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99% 2N 99.9% 3N     99.99% 4N   99.999% 5N     99.9999% 6N 

Solar Energy
AE Solar Energy ™

32.4 (A)/00.022


Hydrogen                                 Helium
Lithium Beryllium                     Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium                     Aluminum Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Cesium Barium Lanthanum Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury Thallium Lead Bismuth Polonium Astatine Radon
                                   
    Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium    
    Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawerencium      

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Safety data, research and properties for AE Solar Energy™ materials are provided below.  American Elements is a manufacturer and supplier specializing in materials essential to several solar energy technologies.

The history of solar energy materials began in the 1970s with the first silicon-based photovoltaic (PV) cells. These basic cells were created by doping silicon to form two oppositely charged layers. A positively charged or p-type layer underneath a negatively charged or n-type layer. In first configurations the p-type layer was doped with Boron to create the positive charge and n-type layer was doped with phosphorous.

When the sun's energy in the form of photons collects in the cell layers in a volume sufficient to force electrons in the layer materials from their "Valence Band" to their "Conduction Band", electrons from the layers are released. This energy threshold is referred to as the "Band Gap". These freed electrons naturally attempt to flow from the negatively charge N-type layer to the positively charged P-type layer. For this reason, the P-type layer is also sometimes called the "Absorption Layer" and the N-Type layer is called the "Emitter Layer".

However, the boundary between these two layers, which is called the "P-N Junction" or "Adhesion Layer" blocks their flow. Collection circuits are attached from the N-type layer to the P-type layer to allow for the electrons to reach their target and complete the circuit. Energy in the form of electricity is collected or harvested from this external circuit.

These silicon based photovoltaic cells have gone through several generations of development designed to reduce production costs. Originally the layers were produced by growing and slicing doped single crystals of silicon. To save cost producers began casting shapes using polycrystalline silicon. While less expensive to produce, efficiencies are also lower. A silicon single crystal may have as high as 30% efficiency; polycrystalline silicon might reach 10-15%. The least expensive approach but also the least efficient cell (approximately 5%) is produced through thin film deposition of amorphous silicon using sputtering techniques.

Presently, most silicon-based PV solar cells are produced from polycrystalline silicon with single crystal systems the next most common.

All silicon-based photovoltaic solar energy collectors however suffer from their ability to absorb energy from a relatively narrow range of the sun's light wave emission. Substantial research ha gone into developing materials that can either expand the band gap or create multiple band gaps in order to absorb a greater portion of the solar energy spectrum. This has lead to the development of PV cells based on Copper Indium Selenide (CuInSe2) or "CIS" Absorption Layers which can capture energy from portions of the light's spectrum not collected by silicon-based PV cells. Doping CIS with Gallium increases the band gap even further and as such most PV cells are now based on Copper Indium Gallium Selenide (CuInGaSe2) and are referred to as "CIGS".

In the typical CIGS photovoltaic cell, the CIGS layer acts as the the P-type or absorption layer. A second material, Cadmium Selenide (CdSe) functions as the emitter or N-type layer. Because two different materials are uses these are sometimes referred to as "Heterojunction" systems. The external circuit is provided by a zinc oxide contact layer on the N-Type layer and a Molybdenum metal contact layer on the P-Type layer.

CIGS based solar cells are a rapidly growing segment of the solar energy market. Besides being more efficient that silicon-based solar cells and therefore less expensive per watt of energy generated, they can be designed to bend to complex geometries and are very light weight. Due to their high efficiency, layers can be achieved using thin film techniques. Thin film deposition of Silicon Nanoparticle quantum dots on the polycrystalline silicon substrate of a photovoltaic (solar) cell increases voltage output as much as 60% by fluorescing the incoming light prior to capture.

Other promising designs include cells based on III-IV Nitride materials and research on Zinc Manganese Telluride, Cadmium Telluride (CdTe) and Gallium Selenide P-Type layers.

The band gap for III-IV Nitride materials, such as Gallium Indium Nitride, covers nearly the entire energy spectrum of the sun because of multiple band gaps in the semiconductor materials. Similarly, Zinc Manganese Telluride crystals have three band gaps which can absorb greater than 50% of the solar energy spectrum.

Further important research involves nanotechnology approaches using nanoparticles of the above materials. Below please find further technical and safety information on solar energy materials manufactured by American Elements' AE Solar EnergyT group.



