Anodic Aluminum Oxide Template Research Articles

Efficient concentration of trace analyte with ordered hotspot construction for a robust and sensitive SERS platform

Surface-enhanced Raman scattering (SERS) platform, which enables trace analyte detection, has important application prospects. By structuring/modifying the surface of the SERS substrate, analyte in highly diluted solutions can be concentrated into localized active areas for highly sensitive detection. However, subject to the difficulty of the fabrication process, it remains challenging to balance hot-spot construction and the concentration capacity of analyte simultaneously. Therefore, preparing SERS substrates with densely ordered hot spots and efficient concentration capacity is of great significance for highly sensitive detection. Herein, we propose an Ag and fluoroalkyl-modified hierarchical armour substrate (Ag/F-HA), which has a double-layer stacking design to combine analyte concentration with hotspot construction. The microarmour structure is fabricated by femtosecond-laser processing to serve as a superhydrophobic and low-adhesive surface to concentrate analyte, while the anodic aluminium oxide (AAO) template creates a nanopillar array serving as dense and ordered hot spots. Under the synergistic action of hot spots and analyte concentration, Ag/F-HA achieves a detection limit down to 10−7 M doxorubicin (DOX) molecules with a RSD of 7.69%. Additionally, Ag/F-HA exhibits excellent robustness to resist external disturbances such as liquid splash or abrasion. Based on our strategy, SERS substrates with directional analyte concentrations are further explored by patterning microcone arrays with defects. This work opens a way to the realistic implementation of SERS in diverse scenarios.

Modulated critical currents of spin-transfer torque-induced resistance changes in NiCu/Cu multilayered nanowires.

We present a novel method combining anodic aluminum oxide template synthesis and nanolithography to selectively deposit vertically patterned magnetic nanowires on a Si substrate. With this approach we fabricated three-dimensional nanowire-based spin valve devices without the need of complex etching processes or additional spacer coating. Through this method, we successfully obtained NiCu/Cu multilayered nanowire arrays with a controlled sequence along the long axis of the nanowires. Both magnetic switching and excitation phenomena driven by spin-polarized currents were clearly demonstrated in our NiCu/Cu multilayered nanowires. Moreover, the critical currents for switching and excitation were observed to be modulated in an oscillatory manner by the magnetic field in the nanowire-based devices. We present a toy model to qualitatively explain these observations.

ReS2-MoS2 heterojunction nanotube FET with superlattice structures for ultrasensitive detection of miRNA

Ultrasensitive detection of cancer biomarkers holds immense importance in facilitating the early diagnosis and treatment of cancer. Compared to conventional detection techniques, field-effect transistor (FET) biosensors have demonstrated substantial potential in achieving sensitive detection of cancer biomarkers. However, the ultrasensitive FET still remains great challenges due to the limited electron transport capacity and sensitivity of channel materials. Herein, we employed rhenium disulfide-molybdenum disulfide nanotube (ReS2-MoS2 NT) featuring superlattice structures as channel materials in FET biosensors for the highly sensitive detection of cancer biomarker miRNA-21. More concretely, ReS2-MoS2 NT featuring superlattice structures was synthesized using the anodic aluminum oxide (AAO) template sacrifice method and atomic layer deposition (ALD) method. The electrical properties of single ReS2-MoS2 NT FET were regulated by adjusting the total layers and number of heterojunction interfaces, and the optimal number of heterojunction interfaces of 7 was obtained. Finally, FET biosensors utilizing the network ReS2-MoS2 NT as the channel materials were fabricated and exhibited remarkable sensitivity in detecting miRNA-21 under an external light source. The linear range for detection spanned from 10 aM to 1 nM, with an exceptionally low detection limit of 2.1 aM. This study holds promise for replacing current channel materials and surpassing the detection threshold of cancer biomarkers in the future.

The glass transition and enthalpy recovery of polystyrene nanorods using Flash differential scanning calorimetry.

