1D MXenes: Synthesis, Properties, and Applications.

The fascinating properties and versatile nature of 2D MXenes have generated significant interest in the scientific community. This has led to extensive research on expanding these materials into 1D and 0D forms. This review investigates the synthesis, properties, and applications of 1D MXenes, elucidating their potential across various fields. 1D MXenes, including nanowires, nanoribbons, nanorods, and nanotubes, inherit the remarkable properties of their 2D counterparts while also exhibiting unique anisotropic characteristics that enhance their performance in various applications. The review explores various methods for synthesizing 1D MXenes and examines their structural, electronic, and optical properties. The transition from 2D to 1D results in MXenes that offer superior properties, which are advantageous for various next-generation systems. The increased aspect ratio and surface area of 1D MXenes broaden their usage in energy storage, photothermal therapy, oxygen evolution reactions (OER), hydrogen evolution reactions (HER), oxygen reduction reactions (ORR), microwave absorption, filtration membranes, gas sensors, metal detection, etc. The review also addresses the challenges associated with 1D MXenes, such as limited synthesis methods, scalable production, size customization, preservation of structural integrity, and stability. Furthermore, potential opportunities and future directions in the field of 1D MXenes have also been proposed.

In Situ Nanomechanics: Opportunities Based on Superplastic Nanomolding.

In situ nanomechanics, referring to the real-time monitoring of nanomechanical deformation during quantitative mechanical testing, is a key technology for understanding the physical and mechanical properties of nanoscale materials. This perspective reviews the progress of in situ nanomechanics from the aspects of preparation and testing of nanosamples, with a major focus on one-dimensional (1D) nanostructures and discussions of their challenges. We highlight the opportunities provided by in situ nanomechanics combined with the superplastic nanomolding technique, especially in the aspects of regulating physical and chemical properties which are highly exploitable for mechanoelectronics, mechanoluminescence, piezoelectronics, piezomagnetism, piezothermography, and mechanochemistry.

Low-Temperature Ethanol Sensor via Defective Multiwalled Carbon Nanotubes.

This paper focuses on the fabrication of defective-induced nanotubes via the catalytic chemical vapor deposition method and the investigation of their properties toward gas sensing. We have developed defective multi-walled carbon nanotubes with porous and crystalline structures. The catalyst layer used in CNTs' growth here was based on 18 and 24 nm of Ni, and 5 nm of Cr deposited by the dc-sputtering technique. The CNTs' defects were characterized by observing the low graphite peak (G-band) and higher defect peaks (D-band) in the Raman spectrum. The defectives sites are the main source of the sensitivity of materials toward different gases. Thus, the current product was used for sensing devices. The device was subjected to various gases such as NO, NO2, CO, acetone, and ethanol at a low operating temperature of 30 °C and a concentration of 50 ppm. The sensor was observed to be less sensitive to most gas while showing the highest response towards ethanol gas. The sensor showed the highest response of 8.8% toward ethanol at 30 °C of 50 ppm, and a low response of 2.8% at 5 ppm, which was investigated here. The signal repeatability of the present sensor showed its capability to detect ethanol at much lower concentrations and at very low operating temperatures, resulting in reliability and saving power consumption. The gas sensing mechanism of direct interaction between the gas molecules and nanotube surface was considered the main. We have also proposed a sensing mechanism based on Coulomb dipole interaction for the physical adsorption of gas molecules on the surface.

One-Dimensional Nanoscale Si/Co Based on Layered Double Hydroxides towards Electrochemical Supercapacitor Electrodes.

