Inorganic Nanowires Research Articles

A biodegradable piezoelectric scaffold promotes spinal cord injury nerve regeneration

Neural repair and regeneration remain one of the greatest challenges in regenerative medicine. The incorporation of intelligent scaffolds with noninvasive in vivo electrical stimulation illustrates considerable potential for tissue repair and regeneration. Nevertheless, the development of biomaterials that possess both biodegradable tissue scaffolds and electrical stimulation capabilities at a high level remains a significant obstacle. In this study, we effectively integrated the organic piezoelectric material poly-L-lactic acid (PLLA) with inorganic piezoelectric nanowires (potassium sodium niobate coated with polydopamine, KNN@PDA) to fabricate PLLA/KNN@PDA piezoelectric composite fibers. These fibers exhibit in-situ electrical stimulation capabilities, rendering them suitable for direct application in living tissues. The PLLA/KNN@PDA piezoelectric composite fibers not only function as biodegradable scaffolds for regenerative tissue engineering and platforms for in-situ electrical stimulation to enhance dorsal root ganglion axon growth, proliferation, and neuronal differentiation but also serve as versatile scaffolds for broader tissue engineering applications. In the complete spinal cord transection rat model, the piezoelectric scaffold enabled the recovery of rat motor function, indicating its significant ability to promote tissue formation and regeneration. Therefore, combining biodegradable piezoelectric tissue scaffolds with in situ electrical stimulation has significant therapeutic advantages for spinal cord injury repair and may be extended to other damaged tissues regeneration.

Spatiotemporally modulated full-polarized light emission for multiplexed optical encryption

Spatiotemporal control of full freedoms of polarized light emission is crucial in multiplexed optical computing, encryption and communication. Although recent advancements have been made in active emission or passive conversion of polarized light through solution-processed nanomaterials or metasurfaces, these design paths usually encounter limitations, such as small polarization degrees, low light utilization efficiency, limited polarization states, and lack of spatiotemporal control. Here, we addressed these challenges by integrating the spatiotemporal modulation of the LED device, the precise control and efficient polarization emission through nanomaterial assembly, and the programmable patterning/positioning using 3D printing. We achieved an extremely high degree of polarization for both linearly and circularly polarized emission from ultrathin inorganic nanowires and quantum nanorods thanks to the shear-force-induced alignment effect during the protruding of printing filaments. Real-time polarization modulation covering the entire Poincaré sphere can be conveniently obtained through the programming of the on-off state of each LED pixel. Further, the output polarization states can be encoded by an ordered chiral plasmonic film. Our device provides an excellent platform for multiplexing spatiotemporal polarization information, enabling visible light communication with an exceptionally elevated level of physical layer security and multifunctional encrypted displays that can encode both 2D and 3D information.

Ultra-Long Carrier Lifetime of Spiral Perovskite Nanowires Realized through Cooperative Strategy of Selective Etching and Passivation.

Spiral inorganic perovskite nanowires (NWs) possess unique morphologies and properties that allow them highly attractive for applications in optoelectronic and catalytic fields. In popular solution-based synthesis methodology, however, challenges persist in simultaneously achieving precise and facile control over morphological twisting and fantastic carrier lifetimes. Here, a cooperative strategy of concurrently employing selective etching and ligand engineering is applied to facilitate the formation of spiral CsPbBr3 perovskite NWs with an ultralong carrier lifetime of ≈2 µs. Specifically, a novel amine of 1-(p-tolyl)ethanamine is introduced to functionalize as both a selective etchant and the source of forming an effective ligand to passivate the exposed facets, favoring the structural twisting and the enhancement of carrier lifetimes. The twisting behaviors are dependent on the etch ratios, which are essentially associated with the densities of grain boundaries and dislocations in the NWs. The ultralong carrier lifetime and long-term stability of the spiral NWs open up new possibilities for all-inorganic perovskites in optoelectronic and photocatalytic fields, while the cooperative synthesis strategy paves the way for exploring complex spiral structures with tunable morphology and functionality.