The glass transition (Tg) behavior and enthalpy recovery of polystyrene nanorods within an anodic aluminum oxide (AAO) template (supported nanorods) and after removal from AAO (unsupported nanorods) is studied using Flash differential scanning calorimetry. Tg is found to be depressed relative to the bulk by 20 ± 2K for 20 nm-diameter unsupported polystyrene (PS) nanorods at the slowest cooling rate and by 9 ± 1K for 55 nm-diameter rods. On the other hand, bulk-like behavior is observed in the case of unsupported 350 nm-diameter nanorods and for all supported rods in AAO. The size-dependent Tg behavior of the PS unsupported nanorods compares well with results for ultrathin films when scaled using the volume/surface ratio. Enthalpy recovery was also studied for the 20 and 350nm unsupported nanorods with evolution toward equilibrium found to be linear with logarithmic time. The rate of enthalpy recovery for the 350nm rods was similar to that for the bulk, whereas the rate of recovery was enhanced for the 20nm rods for down-jump sizes larger than 17K. A relaxation map summarizes the behavior of the nanorods relative to the bulk and relative to that for the 20 nm-thick ultrathin film. Interestingly, the fragility of the 20 nm-diameter nanorod and the 20nm ultrathin film are identical within the error of measurements, and when plotted vs departure from Tg (i.e., T - Tg), the relaxation maps of the two samples are identical in spite of the fact that the Tg is depressed 8K more in the nanorod sample.

Polarized emission of Cs3Cu2I5 nanowires embedded in nanopores of an anodic aluminum oxide template.

Due to the intrinsic polarized emission property, polarized emissive materials with anisotropic nanostructures are expected to be potential substitutes for polarizers. Herein, by the template-assisted strategy, well-aligned lead-free metal halide Cs3Cu2I5 nanowire (NW) arrays are fabricated by evaporating the precursor ink in the anodic aluminum oxide (AAO) for polarized emission. The Cs3Cu2I5/AAO composite film emits highly polarized light with a degree of polarization (DOP) of 0.50. Furthermore, by changing the molar ratio of CsI/CuI, the stability of Cs3Cu2I5 precursor inks is improved. Finally, an ultraviolet (UV) light-emitting diode (LED) is adopted to pump the composite film to achieve a blue LED device. The reported Cs3Cu2I5/AAO composite film with highly polarized light emissions will have great potential for polarized emission applications such as liquid crystal display backlights, waveguides, and lasers.

Au nanostructures with controllable morphology in porous anodic aluminum oxide templates

We report the controllable fabrication of Au nanostructures with different morphology inside the nanochannels of the Al-surrounded porous anodic aluminum oxide (AAO) templates. It has been found that the morphology of the Au nanostructures is influenced by the pore diameter of the AAO templates and the bottom Au layer sputtering on the surface of the AAO templates. Au nanowires are formed in the AAO templates with smaller pore diameters (40–60 nm), and rice spike-like Au nanostructures are formed in the AAO templates with larger pore diameters (∼130 nm). When the AAO templates with bottom Au layer were used, almost all of the nanochannels were filled with Au nanostructures. As the AAO templates without bottom Au layer were employed, longer Au nanostructures are formed inside some nanochannels near the Al-AAO boundary.

Nanocontrolled thinning of the barrier layer thickness of porous anodic films using galvanodynamic polarization of aluminum alloys

Thinning the barrier layer thickness of anodic films prepared on refined aluminum substrates (4 N or 5 N) was usually performed to elaborate -after the usual two-step anodizing method- anodic aluminum oxide (AAO) templates with pores opened at both sides, allowing the subsequent nanodevices synthesis. By contrast, there is a lack of studies concerning similar barrier layer thinning for anodic films grown -by a single-step anodizing - on commercial low alloyed aluminum substrates (1XXX series) or other more complex aluminum alloys (AA 2XXX-8XXX). Yet such a need is now emerging, particularly for future applications requiring transverse electrical conductivity of usual anodic films toward the aluminum alloy substrate.This work aims to study and to master a simple and cheap method for thinning the barrier layer thickness of such anodic films on commercial aluminum alloys. Here, the thinning is studied using a current density decrease (at a constant rate) after the anodic film growth in phosphoric acid-based electrolyte, using the conjunction of in-situ accurate electrochemical follow-up and ex-situ FE-SEM morphological observations. Variation of current density scan rate highlights that fast processes lead to no barrier layer thinning, and slow ones to the detachment of the whole oxide film. However, by choosing the right scan rate range, it is possible to successfully obtain, in a straightforward manner, anodic films still supported on aluminum alloy substrates, but with barrier layer thickness tuned at the nanoscale.