It is well known that layered double hydroxides (LDHs) are two-dimensional (2D) layered compounds. However, we modified these 2D layered compounds to become one-dimensional (1D) nanostructures destined for high-performance supercapacitors applications. In this direction, silicon was inserted inside the nanolayers of Co-LDHs producing nanofibers of Si/Co LDHs through the intercalation of cyanate anions as pillars for building nanolayered structures. Additionally, nanoparticles were observed by controlling the preparation conditions and the silicon percentage. Scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy and thermal analyses have been used to characterize the nanolayered structures of Si/Co LDHs. The electrochemical characterization was performed by cyclic voltammetry and galvanic charge-discharge technique in 2M KOH electrolyte solution using three-electrode cell system. The calculated specific capacitance results indicated that the change of morphology from nanoparticles or plates to nanofibers had a positive effect for improving the performance of specific capacitance of Si/Co LDHs. The specific capacitance enhanced to be 621.5 F g-1 in the case of the nanofiber of Si/Co LDHs. Similarly, the excellent cyclic stability (84.5%) was observed for the nanofiber. These results were explained through the attribute of the nanofibrous morphology and synergistic effects between the electric double layer capacitive character of the silicon and the pseudo capacitance nature of the cobalt. The high capacitance of ternary Si/Co/cyanate LDHs nanocomposites was suggested to be used as active electrode materials for high-performance supercapacitors applications.

Growth of 1D TiO2nanostructures on Ti substrates incorporated with residual stress through humid oxidation and their characterizations.

Different Ti substrates, such as particles (as-received and ball milled), plate and TEM grid were oxidized for the growth of one dimensional (1D) TiO2nanostructures. The Ti substrates were oxidized for 4 h at temperatures of 700 °C-750 °C in humid and dry Ar containing 5 ppm of O2. The effects of residual stress on the growth of 1D TiO2nanostructures were investigated. The residual stress inside the Ti particles was measured by XRD-sin2ψtechnique. The oxidized Ti substrates were characterized using field emission scanning electron microscope equipped with energy dispersive x-ray spectroscope, transmission electron microscope, x-ray diffractometer and x-ray photoelectron spectroscope. Results revealed that humid environment enhances the growth of 1D TiO2nanostructures. Four different types of 1D morphologies obtained during humid oxidation, e.g. stacked, ribbon, plateau and lamp-post shaped nanostructures. The presence of residual stress significantly enhances the density and coverage of 1D nanostructures. The as-grown TiO2nanostructures possess tetragonal rutile structure having length up to 10µm along the 〈1 0 1〉 directions. During initial stage of oxidation, a TiO2layer is formed on Ti substrate. Lower valence oxides (Ti3O5, Ti2O3and TiO) then form underneath the TiO2layer and induce stress at the interface of oxide layers. The induced stress plays significant role on the growth of 1D TiO2nanostructures. The induced stress is relaxed by creating new surfaces in the form of 1D TiO2nanostructures. A diffusion based model is proposed to explain the mechanism of 1D TiO2growth during humid oxidation of Ti. The 1D TiO2nanostructures and TiO2layer is formed by the interstitial diffusion of Ti4+ions to the surface and reacts with the surface adsorbed hydroxide ions (OH-). Lower valence oxides are formed at the metal-oxide interface by the reaction between diffused oxygen ions and Ti ions.

Synthesis of Co-Fe 1D Nanocone Array Electrodes Using Aluminum Oxide Template.

Porous anodic alumina oxide (AAO) obtained via two-step anodization is a material commonly used as a template for fabricating 1D nanostructures. In this work, copper and cobalt-iron 1D nanocones were obtained by an electrodeposition method using AAO templates. The templates were produced using two-step anodization in H2C2O4. The Co-Fe nanostructures are characterized by homogeneous pore distribution. The electrocatalytic activity of the produced nanomaterials was determined in 1 M NaOH using the linear sweep voltammetry (LSV) and chronopotentiometry (CP) methods. These materials can be used as catalysts in the water-splitting reaction. The sample's active surface area was calculated and compared with bulk materials.

Mechanical design of brush coating technology for the alignment of one-dimension nanomaterials.

Widespread approaches to fabricate surfaces with aligned nanostructured topographies have been stimulated by opportunities to enhance interface performance by combing physical and chemical effects, in which brush-coating technology (BCT) is a cost-effective and feasible method for aligned film and large-scale production. Here, we reported a BCT process to realize the alignment of various 1D nanostructures through mechanical design that provides a more precise and higher shear force. By regulating the viscosity of dispersion, shear force is proved to be 24 and 20.3 times larger (when the volume ratio of water and glycerol is 1:3) according to the theoretical calculation and ANSYS simulating calculation results respectively, which plays a vital role in brush coating process. The universality was demonstrated by the alignment of one-dimension nanomaterials with different diameters, including silver nanowires (~80 nm), molybdenum trioxide nanobelts (~150 nm), vanadium pentoxide nanobelts (~150 nm) and bismuth sulfide nanobelts (~200 nm), et al., which in consequence have different alignment ratios. Meanwhile, anisotropic and flexible electrical conductors (the resistance anisotropic ratio was 2) and thermoelectric films (Seebeck coefficient was calculated to be 56.7 µV/K) were demonstrated.

