Plasma‐Induced Hetero‐Nanostructures on a Polymer with Selective Metal Co‐Deposition

Plasma‐induced pattern formation is explored on polyethylene terephthalate (PET) using an oxygen plasma glow discharge. The nanostructures on PET are formed through preferential etching directed by the co‐deposition of metallic elements, such as Cr or Fe, sputtered from a stainless‐steel cathode. The local islands formed by metal co‐deposition have significantly slower etching rates than those of the pristine regions on PET, generating anisotropic nanostructures in pillar‐ or hair‐like form during plasma etching. By covering the cathode with the appropriate material, the desired metallic or polymeric elements can be co‐deposited onto the target surfaces. When the cathode is covered by a relatively soft material composed of only carbon and hydrogen, such as polystyrene, nanostructures typically induced by preferential etching are not observed on the PET surface, and the surfaces are uniformly etched. A variety of metals, such as Ag, Cu, Pt, or Si, can be successfully co‐deposited onto the PET surfaces by simply using a cathode covered in the desired metal; high‐aspect‐ratio nanostructures coated with the co‐deposited metal are subsequently formed. Therefore this simple single‐step method for forming hetero‐nanostructures—that is, nanoscale hair‐like polymer structures decorated with metals—can be used to produce nanostructures for various applications, such as catalysts, sensors, or energy devices.     

Large Photothermal Effect in Sub‐40 nm h‐BN Nanostructures Patterned Via High‐Resolution Ion Beam

The controlled nanoscale patterning of 2D materials is a promising approach for engineering the optoelectronic, thermal, and mechanical properties of these materials to achieve novel functionalities and devices. Herein, high‐resolution patterning of hexagonal boron nitride (h‐BN) is demonstrated via both helium and neon ion beams and an optimal dosage range for both ions that serve as a baseline for insulating 2D materials is identified. Through this nanofabrication approach, a grating with a 35 nm pitch, individual structure sizes down to 20 nm, and additional nanostructures created by patterning crystal step edges are demonstrated. Raman spectroscopy is used to study the defects induced by the ion beam patterning and is correlated to scanning probe microscopy. Photothermal and scanning near‐field optical microscopy measure the resulting near‐field absorption and scattering of the nanostructures. These measurements reveal a large photothermal expansion of nanostructured h‐BN that is dependent on the height to width aspect ratio of the nanostructures. This effect is attributed to the large anisotropy of the thermal expansion coefficients of h‐BN and the nanostructuring implemented. The photothermal expansion should be present in other van der Waals materials with large anisotropy and can lead to applications such as nanomechanical switches driven by light.     

Metasurface Enabled Wide‐Angle Fourier Lens

Fourier optics, the principle of using Fourier transformation to understand the functionalities of optical elements, lies at the heart of modern optics, and it has been widely applied to optical information processing, imaging, holography, etc. While a simple thin lens is capable of resolving Fourier components of an arbitrary optical wavefront, its operation is limited to near normal light incidence, i.e., the paraxial approximation, which puts a severe constraint on the resolvable Fourier domain. As a result, high‐order Fourier components are lost, resulting in extinction of high‐resolution information of an image. Other high numerical aperture Fourier lenses usually suffer from the bulky size and costly designs. Here, a dielectric metasurface consisting of high‐aspect‐ratio silicon waveguide array is demonstrated experimentally, which is capable of performing 1D Fourier transform for a large incident angle range and a broad operating bandwidth. Thus, the device significantly expands the operational Fourier space, benefitting from the large numerical aperture and negligible angular dispersion at large incident angles. The Fourier metasurface will not only facilitate efficient manipulation of spatial spectrum of free‐space optical wavefront, but also be readily integrated into micro‐optical platforms due to its compact size.     

Controlled Synthesis of One‐Dimensional Inorganic Nanostructures Using Pre‐Existing One‐Dimensional Nanostructures as Templates

Template‐directed strategy has become one of the most popular methods for the fabrication of one‐dimensional (1D) nanostructures with uniform size and controllable physical dimensions in recent years. This Review article describes the recent progress in the synthesis of 1D inorganic nanostructures by using suitable templates. A brief survey on the templating method based on the organic templates and porous membrane is firstly given. Then, the article is focused on recent emerging synthetic strategies by templating against the pre‐existing 1D nanostructures using different physical and chemical transformation techniques, including epitaxial growth, nonepitaxial growth, direct chemical transformation, solid‐state interfacial diffusion reaction, and so on. The important reactivity role of the 1D nanostructures will be emphasized in such transformation process. Finally, we conclude this paper with some perspectives and outlook on this research topic.     

