- Award ID(s):
- 1659512
- PAR ID:
- 10207654
- Date Published:
- Journal Name:
- Nanoscale
- Volume:
- 12
- Issue:
- 11
- ISSN:
- 2040-3364
- Page Range / eLocation ID:
- 6438 to 6448
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Abstract Silver nanowires (AgNWs) hold great promise for applications in wearable electronics, flexible solar cells, chemical and biological sensors, photonic/plasmonic circuits, and scanning probe microscopy (SPM) due to their unique plasmonic, mechanical, and electronic properties. However, the lifetime, reliability, and operating conditions of AgNW-based devices are significantly restricted by their poor chemical stability, limiting their commercial potentials. Therefore, it is crucial to create a reliable oxidation barrier on AgNWs that provides long-term chemical stability to various optical, electrical, and mechanical devices while maintaining their high performance. Here we report a room-temperature solution-phase approach to grow an ultra-thin, epitaxial gold coating on AgNWs to effectively shield the Ag surface from environmental oxidation. The Ag@Au core-shell nanowires (Ag@Au NWs) remain stable in air for over six months, under elevated temperature and humidity (80 °C and 100% humidity) for twelve weeks, in physiological buffer solutions for three weeks, and can survive overnight treatment of an oxidative solution (2% H 2 O 2 ). The Ag@Au core-shell NWs demonstrated comparable performance as pristine AgNWs in various electronic, optical, and mechanical devices, such as transparent mesh electrodes, surface-enhanced Raman spectroscopy (SERS) substrates, plasmonic waveguides, plasmonic nanofocusing probes, and high-aspect-ratio, high-resolution atomic force microscopy (AFM) probes. These Au@Ag core-shell NWs offer a universal solution towards chemically-stable AgNW-based devices without compromising material property or device performance.more » « less
-
Abstract Carbon nanotubes (CNTs) possess extremely anisotropic electronic, thermal, and optical properties owing to their 1D character. While their linear optical properties have been extensively studied, nonlinear optical processes, such as harmonic generation for frequency conversion, remain largely unexplored in CNTs, particularly in macroscopic CNT assemblies. In this work, macroscopic films of aligned and type‐separated (semiconducting and metallic) CNTs are synthesized and polarization‐dependent third‐harmonic generation (THG) from the films with fundamental wavelengths ranging from 1.5 to 2.5 µm is studied. Both films exhibited strongly wavelength‐dependent, intense THG signals, enhanced through exciton resonances, and third‐order nonlinear optical susceptibilities of 2.50 × 10−19 m2 V−2(semiconducting CNTs) and 1.23 × 10−19 m2 V−2(metallic CNTs), respectively are found, for 1.8 µm excitation. Further, through systematic polarization‐dependent THG measurements, the values of all elements of the susceptibility tensor are determined, verifying the macroscopically 1D nature of the films. Finally, polarized THG imaging is performed to demonstrate the nonlinear anisotropy in the large‐size CNT film with good alignment. These findings promise applications of aligned CNT films in mid‐infrared frequency conversion, nonlinear optical switching, polarized pulsed lasers, polarized long‐wave detection, and high‐performance anisotropic nonlinear photonic devices.
-
Chemically-synthesized single-crystalline silver nanowire (AgNW) probes can combine the scanning tunneling microscopy (STM) technique with tip-enhanced Raman scattering spectroscopy (TERS) for complementary morphological and chemical information with nanoscale spatial resolution. However, its performance has been limited by the blunt nanowire tip geometry, the insulating surfactant layer coating AgNW surfaces, and the thermal-induced mechanical vibrations. Here, we report a reproducible fabrication method for the preparation of sharp-tip AgNW-based TERS probes. By removing the polyvinylpyrrolidone (PVP) surfactant molecules from the AgNW surfaces for stable electrical conductivity and controlling the protruding length with μm-level accuracy for improved mechanical stability, we demonstrate atomic-resolution STM imaging with the sharp-tip AgNW probe. Furthermore, the sharp-tip AgNW has an excellent TER enhancement (∼1.1 × 10 6 ), which is about 66 folds of that achieved by regular AgNWs. Our experiments demonstrate that AgNWs with clean interfaces and the proper tip geometry can provide reliable and reproducible STM and TER characterizations, which remove the hurdles preventing the implementation of AgNW in STM-based near-field optical applications for a broad community.more » « less
-
Abstract This study describes the production of biodegradable and recyclable flexible electronic devices created by screen‐printing silver nanowires (AgNWs) onto regenerated cellulose films (RCFs). RCFs, derived from microcrystalline cellulose (MCC), are developed and further enhanced for flexibility with additives such as glycerol and poly(ethylene glycol) diglycidyl ether (PEGDE). The resulting cellulose films display relatively high tensile strength (up to 120 MPa), low Young's Modulus (down to 1500 MPa), and 90% optical transparency. Ink with AgNWs and poly(ethylene oxide) (PEO) as a binder is screen‐printed on regenerated cellulose films. The printed AgNWs patterns exhibit high electrical conductivity, excellent electromechanical performance, and strong interfacial adhesion with RCFs. To demonstrate the application of printed AgNWs on RCFs for soft electronics, transparent conductive electrodes (TCEs) are fabricated. Grid and honeycomb structures are printed separately and evaluated in terms of sheet resistance and optical transparency. TCEs with ≈80% transparency and very low sheet resistance (0.045 Ω sq−1) are obtained. Furthermore, enzymatic hydrolysis of the cellulose substrate and the recovery for reuse of the AgNWs are demonstrated, showing the potential of integrating natural polymers and recyclable nanomaterials for eco‐friendly and sustainable soft flexible electronics.
-
Abstract We present 870
μ m Atacama Large Millimeter/submillimeter Array polarization observations of thermal dust emission from the iconic, edge-on debris diskβ Pic. While the spatially resolved map does not exhibit detectable polarized dust emission, we detect polarization at the ∼3σ level when averaging the emission across the entire disk. The corresponding polarization fraction isP frac= 0.51% ± 0.19%. The polarization position angleχ is aligned with the minor axis of the disk, as expected from models of dust grains aligned via radiative alignment torques (RAT) with respect to a toroidal magnetic field (B -RAT) or with respect to the anisotropy in the radiation field (k -RAT). When averaging the polarized emission across the outer versus inner thirds of the disk, we find that the polarization arises primarily from the SW third. We perform synthetic observations assuming grain alignment via bothk -RAT andB -RAT. Both models produce polarization fractions close to our observed value when the emission is averaged across the entire disk. When we average the models in the inner versus outer thirds of the disk, we find thatk -RAT is the likely mechanism producing the polarized emission inβ Pic. A comparison of timescales relevant to grain alignment also yields the same conclusion. For dust grains with realistic aspect ratios (i.e.,s > 1.1), our models imply low grain-alignment efficiencies.