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International audience; We have identified modifications of material distributions in inverted organic solar cell structures during accelerated aging processes that are potentially linked to the loss of the mechanical integrity of the devices. Non-encapsulated devices were treated with ISOS-D-3 ageing (the so called damp heat exposure at 85 °C/85% room humidity in the dark). After performing pull-off tests, the exposed surfaces were analyzed by X-ray photoemission spectroscopy and atomic force microscopy. For fresh devices, the results revealed that mechanical failure occurs close to the PEDOT:PSS/P3HT:PCBM interface, in agreement with the literature. However, after a short exposure to damp heat, XPS investigations indicate an enrichment of PCBM at the PEDOT:PSS/P3HT:PCBM interface and a change in the 2 PEDOT:PSS surface composition. Both phenomena may explain the rapid drop in device performances and the increased tendency towards delamination.

International audience; The photooxidation of a polymer blend film used in efficient solar cells based on poly[(4,40-bis(2-ethylhexyl)dithieno[3,2-b:20,30- d]silole)-2,6-diylalt-(2,1,3-benzothiadiazole)-4,7-diyl], (Si-PCPDTBT) and [6,6]-phenyl-C71-butyric acid methyl (PC70BM) has been investigated. A set of experiments from complementary techniques was developed to monitor the modifications during ageing that occur not only in the bulk but also at the surface. The surface analyses were performed by X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM), and the bulk analyses by UV–visible spectroscopy and infrared (IR) spectroscopy. The results reveal that the silicon bridge atom is the first target of degradation. We have identified the existence of a photooxidation profile within the 300 nm thick film. Such a heterogeneous degradation was confirmed by time-of-flight secondary ion mass spectrometry (TOF-SIMS) depth profiling.

International audience; In the printing industry, the exploitation of triggerable materials that can have their surface properties altered on application of a post-deposition external stimulus has been crucial for the production of robust layers and patterns. To this end, herein, a series of clickable poly(R-alkyl p-styrene sulfonate) homopolymers, with systematically varied thermally-labile protecting groups, has been synthesised via reversible addition-fragmentation chain transfer (RAFT) polymerisation. The polymer range has been designed to offer varied post-deposition thermal treatment to switch them from hydrophobic to hydrophilic. Suitable RAFT conditions have been identified to produce well-defined homopolymers (Đ, Mw/Mn < 1.11 in all cases) at high monomer conversions (>80% for all but one monomer) with controllable molar mass. Poly(p-styrene sulfonate) with an isobutyl protecting group has been shown to be the most readily thermolysed polymer that remains stable at room temperature, and was thus investigated further by incorporation into a diblock copolymer, P3HT-b-PiBSS, by click chemistry. The strategy for preparation of thermal modifiable block copolymers exploiting R-protected p-styrene sulfonates and azide-alkyne click chemistry presented herein allows the design of new, roll-to-roll processable materials for potential application in the printing industry, particularly organic electronics.