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Much effort has been made recently to develop future devices or sensors comprising nanoscale building blocks such as nanowires, carbon nanotubes, DNA, proteins, and nanoparticles. One of the key requirements to realize these devices/sensors is the capability to place individual nanoscale building blocks onto exact substrate locations. This article will review recent progress in various approaches exploited to place or assemble nanoscale building blocks in a controlled way.

We demonstrate a large-scale placement of nanoparticles through a scheme named "electrostatic funneling", in which charged nanoparticles are guided by an electrostatic potential energy gradient and placed on targeted locations with nanoscale precision. The guiding electrostatic structures are defined using current CMOS fabrication technology. The effectiveness of this scheme is demonstrated for a variety of geometries including one-dimensional and zero-dimensional patterns as well as three-dimensional step structures. Placement precision of 6 nm has been demonstrated using a one-dimensional guiding structure comprising alternatively charged lines with line width of approximately 100 nm. Detailed calculations using DLVO theory agree well with the observed long-range interactions and also estimate lateral forces as strong as (1-3) x 10(-7) dyn, which well explains the observed guided placement of Au nanoparticles.

Devices in which the transport and storage of single electrons are systematically controlled could lead to a new generation of nanoscale devices and sensors. The attractive features of these devices include operation at extremely low power, scalability to the sub-nanometre regime and extremely high charge sensitivity. However, the fabrication of single-electron devices requires nanoscale geometrical control, which has limited their fabrication to small numbers of devices at a time, significantly restricting their implementation in practical devices. Here we report the parallel fabrication of single-electron devices, which results in multiple, individually addressable, single-electron devices that operate at room temperature. This was made possible using CMOS fabrication technology and implementing self-alignment of the source and drain electrodes, which are vertically separated by thin dielectric films. We demonstrate clear Coulomb staircase/blockade and Coulomb oscillations at room temperature and also at low temperatures.

The capability of placing individual nanoscale building blocks on exact substrate locations in a controlled manner is one of the key requirements to realize future electronic, optical, and magnetic devices and sensors that are composed of such blocks. This article reviews some important advances in the strategies for controlled placement of nanoscale building blocks. In particular, we will overview template assisted placement that utilizes physical, molecular, or electrostatic templates, DNA-programmed assembly, placement using dielectrophoresis, approaches for non-close-packed assembly of spherical particles, and recent development of focused placement schemes including electrostatic funneling, focused placement via molecular gradient patterns, electrodynamic focusing of charged aerosols, and others.

Self-assembly of one-dimensional surface structures is examined by tracking single Ir and Pd atoms on W(110) as they incorporate into chains of Ir and Pd, respectively. Ir adatoms move parallel to the chains, but do not come close to the chain sides; incorporation occurs only at the ends. Pd adatoms also migrate parallel to Pd chains, and incorporate at the ends. Occasionally, in the end region, they do jump to the side of a chain, and migrate there until they find an end site. Incorporation behavior for both Ir and Pd is driven by highly anisotropic, long-ranged interactions between atoms on the surface.

This letter reports single-particle placement in which exactly one nanoparticle is electrostatically guided and placed onto a target location. Using an ∼20 nm Au nanoparticle colloid as a model system, we demonstrate that self-limiting interactions between a charged nanoparticle and a charged substrate surface are extremely effective in positioning a single Au nanoparticle on each target location. Detailed theoretical calculations revealed that the self-limiting capability in the nanoparticle positioning is due to an increase in the free energy barrier after the first nanoparticle lands on a target position, effectively blocking the approach of other nanoparticles.