To date, no large-scale preparative method for arrays of nanotube enables the experimentalist to arbitrarily define changes in the tubes' diameter along their length. To this goal, we start with anodic alumina substrates displaying controlled modulations in pore diameter obtained by alternating "mild" and "hard" electrochemical etching conditions. We then utilize atomic layer deposition (ALD) to coat the internal pore walls with conformal layers of an oxide. Ferromagnetic Fe(3)O(4) tubes of 10 nm wall thickness and 10-30 microm in length are thus prepared, which replicate the modulated silhouette of the template. Their magnetic properties strongly depend on the presence of diameter modulations. Introducing one or several very short segments of large diameter (150 nm) into an otherwise thin tube (70 nm diameter) brings its initially large coercive field down to a value close to the case of a homogeneously thick tube. Theoretical modeling emphasizes the major influence of the magnetostatic interactions between neighboring tubes. They are enhanced locally at the sites of diameter modulations, which directly translates into a reduction in coercive field.

Low-temperature atomic layer deposition (ALD) of TiO2, SiO2, and Al2O3 was applied to modify the surface and to tailor the diameter of nanochannels in etched ion-track polycarbonate membranes. The homogeneity, conformity, and composition of the coating inside the nanochannels are investigated for different channel diameters (18-55 nm) and film thicknesses (5-22 nm). Small angle x-ray scattering before and after ALD demonstrates conformal coating along the full channel length. X-ray photoelectron spectroscopy and energy dispersive x-ray spectroscopy provide evidence of nearly stoichiometric composition of the different coatings. By wet-chemical methods, the ALD-deposited film is released from the supporting polymer templates providing 30 μm long self-supporting nanotubes with walls as thin as 5 nm. Electrolytic ion-conductivity measurements provide proof-of-concept that combining ALD coating with ion-track nanotechnology offers promising perspectives for single-pore applications by controlled shrinking of an oversized pore to a preferred smaller diameter and fine-tuning of the chemical and physical nature of the inner channel surface.

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In this work heteroepitaxial stabilization with nanoscale control of the magnetic Co2FeO4 phase at 250 °C is reported. Ultrasmooth and pure Co2FeO4 thin films (5–25 nm) with no phase segregation are obtained on perovskite SrTiO3 single crystal (100) and (110) oriented substrates by atomic layer deposition (ALD). High resolution structural and chemical analyses confirm the formation of the Co‐rich spinel metastable phase. The magneto‐crystalline anisotropy of the Co2FeO4 phase is not modified by stress anisotropy because the films are fully relaxed. Additionally, high coervice fields, 15 kOe, and high saturation of magnetization, 3.3 μB per formula unit (at 10 K), are preserved down to 10 nm. Therefore, the properties of the ALD‐Co2FeO4 films offer many possibilities for future applications in sensors, actuators, microelectronics, and spintronics. In addition, these results are promising for the use of ALD compared to the existing thin‐film deposition techniques to stabilize epitaxial multicomponent materials with nanoscale control on a wide variety of substrates for which the processing temperature is a major drawback.