AVS 55th International Symposium & Exhibition
    Energy Science and Technology Focus Topic Thursday Sessions
       Session EN+EM+NS+P+A+T+V-ThM

Paper EN+EM+NS+P+A+T+V-ThM3
Endohedral Metallofullerenes as Improved Acceptor Materials for Organic Solar Cells

Thursday, October 23, 2008, 8:40 am, Room 203

Session: Energy: Tools and Approaches
Presenter: B.C. Holloway, Luna Innovations Incorporated
Authors: M. Drees, Luna Innovations Incorporated
R. Ross, Georgetown University
C. Cardona, Luna Innovations Incorporated
E. Van Keuren, Georgetown University
D. Guldi, Friedrich-Alexander-Universitat Erlangen-Nurnberg, Germany
B.C. Holloway, Luna Innovations Incorporated
Correspondent: Click to Email

Cost factors in inorganic solar cells have opened up a new path to less expensive manufacturing techniques using bulk heterojunction polymer/fullerene based solar cells. Using empty cage fullerene derivatives as the acceptor material, state-of-the-art organic photovoltaics currently display ~5% overall conversion efficiency. One of the main factors limiting the efficiency in organic solar cells is the low open circuit voltage. The open circuit voltage is governed by the molecular orbitals of the donor and acceptor material; therefore better matching of the orbitals will lead to improved voltages. Here we present a novel acceptor material based on Trimetasphere® carbon nanomaterials (TMS). Trimetaspheres® are endohedral metallofullerenes that consist of a trimetal nitride cluster enclosed in a C80 cage. First-generation Trimetasphere® carbon nanomaterial derivatives have been synthesized and show behavior consistent with C60 but with improved molecular orbitals. Electrochemical data suggests a maximum voltage increase of up to 280 mV over C60-PCBM-based devices and photophysical characterization of shows efficient and stable charge separation. Initial bulk-heterojunction devices have been synthesized with open circuit voltages that are 280 mV higher than reference devices using C60-PCBM and conversion efficiencies exceeding 3.1%.