<?xml version="1.0" encoding="UTF-8" ?>
<rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcq="http://purl.org/dc/terms/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#">
     <records>
	  <record>
	       <dc:title>Application of highly-ordered TiO{sub 2} nanotube-arrays in heterojunction dye-sensitized solar cells</dc:title>
	       <dc:creator>Paulose, Maggie; Shankar, Karthik; Varghese, Oomman K; Mor, Gopal K; Grimes, Craig A [Department of Electrical Engineering, Department of Material Science and Engineering, The Pennsylvania State University, University Park, PA 16802 (United States)]</dc:creator>
	       <dc:subject>75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; ACETONITRILE; ANODIZATION; CARBOXYLIC ACIDS; CRYSTALLIZATION; CURRENT DENSITY; DOPED MATERIALS; ELECTRIC POTENTIAL; ELECTRICAL FAULTS; ELECTROLYTES; FILL FACTORS; FLUORINE; HETEROJUNCTIONS; NANOTUBES; RUTHENIUM; SOLAR CELLS; THIN FILMS; TIN OXIDES; TITANIUM; TITANIUM CHLORIDES; TITANIUM OXIDES</dc:subject>
	       <dc:subjectRelated></dc:subjectRelated>
	       <dc:description>Highly-ordered TiO{sub 2} nanotube arrays are made by potentiostatic anodization of a titanium film in a fluoride containing electrolyte. Here we describe the application of this unique material architecture in both front-side and back-side illuminated dye-sensitized solar cells (DSSCs). The back-side illuminated solar cells are based on the use of 6.2 {mu}m long (110 nm pore diameter, 20 nm wall thickness) highly-ordered nanotube-array films made by anodization of a 250 {mu}m thick Ti foil in a KF electrolyte. Front-side illuminated solar cells use a negative electrode composed of optically transparent nanotube arrays, approximately 3600 nm in length (46 nm pore diameter, 17 nm wall thickness), grown on a fluorine doped tin oxide coated glass substrate by anodic oxidation of a previously deposited RF-sputtered titanium thin film in a HF electrolyte. After crystallization by oxygen annealling the nanotube-arrays are treated with TiCl{sub 4} to enhance photocurrent amplitudes. The arrays are then sensitized by a self-assembled monolayer of bis(tetrabutylammonium)-cis-(dithiocyanato)-N, N'- bis(4-carboxylato-4'-carboxylic acid-2, 2'-bipyridine)ruthenium(II) (commonly called 'N719'). Superior photoresponse is obtained using acetonitrile as the dye solvent. Voltage decay measurements indicate that the highly-ordered TiO{sub 2} nanotube-arrays, in comparison with nanoparticulate systems, provide excellent pathways for electron percolation with superior electron lifetimes. The front-side illuminated DSSCs, show a typical AM 1.5 photocurrent of 10.3 mA cm{sup -2}, open circuit voltage of 0.84 V, 0.54 fill factor, and 4.7% efficiency although the transparent nanotube-array negative electrode is only 360 nm thick. The back-side illuminated DSSCs show an AM 1.5 short-circuit current density of 10.6 mA cm{sup -2}, 0.82 V open circuit potential and a 0.51 fill factor yielding a solar conversion efficiency of 4.4%.</dc:description>
	       <dcq:publisher></dcq:publisher>
	       <dcq:publisherResearch></dcq:publisherResearch>
	       <dcq:publisherAvailability>Available online at http://stacks.iop.org/0022-3727/39/2498/d6_12_005.pdf or at the Web site for the Journal of Physics. D, Applied Physics (ISSN 1361-6463) http://www.iop.org/;INIS</dcq:publisherAvailability>
	       <dcq:publisherSponsor></dcq:publisherSponsor>
	       <dcq:publisherCountry>United Kingdom</dcq:publisherCountry>
		   <dc:contributingOrganizations></dc:contributingOrganizations>
	       <dc:date>2006-06-21</dc:date>
	       <dc:language>English</dc:language>
	       <dc:type>Journal Article</dc:type>
	       <dcq:typeQualifier></dcq:typeQualifier>
	       <dc:relation>Journal Name: Journal of Physics. D, Applied Physics; Journal Volume: 39; Journal Issue: 12; Other Information: PII: S0022-3727(06)15255-9; DOI: 10.1088/0022-3727/39/12/005; Country of input: International Atomic Energy Agency (IAEA)</dc:relation>
	       <dc:coverage></dc:coverage>
	       <dc:format>Medium: X; Size: page(s) 2498-2503</dc:format>
	       <dc:doi>https://doi.org/10.1088/0022-3727/39/12/005; COUNTRY OF INPUT: INTERNATIONAL ATOMIC ENERGY AGENCY (IAEA)</dc:doi>
	       <dc:identifier></dc:identifier>
		   <dc:journalName>[]</dc:journalName>
		   <dc:journalIssue>12</dc:journalIssue>
		   <dc:journalVolume>39</dc:journalVolume>
	       <dc:identifierReport></dc:identifierReport>
	       <dcq:identifierDOEcontract></dcq:identifierDOEcontract>
	       <dc:identifierOther>Journal ID: ISSN 0022-3727; JPAPBE; TRN: GB06Q0645001249</dc:identifierOther>
	       <dc:source>GBN</dc:source>
	       <dc:rights></dc:rights>
	       <dc:dateEntry>2010-12-31</dc:dateEntry>
	       <dc:dateAdded></dc:dateAdded>
	       <dc:ostiId>20825841</dc:ostiId>
	       <dcq:identifier-purl></dcq:identifier-purl>
	  </record>
     </records>
</rdf:RDF>