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Dye-sensitized solar cells (DSSCs) based on Cu-II/I bipyridyl or phenanthroline complexes as redox shuttles have achieved very high open-circuit voltages (V-OC, more than 1 V). However, their short-circuit photocurrent density (J(SC)) has remained modest. Increasing the J(SC) is expected to extend the spectral response of sensitizers to the red or NIR region while maintaining efficient electron injection in the mesoscopic TiO2 film and fast regeneration by the Cu-I complex. Herein, we report two new D-A-pi-A-featured sensitizers termed HY63 and HY64, which employ benzothiadiazole (BT) or phenanthrene-fused-quinoxaline (PFQ), respectively, as the auxiliary electron-withdrawing acceptor moiety. Despite their very similar energy levels and absorption onsets, HY64-based DSSCs outperform their HY63 counterparts, achieving a power conversion efficiency (PCE) of 12.5 %. PFQ is superior to BT in reducing charge recombination resulting in the near-quantitative collection of photogenerated charge carriers.

Semitransparent dye-sensitized solar cells (DSCs) are appealing as aesthetically pleasing and colorful see-through photovoltaics. Green semitransparent DSCs have been presented, but the best ones rely on green zinc porphyrin photosensitizers and high volatile electrolytes. For potential outdoor applications, the zinc porphyrin DSCs employing ionic liquid electrolytes merely reached a power conversion efficiency (PCE) of 6.3% even with opaque mesoporous TiO2 films. Herein, the new green DSC is realized by using a blue organic photosensitizer in conjunction with an orange ionic-liquid-based electrolyte, presenting a simple and an effective path for color tuning of photovoltaics. The new approach allows for broadly modulating the color from spring green to cyan by tuning the contributions of the light absorption by the dye-sensitized TiO2 film and the electrolyte layer. The new semitransparent DSCs with spring green to cyan colors have PCEs ranging from 6.7% to 8.1% and show stability for 1000 h under accelerated ageing test at 80 degrees C, superior to the zinc porphyrin DSCs. The findings pave a new way to achieve efficient and stable colorful solar cells.

Over the past three decades, dye-sensitized solar cells (i. e. Gratzel cells) have evolved from a pioneering concept of molecular photovoltaics to large-scale industrial deployment. In this review article, we provide a historical overview of the developments with a focus on the scientific advancements that have set the stage for this technology to emerge and thrive. This involves insights into the (photo)electrochemistry of the underlying processes, molecular engineering of dyes, redox shuttles, and hole-transporting materials, as well as their implementation into solar cells. We further outline applications and future perspectives, involving the long-lasting objective to develop efficient solid-state alternatives to conventional dye-sensitized solar cells.

Long-term durability is critically important for the commercialization of perovskite solar cells (PSCs). The ionic character of the perovskite and the hydrophilicity of commonly used additives for the hole-transporting layer (HTL), such as lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) and tert-butylpyridine (tBP), render PSCs prone to moisture attack, compromising their long-term stability. Here we introduce a trifluoromethylation strategy to overcome this drawback and to boost the PSC's solar to electric power conversion efficiency (PCE). We employ 4-(trifluoromethyl)benzylammonium iodide (TFMBAI) as an amphiphilic modifier for interfacial defect mitigation and 4-(trifluoromethyl)pyridine (TFP) as an additive to enhance the HTL's hydrophobicity. Surface treatment of the triple-cation perovskite with TFMBAI largely suppressed the nonradiative charge carrier recombination, boosting the PCE from 20.9% to 23.9% and suppressing hysteresis, while adding TFP to the HTL enhanced the PCS's resistance to moisture while maintaining its high PCE. Taking advantage of the synergistic effects resulting from the combination of both fluoromethylated modifiers, we realize TFMBAI/TFP-based highly efficient PSCs with excellent operational stability and resistance to moisture, retaining over 96% of their initial efficiency after 500 h maximum power point tracking (MPPT) under simulated 1 sun irradiation and 97% of their initial efficiency after 1100 h of exposure under ambient conditions to a relative humidity of 60-70%.

Dye-sensitized solar cells (DSCs) based on copper(II/I) redox mediators have recently achieved notable performance progress through tailoring the ligand structure of the copper complexes, exploiting cosensitization, and introducing an advanced device structure. In order to further improve the power conversion efficiency (PCE), it is imperative to develop wide spectral-response photo- sensitizers compatible with the copper(II/I) redox mediators while attaining a high Voc. Herein, a blue photosensitizer coded R7 is reported, which is purposely designed for highly efficient DSCs with copper-based electrolytes. R7 features a strong electron-donating segment of 9,19-dihydrobenzo[1′,10′ ] phenanthro[3′,4′:4,5]thieno[3,2-b]benzo[1,10]phenanthro[3,4-d]thiophene conjugated with a bulky auxiliary donor N-(2,4′-bis(hexyloxy)-[1,1′-biphenyl]-4- yl)-2,4′-bis(hexyloxy)-N-methyl-[1,1′-biphenyl]-4-amine and the electron acceptor 4-(7-ethynylbenzo[c][1,2,5]thiadiazol-4-yl)benzoic acid. The blue dye R7 with bulkier auxiliary donor moiety in the DSC largely outperforms the reference dye R6, which has a smaller bis(4-(hexyloxy)phenyl)amine donor unit. Transient absorption spectroscopy and electrochemical impedance spectroscopy meas- urements show that the R7 based DSC has a higher charge separation yield, a higher charge collection efficiency, and lower charge recombination with the copper electrolyte than the R6 based counterpart. A cosensitized system of R7 and Y123 for the DSC presents an outstanding PCE of 12.7% and retains 90% of its initial value after 1000 h of light soaking under 1 sun at 45 °C.