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With the burgeoning of the microelectronics industry, in order to improve the transmission speed between chips in large-scale integrated circuits to meet the demands of high integration, it is necessary for interlayer insulation materials to possess a lower dielectric constant (k). Polyimide (PI) has been widely used as interlayer insulation materials for large-scale integrated circuits, and the exploration on reducing their dielectric constant has attracted extensive attention in recent years. In this work, porous PI-based composites with a low dielectric constant are mainly reviewed. The application of porous SiO2, graphene derivatives, polyoxometalates, polyhedral oligomeric silsesquioxane and hyperbranched polysiloxane in reducing the dielectric constant of PI is emphatically introduced. The key technical problems and challenges in the current research of porous polyimide materials are summarized, and the development prospect of low k polyimide is also expounded.
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Bismuth-based double perovskite Cs2AgBiBr6 shows promise as a photodetection material. However, its detection performance and application are limited by high-exciton binding energy and poor carrier mobility. In this study, we address these limitations by delicately designing a solution-based method for incorporating A-site Rubidium (Rb) substitution into Cs2AgBiBr6 double perovskite films. The introduction of Rb resulted in a significant decrease in trap defect density and an improvement in film quality. The trap-filled limit voltage (VTFL) of pure and Rb-doped CABB film is determined to be 1.71 V and 0.48 V, respectively. Subsequently, by introducing an ultrathin atomic-layer-deposited (ALD) TiO2 films, the fabricated CABB photodetectors exhibit significantly improved photoresponse performance. The response speed and -3dB bandwidth are boosted from â¼93 ms to â¼350 µs and broadened from 1.4 kHz to 17 kHz, respectively. Density Functional Theory (DFT) calculations indicate Rb-substitution shortens the bond length and weaken exciton binding energy. Furthermore, we demonstrate a wireless near ultraviolet (UV) light communication system using CABB photodetectors as light receivers. Our findings provide an efficient approach to utilize A-site cation substitution as a tuning parameter for photodetection in high-exciton binding energy perovskite materials, thereby extending the potential applications of other functional perovskites.
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There are two primary types of photoreceptor cells in the human eye: cone cells and rod cells that enable color vision and night vision, respectively. Herein, inspired by the function of human visual cells, we develop a high-resolution perovskite-based color camera using a set of narrowband red, green, blue, and broadband white perovskite photodetectors as imaging sensors. The narrowband red, green, and blue perovskite photodetectors with color perceptions mimic long-, medium-, and short-wavelength cones cells to achieve color imaging ability. Also, the broadband white perovskite photodetector with better detectivity mimics rod cells to improve weak-light imaging ability. Our perovskite-based camera, combined with predesigned pattern illumination and image reconstruction technology, is demonstrated with high-resolution color images (up to 256 × 256 pixels) in diffuse mode. This is far beyond previously reported advanced perovskite array image sensors that only work in monochrome transmission mode. This work shows a new approach to bio-inspired cameras and their great potential to strongly mimic the ability of the natural eye.
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Nickel sulfide based anode materials, featuring rich types, high specific capacities and favorable conversion kinetics, have been proved to be promisingly applied in high-performance sodium-ion batteries (SIBs). Unfortunately, the poor electronic/ionic conductivity, together with the structure change induced degraded capacity upon cycling, restricts their further development. In this work, heazlewoodite nanoparticles decorated on nitrogen doped reduced graphene oxide (Ni3S2/NrGO) were fabricated via a facile combined approach with freeze-drying and subsequent in-situ sulfidation. In the obtained hybrid structure, the synergistic effect between Ni3S2 and NrGO endows the composite with highly conductive pathways, thus accelerating the charge transfer. Benefitting from the buffering matrix offered by NrGO as well as the tight combination between Ni3S2 and NrGO, this novel Ni3S2/NrGO demonstrates satisfying sodium storage performance, with a stable reversible capacity of 299.2 mAh g-1 up to 100 cycles (0.1 A g-1) and a high initial Coulombic efficiency of 76.8%. Importantly, the rational structure design and synthesis method, as well as the insights on the improved electrochemical performance reported in this work, should be helpful for the development of new-type host materials with high performance for SIBs.
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The development of battery systems with high specific capacity and power density could fuel various energy-related applications from personal electronics to grid storage. (Fe2.5Ti0.5)1.04O4 possessing high theoretical specific capacity has been considered as a promising high rate anode material for lithium ion batteries due to the replacement of Fe3+ (0.64 Å) by Ti4+ (0.68 Å) with a larger radius to expand the interlayer space for ion intercalation. However, its extreme volume variation upon cycling as well as poor electrical conductivity hinder its further application. To tackle the above problems, in this work, we successfully synthesized two-dimensional (2D) (Fe2.5Ti0.5)1.04O4/C/MXene architecture derived from Ti3C2Tx MXene via solvo-hydrothermal, ultrasound hybridizing and high temperature annealing processes. The (Fe2.5Ti0.5)1.04O4/C/MXene shows a high discharge capacity of 757.2 mAh g-1 after 800 cycles at a current density of 3 A g-1 with excellent rate performance. The superior electrochemical performances are triggered primarily by the incorporation of carbon and MXene into (Fe2.5Ti0.5)1.04O4 moiety to construct a 2D layered structure, which can improve the ion diffusion and electron transport. In addition, the synergistic contributions from diffusion controlled and capacitive processes for (Fe2.5Ti0.5)1.04O4/C/MXene improve the ion diffusion rate and offer high specific capacity at high current density. The MXene-derived synthesis strategy in this work should be a promising pathway to synthesize other anode materials with 2D layered architecture for high performance lithium storage.