High‐Gain 200 ns Photodetectors from Self‐Aligned CdS–CdSe Core–Shell Nanowalls

1D core–shell heterojunction nanostructures have great potential for high‐performance, compact optoelectronic devices owing to their high interface area to volume ratio, yet their bottom‐up assembly toward scalable fabrication remains a challenge. Here the site‐controlled growth of aligned CdS–CdSe core–shell nanowalls is reported by a combination of surface‐guided vapor–liquid–solid horizontal growth and selective‐area vapor–solid epitaxial growth, and their integration into photodetectors at wafer‐scale without postgrowth transfer, alignment, or selective shell‐etching steps. The photocurrent response of these nanowalls is reduced to 200 ns with a gain of up to 3.8 × 10³ and a photoresponsivity of 1.2 × 10³ A W^?1, the fastest response at such a high gain ever reported for photodetectors based on compound semiconductor nanostructures. The simultaneous achievement of sub‐microsecond response and high‐gain photocurrent is attributed to the virtues of both the epitaxial CdS–CdSe heterojunction and the enhanced charge‐separation efficiency of the core–shell nanowall geometry. Surface‐guided nanostructures are promising templates for wafer‐scale fabrication of self‐aligned core–shell nanostructures toward scalable fabrication of high‐performance compact photodetectors from the bottom‐up.     

Process optimization and microstructural analysis of aluminum based composite reinforced by multi‐walled carbon nanotubes with various aspect ratios

The dispersion of carbon nanostructures in metallic matrix with strong bonding is a very important challenge to achieve a composite with high mechanical properties. In this work, the effect of aspect ratio of reinforcement phase, weight percent and using improved mechanical alloying process and sonication on the well dispersion of multiwalled carbon nanostructures (MWCNTs) were investigated. Moreover, the hot pressing conditions were optimized by factorial design technique to achieve the highest relative density. Field emission scanning electron microscopy (FE‐SEM), transmission electron microscopy (TEM) and X‐ray diffraction were used to analyse the microstructure. Also, the particle size of the grain structure of composite containing multi‐walled carbon nanotubes determined for evaluating the influence of aspect ratio on grain growth. The results verified that by using conventional method of alloying, grinding process and agglomeration of 2 wt% multi‐walled carbon nanotubes with long length can be occurred. By decreasing the weight percent of multi‐walled carbon nanotubes to 1 wt%, dispersion process progressed slightly. Short length multi‐walled carbon nanotubes showed more clustering and minor damage in both 1 and 2 wt%. By using modified design of alloying (using magnet), both types of multi‐walled carbon nanotubes dispersed better than conventional design in the matrix with good bonding at initial times.     

Phonon‐Assisted Electro‐Optical Switches and Logic Gates Based on Semiconductor Nanostructures

High‐performance nanostructured electro‐optical switches and logic gates are highly desirable as essential building blocks in integrated photonics. In contrast to silicon‐based optoelectronic devices, with their inherent indirect optical bandgap, weak light‐modulation mechanism, and sophisticated device configuration, direct‐bandgap‐semiconductor nanostructures with attractive electro‐optical properties are promising candidates for the construction of nanoscale optical switches for on‐chip photonic integrations. However, previously reported semiconductor‐nanostructure optical switches suffer from serious drawbacks such as high drive voltage, limited operation spectral range, and low modulation depth. High‐efficiency electro‐optical switches based on single CdS nanobelts with low drive voltage, ultra‐high on/off ratio, and broad operation wavelength range, properties resulting from unique electric‐field‐dependent phonon‐assisted optical transitions, are demonstrated. Furthermore, functional NOT, NOR, and NAND optical logic gates are demonstrated based on these switches. These switches and optical logic gates represent an important step toward integrated photonic circuits.     