Unidirectional Magnetic Anisotropy in Dense Vertically-Standing Arrays of Passivated Nickel Nanotubes.

We report the facile and low-cost preparation as well as detailed characterization of dense arrays of passivated ferromagnetic nickel (Ni) nanotubes (NTs) vertically-supported onto solid Au-coated Si substrates. The proposed fabrication method relies on electrochemical synthesis within the nanopores of a supported anodic aluminum oxide (AAO) template and allows for fine tuning of the NTs ferromagnetic walls just by changing the cathodic reduction potential during the nanostructures' electrochemical growth. Subsequently, the experimental platform allowed further passivation of the Ni NTs with the formation of ultra-thin antiferromagnetic layers of nickel oxide (NiO). Using adequately adapted magnetic measurements, we afterwards demonstrated that the thickness of the NT walls and of the thin antiferromagneticNiO layer, strongly influences the magnetic behavior of the dense array of exchange-coupled Ni/NiO NTs. The specific magnetic properties of these hybrid ferromagnetic/antiferromagnetic nanosystems were then correlated with the morpho-structural and geometrical parameters of the NTs, as well as ultimately strengthened by additionally-implemented micromagnetic simulations. The effect of the unidirectional anisotropy strongly amplified by the cylindrical geometry of the ferromagnetic/antiferromagnetic interfaces has been investigated with the magnetic field applied both parallel and perpendicular to the NTs axis.

One-Dimensional Nanostructures of Polypyrrole for Shielding of Electromagnetic Interference in the Microwave Region.

Polypyrrole one-dimensional nanostructures (nanotubes, nanobelts and nanofibers) were prepared using three various dyes (Methyl Orange, Methylene Blue and Eriochrome Black T). Their high electrical conductivity (from 17.1 to 60.9 S cm-1), good thermal stability (in the range from 25 to 150 °C) and resistivity against ageing (half-time of electrical conductivity around 80 days and better) were used in preparation of lightweight and flexible composites with silicone for electromagnetic interference shielding in the C-band region (5.85-8.2 GHz). The nanostructures' morphology and chemical structure were characterized by scanning electron microscopy, Brunauer-Emmett-Teller specific surface measurement and attenuated total reflection Fourier-transform infrared spectroscopy. DC electrical conductivity was measured using the Van der Pauw method. Complex permittivity and AC electrical conductivity of respective silicone composites were calculated from the measured scattering parameters. The relationships between structure, electrical properties and shielding efficiency were studied. It was found that 2 mm-thick silicone composites of polypyrrole nanotubes and nanobelts shield almost 80% of incident radiation in the C-band at very low loading of conductive filler in the silicone (5% w/w). Resulting lightweight and flexible polypyrrole composites exhibit promising properties for shielding of electromagnetic interference in sensitive biological and electronic systems.

One Dimensional ZnO Nanostructures: Growth and Chemical Sensing Performances.

Recently, one-dimensional (1D) nanostructures have attracted the scientific community attention as sensitive materials for conductometric chemical sensors. However, finding facile and low-cost techniques for their production, controlling the morphology and the aspect ratio of these nanostructures is still challenging. In this study, we report the vapor-liquid-solid (VLS) synthesis of one dimensional (1D) zinc oxide (ZnO) nanorods (NRs) and nanowires (NWs) by using different metal catalysts and their impact on the performances of conductometric chemical sensors. In VLS mechanism, catalysts are of great interest due to their role in the nucleation and the crystallization of 1D nanostructures. Here, Au, Pt, Ag and Cu nanoparticles (NPs) were used to grow 1D ZnO. Depending on catalyst nature, different morphology, geometry, size and nanowires/nanorods abundance were established. The mechanism leading to the VLS growth of 1D ZnO nanostructures and the transition from nanorods to nanowires have been interpreted. The formation of ZnO crystals exhibiting a hexagonal crystal structure was confirmed by X-ray diffraction (XRD) and ZnO composition was identified using transmission electron microscopy (TEM) mapping. The chemical sensing characteristics showed that 1D ZnO has good and fast response, good stability and selectivity. ZnO (Au) showed the best performances towards hydrogen (H2). At the optimal working temperature of 350 °C, the measured response towards 500 ppm of H2 was 300 for ZnO NWs and 50 for ZnO NRs. Moreover, a good selectivity to hydrogen was demonstrated over CO, acetone and ethanol.