Polybenzimidazole dispersed polymer coated nanowires as efficient electrolytes for proton exchange membrane fuel cells

In this study, polymer-coated anisotropic inorganic nanowires dispersed in PBI matrix were introduced to construct 1D proton conducting channels within PBI. Ionic-liquid and solvothermal methods were used for the synthesis of ZrO2 and W18O49 NWs, which were coated with PVPA and PDDA polymers to increase their proton conductivity. Our results showed that, prepared membranes have amorphous nature due to the dominating presence of PBI. SEM analysis revealed the average thickness of membrane of about 36 µm. TG/DTA analysis detected lower weight loss of W18O49 NWs (total 2.8%) compared to ZrO2 NWs (18%). Proton conductivity analysis showed that, PDDA/W18O49 NWs possess relatively 4 times higher proton conductivity (4×\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ \ imes $$\\end{document}10−4 Scm−1) compared to PDDA/ZrO2 NWs (1×\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ \ imes $$\\end{document}10−4 Scm−1) at 80 ℃. In addition, PDDA-coated W18O49 NWs dispersed PBI membranes showed the highest fuel cell current density (1.2 A/cm2) and power density (215 mW/cm2) at 150 ℃ after 24 h which is nearly 2.5 times higher than pure PBI membrane. In addition, they exhibited the lowest in-situ proton resistance of about (0.47 Ω) compared with that of pure PBI membrane (0.8 Ω). Our results are introducing new concepts towards the development of thin and efficient polymer electrolyte membranes for PEM fuel cells.

Ultralong Nanowires of Cadmium Phosphate Hydroxide Synthesized Using a Cadmium Oleate Precursor Hydrothermal Method and Sulfidation Conversion to Ultralong CdS Nanowires.

Ultralong nanowires with ultrahigh aspect ratios exhibit high flexibility, and they are promising for applications in various fields. Herein, a cadmium oleate precursor hydrothermal method is developed for the synthesis of ultralong nanowires of cadmium phosphate hydroxide. In this method, water-soluble cadmium salt is used as the cadmium source, water-soluble phosphate is used as the phosphorus source, and sodium oleate is adopted as a reactant to form cadmium oleate precursor and as a structure-directing agent. By using this method, ultralong nanowires of cadmium phosphate hydroxide are successfully synthesized using CdCl2, sodium oleate, and NaH2PO4 as reactants in an aqueous solution by hydrothermal treatment at 180 °C for 24 h. In addition, a new type of flexible fire-resistant inorganic paper with good electrical insulation performance is fabricated using ultralong nanowires of cadmium phosphate hydroxide. As an example of the extended application of this synthetic method, ultralong nanowires of cadmium phosphate hydroxide can be converted to ultralong CdS nanowires through a convenient sulfidation reaction. In this way, ultralong CdS nanowires are successfully synthesized by simple sulfidation of ultralong nanowires of cadmium phosphate hydroxide under mild conditions. The as-prepared ultralong nanowires of cadmium phosphate hydroxide are promising for applications as the precursors and templates for synthesizing other inorganic ultralong nanowires and have wide applications in various fields.

First-principles calculations of inorganic metallocene nanowires.

Inspired by the recently synthesized inorganic metallocene derivatives Fe(P4)22-, we have identified four stable inorganic metallocene nanowires, MP4 (M = Sc, Ti, Cr and Fe) in configurations of either regular quadrangular prism (Q-type) or anticube (A-type), and further investigated their magnetic and electronic characteristics utilizing the first-principles calculation. It shows that CrP4 is a ferromagnetic metal, while other nanowires are semiconducting antiferromagnets with bandgaps of 0.44, 1.88, and 2.29 eV within the HSE06 level. It also shows that both ScP4 and TiP4 can be stabilized in the Q-type and A-type, corresponding to the antiferromagnetic and ferromagnetic ground states, respectively, indicating a configuration-dependent magnetism. The thermodynamic and lattice stabilities are confirmed by the ab initio molecular dynamics and phonon spectra. This study has unmasked the structural and physical properties of novel inorganic metallocene nanowires, and revealed their potential application in spintronics.

The transformation of lepidocrocite (γ-FeOOH) with Fe(ii)(aq) in slightly acidic media: intermediate pathways and biomimetic behavior

Lepidocrocite catalysis with Fe(ii)(aq) was found to produce Christmas tree particles formed via a bacterial-like mechanism guided by inorganic nanowire antennas through an electron transparent film.