Silicon-Based PV Cells
(P and N Type)
CIS and CIGS-Based PV Cells Other PV Cell Technologies
Single Crystal Silicon Ingot Copper Indium Selenide Single Crystal Zinc Manganese Telluride
Polycrystalline Silicon Powder Copper Indium Selenide Powder Cadmium Telluride
Amorphous Silicon Powder Copper Indium Selenide Sputtering Target Gallium Selenide Single Crystal
Silicon Sputtering Target Copper Indium Selenide Nanoparticles Gallium Selenide Sputtering Target
Silicon Rod Copper Indium Gallium Selenide Single Crystal Gallium Arsenide
Silicon Pellets Copper Indium Gallium Selenide Powder  
Silicon Nanoparticles Copper Indium Gallium Selenide Nanoparticles  
  Copper Selenide Sputtering Target  
  Indium Selenide Sputtering Target  
  Copper Gallium Selenide Sputtering Target  
  Molybdenum Sputtering Target  
  Zinc Oxide Sputtering Target  
  Zinc Oxide Nanopowder, Z-MiteT  


PRODUCT CATALOG Price Quote Submicron & Nanopowder Tolling Ultra High Purity Sputtering Target Crystal Growth Advanced Materials Information Center

 

 

 

 

Recent Research & Development for Solar Energy

  • Survival of enteric microorganisms on grass surfaces irrigated with treated effluent. J Water Health. 2008 Jun;6(2):255-62.

  • Leaf physiological versus morphological acclimation to high-light exposure at different stages of foliar development in oak. Tree Physiol. 2008 May;28(5):761-71.

  • Vitamin D status of apparently healthy schoolgirls from two different socioeconomic strata in Delhi: relation to nutrition and lifestyle. Br J Nutr. 2008 Apr;99(4):876-82. Epub 2007 Oct 1.

  • Ultraviolet light exposure triggers nuclear accumulation of p21(WAF1) and accelerated senescence in human normal and nucleotide excision repair-deficient fibroblast strains. J Cell Physiol. 2008 Apr;215(1):55-67.

  • Focusing the view on nature's water-splitting catalyst. Philos Trans R Soc Lond B Biol Sci. 2008 Mar 27;363(1494):1167-77.

  • A dicyanotriterpenoid induces cytoprotective enzymes and reduces multiplicity of skin tumors in UV-irradiated mice. Biochem Biophys Res Commun. 2008 Mar 21;367(4):859-65. Epub 2008 Jan 17.

  • Solar one-way photoisomerisation of 5',8-cyclo-2'-deoxyadenosine. Org Biomol Chem. 2008 Mar 21;6(6):1083-6. Epub 2008 Feb 14.

  • Oligothiophene dendrimers as new building blocks for optical applications. J Phys Chem A. 2008 Mar 13;112(10):2018-26. Epub 2007 Nov 29.

  • Association of race, body fat, and season with vitamin D status among young women: A cross-sectional study. Clin Endocrinol (Oxf). 2008 Mar 10; [Epub ahead of print]

  • Rapid repair of UVA-induced oxidized purines and persistence of UVB-induced dipyrimidine lesions determine the mutagenicity of sunlight in mouse cells. FASEB J. 2008 Mar 7; [Epub ahead of print]

  • Plant/microbe cooperation for electricity generation in a rice paddy field. Appl Microbiol Biotechnol. 2008 Mar 5; [Epub ahead of print]

  • Design and analysis of a solar reactor for anaerobic wastewater treatment. Bioresour Technol. 2008 Mar 5; [Epub ahead of print]

  • Is Sunlight Important to Melanoma Causation? Cancer Epidemiol Biomarkers Prev. 2008 Mar 4; [Epub ahead of print] No abstract available.

  • In vitro phototoxicity of dihydropyridine derivatives: A photochemical and photobiological study. Eur J Pharm Sci. 2008 Mar 3;33(3):262-270. Epub 2007 Dec 23.

  • Simulated solar light-induced p53 mutagenesis in SKH-1 mouse skin: A dose-response assessment. Mol Carcinog. 2008 Mar 3; [Epub ahead of print]

  • Diagnosis and management of sebaceous carcinoma: an Australian experience. ANZ J Surg. 2008 Mar;78(3):158-63.

  • Up-regulation of hyaluronan synthase genes in cultured human epidermal keratinocytes by UVB irradiation. Arch Biochem Biophys. 2008 Mar 1;471(1):85-93. Epub 2007 Dec 15.

  • Induction of ErbB2 by ultraviolet A irradiation: potential role in malignant transformation of keratinocytes. Cancer Sci. 2008 Mar;99(3):502-9. Epub 2008 Jan 2.

  • Photocatalytic oxidation of gas-phase elemental mercury by nanotitanosilicate fibers. Chemosphere. 2008 Mar;71(5):969-74. Epub 2008 Jan 10.

  • Photolysis of (14)C-sulfadiazine in water and manure. Chemosphere. 2008 Mar;71(4):717-25. Epub 2008 Feb 20.


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