For the Bright Future—Bulk Heterojunction Polymer Solar Cells with Power Conversion Efficiency of 7.4%

• DOI: 10.1002/adma.200903528
• Publication Date: 2010-01-04T13:38:13Z
• Authors: Yongye Liang; Zheng Xu; Jiangbin Xia; Szu‐Ting Tsai; Yue Wu; Gang Li; Claire Ray; Luping Yu
• Keywords: Polymers; Solar Energy; Thiophenes; 02 engineering and technology; 0210 nano-technology; 7. Clean energy; 12. Responsible consumption

Sun is the largest carbon-neutral energy source that has not been fully utilized. Although there are solar cell devices based on inorganic semiconductor to efficiently harvest solar energy, the cost of these conventional devices is too high to be economically viable. This is the major motivation for the development of organic photovoltaic (OPV) materials and devices, which are envisioned to exhibit advantages such as low cost, flexibility, and abundant availability. [1] The past success in organic light-emitting diodes provides scientists with confidence that organic photovoltaic devices will be a vital alternate to the inorganic counterpart. At the heart of the OPV technology advantage is the easiness of the fabrication, which holds the promise of very low-cost manufacturing process. A simple, yet successful technique is the solution-processed bulk heterojunction (BHJ) solar cell composed of electron-donating semiconducting polymers and electron-withdrawing fullerides as active layers. [2] The composite active layer can be prepared as a large area in a single step by using techniques such as spin-coating, inkjet-printing, spraycoating, gravure-coating, roller-casting etc. [3] In the last fifteen years, a significant progress has been made on the improvement of the power-conversion efficiency (PCE) of polymer BHJ solar cells, and the achieved efficiencies have evolved from less than 1% in the poly(phenylene vinylene) (PPV) system in 1995, [2] to 4‐5% in the poly(3-hexylthiphene) (P3HT) system in 2005, [4] to around 6%, as reported recently. [5] However, the efficiency of polymer solar cells is still significantly lower than their inorganic counterparts, such as silicon, CdTe and CIGS, which prevents practical applications in large scale.