Silica nanowires-reinforced silica aerogels with outstanding thermal insulation, thermal stability and mechanical properties

Silica aerogels possess extremely low thermal conductivity, low density and high porosity, which can be regarded as candidates for new thermal insulation materials. However, silica aerogels suffer from low strength, brittleness, modeling difficulties and high moisture absorption. In this work, compatible inorganic silica nanowires are introduced as one-dimensional reinforcing materials, and silica nanowires-reinforced silica aerogels (SiO2NWs-MSAs) are synthesized using a two-step acid-base catalytic in-situ sol-gel method combined with atmospheric pressure drying, aiming to improve the comprehensive performances of the composite aerogels. The composite aerogels exhibit good mechanical properties, and the composite aerogel has a compressive strength of 1.379 MPa at a strain of 60 % when the doping amount of silica nanowires is 11 %. The volumetric shrinkage of the composite aerogels varies between 11.58 and 12.81 % and the density ranges from 0.11 to 0.13 g cm−3. SiO2NWs-MSA2 has a low thermal conductivity and good high-temperature insulation properties with thermal conductivity of 0.039 W m−1 K−1 at 25 °C and 0.046 W m−1 K−1 at 150 °C. The thermal stability of the composite aerogels is improved, and the thermal decomposition temperature reaches 500 °C. Meanwhile, the water contact angles of the composite aerogels all exceed 140°. In addition, the composite aerogels can maintain the amorphous state at 1200 °C, and the microstructure remains basically unchanged at 1000 °C, showing excellent high-temperature resistance.

Robust, biodegradable and flame-retardant nanocomposite films based on TEMPO-oxidized cellulose nanofibers and hydroxyapatite nanowires

Flammability is a fatal drawback for sustainable packaging materials made from cellulose and its derivatives. Incorporating inorganic nanomaterials is a viable approach to improve the fire-resistant property. However, due to the aggregation of inorganic fillers and weak interactions between components, incorporating inorganic nanomaterials always had an adverse impact on the mechanical properties and optical transparency of cellulose-based nanocomposites. Herein, we presented a robust, biodegradable, and flame-retardant nanocomposite film composed of TEMPO-oxidized cellulose nanofibers (TOCNFs) and inorganic hydroxyapatite nanowires (HNWs). Both TOCNFs and HNWs possessed one-dimensional microstructure and could form unique organic-inorganic networks microstructure. The organic-inorganic networks interact through physical intertwinement and multiple chemical bonds, endowing nanocomposite film with outstanding mechanical properties. This nanocomposite film showed a tensile strength of 223.68 MPa and Young's modulus of 9.18 GPa, which were superior to most reported cellulose-based nanocomposite. Furthermore, this nanocomposite film demonstrated exceptional thermal stability and flame-retardant feature attributed to the inorganic framework formed by HNWs. This nanocomposite film also possessed a high optical transmittance even when HNWs content reached 30 % and could be decomposed quickly in soil. By employing organic-inorganic interpenetrating network structure design and multiple bonding interaction, cellulose-based nanocomposites can overcome inherent limitations and attain desirable comprehensive properties.

Regulating the Conformational and Macroscopic Properties of Inorganic Nanowires by Polymer Grafts

AbstractUltrathin inorganic nanowires are an emerging class of building blocks for creating functional materials and devices, but there remains challenging to fine‐tune the structure and property of the nanowires at the molecular level. Here, this work shows that ultrathin polymer‐grafted gold nanowires (PG‐AuNWs) can exhibit bottlebrush polymer‐like physical behaviors and macroscopic properties. The hybrid PG‐AuNWs in solutions show polymer‐like viscoelasticity which can be finely regulated by controlling the structural parameters (e.g., length of the AuNWs, molecular weight of grafted polymers) of the PG‐AuNWs, the environmental conditions (e.g., temperature, solvent compositions), and the aging time. Furthermore, this work unravels at the molecular level that the conformational properties (e.g., contour length, persistence length, and mean‐squared radius of gyration) of the PG‐AuNWs can be correlated to their structural parameters following similar power‐law relations as molecular bottlebrush polymers. This work bridges the fundamental gap between polymer‐like inorganic nanowires and bottlebrush polymers, thus accelerating the development of new nanowire‐based functional hybrid materials and devices.

