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dc.contributor.advisorMarc A. Baldo.en_US
dc.contributor.authorMapel, Jonathan Kingen_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science.en_US
dc.date.accessioned2009-03-20T19:30:45Z
dc.date.available2009-03-20T19:30:45Z
dc.date.copyright2008en_US
dc.date.issued2008en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/44904
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2008.en_US
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.descriptionIncludes bibliographical references (p. 158-169).en_US
dc.description.abstractThe separation of light harvesting and charge generation offers several advantages in the design of organic photovoltaics and organic solar concentrators for the ultimate end goal of achieving a lower cost solar electric conversion. In this work, we explore two new device architectures. In antenna organic solar cells, we utilize external energy transfer mediated by surface plasmon polaritons to increase the efficiency of existing organic photovoltaic devices limited in performance by the exciton diffusion bottleneck. This unique architecture is analyzed for its functionality and the efficiencies of each added step is quantified. Although the introduction of additional energy transduction will ultimately introduce more losses, bypassing the exciton diffusion bottleneck offers the potential for increased efficiency through judicious device design. We also seek to enable the use of high efficiency inorganic solar cells in organic solar concentrators which aim to exploit high performance of the PV cells in low cost, nontracking configurations. By utilizing thin films of organic chromophores on high refractive index glass substrates, we are able to apply the recent advances of organic optoelectonics to the fluorescent concentrator platform, including near field energy transfer, solid state solvation, and phosphorescence. By reducing self-absorption losses, we demonstrate optical flux gains an order of magnitude greater than previously published results and thereby reduce the effective cost of inorganic solar cells by at least a factor of ten. Combined with the potential for low cost solution processing, the high flux gains and power efficiencies realized here should enable a new source of inexpensive solar power.en_US
dc.description.statementofresponsibilityby Jonathan King Mapel.en_US
dc.format.extent169 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectElectrical Engineering and Computer Science.en_US
dc.titleOrganic photovoltaics and concentratorsen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
dc.identifier.oclc297540223en_US


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