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Supercapacitors, also known as electrochemical capacitors, are attracting much research attention owing to their high power density, long-term cycling stability, as well as exceptional safety compared with rechargeable batteries, although the globally accepted quantitative benchmarks on the power density, cycling stability, and safety are yet to be established. However, it should be noted that the supercapacitors generally exhibit low energy density, which cannot satisfy the demands where both high energy density and power density are needed. To date, various methods have been employed to improve the electrochemical performances of supercapacitors. Among them, introducing redox additives (or redox mediators) into conventional aqueous electrolyte is regarded as one of the most promising strategies. The redox additives in aqueous electrolyte are widely demonstrated to be able to increase the charge storage capability via redox transformation and thus enhance the electrochemical performances. Herein, we present a brief review on the classification, state-of-the-art progress, challenges, and perspectives of the redox additives in aqueous electrolyte for high performance supercapacitors.
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Carbon microspheres (CSs) were successfully fabricated and used as counter electrodes of dye-sensitized solar cells (DSSCs). CSs were obtained through a fast microwave-assisted approach using sucrose as the precursor in a microwave system and subsequent thermal treatment at 600, 800 and 1000°C. A maximum photovoltaic conversion efficiency of 5.5% is achieved for DSSCs based on the CSs counter electrodes, which is comparable to the cell based on conventional Pt counter electrode at one sun (AM 1.5 G, 100 mW cm(-2)). The results suggest the CSs to be a potential candidate for counter electrodes of DSSCs.
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Long afterglow Sr4Al14O25:Eu,Dy phosphors were introduced into the TiO2 photoanode of CdS quantum dot-sensitized solar cells (QDSSCs) as both a scattering and down converting layer, and the photovoltaic performances of the cells were investigated. The results show that the cell with Sr4Al14O25:Eu,Dy achieves a power conversion efficiency of 1.40%, which is an increase of 38% compared to the cell without Sr4Al14O25:Eu,Dy (1.02%). The performance improvement is attributed to enhanced light harvesting via improved light absorption and scattering processes. After a single sun illumination for 1 min and subsequent removal of the light source, the cell with Sr4Al14O25:Eu,Dy could be driven even in the dark by the long persistent light from Sr4Al14O25:Eu,Dy.
RESUMEN
CdSe quantum dot-sensitized solar cells based on an efficient bifunctional structured layer composed of long afterglow SrAl2O4:Eu,Dy phosphors on top of a transparent layer of nanocrystalline TiO2 were fabricated and their photovoltaic performances were investigated. The results show that a high power conversion efficiency of 1.22% is achieved for the cell with SrAl2O4:Eu,Dy at one sun illumination (AM 1.5 G, 100 mW cm(-2)), which is an increase of 48% compared to the cell without SrAl2O4:Eu,Dy (0.82%). After one sun illumination for 1 min and subsequent turn off of the light source, the cell with SrAl2O4:Eu,Dy still shows an efficiency of 0.04% under dark condition due to the irradiation by the long persistent light from SrAl2O4:Eu,Dy. The present strategy should provide a possibility to fulfill the operation of solar cells even in the dark.
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A reduced graphene (RG)-Au nanoparticle composite film is successfully fabricated by electrophoretic deposition and used as counter electrode for quantum dot-sensitized solar cells. The RG-Au composite is prepared by one-step microwave-assisted reduction of chloroaurate in alkaline solution with graphite oxide dispersion. Under one sun illumination (AM 1.5 G, 100 mW cm(-2)), the cell with a RG-Au counter electrode shows an energy conversion efficiency of 1.36 %, which is higher than those of cells employing conventional Pt or Au counter electrodes, due to the superior combination of highly catalytic Au nanoparticles and the conductive graphene network structure.
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Y(3)Al(5)O(12):Ce phosphors have been prepared and used as an effective scattering layer on top of a transparent layer of nanocrystalline TiO(2) for dye sensitized solar cells (DSSCs). The Y(3)Al(5)O(12):Ce scattering layer increases the photocurrent of DSSCs due to the enhanced light harvesting mainly via the improved light absorption and scattering. Under one sun illumination (AM 1.5G, 100 mW cm(-2)), a high efficiency of 7.91% was achieved for the cell with a Y(3)Al(5)O(12):Ce scattering layer, which is an increase of 13.5% compared to the cell without a scattering layer (6.97%).
