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High-quality-factor microring resonators are highly desirable in many applications. Fabricating a microring resonator typically requires delicate instruments to ensure a smooth side wall of waveguides and 100-nm critical feature size in the coupling region. In this work, we demonstrate a new method "damascene soft nanoimprinting lithography" that can create high-fidelity waveguide by simply backfill an imprinted cladding template with a high refractive index polymer core. This method can easily realize high Q-factor polymer microring resonators (e.g., ~5 x 105 around 770 nm wavelength) without the use of any expensive instruments and can be conducted in a normal lab environment. The high Q-factors can be attributed to the residual layer-free feature and controllable meniscus cross-section profile of the filled polymer core. Furthermore, the new method is compatible with different polymers, yields low fabrication defects, enables new functionalities, and allows flexible substrate. These benefits can broaden the applicability of the fabricated microring resonator.
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Printed electronics have made remarkable progress in recent years and inkjet printing (IJP) has emerged as one of the leading methods for fabricating printed electronic devices. However, challenges such as nozzle clogging, and strict ink formulation constraints have limited their widespread use. To address this issue, a novel nozzle-free printing technology is explored, which is enabled by laser-generated focused ultrasound, as a potential alternative printing modality called Shock-wave Jet Printing (SJP). Specifically, the performance of SJP-printed and IJP-printed bottom-gated carbon nanotube (CNT) thin film transistors (TFTs) is compared. While IJP required ten print passes to achieve fully functional devices with channel dimensions ranging from tens to hundreds of micrometers, SJP achieved comparable performance with just a single pass. For optimized devices, SJP demonstrated six times higher maximum mobility than IJP-printed devices. Furthermore, the advantages of nozzle-free printing are evident, as SJP successfully printed stored and unsonicated inks, delivering moderate electrical performance, whereas IJP suffered from nozzle clogging due to CNT agglomeration. Moreover, SJP can print significantly longer CNTs, spanning the entire range of tube lengths of commercially available CNT ink. The findings from this study contribute to the advancement of nanomaterial printing, ink formulation, and the development of cost-effective printable electronics.
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Decorative chrome plating (DCP) continues to be ubiquitous in creating highly appealing metal finishings and coatings, beating out other organic dye-based finishes. However, the hazardous chrome plating process is fraught with adverse health effects for the workers involved and causes significant environmental damage. In this work, we present a multilayer thin film structure to mimic the chrome appearance. To find a design efficiently, we employ a reinforcement learning (RL) algorithm to perform an automatic inverse design. This results in structures composed of environmentally friendly materials that not only have the chrome color but can also achieve additional functions beyond decoration. As an example, one structure is designed to have high transmission in the radio frequency regime, a property that general metals cannot have, which can broaden the decorative chrome applications to include microwave operating devices. The experimental structures are fabricated by physical vapor deposition to demonstrate the indistinguishable chrome color and validate the effectiveness of the RL inverse design approach.
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The increasing demand for cost-efficient and user-friendly wearable electronic devices has led to the development of stretchable electronics that are both cost-effective and capable of maintaining sustained adhesion and electrical performance under duress. This study reports on a novel physically crosslinked poly(vinyl alcohol) (PVA)-based hydrogel that serves as a transparent, strain-sensing skin adhesive for motion monitoring. By incorporating Zn2+ into the ice-templated PVA gel, a densified amorphous structure is observed through optical and scanning electron microscopy, and it is found that the material can stretch up to 800% strain according to tensile tests. Fabrication in a binary glycerol:water solvent results in electrical resistance in the kΩ range, a gauge factor of 0.84, and ionic conductivity on the scale of 10-4 S cm-1 , making it a potentially low-cost candidate for a stretchable electronic material. This study characterizes the relationship between improved electrical performance and polymer-polymer interactions through spectroscopic techniques, which play a role in the transport of ionic species through the material.
