Self-Assembled Three-Dimensional Nanocrown Array

Although an ordered nanoplasmonic probe array will have a huge impact on light harvesting, selective frequency response (<i>i.e.</i>, nanoantenna), and quantitative molecular/cellular imaging, the realization of such an array is still limited by conventional techniques due to the serial processing or resolution limit by light diffraction. Here, we demonstrate a thermodynamically driven, self-assembled three-dimensional nanocrown array that consists of a core and six satellite gold nanoparticles (GNPs). Our ordered nanoprobe array is fabricated over a large area by thermal dewetting of thin gold film on hexagonally ordered porous anodic alumina (PAA). During thermal dewetting, the structural order of the PAA template dictates the periodic arrangement of gold nanoparticles, rendering the array of gold nanocrown. Because of its tunable size (<i>i.e.</i>, 50 nm core and 20 nm satellite GNPs), arrangement, and periodicity, the nanocrown array shows multiple optical resonance frequencies at visible wavelengths as well as angle-dependent optical properties

Omnidirectionally Stretchable and Transparent Graphene Electrodes

Stretchable and transparent electrodes have been developed for applications in flexible and wearable electronics. For customer-oriented practical applications, the electrical and optical properties of stretchable electrodes should be independent of the directions of the applied stress, and such electrodes are called omnidirectionally stretchable electrodes. Herein, we report a simple and cost-effective approach for the fabrication of omnidirectionally stretchable and transparent graphene electrodes with mechanical durability and performance reliability. The use of a Fresnel lens-patterned electrode allows multilayered graphene sheets to achieve a concentric circular wavy structure, which is capable of sustaining tensile strains in all directions. The as-prepared electrodes exhibit high optical transparency, low sheet resistance, and reliable electrical performances under various deformation (<i>e</i>.<i>g</i>., bending, stretching, folding, and buckling) conditions. Furthermore, computer simulations have also been carried out to investigate the response of a Fresnel lens-patterned structure on the application of mechanical stresses. This study can be significant in a large variety of potential applications, ranging from stretchable devices to electronic components in various wearable integrated systems

Plasmonic Optical Interference

Understanding optical interference is of great importance in fundamental and analytical optical design for next-generation personal, industrial, and military applications. So far, various researches have been performed for optical interference phenomena, but there have been no reports on plasmonic optical interference. Here, we report that optical interference could be effectively coupled with surface plasmons, resulting in enhanced optical absorption. We prepared a three-dimensional (3D) plasmonic nanostructure that consists of a plasmonic layer at the top, a nanoporous dielectric layer at the center, and a mirror layer at the bottom. The plasmonic layer mediates strong plasmonic absorption when the constructive interference pattern is matched with the plasmonic component. By tailoring the thickness of the dielectric layer, the strong plasmonic absorption can facilely be controlled and covers the full visible range. The plasmonic interference in the 3D nanostructure thus creates brilliant structural colors. We develop a design equation to determine the thickness of the dielectric layer in a 3D plasmonic nanostructure that could create the maximum absorption at a given wavelength. It is further demonstrated that the 3D plasmonic nanostructure can be realized on a flexible substrate. Our 3D plasmonic nanostructures will have a huge impact on the fields of optoelectronic systems, biochemical optical sensors, and spectral imaging

Asymmetrically Coupled Plasmonic Core and Nanotriplet Satellites

Here, we report asymmetrical multiple electromagnetic coupling of plasmonic core and nanotriplet satellites. Within the plasmonic core and nanotriplet satellites, an enhanced local field is generated which expands across the core due to multiple electromagnetic coupling between a core and nanotriplets. Based on 3D simulations of our plasmonic nanosystem, the overall local field enhancement reaches to over 10⁴ times, compared with that of a single nanoparticle array. A strong local field distribution across the core to nanotriplets as well as the critical role of the plasmonic core is demonstrated through the 3D simulations. It is proposed that a self-assembled nanotriplet array is completed through two stages of dewetting of a gold thin film on an anodic aluminum oxide (AAO) template. Formation of the core–nanotriplet satellites is significantly influenced by geometrical parameters (i.e., the pore diameter and depth) of the AAO template. Our experimental results show that the local field of our plasmonic nanostructures is amplified up to ∼110 times by adopting a core into the nanotriplet satellites, compared with that of the nanotriplets array without a core. This approach offers a promising strategy for creating an advanced nanoplasmonic platform with strong local field distribution and high-throughput production

