Assemblies of anisotropic nanoparticles

1. A method comprising:

forming a substantially close packed dense layer by assembling a plurality of anisotropic nanoparticles wherein the plurality of nanoparticles includes a member selected from the group consisting of (In,Ga) y (S,Se) 1-y , an In 2 Se 3 stable wurtzite structure that defines a hexagonal rod nanoparticle, Cu x (Se) 1-x , and Cu(In,Ga) y (S,Se) 1-y , each of the plurality of anisotropic nanoparticles having a) a first dimension that is substantially different than both a second dimension and a third dimension and b) a non-random nanoparticle crystallographic orientation that is substantially aligned with a first direction, wherein assembling includes mechanically interacting the plurality of anisotropic nanoparticles by

imposing a delocalized force that defines a direction that is substantially perpendicular to a basal plane of the substantially close packed dense layer; and

imposing a fluctuating force to which the anisotropic nanoparticles respond, wherein fluctuations in a magnitude of the imposed force are sufficient to overcome a short range weak attractive force between members of the plurality of anisotropic nanoparticles with respect to anisotropic nanoparticles that are not substantially overlapping, and wherein assembling further includes arranging the plurality of anisotropic nanoparticles to define an order having one-dimensional translational periodicity and a rotational symmetry selected from the group consisting of eight fold, ten fold and twelve fold with respect to a normal to the basal plane of the substantially close packed dense layer, and

wherein the plurality of anisotropic nanoparticles are substantially aligned with respect to each other to define the substantially close packed dense layer and the substantially close packed dense layer has a non-random shared crystallographic orientation that is substantially aligned with the basal plane of the substantially close packed dense layer.

2. The method of claim 1 , wherein the substantially close packed dense layer is characterized by a packing factor that is within at least 10% of a maximum packing factor.

3. The method of claim 1 , wherein the delocalized force includes at least one member selected from the group consisting of gravity, magnetic, electrostatic and electromagnetic.

4. The method of claim 1 , further comprising stabilized the non-random shared crystallographic orientation.

5. The method of claim 4 , wherein stabilizing includes fusing the plurality of anisotropic nanoparticles.

6. The method of claim 4 , wherein stabilizing includes changing a chemical composition of the substantially close packed dense layer.

7. The method of claim 6 , wherein changing includes volatilization of a solvent.

8. The method of claim 6 , wherein the plurality of anisotropic nanoparticles include polar crystals.

9. The method of claim 4 , wherein stabilizing includes changing a local ionic concentration within the substantially close packed dense layer by forming a Helmholtz double layer, wherein the substantially close packed dense layer is located in one layer of the Helmholtz double layer.

10. The method of claim 4 , wherein stabilizing includes changing a composition of a medium that is coupled to the substantially close packed dense layer.

11. The method of claim 4 , wherein stabilizing includes changing a pH of a medium that is coupled to the substantially close packed dense layer.

12. The method of claim 4 , wherein the short range weak attractive force includes Van der Waals attractive forces.

13. The method of claim 1 , where imposing the fluctuating force includes exciting the plurality of anisotropic nanoparticles with at least one activation energy source selected from the group consisting of electric, magnetic, electrostatic, electromagnetic, ultrasonic, acoustic and actinic.

14. The method of claim 1 , further comprising providing a plurality of isotropic nanoparticles coupled to the plurality of anisotropic nanoparticles.

15. The method of claim 1 , wherein each of the plurality of anisotropic nanoparticles defines a platelet having a) an aspect ratio of less than approximately 0.20 and b) a principle plane that is substantially parallel to the basal plane.

16. The method of claim 1 , wherein the plurality of anisotropic nanoparticles includes a first set of anisotropic nanoparticles and a second set of anisotropic nanoparticles, wherein the first set of anisotropic nanoparticles and the second set of anisotropic nanoparticles are different from one another with regard to at least one state variable selected from the group consisting of principle plane plan, minor plane profile, impurity presence, edge electrostatic charge, surface electrostatic charge, edge acidity, surface acidity, edge hydrophilicity and surface hydrophilicity.

17. The method of claim 1 , wherein arranging the plurality of anisotropic nanoparticles includes arranging the plurality of anisotropic nanoparticles to define a ten fold rotational symmetry with respect to a normal to the basal plane.

18. The method of claim 1 , wherein assembling includes arranging the plurality of anisotropic nanoparticles to define an order having three-dimensional translational periodicity and a rotational symmetry selected from the group consisting of four fold and a six fold, with respect to a normal to the basal plane of the substantially close packed dense layer.

19. The method of claim 1 , wherein assembling includes arranging the plurality of anisotropic nanoparticles to have a local impurity concentration by volume of no more than approximately 25% different than an average impurity concentration by volume with respect to the substantially close packed dense layer.

20. The method of claim 19 , wherein the local impurity concentration is sodium per unit volume.

21. The method of claim 1 wherein the plurality of anisotropic nanoparticles ordered with respect to basal spatial location on a scale that is substantially a multiple of approximately five nanometers.