Flexible dye solar cells with TiO2 nanopaper and Ti back contact electrodes

Flexible dye solar cells (F-DSCs) have attracted great attention because of their low cost, flexibility and lightweight, and their advantages for wearable electronic devices and other applications. We propose here a novel structure of F-DSCs using flexible TiO2 nanopapers as substrates and Ti back contact electrodes(Ti BCE) as electron collection electrodes. By combining the high-temperature hydrothermal nanowire synthesis with conventional paper preparation, TiO2 nanopapers (long nanowire TiO2 free-standing membranes) with good mechanical strength and flexibility were prepared. This TiO2 nanopapers from pure long inorganic nanowires, can be used as an ideal flexible substrate for Ti BCE and nanocrystalline TiO2 films, because they retain their excellent mechanical strength and flexibility at high temperatures. The PCE of F-DSCs with TiO2 nanopaper substrate and the porous Ti BCE reached 4.38% under AM 1.5G and 100 mW cm−2 simulated solar irradiation. The F-DSCs remained stable after 100 bending tests at 16 mm bending radius.

Mixed-Dimensional Nanoparticle-Nanowire Channels for Flexible Optoelectronic Artificial Synapse with Enhanced Photoelectric Response and Asymmetric Bidirectional Plasticity.

A mixed-dimensional dual-channel synaptic transistor composed of inorganic nanoparticles and organic nanowires was fabricated to expand the photoelectric gain range. The device can actualize the sensitization features of the nociceptor and shows improved responsiveness to visible light. Under electrical pulses with different polarities, the apparatus exhibits reconfigurable asymmetric bidirectional plasticity. Moreover, the devices demonstrate good operational tolerance and mechanical stability, retaining more than 60% of their maximum responsiveness after 100 consecutive/bidirectional and 1000 flex/flat operations. The improved photoelectric response of the device endows a high image recognition accuracy of greater than 80%. Asymmetric bidirectional plasticity is used as punishment/reward in a psychological experiment to emulate the improvement of learning motivation and enables real-time forward and backward deflection (+7 and -25°) of artificial muscle. The mixed-dimensional optoelectronic artificial synapses with switchable behavior and electron/hole transport type have important prospects for neuromorphic processing and artificial somatosensory nerves.

Out-of-Plane Electronics on Flexible Substrates Using Inorganic Nanowires Grown on High-Aspect-Ratio Printed Gold Micropillars.

Out-of-plane or3Delectronics on flexible substrates are an interesting direction that can enable novel solutions such as efficient bioelectricity generation and artificial retina. However, the development of devices with such architectures is limited by the lack of suitable fabrication techniques. Additive manufacturing (AM) can but often fail to provide high-resolution, sub-micrometer 3D architectures. Herein, the optimization of a drop-on-demand (DoD), high-resolution electrohydrodynamic (EHD)-based jet printing method for generating 3D gold (Au) micropillars is reported. Libraries of Au micropillar electrode arrays (MEAs) reaching a maximum height of 196µm and a maximum aspect ratio of 52 are printed. Further, by combining AM with the hydrothermal growth method, a seedless synthesis of zinc oxide (ZnO) nanowires (NWs) on the printed Au MEAs is demonstrated. The developed hybrid approach leads to hierarchical light-sensitive NW-connected networks exhibiting favorable ultraviolet (UV) sensing as demonstrated via fabricating flexible photodetectors (PDs). The 3D PDs exhibit an excellent omnidirectional light-absorption ability and thus, maintain high photocurrents over wide light incidence angles (±90°). Lastly, the PDs are tested under both concave and convex bending at 40mm, showing excellent mechanical flexibility.

Multicolor Circularly Polarized Luminescence from Inorganic Crystalline Nanostructures Induced by Atomic Chirality.

Circularly polarized luminescence (CPL) is well-studied in molecular systems but has been rarely reported in pure inorganic nanoscale crystals. Herein, we develop a family of pure inorganic rare-earth nanowires with robust and color-tunable CPL emissions. The chiral rare earth nanowires possess intrinsic atomic chirality with controlled handedness that is guided by the enantiomers with molecular chirality in the synthesis. By varying luminescent ions incorporated in the crystal lattice, color-tunable CPL can be achieved and is thermally robust, preserving emission over 300 °C, distinct from existing CPL-active materials. Moreover, as a proof of concept, we demonstrate that the synthesized nanostructures can be easily dispersed in a polymer matrix to enable transparent and flexible CPL films. This study opens up a promising avenue to design robust and tunable CPL materials helpful to the understanding of inorganic chiral information and capable of further applications in novel optoelectronic devices.

