{"id":2892,"date":"2011-06-24T15:26:22","date_gmt":"2011-06-24T15:26:22","guid":{"rendered":"https:\/\/mtlsites.mit.edu\/annual_reports\/2011\/?p=2892"},"modified":"2011-07-19T18:38:19","modified_gmt":"2011-07-19T18:38:19","slug":"ternary-mixtures-for-improved-performance-in-p3htpcbm-bulk-heterojunction-solar-cells","status":"publish","type":"post","link":"https:\/\/mtlsites.mit.edu\/annual_reports\/2011\/ternary-mixtures-for-improved-performance-in-p3htpcbm-bulk-heterojunction-solar-cells\/","title":{"rendered":"Ternary Mixtures for Improved Performance in P3HT\/PCBM Bulk Heterojunction Solar Cells"},"content":{"rendered":"

Photovoltaic cells containing nanoscale phase separated mixtures of a poly(thiophene) donor and a fullerene acceptor in the active layer have proven to be a attractive class of low-cost solar energy harvesting devices. The benchmark polymer solar cell (PSC) is one fabricated with poly(3-hexylthiophene) (P3HT) and PCn<\/sub>BM (n = 61, 71, Figure 1), which displays power conversion efficiencies of approximately 5% [1<\/a>] <\/sup>. Extensive optimization of the polymeric donor component has lead to the evolution of PSCs with power conversion efficiencies of approximately 8% [2<\/a>] <\/sup>; however, soluble fullerene derivatives remain the primary choice for the donor component in bulk heterojunctions. We have demonstrated that select small-molecule acceptors can serve as fullerene substitutes in P3HT\/PC61<\/sub>BM bulk heterojunctions and can increase the power conversion efficiencies of the resulting solar cells (Figure 2). Ternary mixtures containing 6,6-dicyanofulvenes [3<\/a>] <\/sup>, such as DCF (Figure 1), yield average power conversion efficiencies of 4%. Moreover, ternary mixtures containing stable organic radicals, such as TEMPO and DPPH, also augment the performance of P3HT\u2013PC61<\/sub>BM solar cells and result in power conversion efficiencies of up to 3.4%.<\/p>\n\n\t\t