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Álcool de Polivinil , Dispositivos Eletrônicos Vestíveis , Polímeros , Movimento (Física) , Condutividade Elétrica , Hidrogéis/química , ÍonsRESUMO
Polymers with broad infrared emission and negligible solar absorption have been identified as promising radiative cooling materials to offer a sustainable and energy-saving venue. Although practical applications desire color for visual appearance, the current coloration strategies of polymer-based radiative cooling materials are constrained by material, cost, and scalability. Here, we demonstrate a universally applicable coloration strategy for polymer-based radiative cooling materials by nanoimprinting. By modulating light interference with periodic structures on polymer surfaces, specular colors can be induced while maintaining the hemispheric optical responses of radiative cooling polymers. The retrofit strategy is exemplified by four different polymer films with a minimum impact on optical responses compared to the pristine films. Polymer films feature low solar absorption of 1.7-3.7%, and daytime sub-ambient cooling is exemplified in the field test. The durability of radiative cooling and color are further validated by dynamic spectral analysis. Finally, the potential roll-to-roll manufacturing empowers a scalable, low-cost, and easy-retrofitting solution for colored radiative cooling films.
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Mechanical energy harvesting by piezoelectric materials to drive catalysis reactions received extensive attention for environmental remediation. In this work, SbSI/Sb2S3 nanocomposites were synthesized as a catalyst. ZrO2 balls were used as an alternative mechanical force to ultrasonic for stimulating the piezocatalyst for the first time. The kinetics and thermodynamics of the piezo degradation of methylene blue (MB) were studied deeply. Besides the effect of the type of mechanical force, the number of ZrO2 balls, and temperature of the reaction on the degradation efficiency were studied. Here mechanical energy came from the collision of the ZrO2 balls with the catalyst particles. Using ZrO2 balls instead of ultrasonic vibration led to enhance degradation efficiency by 47% at 30 ± 5 °C. A kinetic study revealed that piezo degradation of methylene blue (MB) by SbSI/Sb2S3 catalyst followed pseudo-second-order kinetics. Based on thermodynamic results piezo degradation of MB was an exothermic reaction.
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We demonstrate tunable structural color patterns that span the visible spectrum using atomic layer deposition (ALD). Asymmetric metal-dielectric-metal structures were sequentially deposited with nickel, zinc oxide, and a thin copper layer to form an optical cavity. The color response was precisely adjusted by tuning the zinc oxide (ZnO) thickness using ALD, which was consistent with model predictions. Owing to the conformal nature of ALD, this allows for uniform and tunable coloration of non-planar three-dimensional (3D) objects, as exemplified by adding color to 3D-printed parts produced by metal additive manufacturing. Proper choice of inorganic layered structures and materials allows the structural color to be stable at elevated temperatures, in contrast to traditional paints. To print multiple colors on a single sample, polymer inhibitors were patterned in a desired geometry using electrohydrodynamic jet (e-jet) printing, followed by area-selective ALD in the unpassivated regions. The ability to achieve 3D color printing, both at the micro- and macroscales, provides a new pathway to tune the optical and aesthetic properties during additive manufacturing.
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Designing optical structures for generating structural colors is challenging because of the complex relationship between the optical structures and the color perceived by human eyes. Machine learning-based approaches have been developed to expedite this design process. However, existing methods solely focus on structural parameters of the optical design, which could lead to suboptimal color generation because of the inability to optimize the selection of materials. To address this issue, an approach known as Neural Particle Swarm Optimization is proposed in this paper. The proposed method achieves high design accuracy and efficiency on two structural color design tasks; the first task is designing environment-friendly alternatives to chrome coatings, and the second task concerns reconstructing pictures with multilayer optical thin films. Several designs that could replace chrome coatings have been discovered; pictures with more than 200,000 pixels and thousands of unique colors can be accurately reconstructed in a few hours.