Eutectic Combinations as a Pathway to the Formation of Substrate‐Based Au‐Ge Heterodimers and Hollowed Au Nanocrescents with Tunable Optical Properties

Pairs of immiscible elements with deep eutectics are used to synthesize periodic arrays of heterodimers and hollowed metal nanocrescents. In the devised route, substrate‐immobilized Au or Ag nanostructures act as heterogeneous nucleation sites for Ge adatoms. At elevated temperatures the adatoms collect in sufficient quantities to transform each site into a AuGe liquid alloy which, upon cooling, phase separates into elemental components sharing a common interface. The so‐formed Au‐Ge and Ag‐Ge heterodimers exhibit a complex morphology characterized by a noble metal nanocrescent which partially encapsulates one end of the Ge domain. Through the use of a selective etch the Ge component is removed, leaving behind a periodic array of hollow noble metal nanocrescents on the surface of the substrate. Optical characterization of both the heterodimers and nanocrescents indicates that the presence of Ge gives rise to a relative blue‐shift in the localized surface plasmon peak, a result that is in stark contrast to the red‐shifts typically observed when plasmonic nanostructures are in contact with a dielectric medium. Simulations are used to both rationalize the observed shift and show the potential for deriving unexpected behaviors when semishell‐like noble metal structures are in contact with high permittivity dielectric mediums.     

A Template‐Free Method Towards Conducting Polymer Nanostructures

Conducting polymer nanostructures have recently received special attention in nanoscience and nanotechnology because of their highly π‐conjugated polymeric chains and metal‐like conductivity, such that they can be regarded not only as excellent molecular wires, but also as basic units for the formation of nanodevices. Although various approaches, such as hard‐template methods, soft‐template methods, electrospinning technology, and so on are widely employed to synthesize or fabricate conducting polymer nanostructures and their composite nanostructures, each of the currently used methods possess disadvantages. Therefore, finding a facile, efficient, and controlled method of forming conducting polymer nanostructures is desirable. Similar to other nanomaterials, the effect of size (in these cases 1–100 nm) on the properties of the conducting polymer nanostructures must be considered. Electrical measurements of single nanotubes or nanowires are desirable in order to be able to understand the pure electrical properties of conducting polymer nanostructures. Compared with bulk conducting polymers, conducting polymer nanostructures are expected to display improved performance in technological applications because of the unique properties arising from their nanometer‐scaled size: high conductivity, large surface area, and light weight. Thus, it is also desirable to develop promising applications for conducting polymer nanostructures. In accordance with the issues described above, our research focuses on a new synthesis method to form conducting polymer nanostructures and on the related formation mechanism of the resultant nanostructures. The electrical and transport properties of single nanotubes of conducting polymer, measured by a four‐probe method, and promising applications of such template‐free‐synthesized conducting polymer nanostructures as new microwave absorbing materials and sensors guided by a reversible wettability are also of interest. This article reports some of our main results and reviews some important contributions of others.

     

3D Direct Laser Writing of Nano‐ and Microstructured Hierarchical Gecko‐Mimicking Surfaces

Applying 3D direct laser writing, artificial hierarchical gecko‐type structures are designed and fabricated down to nanometer dimensions. In this way, the elastic modulus and the length scale of the gecko's setae are very closely matched. Direct laser writing is a very flexible rapid prototyping method allowing the fabrication of arbitrary nanostructures. Since the parameters of the structures can be easily changed, this technique is perfect for design studies of dry adhesives. Measuring the adhesional forces by atomic force microscopy, the influence of several design parameters like density, aspect ratio, and tip‐shape on dry adhesion performance are systematically examined. In this way, it is revealed that hierarchy is favorable for artificial gecko‐inspired dry adhesives made of stiff materials on the nanometer scale.     