Aerobic Oil-Phase Cyclic Magnetic Adsorption to Synthesize 1D Fe2O3@TiO2 Nanotube Composites for Enhanced Visible-Light Photocatalytic Degradation.

In this work, Fe2O3@TiO2 nanostructures with staggered band alignment were newly designed by an aerobic oil-phase cyclic magnetic adsorption method. XRD and TEM analyses were performed to verify the uniform deposition of Fe2O3 nanoparticles on the nanotube inner walls of TiO2. The steady-state degradation experiments exhibited that 1FeTi possessed the most superior performance, which might be ascribable to the satisfying dark adsorption capacity, efficient photocatalytic activity, ease of magnetic separation, and economic efficiency. These results indicated that the deposition of Fe2O3 into TiO2 nanotubes significantly enhanced the activity of Fe2O3, which was mainly ascribed to the Fe2O3-induced formation of staggered iron oxides@TiO2 band alignment and thus efficient separation of h+ and e-. Furthermore, the PL intensity and lifetime of the decay curve were considered as key criterions for the activity's evaluation. Finally, the leaching tests and regeneration experiments were also performed, which illustrated the inhibited photodissolution compared with TiO2/Fe3O4 and stable cycling ability, enabling 1FeTi to be a promising magnetic material for photocatalytic water remediation.

High-Efficiency Perovskite Solar Cells Enabled by Anatase TiO2 Nanopyramid Arrays with an Oriented Electric Field.

One-dimensional (1D) nanostructured oxides are proposed as excellent electron transport materials (ETMs) for perovskite solar cells (PSCs); however, experimental evidence is lacking. A facile hydrothermal approach was employed to grow highly oriented anatase TiO2 nanopyramid arrays and demonstrate their application in PSCs. The oriented TiO2 nanopyramid arrays afford sufficient contact area for electron extraction and increase light transmission. Moreover, the nanopyramid array/perovskite system exhibits an oriented electric field that can increase charge separation and accelerate charge transport, thereby suppressing charge recombination. The anatase TiO2 nanopyramid array-based PSCs deliver a champion power conversion efficiency of approximately 22.5 %, which is the highest power conversion efficiency reported to date for PSCs consisting of 1D ETMs. This work demonstrates that the rational design of 1D ETMs can achieve PSCs that perform as well as typical mesoscopic and planar PSCs.

Co-Evaporated CuO-Doped In2O3 1D-Nanostructure for Reversible CH4 Detection at Low Temperatures: Structural Phase Change and Properties.

In order to improve the sensitivity and to reduce the working temperature of the CH4 gas sensor, a novel 1D nanostructure of CuO-doped In2O3 was synthesized by the co-evaporation of Cu and In granules. The samples were prepared with changing the weight ratio between Cu and In. Morphology, structure, and gas sensing properties of the prepared films were characterized. The planned operating temperatures for the fabricated sensors are 50-200 °C, where the ability to detect CH4 at low temperatures is rarely reported. For low Cu content, the fabricated sensors based on CuO-doped In2O3 showed very good sensing performance at low operating temperatures. The detection of CH4 at these low temperatures exhibits the potential of the present sensors compared to the reported in the literature. The fabricated sensors showed also good reversibility toward the CH4 gas. However, the sensor fabricated of CuO-mixed In2O3 with a ratio of 1:1 did not show any response toward CH4. In other words, the mixed-phase of p- and n-type of CuO and In2O3 materials with a ratio of 1:1 is not recommended for fabricating sensors for reducing gas, such as CH4. The gas sensing mechanism was described in terms of the incorporation of Cu in the In2O3 matrix and the formation of CuO and In2O3 phases.

