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Cell–material interactions play an essential role in the development of scaffold-based tissue engineering strategies. Cell therapies are still limited in treating injuries when severe damage causes irreversible loss of muscle cells. Electroactive biomaterials and, in particular, piezoelectric materials offer new opportunities for skeletal muscle tissue engineering since these materials have demonstrated suitable electroactive microenvironments for tissue development. In this study, the influence of the surface charge of piezoelectric poly(vinylidene fluoride) (PVDF) on cell adhesion was investigated. The cytoskeletal organization of C2C12 myoblast cells grown on different PVDF samples was studied by immunofluorescence staining, and the interactions between single live cells and PVDF were analyzed using an atomic force microscopy (AFM) technique termed single-cell force spectroscopy. It was demonstrated that C2C12 myoblast cells seeded on samples with net surface charge present a more elongated morphology, this effect being dependent on the surface charge but independent of the poling direction (negative or positive surface charge). It was further shown that the cell deadhesion forces of individual C2C12 cells were higher on PVDF samples with an overall negative surface charge (8.92 ± 0.45 nN) compared to those on nonpoled substrates (zero overall surface charge) (4.06 ± 0.20 nN). These findings explicitly demonstrate that the polarization/surface charge is an important parameter to determine cell fate as it affects C2C12 cell adhesion, which in turn will influence cell behavior, namely, cell proliferation and differentiation, Portuguese Foundation for Science and Technology (FCT) in the framework of the Strategic Funding UID/FIS/04650/2019, UID/BIA/04050/2013, UID/BIO/04469, project POCI-01-0145-FEDER-028237 and under BioTecNorte operation (NORTE-01-0145-FEDER-000004). The authors also thank the FCT for the SFRH/BD/111478/2015 (S.R.) and SFRH/BPD/90870/2012 (C.R.) grants. Funds provided by FCT in the framework of EuroNanoMed 2016 call, Project LungChek ENMed/0049/2016 are also gratefully acknowledged. The authors acknowledge funding by the Spanish Ministry of Economy and Competitiveness (MINECO) through the project MAT2016-76039-C4-3-R (AEI/FEDER, UE) and from the Basque Government Industry and Education Department under the ELKARTEK, HAZITEK and PIBA (PIBA-2018-06)

In this work, we proposed an efficient heterostructure photocatalyst by integrating the ferroelectric BaTiO3 (BTO) layer with the semiconductor MoO3 layer, availing the ferroelectric polarization of BaTiO3 and high generation of photoinduced charge carriers in the MoO3 layer. The effect of MoO3 layer thickness (tMoO3) on the photocatalytic efficiency of the BTO/MoO3 heterostructures is found to be optimum at tMoO3 = 67 nm as tMoO3 varies from 40 to 800 nm. The BTO/MoO3 heterostructure with tMoO3 = 67 nm exhibits a high efficiency of 86% for the degradation of rhodamine B (RhB) under the exposure of UV-visible light for 60 min. The photocatalysis rate kinetics analysis reveals that the rate constant in the heterostructure is 1.7 times of pure BTO and 3.2 times of pure MoO3 films. The enhanced photocatalytic activity in the heterostructures is attributed to the electric field-driven carrier separation due to the ferroelectric polarization and the heterojunction band bending. The charge coupling effect between BaTiO3 and MoO3 is evident from the current-voltage characteristics. The maximum lattice strain in the heterostructure with tMoO3 = 67 nm as evident from X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and photoluminescence (PL) analysis further confirms the charge transfer between the layers. The degradation as well as decolorization efficiency of the BTO/MoO3 heterostructure is higher than that of pure BTO and MoO3 films. Radical trapping experiments reveal that electrons are the major contributors to the photocatalytic activity of the BTO/MoO3 heterostructure. The reusability test shows only a reduction of 5% in the efficiency of the heterostructure after five photocatalysis cycles. The heterostructure can also efficiently decompose the other dyes such as rose bengal and methyl violet. Thus, our findings prove that an efficient and reusable photocatalyst can be designed through the integration of the ferroelectrics with the semiconductor layers., This work was financially supported by UGC and DST-SERB, Govt. of India through grants no. F.4-5(59-FRP/2014(BSR)) and ECR/2017/000068. K.V.A. acknowledges DST, Govt. of India for the Inspire fellowship (IF170601). A. R. Jayakrishnan acknowledges Central University of Tamil Nadu, India for his Ph.D. fellowship. K.K. acknowledges the DST-SERB, Govt of India for the financial support through grant no: ECR/2017/ 002537. J.P.B.S. is grateful for the financial support by the Portuguese Foundation for Science and Technology (FCT) in the framework of the Strategic Funding UID/FIS/04650/ 2019. Authors acknowledge A. Sulthan Ibrahim (Technical Assistant, Dept. of Physics, Central University of Tamil Nadu), Ajeesh Kumar S. (Technical Assistant, SPAP, M.G. University, Kerala), and Dheepika R (Research Scholar, Dept. of Chemistry, Central University of Tamil Nadu) for their timely help in various characterizations.

