Publications by authors named "Johann Boucle"

Double halide perovskites have received massive attention due to their low toxicity, tunable bandgap, structural flexibility, and stability as compared to conventional 3D lead halide perovskites. Particularly, newly discovered formamidinium germanium-antimony halide (FAGeSbCl) double perovskites offer an excellent bandgap (∼1.3 eV) for solar cell (SC) applications.

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Donor−acceptor (D−A) small molecules are regarded as promising hole-transporting materials for perovskite solar cells (PSCs) due to their tunable optoelectronic properties. This paper reports the design, synthesis and characterization of three novel isomeric D-π-A small molecules PY1, PY2 and PY3. The chemical structures of the molecules consist of a pyrazolo[1,5-a]pyrimidine acceptor core functionalized with one 3,6-bis(4,4′-dimethoxydiphenylamino)carbazole (3,6-CzDMPA) donor moiety via a phenyl π-spacer at the 3, 5 and 7 positions, respectively.

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CaTiFe O perovskite oxide films are promising candidate materials for p-type interlayers of third generation solar cells or light-emitting devices. The impact of atomic Ti substitutions by Fe on electrical and optical properties of CaTiFeO perovskite films have been studied. The best compromise between a high transmission coefficient and the suitable electrical conductivity is obtained for a specific atomic composition of Ca (1) Ti (0.

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Electron and hole transport layers (ETL and HTL) play an essential role in shaping the photovoltaic performance of perovskite solar cells. While compact metal oxide ETL have been largely explored in planar device architectures, aligned nanowires or nanorods remain highly relevant for efficient charge extraction and directional transport. In this study, we have systematically grown ZnO nanowires (ZnO NWs) over aluminum-doped zinc oxide (AZO) substrates using a low-temperature method, hydrothermal growth (HTG).

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For the first time, an original compound belonging to the heptazine family has been deposited in the form of thin layers, both by thermal evaporation under vacuum and spin-coating techniques. In both cases, smooth and homogeneous layers have been obtained, and their properties evaluated for eventual applications in the field of organic electronics. The layers have been fully characterized by several concordant techniques, namely UV-visible spectroscopy, steady-state and transient fluorescence in the solid-state, as well as topographic and conductive atomic force microscopy (AFM) used in Kelvin probe force mode (KPFM).

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Chlorophyll derivatives were integrated in "all solid-state" dye sensitized solar cells (DSSCs) with a mesoporous TiO electrode and 2',2',7,7'-tetrakis[,-di(4-methoxyphenyl)amino]-9,9'-spirobifluorene as the hole-transport material. Despite modest power conversion efficiencies (PCEs) between 0.26% and 0.

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Laser synthesis was used for one-step synthesis of titania/graphene composites (G-TiO (C)) from a suspension of 0.04 wt% commercial reduced graphene oxide (rGO) dispersed in liquid titanium tetraisopropoxide (TTIP). Reference titania sample (TiO(C)) was prepared by the same method without graphene addition.

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This work presents an original synthesis of TiO/graphene nanocomposites using laser pyrolysis for the demonstration of efficient and improved perovskite solar cells. This is a one-step and continuous process known for nanoparticle production, and it enables here the elaboration of TiO nanoparticles with controlled properties (stoichiometry, morphology, and crystallinity) directly grown on graphene materials. Using this process, a high quality of the TiO/graphene interface is achieved, leading to an intimate electronic contact between the two materials.

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Solid-state dye-sensitized solar cells (ssDSSC) constitute a major approach to photovoltaic energy conversion with efficiencies over 8% reported thanks to the rational design of efficient porous metal oxide electrodes, organic chromophores, and hole transporters. Among the various strategies used to push the performance ahead, doping of the nanocrystalline titanium dioxide (TiO₂) electrode is regularly proposed to extend the photo-activity of the materials into the visible range. However, although various beneficial effects for device performance have been observed in the literature, they remain strongly dependent on the method used for the production of the metal oxide, and the influence of nitrogen atoms on charge kinetics remains unclear.

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This study demonstrates that the concept of molecular antenna is a relevant strategy to improve the power conversion efficiency of solid-state dye-sensitized solar cells by extending their spectral sensitivity over a broad region of the solar spectrum. In this work, we have associated a BODIPY antenna to a bi-chromophoric sensitizer made of a squaraine unit linked to a zinc porphyrin by axial ligation onto the zinc. Using steady-state and transient photoluminescence spectroscopy, we demonstrate that efficient energy transfers occur from the antenna to the dyad, extending its visible photosensitivity.

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This paper presents the continuous-flowand single-step synthesis of a TiO2/MWCNT (multiwall carbon nanotubes) nanohybrid material. The synthesis method allows achieving high coverage and intimate interface between the TiO2particles and MWCNTs, together with a highly homogeneous distribution of nanotubes within the oxide. Such materials used as active layer in theporous photoelectrode of solid-state dye-sensitized solar cells leads to a substantial performance improvement (20%) as compared to reference devices.

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A new approach for developing solid-state dye-sensitised solar cells (DSSCs) on glass/ITO and plastic substrates (PEN/ITO) is presented in this manuscript. A two step electrodeposition technique has been employed to realize the ZnO photoelectrodes. First a ZnO thin film is deposited on the ITO substrate and subsequently on this buffer layer 650 nm long ZnO nanowires are grown.

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