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Recent decades have witnessed flourishing prosperity of III-nitride emitters in solid-state lighting and high-resolution displays. As one of the widely used substrates, sapphire shows superiority for heteroepitaxial growth of III-nitride light-emitting diode (LED) structure, due to the advantages of stability, low cost, high mechanical strength, as well as mature fabrication technology. However, realization of efficient LEDs grown on sapphire substrate is impeded by high density of defects in epilayers and low light extraction efficiency. The emergence of patterned sapphire substrate (PSS) turns out to be a promising and effective technology to overcome these problems and enhance the LED performances. In this review, we first introduce the background and recent advances of PSS applied in III-nitride visible and ultraviolet LEDs are. Then, we summarize the fabrication methods of PSS, together with novel methods to define nanometre-scale patterned structures. We further demonstrate the effect of PSS that contributes to reduce the threading dislocation density (TDD) of epilayers in detail. Meanwhile, mechanism of light extraction efficiency enhancement by adopting PSS is presented based on numerical analysis. Next, we explore the influence of PSS structural parameters (e.g. pattern size, pattern shape and aspect ratio) on LED performances, spanning from visible to deep ultraviolet UV emission region. Finally, challenges and potential prospects in PSS for future LED development are proposed and forecasted as well.
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With increasing demands and interest in flexible and foldable devices, much effort has been devoted to the development of flexible transparent electrodes. An in-depth understanding of failure mechanisms in nanoscale structure is crucial in developing stable, flexible electronics with long-term durability. The present work investigated the mechanoelectric characteristics of transparent conductive electrodes in the form of dielectric/metal/dielectric (DMD) sandwich structures under bending, including one time and repeated cyclic bending test, and provides an explanation of their failure mechanism. We demonstrate how a thin metallic layer helps to enhance the mechanical robustness of the DMD as compared with that without, tune the mechanical properties of the cohesive layer, and improve the electrode fracture resistance. Abnormal crack propagation and toughening of multilayer DMD structures are analyzed, and its underlying mechanisms are explained. We consider the knowledge of the failure mechanisms of transparent conductive electrodes gained from the present study as a foundation for future design improvements.
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High-quality transparent conductive materials are beneficial to improve the charge transfer and light transmittance and reduce the interface defects as well as the production cost of optoelectronic devices. A high threshold thickness of metal layer in oxide/metal/oxide (OMO) compound thin films leads to strong reflectance, especially in the near-infrared region, limiting the broad-spectrum device applications. Here, we propose a novel Zn doping strategy using the low-cost single-target sputtering technology to achieve the growth of Ag-Zn thin films (i.e., Zn-doped Ag) and introduce a trace amount of O2 to further obtain ultrathin Ag-Zn(O) films (thin-film thickness d ≤ 5 nm), which greatly improves the broad-spectrum characteristics of OMO films. Heterogeneous metal and gas doping technology effectively promotes the formation of two-dimensional continuous film growth. By combining the ultrathin Ag-Zn(O) layer with the MGZO (i.e., Mg- and Ga co-doped ZnO) oxide film grown by reactive plasma deposition, a typical broad-spectrum MGZO/Ag-Zn(O)/MGZO (50/5/50 nm)-OMO compound thin film exhibits an average transmittance of 91.6% in the wavelength range of 400-1200 nm and low sheet resistance. The broad-spectrum organic solar cells based on MGZO/Ag-Zn(O)/MGZO electrodes present a high power conversion efficiency of 15.35%, superior to those devices based on single-layer oxide electrodes. The distinguished performances are attributed to the ultrathin Ag-Zn(O) films in OMO, paving the way for applications in broad-spectrum optoelectronic and flexible electronic devices.
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We have developed a single-step, high-throughput methodology to selectively confine sub-micrometer particles of a specific size into sequentially inscribed nanovoid patterns by utilizing electrostatic and entropic particle-void interactions in an ionic solution. The nanovoid patterns can be rendered positively charged by coating with an aluminum oxide layer, which can then localize negatively charged particles of a specific size into ordered arrays defined by the nanovoid topography. On the basis of the Poisson-Boltzmann model, the size-selective localization of particles in the voids is directed by the interplay between particle-nanovoid geometry, electrostatic interactions, and ionic entropy change induced by charge regulation in the electrical double layer overlapping region. The underlying principle and developed method could potentially be extended to size-selective trapping, separation, and patterning of many other objects including biological structures.
