Zhaoqin Chu

Preparation and characterization of amorphous SiOx nanowires

Abstract Large-scale synthesis of amorphous silicon oxide nanowires (SiONWs) was achieved by using simple physical evaporation of the mixture of silica xerogel containing Fe nanoparticles and silicon powder. Transmission electron microscopy (TEM) observations showed that the amorphous SiONWs have a length of up to several tens of micrometers and a diameter of 10–40 nm. Energy-dispersed X-ray spectrometry (EDX) analysis revealed that the SiONWs consist of Si and O elements in atomic ratio approximately to 1:1.4. Different morphologies of nanowires such as straight, smoothly curved, braided and helical shapes were observed. The formation process of SiONWs was closely related to the VLS growth mechanism. Raman scattering spectrum of amorphous SiONWs showed that there is an asymmetric, broadened linewidth Raman peak at 502 cm −1 greatly different from that of bulk SiO 2 non-crystalline solids.

A General Synthetic Approach to Interconnected Nanowire/Nanotube and Nanotube/Nanowire/Nanotube Heterojunctions with Branched Topology

Heterojunctions between nanotubes (NTs) and nanowires (NWs) could provide building blocks for nanoelectronics and nanophotonics, with other applications in barcodes, optical readout, biomolecular separation, catalysis, selfassembly, and magnetic manipulation. Although hybrid NWs (metal/polymer, semiconductor/semiconductor, 9] metal/semiconductor, and metal/metal ), hybrid NTs (metal/metal), NT/NW heterojunctions, and tree-like nano-heterojunctions have beenmade, the corresponding studies demonstrated limited control over the geometry and complexity of the nano-heterojunctions, which ultimately are central to the design of building blocks for nanocircuits, nanodevices, and nanosystems. Herein we show a general synthetic approach to various branched two-segment NW/NT and three-segment NT/NW/NT heterojunctions, based on a combinatorial process of electrodepositing NWs within the branched channels of anodic aluminum oxide (AAO) templates, selectively etching part of the electrodeposited NWs, and growing NTs on the ends of the NWs. The NWs can be metallic or semiconducting, while the NTs can consist of carbon, silicon, and silica; the two NT segments in threesegment NT/NW/NT nanoarchitectures can comprise either the same or different materials. This approach enables excellent control over the geometry, chemical composition, and complexity of the hetero-nanoarchitectures that can be the framework for nanoscale devices and systems. Figure 1 shows schematic depictions of the basic heteronanoarchitectures we have made, which consist of various NT and NW segments placed combinatorially in a Y-shaped topology. The synthesis scheme follows a typical buildingblock concept in which a set of different nanoscale components (NTs and NWs of different materials with distinct properties, in linear and branched topologies) can be connected in a predetermined fashion inside the branched

Controlled Synthesis of Germanium Nanowires and Nanotubes with Variable Morphologies and Sizes

We report on the controlled growth of germanium (Ge) nanostructures in the form of both nanowire (NW) and nanotube (NT) with ultrahigh aspect ratios and variable diameters. The nanostructures are grown inside a porous anodic aluminum oxide (AAO) template by low-temperature chemical vapor deposition (CVD) assisted by an electrodeposited metal nanorod catalyst. Depending on the choice of catalytic metals (Au, Ni, Cu, Co) and germane (GeH(4)) concentration during CVD, either Ge NWs or NTs can be synthesized at low growth temperatures (310-370 °C). Furthermore, Ge NWs and NTs with two or more branches can be grown from the same stem while using AAO with branched channels as templates. Transmission electron microscopy studies show that NWs are single crystalline and that branches grow epitaxially from the stem of NWs with a crystalline direction independent of diameter. As-grown NTs are amorphous but can crystallize via postannealing at 400 °C in Ar/H(2) atmosphere, with a wall thickness controllable between 6 and 18 nm in the CVD process. The yield and quality of the NTs are critically dependent on the choice of the catalyst, where Ni appears the best choice for Ge NT growth among Ni, Cu, Co, and Au. The synthesis of structurally uniform and morphologically versatile Ge nanostructures may open up new opportunities for integrated Ge-nanostructure-based nanocircuits, nanodevices, and nanosystems.

Polyacrylic acid sodium salt film entrapped Ag-nanocubes as molecule traps for SERS detection

AbstractSurface-enhanced Raman spectroscopy (SERS) is a fast analytical technique for trace chemicals; however, it requires the active SERS-substrates to adsorb analytes, thus limiting target species to those with the desired affinity for substrates. Here we present networked polyacrylic acid sodium salt (PAAS) film entrapped Ag-nanocubes (denoted as Ag-nanocubes@PAAS) as an effective SERS-substrate for analytes with and without high affinity. Once the analyte aqueous solution is cast on the dry Ag-nanocubes@PAAS substrate, the bibulous PAAS becomes swollen forcing the Ag-nanocubes loose, while the analytes diffuse in the interstices among the Ag-nanocubes. When dried, the PAAS shrinks and pulls the Ag-nanocubes back to their previous aggregated state, while the PAAS network “detains” the analytes in the small gaps between the Ag-nanocubes for SERS detection. The strategy has been proven effective for not only singleanalytes but also multi-analytes without strong affinity for Ag, showing its potential in SERS-based simultaneous multi-analyte detection of both adsorbable and non-adsorbable pollutants in the environment.