25th Anniversary Article: Label‐Free Electrical Biodetection Using Carbon Nanostructures

Nanostructures are promising candidates for use as active materials for the detection of chemical and biological species, mainly due to the high surface‐to‐volume ratio and the unique physical properties arising at the nanoscale. Among the various nanostructures, materials comprised of sp²‐carbon enjoy a unique position due to the possibility to readily prepare them in various dimensions ranging from 0D, through 1D to 2D. This review focuses on the use of 1D (carbon nanotubes) and 2D (graphene) carbon nanostructures for the detection of biologically relevant molecules. A key advantage is the possibility to perform the sensing operation without the use of any labels or complex reaction schemes. Along this spirit, various strategies reported for the label‐free electrical detection of biomolecules using carbon nanostructures are discussed. With their promise for ultimate sensitivity and the capability to attain high selectivity through controlled chemical functionalization, carbon‐based nanobiosensors are expected to open avenues to novel diagnostic tools as well as to obtain new fundamental insight into biomolecular interactions down to the single molecule level.     

Simultaneous Fabrication of Very High Aspect Ratio Positive Nano‐ to Milliscale Structures

A simple and inexpensive technique for the simultaneous fabrication of positive (i.e., protruding), very high aspect (>10) ratio nanostructures together with micro‐ or millistructures is developed. The method involves using residual patterns of thin‐film over‐etching (RPTO) to produce sub‐micro‐/nanoscale features. The residual thin‐film nanopattern is used as an etching mask for Si deep reactive ion etching. The etched Si structures are further reduced in size by Si thermal oxidation to produce amorphous SiO₂, which is subsequently etched away by HF. Two arrays of positive Si nanowalls are demonstrated with this combined RPTO‐SiO₂‐HF technique. One array has a feature size of 150 nm and an aspect ratio of 26.7 and another has a feature size of 50 nm and an aspect ratio of 15. No other parallel reduction technique can achieve such a very high aspect ratio for 50‐nm‐wide nanowalls. As a demonstration of the technique to simultaneously achieve nano‐ and milliscale features, a simple Si nanofluidic master mold with positive features with dimensions varying continuously from 1 mm to 200 nm and a highest aspect ratio of 6.75 is fabricated; the narrow 200‐nm section is 4.5 mm long. This Si master mold is then used as a mold for UV embossing. The embossed open channels are then closed by a cover with glue bonding. A high aspect ratio is necessary to produce unblocked closed channels after the cover bonding process of the nanofluidic chip. The combined method of RPTO, Si thermal oxidation, and HF etching can be used to make complex nanofluidic systems and nano‐/micro‐/millistructures for diverse applications.     

One‐Step Construction of N,P‐Codoped Porous Carbon Sheets/CoP Hybrids with Enhanced Lithium and Potassium Storage

Despite the desirable advancement in synthesizing transition‐metal phosphides (TMPs)‐based hybrid structures, most methods depend on foreign‐template‐based multistep procedures for tailoring the specific structure. Herein, a self‐template and recrystallization–self‐assembly strategy for the one‐step synthesis of core–shell‐like cobalt phosphide (CoP) nanoparticles embedded into nitrogen and phosphorus codoped porous carbon sheets (CoP?NPPCS), is first proposed. Relying on the unusual coordination ability of melamine with metal ions and the cooperative hydrogen bonding of melamine and phytic acid to form a 2D network, a self‐synthesized single precursor can be attained. Importantly, this approach can be easily expanded to synthesize other TMPs?NPPCS. Due to the unique compositional and structural characteristics, these CoP?NPPCSs manifest outstanding electrochemical performances as anode materials for both lithium‐ and potassium‐ion batteries. The unusual hybrid architecture, the high specific surface area, and porous features make the CoP?NPPCS attractive for other potential applications, such as supercapacitors and electrocatalysis.     

Ferrocene‐Incorporated Cobalt Sulfide Nanoarchitecture for Superior Oxygen Evolution Reaction