Ultrabroadband absorptive refractory plasmonics for photocatalytic hydrogen evolution reactions

As an environmentally friendly and renewable method for hydrogen production powered by solar energy, photocatalytic hydrogen evolution reactions (HERs) using broadband absorbers have received much attention. Here, we report the fabrication and characterization of an ultrabroadband absorber for the photocatalytic HER. The absorber is composed of titanium nitride and titanium dioxide heterostructures deposited onto a porous anodized aluminum oxide template. The absorber shows ultrabroadband absorption in both the visible and near-infrared regions (400–2500 nm), with averages of 99.1% and 80.1%, respectively. Additionally, the presence of the TiO2 layer within the absorber extends the lifetime of the hot carriers by 2.7 times longer than that without the TiO2 layer, enhancing the transfer of hot electrons and improving the efficiency of hydrogen production by 1.9 times. This novel ultrabroadband absorber has potential use in advanced photocatalytic HER applications, providing a sustainable and cost-effective route for hydrogen generation from solar energy.

High sensitive SERS film of Ag-coated aggregated nanowire structure and benzene gas detection

A highly sensitive surface-enhanced Raman spectroscopy (SERS) film was fabricated based on anodic aluminum oxide template and Ag coating techniques. The array of alumina nanowires of ∼5 μm length and 26 nm thickness was fabricated and then made collapse to build a micro-scale funnel array, where each cell consists of hundreds of nanowires. Ag film was deposited on the nanowire structure by thermal evaporation. Due to numerous tapered nanogaps and efficient illumination of incident light in the micro-funnel structures, Raman signal enhancement factor (E.F.) as high as ∼1.8 × 107 could be obtained at 785 nm. The SERS film functionalized by 1-propanethiol was used for benzene gas detection, where the sensitivity of <0.3 ppm (3-σ) was realized within 120 s. This nanostructure is expected to be widely used for highly sensitive chemical and bio-sensors and have higher E.F. when the morphology is optimized further.

Enhancement of NaYF&lt;sub&gt;4&lt;/sub&gt;:Yb&lt;sup&gt;3+&lt;/sup&gt;/Er&lt;sup&gt;3+&lt;/sup&gt; up-conversion luminescence based on anodized alumina template

Up-conversion nanoparticle (UCNP) can collect near-infrared (NIR) light and convert it into visible light. Therefore, UCNP has potential applications in fields such as biomedicine, anti-counterfeiting, and solar cells. However, the efficiency of traditional UCNP in the above-mentioned fields is relatively low, greatly limiting its use in related fields. Therefore, enhancing the up-conversion luminescence intensity of up-conversion nanoparticles is particularly important and urgently needed. In this work, anodic alumina templates are used to enhance the luminescence intensity of up-conversion nanocrystals. NaYF&lt;sub&gt;4&lt;/sub&gt;:Yb&lt;sup&gt;3+&lt;/sup&gt;, Er&lt;sup&gt;3+&lt;/sup&gt;with a diameter of 35 nm is prepared by using co-precipitation method. Single pass AAO templates with pore size and pore spacing of 88 nm and 100 nm are prepared by using two-step anodization method. Finally, NaYF&lt;sub&gt;4&lt;/sub&gt;:Yb&lt;sup&gt;3+&lt;/sup&gt;, Er&lt;sup&gt;3+&lt;/sup&gt;/AAO composite structures are formed by using spin coating method. The red green light emission intensity of NaYF&lt;sub&gt;4&lt;/sub&gt;:Yb&lt;sup&gt;3+&lt;/sup&gt;, Er&lt;sup&gt;3+&lt;/sup&gt;/AAO sample can increase 4.4 and 9.0 times that of NaYF&lt;sub&gt;4&lt;/sub&gt;:Yb&lt;sup&gt;3+&lt;/sup&gt;, Er&lt;sup&gt;3+&lt;/sup&gt;/Al reference sample, respectively. The enhancement mechanism is explored by using the finite difference time domain method, and the results show that the primary source of enhancement is the localized surface plasmon resonance effect of the pores in the anodic alumina template. At the same time, the relationship between the up-conversion luminescence intensity of NaYF&lt;sub&gt;4&lt;/sub&gt;:Yb&lt;sup&gt;3+&lt;/sup&gt;, Er&lt;sup&gt;3+&lt;/sup&gt;/AAO sample and the incident angle is investigated. The experimental results show that as the incident angle increases, the luminescence intensity of the red and green light of NaYF&lt;sub&gt;4&lt;/sub&gt;:Yb&lt;sup&gt;3+&lt;/sup&gt;, Er&lt;sup&gt;3+&lt;/sup&gt;/AAO samples first decrease and then increase. Due to the coupling of the local surface plasmon resonance with the excitation wavelength and emission wavelength, the up-conversion luminescence intensity of the sample can be affected. The relationship of AAO channel enhancement factor with incident angle at excitation wavelength and emission wavelength is studied by using the finite difference time domain method. The results indicate that as the incident angle increases, the enhancement factor at the excitation wavelength decreases, while the enhancement factor at the emission wavelength increases after being illuminated at an incident angle of 15°. Therefore, when the incident angle is less than 20°, the electric field intensity at 980 nm dominates, but when it is greater than 20°, the electric field intensity at 540 nm and 650 nm takes precedence. The above results provide a reference for putting them into practical applications in the fields of anti-counterfeiting and solar cells.

