Polymer acceptors based on Y6 derivatives for all-polymer solar cells

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Lateral size reduction of graphene oxide preserving its electronic properties and chemical functionality

Graphene oxide (GO) is widely considered as a graphene precursor when chemically reduced. Nevertheless, through the precise control of two parameters: lateral size and oxidation degree, GO can be useful in many applications as modified graphene oxide or functional reduced graphene oxide. Commonly, the decrease in GO lateral size, involves a change in the C/O ratio and therefore a modification in a large number of characteristics. Here, a simple but effective approach to synthesize GO with lateral dimensions below 100 nm and without modification of its chemical, optical and electronic features is presented. The use of a sonifier at low temperature allows to rapidly reduce the lateral size in similar to 82% while preserving the C/O ratio and consequently the chemical stability, the band gap, the electronic energy levels and the functionality. This method will allow several applications from biomedicine to energy, where reliable reduced size of GO is required

13.4 % Efficiency from All-Small-Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions

How to simultaneously achieve both high open-circuit voltage (Voc) and high short-circuit current density (Jsc) is a big challenge for realising high power conversion efficiency (PCE) in all-small-molecule organic solar cells (all-SM OSCs). Herein, a novel small molecule (SM)-donor, namely FYSM−SiCl, with trialkylsilyl and chlorine substitutions was designed and synthesized. Compared to the original SM-donor FYSM−H, FYSM−Si with trialkylsilyl substitution showed a decreased crystallinity and lower highest occupied molecular orbital (HOMO) level, while FYSM−SiCl had an improved crystallinity, more ordered packing arrangement, significantly lower HOMO level, and predominant “face-on” orientation. Matched with a SM-acceptor Y6, the FYSM−SiCl-based all-SM OSCs exhibited both high Voc of 0.85 V and high Jsc of 23.7 mA cm−2, which is rare for all-SM OSCs and could be attributed to the low HOMO level of FYSM−SiCl donor and the delicate balance between high crystallinity and suitable blend morphology. As a result, FYSM−SiCl achieved a high PCE of 13.4 % in all-SM OSCs, which was much higher than those of the FYSM−H- (10.9 %) and FYSM−Si-based devices (12.2 %). This work demonstrated a promising method for the design of efficient SM-donors by a side-chain engineering strategy via the introduction of trialkylsilyl and chlorine substitutions

In Situ Study the Dynamics of Blade-Coated All-Polymer Bulk Heterojunction Formation and Impact on Photovoltaic Performance of Solar Cells

All-polymer solar cells (all-PSCs) have achieved impressive progress by employing acceptors polymerized from well performing small-molecule non-fullerene acceptors. Herein, the device performance and morphology evolution in blade-coated all-PSCs based on PBDBT:PF5–Y5 blends prepared from two different solvents, chlorobenzene (CB), and ortho-xylene (o-XY) are studied. The absorption spectra in CB solution indicate more ordered conformation for PF5–Y5. The drying process of PBDBT:PF5–Y5 blends is monitored by in situ multifunctional spectroscopy and the final film morphology is characterized with ex situ techniques. Finer-mixed donor/acceptor nanostructures are obtained in CB-cast film than that in o-XY-cast ones, corresponding to more efficient charge generation in the solar cells. More importantly, the conformation of polymers in solution determines the overall film morphology and the device performance. The relatively more ordered structure in CB-cast films is beneficial for charge transport and reduced non-radiative energy loss. Therefore, to achieve high-performance all-PSCs with small energy loss, it is crucial to gain favorable aggregation in the initial stage in solution

10.13% Efficiency All-Polymer Solar Cells Enabled by Improving the Optical Absorption of Polymer Acceptors

The limited light absorption capacity for most polymer acceptors hinders the improvement of the power conversion efficiency (PCE) of all-polymer solar cells (all-PSCs). Herein, by simultaneously increasing the conjugation of the acceptor unit and enhancing the electron-donating ability of the donor unit, a novel narrow-bandgap polymer acceptor PF3-DTCO based on an A–D–A-structured acceptor unit ITIC16 and a carbon–oxygen (C–O)-bridged donor unit DTCO is developed. The extended conjugation of the acceptor units from IDIC16 to ITIC16 results in a red-shifted absorption spectrum and improved absorption coefficient without significant reduction of the lowest unoccupied molecular orbital energy level. Moreover, in addition to further broadening the absorption spectrum by the enhanced intramolecular charge transfer effect, the introduction of C–O bridges into the donor unit improves the absorption coefficient and electron mobility, as well as optimizes the morphology and molecular order of active layers. As a result, the PF3-DTCO achieves a higher PCE of 10.13% with a higher short-circuit current density (Jsc) of 15.75 mA cm−2 in all-PSCs compared with its original polymer acceptor PF2-DTC (PCE = 8.95% and Jsc = 13.82 mA cm−2). Herein, a promising method is provided to construct high-performance polymer acceptors with excellent optical absorption for efficient all-PSCs

Near-infrared absorbing polymer acceptors enabled by selenophene-fused core and halogenated end-group for binary all-polymer solar cells with efficiency over 16%

Due to the vigorous development of polymerized small-molecule acceptors (PSMAs), all-polymer solar cells (all-PSCs) have made tremendous advancement recently. However, their power conversion efficiencies (PCEs) are still restricted by the lack of PSMAs with desirable optoelectronic properties, especially the ability to capture the near-infrared photons. To resolve this, two near-infrared absorbing PSMAs, namely PY2Se-F and PY2Se-Cl, with a selenophene-fused core and halogenated end-group are developed. Combining the synergistic effects of selenium and fluorine (F)/chlorine (Cl) substitutions in broadening absorption and enhancing intermolecular interactions, PY2Se-F and PY2Se-Cl show significantly red-shifted absorption (30-40 nm) and reasonably deep-shifted lowest unoccupied molecular orbital (LUMO) levels compared with the pristine PY2S-H and fluorinated PY2S-F. When replacing F with Cl on the end-group, the PY2Se-Cl shows a better blend morphology with polymer donor PM6, compared with the PY2Se-F-based one, leading to better charge transport. As a result, the PM6:PY2Se-Cl-based all-PSCs achieve an impressive PCE of 16.1% with both high short-circuit current density (J(sc)) of 24.5 mA cm(-2) and fill factor (FF) of 0.743, which are among the highest values in the reported binary all-PSCs so far. Notably, this is the first example of chlorinated end-group derived PSMAs. Combining with the low-cost merit of chlorination, PY2Se-Cl shows great potential in the practical applications of efficient all-PSCs

Fluorinated Photovoltaic Materials for High-Performance Organic Solar Cells

Over the past decade, organic solar cells (OSCs) have achieved a dramatic boost in their power conversion efficiencies from about 6 % to over 16 %. In addition to developments in device engineering, innovative photovoltaic materials, especially fluorinated donors and acceptors, have become the dominant factor for improved device performance. This minireview highlights fluorinated photovoltaic materials that enable efficient OSCs. Impressive OSCs have been obtained by developing some important molds of fluorinated donor and acceptor systems. The molecular design strategy and the matching principle of fluorinated donors and acceptors in OSCs are discussed. Finally, a concise summary and outlook are presented for advances in fluorinated materials to realize the practical application of OSCs