Structural characterization of self-assembled chain like Fe-FeOx Core shell nanostructure.

One of the big challenge of studying the core-shell iron nanostructures is to know the nature of oxide shell, i.e., whether it is γ-Fe2O3 (Maghemite), Fe3O4 (Magnetite), α-Fe2O3 (Hematite), or FeO (Wustite). By knowing the nature of iron oxide shell with zero valent iron core, one can determine the chemical or physical behavior of core-shell nanostructures. Fe core-shell nanochains (NCs) were prepared through the reduction of Fe3+ ions by sodium boro-hydride in aqueous solution at room atmosphere, and Fe NCs were further aged in water up to 240 min. XRD was used to study the structure of Fe NCs. Further analysis of core-shell nature of Fe NCs was done by TEM, results showed increase in thickness of oxide shell (from 2.5, 4, 6 to 10 nm) as water aging time increases (from 0 min, 120 min, 240 min to 360 min). The Raman spectroscopy was employed to study the oxide nature of Fe NCs. To further confirm the magnetite phase in Fe NCs, the Mössbauer spectroscopy was done on Fe NCs-0 and Fe NCs-6. Result shows the presence of magnetite in the sample before aging in water, and the sample after prolonged aging contains pure Hematite phase. It shows that prolonged water oxidation transforms the structure of shell of Fe NCs from mixture of Hematite and Magnetite in to pure hematite shell. The Magnetic properties of the Fe NCs were measured by VSM at 320 K. Because of high saturation magnetization (Ms) values, Fe NCs could be used as r2 contrasts agents for magnetic resonance imaging (MRI) in near future.

1D Carbon-Based Nanocomposites for Electrochemical Energy Storage.

Electrochemical energy storage (EES) devices have attracted immense research interests as an effective technology for utilizing renewable energy. 1D carbon-based nanostructures are recognized as highly promising materials for EES application, combining the advantages of functional 1D nanostructures and carbon nanomaterials. Here, the recent advances of 1D carbon-based nanomaterials for electrochemical storage devices are considered. First, the different categories of 1D carbon-based nanocomposites, namely, 1D carbon-embedded, carbon-coated, carbon-encapsulated, and carbon-supported nanostructures, and the different synthesis methods are described. Next, the practical applications and optimization effects in electrochemical energy storage devices including Li-ion batteries, Na-ion batteries, Li-S batteries, and supercapacitors are presented. After that, the advanced in situ detection techniques that can be used to investigate the fundamental mechanisms and predict optimization of 1D carbon-based nanocomposites are discussed. Finally, an outlook for the development trend of 1D carbon-based nanocomposites for EES is provided.

TiO2 Based Nanostructures for Photocatalytic CO2 Conversion to Valuable Chemicals.

Photocatalytic conversion of CO2 to useful products is an alluring approach for acquiring the two-fold benefits of normalizing excess atmospheric CO2 levels and the production of solar chemicals/fuels. Therefore, photocatalytic materials are continuously being developed with enhanced performance in accordance with their respective domains. In recent years, nanostructured photocatalysts such as one dimensional (1-D), two dimensional (2-D) and three dimensional (3-D)/hierarchical have been a subject of great importance because of their explicit advantages over 0-D photocatalysts, including high surface areas, effective charge separation, directional charge transport, and light trapping/scattering effects. Furthermore, the strategy of doping (metals and non-metals), as well as coupling with a secondary material (noble metals, another semiconductor material, graphene, etc.), of nanostructured photocatalysts has resulted in an amplified photocatalytic performance. In the present review article, various titanium dioxide (TiO2)-based nanostructured photocatalysts are briefly overviewed with respect to their application in photocatalytic CO2 conversion to value-added chemicals. This review primarily focuses on the latest developments in TiO2-based nanostructures, specifically 1-D (TiO2 nanotubes, nanorods, nanowires, nanobelts etc.) and 2-D (TiO2 nanosheets, nanolayers), and the reaction conditions and analysis of key parameters and their role in the up-grading and augmentation of photocatalytic performance. Moreover, TiO2-based 3-D and/or hierarchical nanostructures for CO2 conversions are also briefly scrutinized, as they exhibit excellent performance based on the special nanostructure framework, and can be an exemplary photocatalyst architecture demonstrating an admirable performance in the near future.

