The invention provides a suitable method and an appropriate, PV film structure. This aim is achieved by a room temperature method in which aqueous dispersions are printed onto a substrate and cured by an accompanying reaction. The accompanying reaction forms gradients and also nanoscale structures at the film boundaries, which produce a PV active film having standard performance and a higher stability. At around 10% efficiency, stability and no initial loss in performance in the climatic chamber test can be obtained and over a 20 year test period, consistently less fluctuation can be achieved. The method is free from tempering or sintering steps, enables the use of technically pure, advantageous starting materials and makes the PV film structure available as a finished, highly flexible cell for a fraction of the typical investment in production or distribution.

Chromatic systems and structures are presented that operate without external electrical supply, which enable changes in color or transparency of a substrate material, such as glass. Various configurations provide a mechanism to activate an oxidation-reduction reaction in a chromatic material, so as to change from transparent to opaque or from one color to another. These structures may be used in applications from windows for buildings and homes, camera lenses, automotive displays and windows, mobile device displays, and other applications where chromatic change is desired.

In one form, a photoelectrochemical cell comprising a p-type sensitized photocathode including a sensitizer dye and a water-based electrolyte. In another form, the sensitizer dye and an adjacent semiconductor may have a reduction potential that is sufficiently high to either reduce a desired chemical feedstock in the cell or reduce protons in the water to hydrogen gas. The semiconductor to which the sensitizer dye is affixed may be nickel oxide. The photoelectrochemical cell can include a sensitized photocathode and an electrolyte that contains an electron acceptor, where light illumination of the sensitized photocathode results in reduction of the electron acceptor. The electrolyte can include water.

Provided are a method for manufacturing a perovskite nanocrystal particle light-emitter where an organic ligand is substituted, a light-emitter manufactured thereby, and a light emitting device using the same. A method for manufacturing an organic-inorganic-hybrid perovskite nanocrystal particle light-emitter where an organic ligand is substituted may comprise the steps of: preparing a solution including an organic-inorganic-hybrid perovskite nanocrystal particle light-emitter, wherein the organic-inorganic-hybrid perovskite nanocrystal particle light-emitter comprises an organic-inorganic-hybrid perovskite nanocrystal structure and a plurality of first organic ligands surrounding the organic-inorganic-hybrid perovskite nanocrystal structure; and adding, to the solution, a second organic ligand which is shorter than the first organic ligands or includes a phenyl group or a fluorine group, thereby substitutes the first organic ligands with the second organic ligand. Thus, since energy transfer or charge injection into the nanocrystal structure increases through ligand substitution, it is possible to further increase light emitting efficiency and increase durability and stability by means of a hydrophobic ligand.

Provided are an additive for an electrolytic composition which can suppress the decrease of a short-circuit current and improve an open circuit voltage as compared to the case when conventional 4-TBpy is used as an additive for an electrolytic composition, and an electrolytic composition using this additive and a dye-sensitized solar cell. The additive for an electrolytic composition for use in a dye-sensitized solar cell contains a pyridine derivative having a pyridine ring into which an alkylsilyl group is introduced, and it is preferable that this pyridine derivative has an alkylsilyl group at the 4-position of the pyridine ring, and it is more preferable that the pyridine derivative is 4-(trimethylsilyl) pyridine.

Method and system for generating electrical energy from a volume of water.

An electrolyte solution containing a compound (1) represented by the formula (1):

##STR00001##

wherein R.sup.1 and R.sup.2 are each independently a C1-C4 alkyl group optionally containing an ether bond; and a compound (11) represented by the formula (11):

##STR00002##

wherein R.sup.101 and R.sup.102 are each independently a substituent that is a C1-C7 alkyl group or the like. The substituent optionally contains one or more divalent to hexavalent hetero atoms in its structure, with one or more hydrogen atoms each optionally replaced by a fluorine atom or a C0-C7 functional group. Also disclosed is an electrochemical device containing the electrolyte solution, a lithium ion secondary battery containing the electrolyte solution, and a module including the electrochemical device or the lithium ion secondary battery.

Various embodiments of systems and methods for a thermogalvanic brick are disclosed.

The present disclosure relates to nanocomposites of CuO/Cu.sub.2O and continuous flow solar reactors. The nanocomposites can be utilized as a photocatalyst and can be incorporated into photoelectrochemical devices. The described devices, systems, and methods can be used for converting CO.sub.2 into one or more alcohols and other small organics with the use of solar energy and electricity. Other embodiments are described.

Provided are a method for manufacturing a perovskite nanocrystal particle light-emitter where an organic ligand is substituted, a light-emitter manufactured thereby, and a light emitting device using the same. A method for manufacturing an organic-inorganic-hybrid perovskite nanocrystal particle light-emitter where an organic ligand is substituted may comprise the steps of: preparing a solution including an organic-inorganic-hybrid perovskite nanocrystal particle light-emitter, wherein the organic-inorganic-hybrid perovskite nanocrystal particle light-emitter comprises an organic-inorganic-hybrid perovskite nanocrystal structure and a plurality of first organic ligands surrounding the organic-inorganic-hybrid perovskite nanocrystal structure; and adding, to the solution, a second organic ligand which is shorter than the first organic ligands or includes a phenyl group or a fluorine group, thereby substitutes the first organic ligands with the second organic ligand. Thus, since energy transfer or charge injection into the nanocrystal structure increases through ligand substitution, it is possible to further increase light emitting efficiency and increase durability and stability by means of a hydrophobic ligand.