Comb structure
更新于2025-11-14 17:03:37
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Enhanced visible-light-driven photocatalytic activity of BiFeO3 via electric-field control of spontaneous polarization
摘要： Well-polarized BiFeO3 nanoparticles have been successfully prepared by a facile electrical poling method with the assist of a soluble organic-inorganic composite film. From XRD, TEM and SEM studies, no significant change in the crystal structure or morphology was detected after the electrical poling process. The visible-light driven photocatalytic process of poled BiFeO3 nanoparticles was accelerated by 2 times compared to unpoled BiFeO3. By combining time-resolved photoluminescence (PL), photoinduced silver deposition testing and photoelectrochemical measurements, it can be revealed that the enhanced photocatalytic performance of poled samples can be properly attributed to the promoted separation and prolonged lifetime of the photogenerated carriers caused by the ferroelectric polarization. These findings may offer a new route to promote the photocatalytic or photoelectric performances of BiFeO3 for advanced applications by adjusting the ferroelectric polarization.
关键词： BiFeO3 nanoparticles,Organic-inorganic composite film,Ferroelectric polarization,Electrical poling technology,Photocatalytic activity
更新于2025-11-14 15:24:45
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Mechanism of photoluminescence intermittency in organic-inorganic perovskite nanocrystals
摘要： Lead halide perovskite nanocrystals have demonstrated their potential as active materials for optoelectronic applications over the past few years. Nevertheless one issue which hampers their applicability has to do with the observation of photoluminescence intermittency, commonly referred to as blinking, as in their inorganic counterparts. Such behavior, reported for structures well above the quantum confinement regime, has been discussed to be strongly related with the presence of charge carrier traps. In this work we analyze the characteristics of this intermittency and explore the dependence with the surrounding atmosphere, showing evidence for the critical role played by the presence of oxygen. We discuss a possible mechanism in which a constant creation/annihilation of halide-related carrier traps takes place under light irradiation, the dominant rate being determined by the atmosphere.
关键词： photoluminescence,Hybrid organic inorganic perovskites,spectroscopy,nanocrystal,blinking
更新于2025-09-23 15:23:52
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Sustainable Liquid Luminescent Solar Concentrators
摘要： Luminescent solar concentrators (LSCs) are photovoltaic (PV) complementary devices to overcome the mismatch between the Si-based PV cells, response and the solar spectrum, allowing PV urban integration. Challenges for the luminescent layer include the use of abundant and sustainable natural organic molecules. Here, LSCs composed of a glass container and based on bundles of cylindrical hollow-core plastic optical fibers filled with aqueous solutions of R-phycoerythrin (R-PE), extracted from Gracilaria sp. algae are presented. The R-PE solutions absorb in the UV/visible spectral range (300–550 nm) and convert this radiation into red-emission (550–700 nm) with a maximum absolute quantum yield of ≈0.39. In this work, LSCs with distinct geometries are reported, in which the R-PE emission yields optical conversion efficiency values up to ≈6.88% and ≈4.74% for a planar device and for a bundle of cylindrical LSCs, respectively, which are the largest values known for liquid-based LCSs using sustainable emitting centres. Moreover, the coupling of the LSCs to commercial Si-based PV devices yields power conversion efficiency values of ≈0.27% (planar) and ≈23.03 × 10?3%, (bundle). These values illustrate the potential of this approach for the development of natural-based LSCs meeting the requirements of reliable, sustainable, and competitive energy systems.