Plasmonic–Photonic Interference Coupling in Submicrometer Amorphous TiO₂–Ag Nanoarchitectures

In this study, we report the crystallinity effects of submicrometer titanium dioxide (TiO₂) nanotube (TNT) incorporated with silver (Ag) nanoparticles (NPs) on surface-enhanced Raman scattering (SERS) sensitivity. Furthermore, we demonstrate the SERS behaviors dependent on the plasmonic–photonic interference coupling (P-PIC) in the TNT-AgNP nanoarchitectures. Amorphous TNTs (A-TNTs) are synthesized through a two-step anodization on titanium (Ti) substrate, and crystalline TNTs (C-TNTs) are then prepared by using thermal annealing process at 500 °C in air. After thermally evaporating 20 nm thick Ag on TNTs, we investigate SERS signals according to the crystallinity and P-PIC on our TNT-AgNP nanostructures. (A-TNTs)-AgNP substrates show dramatically enhanced SERS performance as compared to (C-TNTs)-AgNP substrates. We attribute the high enhancement on (A-TNTs)-AgNP substrates with electron confinement at the interface between A-TNTs and AgNPs as due to the high interfacial barrier resistance caused by band edge positions. Moreover, the TNT length variation in (A-TNTs)-AgNP nanostructures results in different constructive or destructive interference patterns, which in turn affects the P-PIC. Finally, we could understand the significant dependency of SERS intensity on P-PIC in (A-TNTs)-AgNP nanostructures. Our results thus might provide a suitable design for a myriad of applications of enhanced EM on plasmonic-integrated devices

P-Type Polymer-Hybridized High-Performance Piezoelectric Nanogenerators

Enhancing the output power of a nanogenerator is essential in applications as a sustainable power source for wireless sensors and microelectronics. We report here a novel approach that greatly enhances piezoelectric power generation by introducing a p-type polymer layer on a piezoelectric semiconducting thin film. Holes at the film surface greatly reduce the piezoelectric potential screening effect caused by free electrons in a piezoelectric semiconducting material. Furthermore, additional carriers from a conducting polymer and a shift in the Fermi level help in increasing the power output. Poly­(3-hexylthiophene) (P3HT) was used as a p-type polymer on piezoelectric semiconducting zinc oxide (ZnO) thin film, and phenyl-C₆₁-butyric acid methyl ester (PCBM) was added to P3HT to improve carrier transport. The ZnO/P3HT:PCBM-assembled piezoelectric power generator demonstrated 18-fold enhancement in the output voltage and tripled the current, relative to a power generator with ZnO only at a strain of 0.068%. The overall output power density exceeded 0.88 W/cm³, and the average power conversion efficiency was up to 18%. This high power generation enabled red, green, and blue light-emitting diodes to turn on after only tens of times bending the generator. This approach offers a breakthrough in realizing a high-performance flexible piezoelectric energy harvester for self-powered electronics

Halide Perovskite Nanopillar Photodetector

Numerous studies have reported the use of halide perovskites as highly functional light-harvesting materials. The development of optimized compositions and deposition approaches has led to impressive improvements; however, no noticeable breakthrough in performance has been observed for these materials recently. Here, a breakthrough that enables the fabrication of vertically grown halide perovskite (VGHP) nanopillar photodetectors <i>via</i> a nanoimprinting crystallization technique is demonstrated. We used engraved nanopatterned polymer stamps to form VGHP nanopillars during the pressurized crystallization of the softly baked gel state of a methylammonium lead iodide (CH₃NH₃PbI₃, denoted MAPI) film. The VGHP films exhibit much lower defect density and higher conductivity, as supported by current–voltage characteristic measurements and conductive atomic force microscopy measurements. Ultimately, two-terminal lateral photodetectors based on the VGHP nanopillar films show a greatly enhanced photoresponse compared with flat film-based photodetectors. We expect that the deposition method presented here will help surpass the technical limits and contribute to further improvements in various halide-perovskite-based devices