Structural transformation of nanorods in artificial nanochannels: Influence of nanochannel size and mass fraction of homopolymer

In this work, various nanorods (NRs) with different structures by self-assembly of copolymer polystyrene-b-poly (4-vinylpyridine) (PS36·5K-b-P4VP16K, SVP-16) and homopolystyrene (hPS3.35k) in cylindrical anodic aluminum oxide (AAO) templates were obtained. Structural transformation in NRs was investigated by varying the AAO nanochannel size and the mass fraction of hPS3.35k. As the mass fraction of hPS3.35k increases, a typical structure change of NRs can be observed, from a continuous concentric lamellar shape to intermittent irregular blocks and finally to dense spherical structures. The AAO channel size also significantly influences the internal structure of the NRs and the arrangement of the P4VP particles, and the ionic current changes remarkably after the self-assembly of SVP-16/hPS3.35k with different weight fractions of hPS3.35k (φhPS). Furthermore, mesoporous nanorods with controlled structures can be obtained by selective swelling of the micro-regional fraction of BCPs in organic solvents. This work provides valuable insights into the structural transformation of self-assembled polymers in artificial nanochannels, benefiting understanding the underlying mechanism of ion transport.

(Invited) Confined and Free-Standing Perovskite Nanowires for X-Ray Detection

Metal halide perovskites (MHPs) have shown excellent results in many applications, including X-ray scintillation detection. Nanowires could offer improved sensitivity by exploiting nanophotonic light guiding, and the MHP stability could be improved by growing nanowires physically protected in anodized aluminum oxide (AAO). We use a one-step solution low-temperature method to grow arrays of long single-crystalline CsPbBr3 nanowires in an AAO template. The diameters can be adjusted by the AAO template, ranging from 30 to 360 nm, and the length can be controlled up to 15 μm (Fig 1(a)) [1]. The nanowires show excellent stability, with no obvious lack in photoluminescence after months of storage in air. The X-ray scintillation shows no systematic degradation over 2 weeks of continuous X-ray exposure, but an unexpected positive correlation with room humidity. The excellent stability allows tomographic 3D X-ray imaging at better than 3 μm resolution [2].Surprisingly, we find that free-standing CsPbBr3 nanowires can be obtained by the same method (Fig 1(b)) [3]. The length of the vertically aligned nanowires is controlled from 1 to 20 μm with the precursor amount. The nanowires are single-crystalline and exhibit excellent photoluminescence and clear light guiding (Fig 1(c)). Lithography methods for MHPs have been limited because of their solubility in polar solvents. However, we show that o-xylene can be used in a perovskite-compatible electron beam lithography (EBL) process based on nonpolar solvents [4]. Combining these results, we demonstrate single nanowire devices with excellent photoresponse. Recently, we have developed a gas-phase halide exchange method based on HCl or Cl2 to convert the green-emitting CsPbBr3 to blue-emitting CsPb(BrxCl1-x)3. [5]. Using the aforementioned EBL process, we