关键词： sustainability,organic–inorganic hybrids,luminescent solar concentrators,R-phycoerythrin,natural optically active center,bundles
更新于2025-09-23 15:23:52
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Super photo-base initiated organic-inorganic hybrid coatings by plural-cure mechanisms
摘要： Free-radical polymerization forms the core chemistry of a majority of commercial UV-curable coating system today. Rapid curing at ambient temperature using stable, single component coating systems form the key value proposition that such coating systems offer. However, owing to their limitations such as oxygen inhibition, volume shrinkage, toxicity profiles of reactive diluents (RD), and the limited chemistry available, efforts are being made to counter these challenges by innovating and exploring new systems that have the potential to replace the existing chemistries. Anionic polymerization is one such promising area that has the potential to introduce a wide variety of chemistries in the field of UV-curable coatings. A significant stride in this field has been the innovation of photo-labile bases in the UV industry and the diverse chemistries that these bases have brought to fore. The primary focus of the present study is use of a super photo-base generator (PBG) in catalyzing concomitant but independent reactions to develop organic-inorganic hybrid (OIH) coating networks by leveraging plural-cure chemistry. The super PBG has been used to initiate both Michael-addition (MA) reaction and sol-gel reaction concurrently, upon exposure to the UV source. Coatings have been formulated using uniquely designed acrylate functional oligomers (MA-acceptor), acetoacetate functional reactive diluents (MA-donors) and organo-silanes (sol-gel precursors), besides super PBG. The study highlights many technical and environmental benefits of these OIH coatings with potential for applications in advanced coatings and additive manufacturing.
关键词： Reactive diluent,Super photo-base,Organic-inorganic hybrid,Michael-Addition
更新于2025-09-23 15:23:52
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Broadband Emission in Hybrid Organic–Inorganic Halides of Group 12 Metals
摘要： We report syntheses, crystal and electronic structures, and characterization of three new hybrid organic?inorganic halides (R)ZnBr3(DMSO), (R)2CdBr4·DMSO, and (R)CdI3(DMSO) (where (R) = C6(CH3)5CH2N(CH3)3, and DMSO = dimethyl sulfoxide). The compounds can be conveniently prepared as single crystals and bulk polycrystalline powders using a DMSO?methanol solvent system. On the basis of the single-crystal X-ray diffraction results carried out at room temperature and 100 K, all compounds have zero-dimensional (0D) crystal structures featuring alternating layers of bulky organic cations and molecular inorganic anions based on a tetrahedral coordination around group 12 metal cations. The presence of discrete molecular building blocks in the 0D structures results in localized charges and tunable room-temperature light emission, including white light for (R)ZnBr3(DMSO), bluish-white light for (R)2CdBr4·DMSO, and green for (R)CdI3(DMSO). The highest photoluminescence quantum yield (PLQY) value of 3.07% was measured for (R)ZnBr3(DMSO), which emits cold white light based on the calculated correlated color temperature (CCT) of 11,044 K. All compounds exhibit fast photoluminescence lifetimes on the timescale of tens of nanoseconds, consistent with the fast luminescence decay observed in π-conjugated organic molecules. Temperature dependence photoluminescence study showed the appearance of additional peaks around 550 nm, resulting from the organic salt emission. Density functional theory calculations show that the incorporation of both the low-gap aromatic molecule R and the relatively electropositive Zn and Cd metals can lead to exciton localization at the aromatic molecular cations, which act as luminescence centers.
关键词： zero-dimensional structures,broadband emission,group 12 metals,exciton localization,photoluminescence quantum yield,hybrid organic?inorganic halides
更新于2025-09-23 15:23:52
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Comprehensive Understanding and Controlling the Defect Structures: An Effective Approach for Organic-Inorganic Hybrid Perovskite-Based Solar-Cell Application
摘要： Understanding the defect structure in organic-inorganic hybrid perovskite material (OHP) is a crucial role to explain several physical properties such as material stability, energy band, carrier mobility, and so on. In the solar-cell applications using OHP, finding, understanding, and controlling defects is essential to making a more advanced device with high efficiency and stability. Naturally, we need to find, understand, and control the possible defects in OHP. However, the defect research field in OHP material is just beginning now. In this short review, we will explore the kinds of defects and their effects on OHP.
关键词： molecular defect,organic-inorganic hybrid perovskite,Schottky/Frankel defect,vacancy,delocalized defect,thin film,defect,solar-cell
更新于2025-09-23 15:21:21
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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