Molecular engineering and sequential cosensitization for preventing the "trade-off" effect with photovoltaic enhancement.

In dye-sensitized solar cells (DSSCs), it is essential to use rational molecular design to obtain promising photosensitizers with well-matched energy levels and narrow optical band gaps. However, the "trade-off" effect between the photocurrent and photovoltage is still a challenge. Here we report four benzoxidazole based D-A-π-A metal-free organic dyes (, , and ) with different combinations of π-spacer units and anchoring-acceptor groups.

High-Performance Porphyrin-Based Dye-Sensitized Solar Cells with Iodine and Cobalt Redox Shuttles.

Recently, enormous research passion has been devoted to enhance the power conversion efficiency (PCE) of porphyrin sensitizers for dye-sensitized solar cells (DSSCs), but the major stumbling block is the absorption defect in the visible-light region. To address this challenge, high-performance DSSCs are reported based on a new donor-π-acceptor sensitizer FW-1, 7H-dibenzo[c,g]carbazole-substituted and fused zinc porphyrin, co-sensitized with a benzotriazole-containing dye (WS-5) in iodine and cobalt redox systems, and high PCEs of 10.21 and 10.

Rational Molecular Engineering of Indoline-Based D-A-π-A Organic Sensitizers for Long-Wavelength-Responsive Dye-Sensitized Solar Cells.

Indoline-based D-A-π-A organic sensitizers are promising candidates for highly efficient and long-term stable dye-sensitized solar cells (DSSCs). In order to further broaden the spectral response of the known indoline dye WS-2, we rationally engineer the molecular structure through enhancing the electron donor and extending the π-bridge, resulting in two novel indoline-based D-A-π-A organic sensitizers WS-92 and WS-95. By replacing the 4-methylphenyl group on the indoline donor of WS-2 with a more electron-rich carbazole unit, the intramolecular charge transfer (ICT) absorption band of dye WS-92 is slightly red-shifted from 550 nm (WS-2) to 554 nm (WS-92).