selectively convert segments of nanowires to CsPb(BrxCl1-x)3 and create axially heterostructured nanowires (Fig 1(d)).1 Z. Zhang, H. Dierks, N. Lamers et al., "Single-Crystalline Perovskite Nanowire Arrays for Stable X-ray Scintillators with Micrometer Spatial Resolution" ACS Applied Nano Materials 5 (1), 881 (2022) http://doi.org/10.1021/acsanm.1c035752 H. Dierks, Z. Zhang, N. Lamers, and J. Wallentin, "3D X-ray microscopy with a CsPbBr3 nanowire scintillator" Nano Res. 16 (1), 1084 (2023) https://doi.org/10.1007/s12274-022-4633-73 Z. Zhang, N. Lamers, C. Sun, C. Hetherington, I. G. Scheblykin, and J. Wallentin, "Free-Standing Metal Halide Perovskite Nanowire Arrays with Blue-Green Heterostructures" Nano Lett. 22 (7), 2941 (2022) http://doi.org/10.1021/acs.nanolett.2c001374 N. Lamers, Z. Zhang, and J. Wallentin, "Perovskite-Compatible Electron-Beam-Lithography Process Based on Nonpolar Solvents for Single-Nanowire Devices" ACS Applied Nano Materials 5 (3), 3177 (2022) http://doi.org/10.1021/acsanm.2c001885 N. Lamers, Z. Zhang, I. G. Scheblykin, and J. Wallentin, "Multisegment Heterostructured CsPb(Br1-xClx)3 Perovskite Nanowires using Gas-Phase Anion Exchange" In review (2023) Figure 1

(Invited) Metal and Nonmetal Plasmonic Nanostructures for Surface-Enhanced Raman Spectroscopy Detection

Toxic small molecules such as pesticides, food additives, plasticizers and dyes have been posing increasing threat to human health. Surface-enhanced Raman scattering spectroscopy (SERS) is a powerful sensing strategy for these small molecules with advantages including fast response, high sensitivity and fingerprint identification.Based on the surface plasmon effect, gold and silver nanostructures are the typical plasmonic sensing materials for rapid detection with SERS. However, the crucial challenges for realizing on-site real detection application is to fabricate reproducible and highly sensitive SERS substrates and portable instrument. We fabricated several long-range ordered sensitive nanostructure arrays based on anodic aluminum oxide templates which could provide reproducible structural patterns. Then, we developed a portable instrument integrated with database of the standard Raman spectra of common contaminants and a software for automatic identification and comparison of the test spectrum with the standard database, which can identify the specific analytes. Combined with the sensitive and reproducible SERS substrates, we realized the on-site and rapid detection of various toxic contaminants.Recently, as an inexpensive candidate, nonmetal plasmonic materials like oxide semiconductors have attracted increasing interests, which induced by the increase of free charge carriers via introducing oxygen vacancies. We synthesized oxygen-deficient WO3-x and NayWO3-x nanosheets and realized the localized surface plasmon resonance (LSPR) band in visible range (~530 nm) as same as the gold nanoparticles, which is the bluest. Then, SERS detection of dyes has also been realized on nonmetal substrate. Moreover, the plasmonic oxygen-deficient oxides showed wide LSPR tuning window from visible to infrared range and plasmon-driven photocatalysis, which may open potentials for biological applications.