Formation of Si Nanorods and Discrete Nanophases by Axial Diffusion of Si from Substrate into Au and AuPt Nanoalloy Nanorods.

Interdiffusion between Si substrate and nanorod arrays of Au, Pt, and AuPt nanoalloys is investigated at temperatures lower than the AuSi eutectic temperature. When the nanorod is pure Au, Si diffusion from the substrate is very rapid. Au atoms are completely replaced by Si, converting the nanostructure into one of Si nanorod arrays. Au is diffused out to the substrate. The Au nanorod arrays on Si are unstable. When the nanorod is pure Pt, however, no diffusion of Si into the nanorod or any silicide formation is observed. The Pt nanorods are stable on Si substrate. When the nanorods are an alloy of AuPt, interesting interactions occur. Si diffusion into the nanorods is rapid but the diffusing Si readily reacts with Pt forming PtSi while Au diffuses out to the substrate. After annealing, nanophases of Au, Pt, PtSi, and Si may be present within the nanorods. When the Pt content of the alloy is low (12 at%) all Pt atoms are converted to silicide and the extra Si atoms remain in elemental form, particularly near the tip of the nanorods. Hence, the presence of Au accelerates Si diffusion and the ensuing reaction to form PtSi, a phenomenon absents in pure Pt nanorods. When the Au content of the alloy is low, the Si diffusion would cease when all Au atoms have diffused out of the nanorod, thereby arresting the silicide formation resulting in excess Pt in elemental form within the nanorod. This is a technique of making Si nanorods with and without embedded PtSi nanophase consisting of heterojunctions which could have unique properties.

Electrospun one-dimensional nanostructures: a new horizon for gas sensing materials.

Electrospun one-dimensional (1D) nanostructures are rapidly emerging as key enabling components in gas sensing due to their unique electrical, optical, magnetic, thermal, mechanical and chemical properties. 1D nanostructures have found applications in numerous areas, including healthcare, energy storage, biotechnology, environmental monitoring, and defence/security. Their enhanced specific surface area, superior mechanical properties, nanoporosity and improved surface characteristics (in particular, uniformity and stability) have made them important active materials for gas sensing applications. Such highly sensitive and selective elements can be embedded in sensor nodes for internet-of-things applications or in mobile systems for continuous monitoring of air pollutants and greenhouse gases as well as for monitoring the well-being and health in everyday life. Herein, we review recent developments of gas sensors based on electrospun 1D nanostructures in different sensing platforms, including optical, conductometric and acoustic resonators. After explaining the principle of electrospinning, we classify sensors based on the type of materials used as an active sensing layer, including polymers, metal oxide semiconductors, graphene, and their composites or their functionalized forms. The material properties of these electrospun fibers and their sensing performance toward different analytes are explained in detail and correlated to the benefits and limitations for every approach.

Stress-Tolerant Nanoporous Germanium Nanofibers for Long Cycle Life Lithium Storage with High Structural Stability.

Nanowires (NWs) synthesized via chemical vapor deposition (CVD) have demonstrated significant improvement in lithium storage performance along with their outstanding accommodation of large volume changes during the charge/discharge process. Nevertheless, NW electrodes have been confined to the research level due to the lack of scalability and severe side reactions by their high surface area. Here, we present nanoporous Ge nanofibers (NPGeNFs) having moderate nanoporosity via a combination of simple electrospinning and a low-energetic zincothermic reduction reaction. In contrast with the CVD-assisted NW growth, our method provides high tunability of macro/microscopic morphologies such as a porosity, length, and diameter of the nanoscale 1D structures. Significantly, the customized NPGeNFs showed a highly suppressed volume expansion of less than 15% (for electrodes) after full lithation and excellent durability with high lithium storage performance over 500 cycles. Our approach offers effective 1D nanostructuring with highly customized geometries and can be extended to other applications including optoelectronics, catalysis, and energy conversion.