Here, ferrocene(Fc)‐incorporated cobalt sulfide (Co_xS_y) nanostructures directly grown on carbon nanotube (CNT) or carbon fiber (CF) networks for electrochemical oxygen evolution reaction (OER) using a facile one‐step solvothermal method are reported. The strong synergistic interaction between Fc‐Co_xS_y nanostructures and electrically conductive CNTs results in the superior electrocatalytic activity with a very small overpotential of ≈304 mV at 10 mA cm^?2 and a low Tafel slope of 54.2 mV dec^?1 in 1 m KOH electrolyte. Furthermore, the Fc‐incorporated Co_xS_y (FCoS) nanostructures are directly grown on the acid pretreated carbon fiber (ACF), and the resulting fabricated electrode delivers excellent OER performance with a low overpotential of ≈315 mV at 10 mA cm^?2. Such superior OER catalytic activity can be attributed to 3D Fc‐Co_xS_y nanoarchitectures that consist of a high concentration of vertical nanosheets with uniform distribution of nanoparticles that afford a large number of active surface areas and edge sites. Besides, the tight contact interface between ACF substrate and Fc‐Co_xS_y nanostructures could effectively facilitate the electron transfer rate in the OER. This study provides valuable insights for the rational design of energy storage and conversion materials by the incorporation of other transition metal into metal sulfide/oxide nanostructures utilizing metallocene.     

SnO2‐Based Nanomaterials: Synthesis and Application in Lithium‐Ion Batteries

The development of new electrode materials for lithium‐ion batteries (LIBs) has always been a focal area of materials science, as the current technology may not be able to meet the high energy demands for electronic devices with better performance. Among all the metal oxides, tin dioxide (SnO₂) is regarded as a promising candidate to serve as the anode material for LIBs due to its high theoretical capacity. Here, a thorough survey is provided of the synthesis of SnO₂‐based nanomaterials with various structures and chemical compositions, and their application as negative electrodes for LIBs. It covers SnO₂ with different morphologies ranging from 1D nanorods/nanowires/nanotubes, to 2D nanosheets, to 3D hollow nanostructures. Nanocomposites consisting of SnO₂ and different carbonaceous supports, e.g., amorphous carbon, carbon nanotubes, graphene, are also investigated. The use of Sn‐based nanomaterials as the anode material for LIBs will be briefly discussed as well. The aim of this review is to provide an in‐depth and rational understanding such that the electrochemical properties of SnO₂‐based anodes can be effectively enhanced by making proper nanostructures with optimized chemical composition. By focusing on SnO₂, the hope is that such concepts and strategies can be extended to other potential metal oxides, such as titanium dioxide or iron oxides, thus shedding some light on the future development of high‐performance metal‐oxide based negative electrodes for LIBs.     

Rapid and Low‐Cost Prototyping of 3D Nanostructures with Multi‐Layer Hydrogen Silsesquioxane Scaffolds

A layer‐by‐layer (LBL) method can generate or approximate any three‐dimensional (3D) structure, and has been the approach for the manufacturing of complementary metal‐oxide‐semiconductor (CMOS) devices. However, its high cost precludes the fabrication of anything other than CMOS‐compatible devices, and general 3D nanostructures have been difficult to prototype in academia and small businesses, due to the lack of expensive facility and state‐of‐the‐art tools. It is proposed and demonstrated that a novel process that can rapidly fabricate high‐resolution three‐dimensional (3D) nanostructures at low cost, without requiring specialized equipment. An individual layer is realized through electron‐beam lithography patterning of hydrogen silsesquioxane (HSQ) resist, followed by planarization via spinning SU‐8 resist and etch‐back. A 4‐layer silicon inverse woodpile photonic crystal with a period of 650 nm and a 7‐layer HSQ scaffold with a period of 300 nm are demonstrated. This process provides a versatile and accessible solution to the fabrication of highly complex 3D nanostructures.     

Atomic‐Layer‐Deposition‐Assisted Formation of Carbon Nanoflakes on Metal Oxides and Energy Storage Application

Nanostructured carbon is widely used in energy storage devices (e.g., Li‐ion and Li‐air batteries and supercapacitors). A new method is developed for the generation of carbon nanoflakes on various metal oxide nanostructures by combining atomic layer deposition (ALD) and glucose carbonization. Various metal oxide@nanoflake carbon (MO@f‐C) core‐branch nanostructures are obtained. For the mechanism, it is proposed that the ALD Al₂O₃ and glucose form a composite layer. Upon thermal annealing, the composite layer becomes fragmented and moves outward, accompanied by carbon deposition on the alumina skeleton. When tested as electrochemical supercapacitor electrode, the hierarchical MO@f‐C nanostructures exhibit better properties compared with the pristine metal oxides or the carbon coating without ALD. The enhancement can be ascribed to increased specific surface areas and electric conductivity due to the carbon flake coating. This peculiar carbon coating method with the unique hierarchical nanostructure may provide a new insight into the preparation of ‘oxides + carbon’ hybrid electrode materials for energy storage applications.     