Orthogonal‐Stacking Integration of Highly Conductive Silicide Nanowire Network as Flexible and Transparent Thin Films

AbstractFlexible and transparent conductive (FTC) thin films are indispensable elements in building high‐performance flexible or soft electronics and displays. Slim inorganic nanowires (NWs), with excellent conductivity and durability, are ideal one‐dimensional ingredients to weave a quasi‐continuous FTC network. However, a precise spatial arrangement of these ultrathin NWs, to form an optimal interconnected network, represents still a difficult challenge. In this work, a catalytic growth of orderly SiNW arrays, via an in‐plane solid‐liquid‐solid mechanism, and an orthogonal‐stacking integration of the SiNWs into a 2‐layer cross‐linked network, followed by a direct alloy formation and soldering of highly conductive SiNi alloy NWs upon a flexible polyimide polymer, is demonstrated. It is also shown that the flexibility of the SiNi FTC network can be significantly enhanced with an elastic spring design of the silicide NW channels, leading to an impressive transmittance of ≈90%, a moderately equivalent sheet resistance of 130 Ω sq−1 and a durable flexibility that can sustain repetitive bending to a 2 mm radius for >1000 cycles. These results highlight the unique capabilities of an optimal spatial arrangement, precise assembly/soldering and elastic geometry design of alloy NWs to enable a new generation of high‐performance FTC thin film material for future flexible electronics, displays, and bio‐interfaced sensors.

Aligned Phthalocyanine Molecular Nanowires by Graphoepitaxial Self‐Assembly and Their In Situ Integration into Photodetector Arrays

AbstractLarge‐scale on‐chip integration of organic nanowire‐based devices requires the deterministic assembly of organic small molecules into highly‐aligned nanowires. In this work, phthalocyanine molecules are self‐assembled into horizontally‐aligned nanowires after generating parallel hydrophobic nanogrooves on a sapphire surface. In contrast to previous self‐oriented inorganic nanowires, these molecular nanowires are separated from their supporting sapphire by an ultrathin amorphous layer, indicating a complete elimination of lattice matching between nanowires and substrates. Therefore, small molecules beyond phthalocyanines hold promise to form aligned nanowires using this graphoepitaxial self‐assembly strategy. The excellent alignment and high crystallinity of these nanowires enable the desired in‐situ integration of nanowire‐based devices without additional postgrowth processing steps. As a proof of concept, self‐oriented CuPc nanowires are integrated into photodetector arrays directly on their growth substrate after electrode arrays are transferred onto the nanowires. Compared to previous CuPc photodetectors constructed using other approaches, these detectors exhibit a faster response to the spectrum in the 488–780 nm range (rise and fall times are 0.05–0.43 s and 0.38–2.34 s, respectively) while offering comparable detectivities (2.49 × 1010 Jones on average). This graphoepitaxial self‐assembly offers new opportunities for the aligned growth of organic crystalline nanowires and their large‐scale in‐situ integration into functional devices.

Perovskite/GaAs-nanowire hybrid structure photodetectors with ultrafast multiband response enhancement by band engineering

We developed a hybrid structure photodetector combining one-dimensional (1D) inorganic GaAs nanowires and two-dimensional (2D) organic perovskite materials, which can achieve various performance enhancements using a relatively simple structure. Via the optical absorption enhancement of perovskite and the type-II energy band structure formed by the heterostructure, the responsivity and detectivity of the photodetector from ultraviolet (UV) to visible (Vis) wavelengths are significantly enhanced, reaching 75 A/W and 1.49×1011 Jones, respectively. The response time of the photodetector was significantly decreased by 3 orders, from 785 ms to 0.5 ms, and the dark current was further reduced to 237 fA. A photodetector was prepared with enhanced responsivity and ultrafast response time in the multiband region from the UV to Vis wavelength. To the best of our knowledge, this is the first time to combine inorganic III-V GaAs nanomaterials with organic perovskite materials, which verifies the effective combination of inorganic and organic materials in a mixed dimension. The excellent photoelectric performance of the perovskite/GaAs-nanowire hybrid structure photodetector makes it a potential candidate material for a wide range of photoelectric applications such as multiband photodetection.

