A new facile method that employs high‐power sonication is used to break up firmly agglutinated nanodiamonds and obtain dispersion just as effectively as stirred‐media milling. The dispersion properties of the de‐agglutinated nanodiamonds in various nonaqueous solvents, and the pH‐dependent dispersion/precipitation behavior of the hydrosols are presented (see figure). The brownish color of the colloids is attributed mostly to the Rayleigh scattering superimposed over the finite absorption in the visible wavelength.

A continuous and wide range control of the diameter (1.9-3.2 nm) and density (0.03-0.11 g cm(-3) ) of single-walled carbon nanotube (SWNT) forests is demonstrated by decoupling the catalyst formation and SWNT growth processes. Specifically, by managing the catalyst formation temperature and H2 exposure, the redistribution of the Fe catalyst thin film into nanoparticles is controlled while a fixed growth condition preserved the growth yield. The diameter and density are inversely correlated, where low/high density forests would consist of large/small diameter SWNTs, which is proposed as a general rule for the structural control of SWNT forests. The catalyst formation process is modeled by considering the competing processes, Ostwald ripening, and subsurface diffusion, where the dominant mechanism is found to be Ostwald ripening. Specifically, H2 exposure increases catalyst surface energy and decreases diameter, while increased temperature leads to increased diffusion on the surface and an increase in diameter.

The magnetism and structure for potassium clusters physisorbed in nanographite-based nanoporous host are investigated. Potassium clusters are subjected to a slight charge transfer to a host nanographite and modify the magnetism of the edge-state spins of nanographite. The localized spins of 4s electrons in the potassium cluster interact with each other through a strong antiferromagnetic interaction. Finite size effect and structural disorder around the cluster surface are responsible for anomalous spin fluctuations in the magnetism.

Understanding the fundamental mechanisms and limiting processes of the growth of single-walled carbon nanotube (SWCNT) would serve as a guide to achieve further control on structural parameters of SWCNT. In this paper, we have studied the growth kinetics of a series of SWCNT forests continuously spanning a wide range of diameters (1.9–3.2 nm), and have revealed an additional fundamental growth limiting process where the mass of the individual SWCNT is determined by the individual catalyst volume. Calculation of the conversion rate of carbon atoms into CNTs per Fe atom is 2 × 102 atoms per second. This rate limiting process provides an important understanding where the larger diameter SWCNT would grow faster, and thus be more suited for mass production.

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