One‐Dimensional Nano‐Interconnection Formation

Interconnection of one‐dimensional nanomaterials such as nanowires and carbon nanotubes with other parts or components is crucial for nanodevices to realize electrical contacts and mechanical fixings. Interconnection has been being gradually paid great attention since it is as significant as nanomaterials properties, and determines nanodevices performance in some cases. This paper provides an overview of recent progress on techniques that are commonly used for one‐dimensional interconnection formation. In this review, these techniques could be categorized into two different types: two‐step and one‐step methods according to their established process. The two‐step method is constituted by assembly and pinning processes, while the one‐step method is a direct formation process of nano‐interconnections. In both methods, the electrodeposition approach is illustrated in detail, and its potential mechanism is emphasized.     

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.     

Low‐Dimensional Nanomaterials Based on Small Organic Molecules: Preparation and Optoelectronic Properties

This article presents a comprehensive review of recent progress of research dedicated to low‐dimensional nanomaterials constructed from functional low‐molecular‐weight organic compounds, whose optoelectronic properties are fundamentally different from those of their inorganic counterparts. After introducing the development of inorganic and organic macromolecular nanomaterials, we begin with a general review of the construction strategies for achieving both zero‐dimensional (0D) and one‐dimensional (1D) nanostructures from small organic functional molecules. We then provide an overview of the unique optoelectronic properties induced by molecular aggregation in the nanostructures. Special emphasis is put on the luminescent properties that are different from those of the corresponding bulk materials, such as aggregation‐induced enhanced emission, fluorescence narrowing, multicolor emission, and tunable and switchable emissions from doped nanostructures. We conclude with a summary and our personal view of the direction of future development of organic opto‐functional nanomaterials and devices.     

One‐Dimensional Hybrid Nanostructures for Heterogeneous Photocatalysis and Photoelectrocatalysis

Semiconductor‐based photocatalysis and photoelectrocatalysis have received considerable attention as alternative approaches for solar energy harvesting and storage. The photocatalytic or photoelectrocatalytic performance of a semiconductor is closely related to the design of the semiconductor at the nanoscale. Among various nanostructures, one‐dimensional (1D) nanostructured photocatalysts and photoelectrodes have attracted increasing interest owing to their unique optical, structural, and electronic advantages. In this article, a comprehensive review of the current research efforts towards the development of 1D semiconductor nanomaterials for heterogeneous photocatalysis and photoelectrocatalysis is provided and, in particular, a discussion of how to overcome the challenges for achieving full potential of 1D nanostructures is presented. It is anticipated that this review will afford enriched information on the rational exploration of the structural and electronic properties of 1D semiconductor nanostructures for achieving more efficient 1D nanostructure‐based photocatalysts and photoelectrodes for high‐efficiency solar energy conversion.     

One‐Dimensional Nanostructures: Synthesis,Characterization, and Applications

This article provides a comprehensive review of current research activities that concentrate on one‐dimensional (1D) nanostructures—wires, rods, belts, and tubes—whose lateral dimensions fall anywhere in the range of 1 to 100 nm. We devote the most attention to 1D nanostructures that have been synthesized in relatively copious quantities using chemical methods. We begin this article with an overview of synthetic strategies that have been exploited to achieve 1D growth. We then elaborate on these approaches in the following four sections: i) anisotropic growth dictated by the crystallographic structure of a solid material; ii) anisotropic growth confined and directed by various templates; iii) anisotropic growth kinetically controlled by supersaturation or through the use of an appropriate capping reagent; and iv) new concepts not yet fully demonstrated, but with long‐term potential in generating 1D nanostructures. Following is a discussion of techniques for generating various types of important heterostructured nanowires. By the end of this article, we highlight a range of unique properties (e.g., thermal, mechanical, electronic, optoelectronic, optical, nonlinear optical, and field emission) associated with different types of 1D nanostructures. We also briefly discuss a number of methods potentially useful for assembling 1D nanostructures into functional devices based on crossbar junctions, and complex architectures such as 2D and 3D periodic lattices. We conclude this review with personal perspectives on the directions towards which future research on this new class of nanostructured materials might be directed.     

Inside Front Cover: One‐Dimensional Plasmon Coupling by Facile Self‐Assembly of Gold Nanoparticles into Branched Chain Networks (Adv. Mater. 21/2005)

Short, single‐particle‐wide chains and complex networks of interconnected chains are easily self‐assembled from 13 nm Au nanoparticles by inducing a surface electrostatic dipolar moment in a controlled manner. Mann and co‐workers further demonstrate both experimentally and theoretically on p. 2553 that efficient surface plasmon coupling takes place in these extensive networks, thus opening a new bottom–up approach to subwavelength optical‐waveguiding devices. The left panel in the image shows isolated 13 nm Au nanoparticles; the back panel, short linear chains; the bottom panel, complex branched network of chains; and the right panel, a graphical rendering of optical spectroscopic properties during the self‐assembly process.     

Anisotropic Wetting Surfaces with One‐Dimesional and Directional Structures: Fabrication Approaches,Wetting Properties and Potential Applications

This review article provides a brief summary of recent research progress on anisotropic wetting on one‐dimensional (1D) and directionally patterned surfaces, as well as the technical importance in various applications. Inspiration from natural structures exhibiting anisotropic wetting behavior is first discussed. Development of fabrication techniques for topographically and chemically 1D patterned surfaces and directional nanomaterials are then reviewed, with emphasis on anisotropic behavior with topographically (structurally) patterned surfaces. The basic investigation of anisotropic wetting behavior and theoretical simulations for anisotropic wetting are also further reviewed. Perspectives concerning future direction of anisotropic wetting research and its potential applications in microfluidic devices, lab‐on‐a‐chip, sensor, microreactor and self‐cleaning are presented.