Push-pull photochromic dyes for semi-transparent solar cells with light-adjustable optical properties and high color-rendering index.

We report the design, synthesis and characterization of push-pull photochromic naphthopyran dyes, incorporating different carbazole moieties as the electron-donor group for use in dye-sensitized solar cells. Compared to a reference dye incorporating a diphenylamine-type donor moiety, the introduction of functionalized carbazoles allows for a hypsochromic shift of the absorption of the coloured isomers of the dyes in the visible region and a better tuning of their spectra to the photopic response of the human eye. Under illumination, the molecules exhibit a broad absorption with a maximum comprised between 546 nm and 571 nm in solution and they reveal relatively fast discoloration kinetics. By using these dyes to fabricate photochromic solar cells whose optical and photovoltaic properties vary with the light exposure, we have achieved a PCE of up to 3% in opaque cells. Using these molecules in semi-transparent solar cells with different electrolytes, a PCE of 2.3% was achieved. We also produced a semi-transparent mini-module with an average visible transmittance varying between 66% and 50% and a colour rendering index around 95 in both the uncoloured and coloured states.

Star-shape non-fullerene acceptor featuring an aza-triangulene core for organic solar cells.

We present the simple synthesis of a star-shape non-fullerene acceptor (NFA) for application in organic solar cells. This NFA possesses a D(A)3 structure in which the electron-donating core is an aza-triangulene unit and we report the first crystal structure for a star shape NFA based on this motive. We fully characterized this molecule's optoelectronic properties in solution and thin films, investigating its photovoltaic properties when blended with PTB7-Th as the electron donor component. We demonstrate that the aza-triangulene core leads to a strong absorption in the visible range with an absorption edge going from 700 nm in solution to above 850 nm in the solid state. The transport properties of the pristine molecule were investigated in field effect transistors (OFETs) and in blends with PTB7-Th following a Space-Charge-Limited Current (SCLC) protocol. We found that the mobility of electrons measured in films deposited from o-xylene and chlorobenzene are quite similar (up to 2.70 × 10-4 cm2 V-1 s-1) and that the values are not significantly modified by thermal annealing. The new NFA combined with PTB7-Th in the active layer of inverted solar cells leads to a power conversion efficiency of around 6.3% (active area 0.16 cm2) when processed from non-chlorinated solvents without thermal annealing. Thanks to impedance spectroscopy measurements performed on the solar cells, we show that the charge collection efficiency of the devices is limited by the transport properties rather than by recombination kinetics. Finally, we investigated the stability of this new NFA in various conditions and show that the star-shape molecule is more resistant against photolysis in the presence and absence of oxygen than ITIC.

Photochromic spiro-indoline naphthoxazines and naphthopyrans in dye-sensitized solar cells.

Photochromic dyes possess unique properties that can be exploited in different domains, including optics, biomedicine and optoelectronics. Herein, we explore the potential of photochromic spiro-indoline naphthoxazine (SINO) and naphthopyran (NIPS) for application in photovoltaics. We designed and synthesized four new photosensitizers with a donor-pi-acceptor structure embedding SINO and NIPS units as photochromic cores. Their optical, photochromic and acidochromic properties were thoroughly studied to establish structure-properties relationships. Then, after unravelling the possible forms adopted depending on the stimuli, their photovoltaic properties were evaluated in DSSCs. Although the photochromic behavior is not always preserved, we elucidate the interplay between photochromic, acidochromic and photovoltaic properties and we demonstrate that these dyes can act as photosensitizers in DSSCs. We report a maximum power conversion efficiency of 2.7% with a NIPS-based dye, a tenfold improvement in comparison to previous works on similar class of compounds. This work opens new perspectives of developments for SINO and NIPS in optical and photovoltaic devices, and it provides novel research directions to design photochromic materials with improved characteristics.

Photochromic naphthopyran dyes incorporating a benzene, thiophene or furan spacer: effect on photochromic, optoelectronic and photovoltaic properties in dye-sensitized solar cells.

We recently demonstrated that diaryl-naphthopyran photochromic dyes are efficient for sensitization of TiO2 mesoporous electrodes, thus allowing the fabrication of photo-chromo-voltaic cells that can self-adapt their absorption of light and their generation of electricity with the light intensity. Herein we report the synthesis, the characterisation of two novel photochromic dyes based on diaryl-naphthopyran core i.e NPI-ThPh and NPI-FuPh for use in Dye Sensitized Solar Cells (DSSCs). Compared to our reference dye NPI, the molecules only vary by the nature of the spacer, a thiophene or a furan, connecting the photochromic unit and the phenyl-cyano-acrylic acid moiety used as the anchoring function. We found that swapping a phenyl for a thiophene or a furan leads to an improvement of the absorption properties of the molecules both in solution and after grafting on TiO2 electrodes, however their photochromic process becomes not fully reversible. Despite better absorption in the visible range, the new dyes show poorer photochromic and photovoltaic properties in devices compared to NPI. Thanks to UV-Vis spectroscopy, DFT calculation, electrical characterization of the cells, and impedance spectroscopy, we unravel the factors limiting their performances. Our study contributes to better understand the connection between photochromic and photovoltaic properties, which is key to develop better performing molecules of this class.

Characterization of Photochromic Dye Solar Cells Using Small-Signal Perturbation Techniques.

Photochromic dye-sensitized solar cells (DSSCs) are novel semi-transparent photovoltaic devices that self-adjust their optical properties to the irradiation conditions, a feature that makes them especially suitable for building integrated photovoltaics. These novel solar cells have already achieved efficiencies above 4%, and there are multiple pathways to improve the performance. In this work, we conduct a full characterization of DSSCs with the photochromic dye NPI, combining electrical impedance spectroscopy (EIS) and intensity-modulated photocurrent spectroscopy (IMPS). We argue that the inherent properties of the photochromic dye, which result in a modification of the functioning of the solar cell by the optical excitation that also acts as a probe, pose unique challenges to the interpretation of the results using conventional models. Absorption of light in the visible range significantly increases when the NPI dye is in the activated state; however, the recombination rate also increases, thus limiting the efficiency. We identify and quantify the mechanism of enhanced recombination when the photochromic dye is activated using a combination of EIS and IMPS. From the comparison to a state-of-the-art reference dye (RK1), we were able to detect a new feature in the IMPS spectrum that is associated with the optical activation of the photochromic dye, providing a useful tool for assessing the electronic behavior of the device under different conditions of light excitation. This study provides guidelines to adequate characterization protocols of photochromic solar cells and essential insights on the interfacial electronic processes.

Push-Pull Zinc Phthalocyanine Bearing Hexa-Tertiary Substituted Carbazolyl Donor Groups for Dye-Sensitized Solar Cells.

An asymmetrical, push-pull phthalocyanine bearing bulky tert-butylcarbazolyl moieties as electron donor and carboxylic acid as anchoring group was synthetized and tested as a photosensitizer in dye-sensitized solar cells (DSSC). The new photosensitizer was characterized by 1H and 13C NMR, UV-Vis and mass spectrometry. The bulky tert-butylcarbazolyl moieties avoid the aggregation of the phthalocyanine dye. DFT studies indicate that the HOMO is delocalized throughout the -electron system of the substituted phthalocyanine and the LUMO is located on the core of the molecule with a sizable electron density distribution on carboxyl groups. The new dye has been used as a photosensitizer in transparent and opaque dye-sensitized solar cells, which exhibit poor efficiencies related to a low Jsc.