Control of Crystallographic Growth Orientation and Twinning Structure in Copper Nanowires by Template-Assisted Electrodeposition

Synthesis and characterization of noble metal nanowires have been a popular topic in the field of microelectronic devices and catalysts. Nanotwinned copper nanowires (nt-CuNWs) possess high mechanical strength, excellent electromigration resistance and low electrical resistivity, which have been considered as a promising interconnect material in ultra-large scale integrated circuits (ICs). Here, we deposited nt-CuNWs in two different anodic aluminum oxide (AAO) templates with respective pore sizes of 70 nm and 35 nm pore by pulse electrodeposition. The influence of thermal treatment on the Cu seed layer deposited on AAO membranes prior to electrodeposition is investigated. Both coarse and thin nt-CuNWs mainly grew in <111> crystallographic direction with (111) texture coefficients (TC(111)) > 2.5, and an aspect ratio (AR) > 100 according to x-ray diffraction analysis. An addition of gelatin (14 ppm) in the copper sulfate electrolyte is found to suppress the growth of (220)-oriented Cu grains in the AAO by forming copper nanowires with large TC(111) > 2.65 and high-density nanotwin structure. This study provides a simple route to tailoring microstructure and physical properties of nanoscale copper wires, which is beneficial for the interconnect technology development in semiconductor IC devices.

Ultrahighly Sensitive Surface-Enhanced Raman Spectroscopy Film of Silver Nanoparticles Dispersed in Three Dimensions on a Thin Alumina Nanowire Framework.

To develop highly sensitive surface-enhanced Raman spectroscopy (SERS) films, various types of aggregated Ag nanowire (NW) and nanoparticle (NP) complex structures were fabricated using anodic aluminum oxide (AAO) templates and thermal evaporation. Aggregated AgNW structures with numerous tapered nanogaps were fabricated via Ag deposition on aggregated thin alumina nanowires of different lengths. AgNP complex structures were obtained by collapsing vertically aligned thin alumina nanowires 1 μm in length and depositing AgNPs on their tops and sides using surface tension during ethanol drying after functionalization. The Raman signal enhancement factors (EFs) of the samples were evaluated by comparing the SERS signal of the thiophenol (TP) self-assembled monolayer (SAM) on the nanostructures with the Raman signal of neat TP. EFs as high as ~2.3 × 107 were obtained for the optimized aggregated AgNW structure (NW length of 1 μm) and ~3.5 × 107 for the optimized AgNP complex structure. The large EF of the AgNP complex film is attributed mainly to the AgNPs dispersed in three dimensions on the sides of the thin alumina nanowires, strongly implying some important, relevant physics yet to be discovered and also a very promising nanostructure scheme for developing ultrahighly sensitive SERS films with EF > 108.

Vertically Aligned Perovskite Laser Arrays for High‐Capacity Anticounterfeiting Labels

AbstractPhysically unclonable functions (PUFs) have emerged as the most effective method against counterfeiting, leveraging the intrinsic randomness of objects to avoid data replication. However, despite their efficacy, the complexity and high cost of most PUF‐based counterfeiting labels hinder their practical application. Here, a high‐capacity PUF label based on vertically aligned perovskite nanowire (NW) arrays is demonstrated. The NW arrays are conveniently constructed using a low‐cost solution process using an anodized aluminum oxide template. Each pixel within the label is composed of closely packed CsPbBr3 NW arrays of different lengths, resulting in varied lasing signals. The collected signal of each pixel emerged from the lasing output of the NW arrays, generating high‐density and nonuniform multiple‐mode lasing to facilitate information encoding. A quaternary encoding mechanism is used to encode the number of laser modes per pixel. Impressively, it exhibits a mapping resolution of 1600 pixels within 400 µm2, achieving an impressive encoding capacity (1.97 × 10963) and a pixel density (4 bits µm−2) in this compact area. This work shows a promising approach for anticounterfeiting applications because of its simplicity, low cost, and high encoding capacity.

Solvent-Tailored Reversible Self-Assembly: Unveiling Ionic Transport Nanochannels in Block Copolymer Composite Electrolytes.