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Ring resonators are well-known optical biosensors thanks to their relatively high Q-factor and sensitivity, in addition to their potential to be fabricated in large arrays with a small footprint. Here, we investigated the characteristics of a polymer ring resonator with a partially tapered waveguide for Biomedical Sensing. The goal is to develop a more sensitive biosensor with an improved figure of merit. The concept is more significant field interaction with the sample under test in tapered segments. Waveguide width is hereby gradually reduced to half. Sensitivity improves from 84.6 to 101.74 [nm/RIU] in a relatively small Q-factor reduction from 4.60 × 103 for a strip waveguide to 4.36 × 103 for a π/4 partially tapered one. After the study, the number of tapered parts from zero to fifteen, the obtained figure of merit improves from 497 for a strip ring to 565 for a π/4 tapered ring close to six tapered ones. Considering the fabrication process, the three-tapered one is suggested. The all-polymer material device provides advantages of a low-cost, disposable biosensor with roll-to-roll fabrication compatibility. This design can also be applied on silicon on isolator, or polymer on silicon-based devices, thereby taking advantage of a higher Q-factor and greater sensitivity.
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Técnicas Biossensoriais , Dispositivos Ópticos , Polímeros , Refratometria , SilícioRESUMO
Conventional waveguide mode decoupling methods for organic light-emitting diodes (OLEDs) are typically not scalable and increase fabrication complexity/cost. Indium-tin-oxide-free transparent anode technologies showed efficiency improvement without affecting other device properties. However, previous works lack rigorous analysis to understand the efficiency improvement. Here, we introduced an ultrathin silver (Ag) film as transparent electrode and conducted systematic modal analysis of OLEDs and report that waveguide mode can be completely eliminated by designing an OLED structure that is below the cutoff thickness of waveguide modes. We also experimentally verified the waveguide mode removal in organic waveguides with the help of index-matching fluid and prism. The negative permittivity, extremely thin thickness (~5 nanometers), and highly conductive properties achieved by a uniform copper-seeded Ag film can suppress waveguide mode formation, enhancing external quantum efficiency without compromising any other characteristics of OLEDs, which paves the way for cost-effective high-efficiency OLEDs in current display industry.
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Glasses-free three-dimensional (3D) display is considered as a potential disruptive technology for display. The issue of visual fatigue, mainly caused by the inaccurate phase reconstruction in terms of image crosstalk, as well as vergence and accommodation conflict, is the critical obstacle that hinders the real applications of glasses-free 3D display. Here we propose a glasses-free 3D display by adopting metagratings for the pixelated phase modulation to form converged viewpoints. When the viewpoints are closely arranged, the holographic sampling 3D display can approximate a continuous light field. We demonstrate a video rate full-color 3D display prototype without visual fatigue under an LED white light illumination. The metagratings-based holographic sampling 3D display has a thin form factor and is compatible with traditional flat panel and thus has the potential to be used in portable electronics, window display, exhibition display, 3D TV, as well as tabletop display.
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The demand for high-performance absorbers in the microwave frequencies, which can reduce undesirable radiation that interferes with electronic system operation, has attracted increasing interest in recent years. However, most devices implemented so far are opaque, limiting their use in optical applications that require high visible transparency. Here, a scheme is demonstrated for microwave absorbers featuring high transparency in the visible range, near-unity absorption (≈99.5% absorption at 13.75 GHz with 3.6 GHz effective bandwidth) in the Ku-band, and hence excellent electromagnetic interference shielding performance (≈26 dB). The device is based on an asymmetric Fabry-Pérot cavity, which incorporates a monolayer graphene and a transparent ultrathin (8 nm) doped silver layer as absorber and reflector, and fused silica as the middle dielectric layer. Guided by derived formulism, this asymmetric cavity is demonstrated with microwaves near-perfectly and exclusively absorbs in the ultrathin graphene film. The peak absorption frequency of the cavity can be readily tuned by simply changing the thickness of the dielectric spacer. The approach provides a viable solution for a new type of microwave absorber with high visible transmittance, paving the way towards applications in the area of optics.
