Perpendicular Magnetization and Generic Realization of the Ising Model in Artificial Spin Ice

PRL 109, 087201 (2012)

We have studied frustrated kagome arrays and unfrustrated honeycomb arrays of magnetostatically
interacting single-domain ferromagnetic islands with magnetization normal to the plane. The measured
pairwise spin correlations of both lattices can be reproduced by models based solely on nearest-neighbor
correlations. The kagome array has qualitatively different magnetostatics but identical lattice topology to
previously studied artificial spin ice systems composed of in-plane moments. The two systems show
striking similarities in the development of moment pair correlations, demonstrating a universality in
artificial spin ice behavior independent of specific realization in a particular material system



Department of Physics and Materials Research Institute, Pennsylvania State University, University Park, Pennsylvania 16802, USA
2
Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, USA
3
Theoretical Division and Center for Nonlinear Studies, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA
(Received 19 March 2012; published 21 August 2012)

Self made Origami structures


Self-Organized Origami Structures via Ion-Induced Plastic Strain


Khattiya   Chalapat  ,   *      Nikolai   Chekurov  ,         Hua   Jiang  ,         Jian   Li  ,         Babak   Parviz  ,
            and   G. S.   Paraoanu





Movement and deformation due to stress relaxation occurs in  a variety of natural or artifi cially-induced processes. In nature,  some plants have evolved their organs as movable origami to
increase their reproductive success. In ice plants, the opening  of the seed capsule is caused by a water-actuated strain mechanism.  After the rain, the cells are full of water, causing the
expansion along the lid axis, and eventually the opening of the seed capsule. Similar to the ice plant seeds, various other objects move and deform through stress relaxation, ranging from
curling of fl owers, self-organization at nanometer scale, to deformation of plasmid DNA in bacteria.



New technique for nanostructure assembly


Self-Assembled Colloidal Superparticles from Nanorods


Science
Vol. 338 no. 6105 pp. 358-363 
DOI: 10.1126/science.1224221

  1. Y. Charles Cao1,*



Colloidal superparticles are nanoparticle assemblies in the form of colloidal particles. The assembly of nanoscopic objects into mesoscopic or macroscopic complex architectures allows bottom-up fabrication of functional materials. We report that the self-assembly of cadmium selenide–cadmium sulfide (CdSe-CdS) core-shell semiconductor nanorods, mediated by shape and structural anisotropy, produces mesoscopic colloidal superparticles having multiple well-defined supercrystalline domains. Moreover, functionality-based anisotropic interactions between these CdSe-CdS nanorods can be kinetically introduced during the self-assembly and, in turn, yield single-domain, needle-like superparticles with parallel alignment of constituent nanorods. Unidirectional patterning of these mesoscopic needle-like superparticles gives rise to the lateral alignment of CdSe-CdS nanorods into macroscopic, uniform, freestanding polymer films that exhibit strong photoluminescence with a striking anisotropy, enabling their use as downconversion phosphors to create polarized light-emitting diodes.

Nanometre optical coatings based on strong interference effects in highly absorbing media



Nature Materials
 
(2012)
 
doi:10.1038/nmat3443
Received
 
Accepted
 
Published online
 

Enzymatic Sculpting of Nanoscale and Microscale Surface Topographies


Angewandte Chemie International Edition

Volume 51Issue 38,pages 9619–9623,September 17, 2012





Lithography-free etching of complex surface features is achieved by harnessing the enzyme proteinase K (PK), controlled by bovine serum albumin (BSA), to digest a biodegradable polymer. This bio-sculpting process is used to construct a membraneless filtration device for the size-based isolation and enrichment of cells from whole blood.

Continuous Evolution Profiles for Electronic-Tongue-Based Analysis†


  1. Dr. Yanxia Hou1,*
  2. Maria Genua1
  3. Dr. Dayane Tada Batista1
  4. Dr. Roberto Calemczuk1
  5. Dr. Arnaud Buhot1
  6. Pauline Fornarelli2
  7. Dr. Jamal Koubachi2
  8. Prof. David Bonnaffé2,*
  9. Els Saesen3
  10. Dr. Cédric Laguri3
  11. Dr. Hugues Lortat-Jacob3
  12. Dr. Thierry Livache1,*
Article first published online: 11 SEP 2012
Licking the problem: A new type of electronic tongue was constructed by self-assembly on the surface of a surface plasmon resonance (SPR) imaging prism with combinations of simple building blocks. The resulting combinatorial array was used to detect proteins in solution (see scheme) using SPR imaging to monitor the interactions. The signal from each spot was dependent on its composition and the protein infused, and correlated with the response of its neighbors.

Direct-Write Patterning of Bacterial Cells by Dip-Pen Nanolithography


Publication Date (Web): September 19, 2012 (Communication)
DOI: 10.1021/ja3073808

J. Am. Chem. Soc., Article ASAP
DOI: 10.1021/ja3073808
Publication Date (Web): September 19, 2012
Copyright © 2012 American Chemical Society

The ability of dip-pen nanolithography (DPN) to generate nano- or microarrays of soft or hard materials (e.g., small molecules, DNA, proteins, nanoparticles, sols, and polymers) in a direct-write manner has been widely demonstrated. The transporting of large-sized ink materials such as bacteria, however, remains a significant challenge with this technique. The size limitation of the water meniscus formed between the DPN tip and the solid surface becomes a bottleneck in such diffusion-based molecular transport experiments. Herein, we report a straightforward “stamp-on” DPN method that uses a nanostructured poly(2-methyl-2-oxazoline) hydrogel-coated tip and carrier agents to generate patterns of micrometer-sizedEscherichia coli JM 109 bacterial cells. We demonstrate that this approach enables the deposition of a single bacterial cell array on a solid surface or arrays of layers of multiple cells by modulating the viscosity of the “ink” solution. Fluorescence microscopy images indicated that the deposited bacterial cells were kept alive on Luria–Bertani-agar layered solid surfaces after DPN patterning.