Rational Design of All-Inorganic Assemblies with Bright Circularly Polarized Luminescence.

Materials with exceptional circularly polarized luminescence (CPL) are important in multi-field applications such as 3D display, anti-counterfeiting, sensing, spin electronics, etc. Although CPL properties have been widely investigated ranging from the traditional chiral organic molecules to the emerging chiral inorganic nanomaterials and their assemblies, a trade-off between the luminescence efficiency (quantum yield, ϕ) and the luminescence dissymmetry factor (glum ) is always the bottleneck for all the chiral luminescent materials, which hinders their practical application. Herein, a new route to overcome the paradox through rationally assembling quantum nanorods and ultrathin inorganic nanowires into ordered multilayer structures is reported, achieving both high ϕ and glum . In these assembled structures, the aligned quantum nanorods emit linearly polarized light that is then transformed to CPL by the aligned ultrathin nanowire assemblies with precisely controlled phase retardation. This method is universal and readily extended to versatile 1D nanomaterials, paving the way for the practical applications of CPL active materials.

Mixed-Dimensional van der Waals Heterostructure for High-Performance and Air-Stable Perovskite Nanowire Photodetectors.

An organic-inorganic hybrid perovskite nanowire (NW), CH3NH3PbI3, shows great potential for high-performance photodetectors due to its excellent photoresponse. However, the inefficient carrier collection between the one-dimensional (1D) NWs and metallic electrodes, as well as degradation of the perovskite, limits the viability of the CH3NH3PbI3 NWs for commercial production. Here, we demonstrate a photodetector with a mixed-dimensional van der Waals heterostructure of hexagonal boron nitride (hBN)/graphene (Gr)/1D CH3NH3PbI3, which exhibits excellent responsivity and specific detectivity of up to 558 A/W and 2.3 × 1012 Jones, owing to the improved carrier extraction at the electrical contact between Gr and the NW. As for the atomic encapsulation of hBN, the device is extremely robust and maintains its outstanding performance for more than 2 months when exposed to air. Moreover, benefitting from the 1D geometry of the CH3NH3PbI3 NW, our device is highly sensitive to polarized light. The mixed-dimensional van der Waals heterostructure, hBN/Gr/1D CH3NH3PbI3, would provide a novel idea and protocol for fabricating high-performance and air-stable photoelectronic devices based on organic-inorganic hybrid perovskite NWs.

Shape memory polymer composites (SMPCs) using interconnected nanowire network foams as reinforcements

Shape memory polymers (SMPs), although offer a suite of advantages such as ease of processability and lower density, lag behind their shape memory alloy counterparts, in terms of mechanical properties such as recovery stress and cyclability. Reinforcing SMPs with inorganic nanowires and carbon nanotubes (CNTs) is a sought-after pathway for tailoring their mechanical properties. Here, inorganic nanowires also offer the added advantage of covalently binding the fillers to the surrounding polymer matrices via organic molecules. The SMP composites (SMPCs) thus obtained have well-engineered nanowire-polymer interfaces, which could be used to tune their mechanical properties. A well-known method of fabricating SMPCs involving casting dispersions of nanowires (or CNTs) in mixtures of monomers and crosslinkers typically results in marginal improvements in the mechanical properties of the fabricated SMPCs. This is owed to the constraints imposed by the rule-of-mixture principles. To circumvent this limitation, a new method for SMPC fabrication is designed and presented. This involves infiltrating polymers into pre-fabricated nanowire foams. The pre-fabricated foams were fabricated by consolidating measured quantities of nanowires and a sacrificial material, such as (NH4)2CO3, followed by heating the consolidated mixtures for subliming the sacrificial material. Similar to the case of traditional composites, use of silanes to functionalize the nanowire surfaces allowed for the formation of bonds between both the nanowire-nanowire and the nanowire-polymer interfaces. SMPCs fabricated using TiO2 nanowires and SMP composed of neopentyl glycol diglycidyl ether and poly(propylene glycol) bis(2-aminopropyl ether) (Jeffamine D230) in a 2:1 molar ratio exhibited a 300% improvement in the elastic modulus relative to that of the SMP. This increase was significantly higher than SMPC made using the traditional fabrication route. Well-known powder metallurgy techniques employed for the fabrication of these SMPCs make this strategy applicable for obtaining other SMPCs of any desired shape and chemical composition.