Electrochromic (EC) technology can adjust optical properties under electrical stimulation with broad applications in smart windows, displays, and camouflage. However, significant challenges remain in developing inorganic EC films with high durability, rapid response, and mechanical flexibility due to intrinsic brittleness and dense microstructure. Herein, a nanostructured quasiplanar heterointerface (Q-PHI) is first introduced into the electrode/EC interlayer to realize a robust, ultrafast switching tungsten trioxide (WO) EC film. The 200 nm-thick Q-PHI WO film exhibits remarkable EC performance, including large optical contrast (81.8% and 83.4% at 700 and 1500 nm), ultrafast switching of 2.4 and 1.8 s, and excellent stability (10,000 cycles with 21.3% optical-contrast loss). A large-area (20 × 15 cm) flexible EC smart window is also successfully achieved. The mechanism lies in the intense built-in electric field and strong interfacial bonding induced by the Q-PHI with unique longitudinal gradient distribution, greatly enhancing the electron/ion transport kinetics, surface ion adsorption, and durability.
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http://dx.doi.org/10.1021/acs.nanolett.4c05696 | DOI Listing |
Nano Lett
January 2025
Key Laboratory of Luminescence Science and Technology, Chinese Academy of Sciences & State Key Laboratory of Luminescence Science and Applications, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun 130033, China.
Electrochromic (EC) technology can adjust optical properties under electrical stimulation with broad applications in smart windows, displays, and camouflage. However, significant challenges remain in developing inorganic EC films with high durability, rapid response, and mechanical flexibility due to intrinsic brittleness and dense microstructure. Herein, a nanostructured quasiplanar heterointerface (Q-PHI) is first introduced into the electrode/EC interlayer to realize a robust, ultrafast switching tungsten trioxide (WO) EC film.
View Article and Find Full Text PDFPhys Rev Lett
December 2024
University of Strathclyde, Institute of Photonics, SUPA Dept of Physics, Glasgow, United Kingdom.
We report a spiking flip-flop memory mechanism that allows controllably switching between neural-like excitable spike-firing and quiescent dynamics in a resonant tunneling diode (RTD) neuron under low-amplitude (<150 mV pulses) and high-speed (ns rate) inputs pulses. We also show that the timing of the set-reset input pulses is critical to elicit switching responses between spiking and quiescent regimes in the system. The demonstrated flip-flop spiking memory, in which spiking regimes can be controllably excited, stored, and inhibited in RTD neurons via specific low-amplitude, high-speed signals (delivered at proper time instants) offers high promise for RTD-based spiking neural networks, with the potential to be extended further to optoelectronic implementations where RTD neurons and RTD memory elements are deployed alongside for fast and efficient photonic-electronic neuromorphic computing and artificial intelligence hardware.
View Article and Find Full Text PDFMetal halide perovskites have unique luminescent properties that make them an attractive alternative for high quality light-emitting devices. However, the poor stability of perovskites with many defects and the long cycle time for the preparation of perovskite nanocomposites have hindered their production and application. Here, we prepared the perovskite mesostructures by embedding MAPbBr nanocrystals in the mesopores on the surface of silica nanospheres and mixing the nanospheres with silver nanowires and poly(methyl methacrylate) (PMMA), and further explored their optical properties.
View Article and Find Full Text PDFEpsilon-near-zero (ENZ) materials, i.e., materials with a vanishing real part of the permittivity, have become an increasingly desirable platform for exploring linear and nonlinear optical phenomena in nanophotonic and on-chip environments.
View Article and Find Full Text PDFChem Sci
January 2025
Department of Chemistry, The University of Adelaide Adelaide South Australia 5005 Australia
Singlet fission (SF) is a process that is potentially beneficial for photovoltaics by producing two triplet excitons from a single photon, but its application is often hindered by the inability to effectively separate the resultant triplet excitons. It has been proposed that an energy gradient can assist in separating triplet excitons through triplet energy transfer between chromophores of different triplet energies, but this approach has only been studied in solution and the efficacy of this strategy in the solid state is under explored. Here, we investigate energy-gradient-driven SF in a disordered solid state, in the form of suspensions of 5,12-bis(triisopropylsilylethnyl)tetracene:6,13-bis(triisopropylsilylethnyl)pentance (TIPS-Tn:TIPS-Pn) blend nanoparticles (NPs).
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