3D Nanoprinting of Perovskites

As competing with the established silicon technology, organic–inorganic metal halide perovskites are continually gaining ground in optoelectronics due to their excellent material properties and low‐cost production. The ability to have control over their shape, as well as composition and crystallinity, is indispensable for practical materialization. Many sophisticated nanofabrication methods have been devised to shape perovskites; however, they are still limited to in‐plane, low‐aspect‐ratio, and simple forms. This is in stark contrast with the demands of modern optoelectronics with freeform circuitry and high integration density. Here, a nanoprecision 3D printing is developed for organic–inorganic metal halide perovskites. The method is based on guiding evaporation‐induced perovskite crystallization in mid‐air using a femtoliter ink meniscus formed on a nanopipette, resulting in freestanding 3D perovskite nanostructures with a preferred crystal orientation. Stretching the ink meniscus with a pulling process enables on‐demand control of the nanostructure's diameter and hollowness, leading to an unprecedented tubular‐solid transition. With varying the pulling direction, a layer‐by‐layer stacking of perovskite nanostructures is successfully demonstrated with programmed shapes and positions, a primary step for additive manufacturing. It is expected that the method has the potential to create freeform perovskite nanostructures for customized optoelectronics.     

Electrocatalytic N‐Doped Graphitic Nanofiber – Metal/Metal Oxide Nanoparticle Composites

Carbon‐based nanocomposites have shown promising results in replacing commercial Pt/C as high‐performance, low cost, nonprecious metal‐based oxygen reduction reaction (ORR) catalysts. Developing unique nanostructures of active components (e.g., metal oxides) and carbon materials is essential for their application in next generation electrode materials for fuel cells and metal–air batteries. Herein, a general approach for the production of 1D porous nitrogen‐doped graphitic carbon fibers embedded with active ORR components, (M/MO_x, i.e., metal or metal oxide nanoparticles) using a facile two‐step electrospinning and annealing process is reported. Metal nanoparticles/nanoclusters nucleate within the polymer nanofibers and subsequently catalyze graphitization of the surrounding polymer matrix and following oxidation, create an interconnected graphite–metal oxide framework with large pore channels, considerable active sites, and high specific surface area. The metal/metal oxide@N‐doped graphitic carbon fibers, especially Co₃O₄, exhibit comparable ORR catalytic activity but superior stability and methanol tolerance versus Pt in alkaline solutions, which can be ascribed to the synergistic chemical coupling effects between Co₃O₄ and robust 1D porous structures composed of interconnected N‐doped graphitic nanocarbon rings. This finding provides a novel insight into the design of functional electrocatalysts using electrospun carbon nanomaterials for their application in energy storage and conversion fields.     

Modulated Triple‐Material Nano‐Heterostructures: Where Gold Influenced the Chemical Activity of Silver in Nanocrystals

For efficient charge separations, multimaterial hetero‐nanostructures are being extensively studied as photocatalysts. While materials with one heterojunction are widely established, the chemistry of formation of multijunction heterostructures is not explored. This needs a more sophisticated approach and modulations. To achieve these, a generic multistep seed mediated growth following controlled ion diffusion and ion exchange is reported which successfully leads to triple‐material hetero‐nanostructures with bimetallic‐binary alloy‐binary/ternary semiconductors arrangements. Ag₂S nanocrystals are used as primary seeds for obtaining AuAg‐AuAgS bimetallic‐binary alloyed metal–semiconductor heterostructures via partial reduction of Ag(I) using Au(III) ions. These are again explored as secondary seeds for obtaining a series of triple‐materials heterostructures, AuAg‐AuAgS‐CdS (or ZnS or AgInS₂), with introduction of different divalent and trivalent ions. Chemistry of each step of the gold ion–induced changes in the rate of diffusion and/or ion exchanges are investigated and the formation mechanism for these nearly monodisperse triple material heterostructures are proposed. Reactions without gold are also performed, and the change in the reaction chemistry and growth mechanism in presence of Au is also discussed.