Thin Au film with highly ordered arrays of hemispherical dots

Thin Au films with highly ordered arrays of hemispherical dots have been fabricated by evaporating Au on the surface of porous anodic alumina template.The hemispherical Au dot arrays arranged in a hexagonal pattern are highly ordered.The densities of the hemispherical Au dots in the array are approximately 1.2=10 m with dot diameters and heights of 12 y2

Crystalline Silicon Nanotubes and Their Connections with Gold Nanowires in Both Linear and Branched Topologies

Silicon, being in the same group in the periodic table as carbon, plays a key role in modern semiconductor industry. However, unlike carbon nanotube (NT), progress remains relatively slow in silicon NT (SiNT) and SiNT-based heteroarchitectures, which would be the fundamental building blocks of various nanoscale circuits, devices, and systems. Here, we report the synthesis of linear and branched crystalline SiNTs via porous anodic aluminum oxide (AAO) self-catalyzed growth and postannealing, and the connection of crystalline SiNTs and gold nanowires (AuNWs) via a combinatorial process of electrodepositing AuNWs with predesired length and location in the channels of the AAO template and subsequent AAO self-catalyzed and postannealing growth of SiNTs in the remaining empty channels adjacent to the AuNWs. Using the approach, a large variety of two-segment AuNW/SiNT and three-segment SiNT/AuNW/SiNT heteronanostructures with both linear and branched topologies have been achieved, paving the way for the rational design and fabrication of SiNT-based nanocircuits, nanodevices, and multifunctional nanosystems in the future.

Nanochannel-Directed Growth of Multi-Segment Nanowire Heterojunctions of Metallic Au1–xGex and Semiconducting Ge

We report on the synthesis of multi-segment nanowire (NW) junctions of Au(1-x)Ge(x) and Ge inside the nanochannels of porous anodic aluminum oxide template. The one-dimensional heterostructures are grown with a low-temperature chemical vapor deposition process, assisted by electrodeposited Au nanowires (AuNWs). The Au-catalyzed vapor-liquid-solid growth process occurs simultaneously in multiple locations along the nanochannel, which leads to multi-segment Au(1-x)Ge(x)/Ge heterojunctions. The structures of the as-grown hybrid NWs, analyzed by using transmission electron microscopy and energy-dispersive X-ray spectroscopy elemental mapping, show clear compositional modulation with variable modulation period and controllable junction numbers. Remarkably, both GeNW and Au(1-x)Ge(x)NW segments are single crystalline with abrupt interfaces and good crystallographic coherences. The electronic and transport properties of individual NW junctions are measured by using a multi-probe scanning tunneling microscope, which confirms the semiconducting nature of Ge segments and the metallic behavior of Au(1-x)Ge(x) segments, respectively. The high yield of multiple segment NW junctions of a metal-semiconductor can facilitate the applications in nanoelectronics and optoelectronics that harness multiple functionalities of heterointerfaces.

A generic approach to nanocables via nanochannel-confined sequential electrodeposition

We have exploited a generic method for nanocables, consisting of two materials that can be obtained via electrodeposition, by first electrodepositing the cable “shells” on the interior walls of nanochannels inside anodic aluminum oxide template with one planar surface side coated with a thin meshlike Au layer and then filling the cavities inside the shells by electrodeposition again to achieve the cable “cores.” The method has been demonstrated for the nanocables of Cu-Bi (Cu shell and Bi core) and Bi-Cu (Bi shell and Cu core). Nanocables of other two materials with tunable shell thickness and inner core diameter can be achieved by modulating the Au-layer thickness, and might have potential in the future nanotechnology.

ERRATUM: Nanocontainers made of Various Materials with Tunable Shape and Size

Nanocontainers have great potentials in targeted drug delivery and nanospace-confined reactions. However, the previous synthetic approaches exhibited limited control over the morphology, size and materials of the nanocontainers, which are crucial in practical applications. Here, we present a synthetic approach to multi-segment linear-shaped nanopores with pre-designed morphologies inside anodic aluminium oxide (AAO), by tailoring the anodizing duration after a rational increase of the applied anodizing voltage and the number of voltage increase during Al foil anodization. Then, we achieve nanocontainers with designed morphologies, such as nanofunnels, nanobottles, nano-separating-funnels and nanodroppers, with tunable sizes and diverse materials of carbon, silicon, germanium, hafnium oxide, silica and nickel/carbon magnetic composite, by depositing a thin layer of materials on the inner walls of the pre-designed AAO nanopores. The strategy has far-reaching implications in the designing and large-scale fabrication of nanocontainers, opening up new opportunities in nanotechnology applications.

A facile low-temperature growth of large-scale uniform two-end-open Ge nanotubes with hierarchical branches

We present a facile approach for the controlled fabrication of well-aligned arrays of Ge nanotubes (GeNTs) with tunable sizes and hierarchical branches inside the pre-designed nanochannels of porous anodic aluminum oxide (AAO) templates. Metal salts, such as nickel nitrate, silver nitrate, cobalt nitrate and copper sulphate are pre-decorated on the inner wall of the AAO nanochannels as catalyst precursors, where they are reduced into nickel, silver, cobalt, and copper clusters, and provide nucleation sites for subsequent Ge growth. GeNTs are formed by confining the Ge growth on the inner walls of the porous AAO template in a low temperature (300–380 °C) chemical vapor deposition process. The as-grown GeNTs have open ends with tailored wall thickness (between 10 and 26 nm), diameter (between 80 and 248 nm), and geometrical configuration (e.g., linear, Y-branching, multi-branching, and various multiple-generation branching). The GeNT formation process is sensitive to the choice of the catalyst precursor. Nickel salts lead to a uniform wall thickness of GeNTs compared with copper, silver, and cobalt salts. And GeNTs grown with copper salts as catalysts are polycrystalline, while nickel, silver and cobalt salts assisted GeNTs are amorphous though they can crystallize via post-annealing at 400 °C in Ar/H2 atmosphere. These open-end hollow nanotubes with tunable sizes and hierarchical branches can serve as nanoscale containers or pipes to deliver fluids and molecular species, and are excellent building blocks for the construction of large-scale nanofluidic systems.