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Organic-inorganic hybrid perovskites have been intensively studied for their use in optoelectronic devices due to their utilization of low-cost, earth-abundant precursors that are solution-processed at low-temperatures into high-quality devices. Despite this progress, interdevice variability and long-term stability have prevented the widespread commercial adoption of perovskite devices, especially for high-energy photon detectors. Using methylammonium lead iodide perovskite single crystals grown via inverse-temperature crystallization, we demonstrate a facile solution-based technique to coat the single-crystalline bulk with a micrometer-scale thick surface layer comprised of a wider band gap two-dimensional Ruddlesden-Popper (RP) hybrid perovskite. The resulting perovskite room-temperature γ-ray detector devices exhibit greatly improved device yield and repeatability from run-to-run and device-to-device within a given processing run. With an energy resolution of under 15% (12.0 keV) for incident 81 keV photons, this solution-based technique resolves interdevice variability concerns and could pave the way for low-cost, scalable manufacturing of optoelectronic devices based on RP hybrid perovskite films.
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Building-integrated photovoltaics employing transparent photovoltaic cells on window panes provide an opportunity to convert solar energy to electricity rather than generating waste heat. Semitransparent organic photovoltaic cells (ST-OPVs) that utilize a nonfullerene acceptor-based near-infrared (NIR) absorbing ternary cell combined with a thin, semitransparent, high conductivity Cu-Ag alloy electrode are demonstrated. A combination of optical outcoupling and antireflection coatings leads to enhanced visible transmission, while reflecting the NIR back into the cell where it is absorbed. This combination of coatings results in doubling of the light utilization efficiency (LUE), which is equal to the product of the power conversion efficiency (PCE) and the average photopic transparency, compared with a conventional semitransparent cell lacking these coatings. A maximum LUE = 3.56 ± 0.11% is achieved for an ST-OPV with a PCE = 8.0 ± 0.2% at 1 sun, reference AM1.5G spectrum. Moreover, neutral colored ST-OPVs are also demonstrated, with LUE = 2.56 ± 0.2%, along with Commission Internationale d'Eclairage chromaticity coordinates of CIE = (0.337, 0.349) and a color rendering index of CRI = 87.
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One key obstacle in fabricating efficient flexible and printable optoelectronic devices is the absence of ideal flexible transparent conductors with superior optical, electrical, and mechanical properties. Here, high-performance flexible transparent conductors are demonstrated using ultrathin (<10 nm) doped silver films, which exhibit an averaged visible transmittance of 80% without any antireflection coating, sheet resistance less than 20 Ω sq-1, and mechanical stability over 1000 bending cycles. The conductor is prepared by doping silver with an additive metal (e.g., nickel, copper, titanium, chromium), and its various properties can be readily tuned by either using different doping metal species or controlling the dopant concentration. Centimeter-size, flexible polymer light-emitting diodes are fabricated using a nickel-doped silver-based electrode, and the devices exhibit 30% enhanced current efficiencies compared to their indium tin oxide counterparts, invariant emission spectra at large viewing angles, and operational stability for over 1200 bending circles. In addition, 6 in. flexible low-emissivity coatings are demonstrated using a copper-doped silver-based conductor, which transmit 85.2% of the visible light while rejecting over 90% of the infrared radiation beyond 1250 nm.
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We demonstrate structural colors produced by a simple, inexpensive, and nontoxic electrodeposition process. Asymmetric metal-dielectric-metal (MDM) multilayered structures were achieved by sequential electrodeposition of smooth gold, thin cuprous oxide, and finally thin gold on conductive substrates, forming an effective optical cavity with angle-insensitive characteristics. Different colors of high brightness were achieved by simply tuning the thickness of the electrodeposited middle cavity layer. This process is compatible with highly nonplanar substrates of arbitrary shape, size, and roughness. This work is the first demonstration of solution-processed, electrodeposited, MDM film stacks that are uniform over large areas and highlights the clear advantages of this approach over traditional deposition or assembly methods for preparing colored films.