Block copolymer composite electrolytes have gained extensive attention for their promising performance in ionic conductivity and mechanical properties, making them valuable for future technologies. The control of the ionic conductivity through the self-assembly of block copolymers, however, remains a great challenge, especially in confined environments. In this study, we prepare block copolymer composite electrolytes using polystyrene-block-poly(ethylene oxide) (PS-b-PEO, SEO) as the polymer matrix and anodic aluminum oxide (AAO) templates as the ceramic skeleton. The self-assembly of SEO creates nanoscale ion transport pathways in the PEO regions through ionic interactions with lithium salts. The nanopores of the AAO templates provide a confined environment for complex phase separation of SEO controlled by selective solvent vapor annealing. Our findings demonstrate that transforming self-assembled SEO structures allows for precise control of ion transport pathways with cylindrical structures exhibiting 20 times higher ionic conductivities than those of helical structures. For AAO templates with pore diameters of 20 nm (SEO-LiTFSI@AAO-20), the ionic conductivities are approximately 410 times higher than those with pore diameters of 200 nm (SEO-LiTFSI@AAO-200), owing to the larger specific surface areas within the smaller nanopores. Utilizing the self-assembly of SEO not only enables the construction of vertically aligned ion transport channels on various scales but also offers a fascinating approach to tailor the conductive capabilities of composite electrolytes, enhancing the ion transport efficiency and allowing for the flexible design of block copolymer composite electrolytes.

The experimental Young’s modulus of polythiophene nanofibers

The Young’s modulus of polythiophene (PT) nanofibers has not been reported so far. In this paper, PT nanofibers were electrolytically prepared from thiophene monomer with a porous anodic aluminum oxide template. The Young's modulus of individual PT nanofibers was measured using atomic force microscopy. The average Young's modulus of PT nanofibers with diameters around 90 nm was 64.5 ± 5.0 GPa, which is an order of magnitude higher than its bulk value. We attribute the high Young’s modulus of PT nanofibers to the alignment of the molecular chain.

Silicon-Based Nanoelectronic Semiconductor Material and Its Surface-Enhanced Raman Image Signals

One-dimensional Zinc Oxide (ZnO) nanomaterials have important applications in devices, such as solar energy, sensors, and piezoelectric materials due to surface effects and quantum size effects. As a semiconductor material, Si has good thermal conductivity and low resistivity. A layer of n-type ZnO nanowires is grown on P-type monocrystalline silicon by transferring the Anodic Aluminum Oxide (AAO) template. The enhanced Raman effect on the surface is attempted by preparing n-type ZnO-P-type Si heterojunction nanostructures. This paper uses Si-based AAO as a template and uses electrochemical deposition method to prepare silicon-based nano-electronic semiconductor material ZnO/AAO/Si. According to SEM analysis, there are uniform pores on the surface of the material, and the cross-section shows that ZnO nanowires have been assembled into the AAO/Si structure. XRD analysis shows that ZnOn nanowires have a hexagonal wurtzite structure. In optoelectronic testing, through PL spectral analysis, the semiconductor material ZnO/AAO/Si has a strong yellow green emission peak near 574 nm. Field emission analysis shows that the β value of the ZnO field enhancement factor in the ZnO/AAO/Si structure is relatively high. The Surface-Enhanced Raman Spectroscopy (SERS) image signal experiment shows that the silicon-based nano-electronic semiconductor material prepared by electrochemical deposition method has good SERS characteristics. The SERS spectral intensity increases with the increase of the concentration of the detected substance and can be used as a SERS substrate to achieve Raman spectral image signal detection of chemical substances with low concentration.

Highly porous and rough polydimethylsiloxane film-based triboelectric nanogenerators and its application for electrochemical cathodic protection

The development and utilization of triboelectric nanogenerator (TENG) are very important for realizing energy cleaning in electrochemical processes. However, limited electrical output performance plays a major stumbling block to this process. Herein, a porous and high-roughness PDMS (PR/PDMS) negative friction layer was obtained by doping PDMS with powdered chitosan and casting using a sacrificial anodic alumina template. A TENG was fabricated by the PR/PDMS with Al film (PR-TENG). The PR-TENG exhibited much better performance than the pure PDMS-based TENG, which was attributed to the porous properties of the PR/PDMS. Under the driving of external mechanical force at 5Hz, the PR-TENG showed a maximum output open-circuit voltage (Voc) and short-circuit current density (Jsc) of 77.1V and 33.9 mA/m2, respectively. To prove the concept, the electrochemical cathodic protection system with PR-TENG was constructed. Ultimately, the application prospects of the PR-TENG as a clean energy source for electrochemical processes were explored and evaluated.