Plasmonic Au nanoparticles (AuNPs) embedded into a TiO2 dielectric matrix were analyzed by combining two-dimensional and three-dimensional electron microscopy techniques. The preparation method was reactive magnetron sputtering, followed by thermal annealing treatments at 400 and 600 degrees C. The goal was to assess the nanostructural characteristics and correlate them with the optical properties of the AuNPs, particularly the localized surface plasmon resonance (LSPR) behavior. High-angle annular dark field scanning transmission electron microscopy results showed the presence of small-sized AuNPs (quantum size regime) in the as-deposited Au-TiO2 film, resulting in a negligible LSPR response. The in-vacuum thermal annealing at 400 degrees C induced the formation of intermediate-sized nanoparticles (NPs), in the range of 10-40 nm, which led to the appearance of a well-defined LSPR band, positioned at 636 nm. Electron tomography revealed that most of the NPs are small-sized and are embedded into the TiO2 matrix, whereas the larger NPs are located at the surface. Annealing at 600 degrees C promotes a bimodal size distribution with intermediate-sized NPs embedded in the matrix and big sized NPs, up to 100 nm, appearing at the surface. The latter are responsible for a broadening and a redshift, to 645 nm, in the LSPR band because of increase of scattering-to-absorption ratio. Beyond differentiating and quantifying the surface and embedded NPs, electron tomography also provided the identification of "hot-spots". The presence of NPs at the surface, individual or in dimers, permits adsorption sites for LSPR sensing and for surface-enhanced spectroscopies, such as surface enhanced Raman scattering., The authors thank the METSA network (FR3507 CNRS) for the financial support for this work, the Clym consortium for granting access to the Jeol 2010F and TITAN 80-300 keV ETEM. S.K. thanks the French Ministry of Higher Education and Research for the financial support during his PhD which was also supported by the LABEX iMUST (ANR-10-LABX-0064) of Universite de Lyon, within the program "Investissements d'Avenir" (ANR-11-IDEX-0007) operated by the French National Research Agency (ANR). This research was partly supported by the 3Dclean ANR-15-CE09-0009 project granted by the ANR. This research was also sponsored by the Portuguese Foundation for Science and Technology (FCT) in the framework of the Strategic Funding UID/FIS/04650/2013 and FCT Project 9471-RIDTI, co-funded by FEDER and with reference PTDC/FIS-NAN/1154/2014. J.B. acknowledges FCT for his Postdoc Grant (SFRH/BPD/117010/2016) and M.S.R. acknowledges FCT for his PhD Grant (SFRH/BD/118684/2016)., info:eu-repo/semantics/publishedVersion

Organic photodetectors (PDs) based on printing technologies will allow to expand the current field of PD applications toward large-area and flexible applications in areas such as medical imaging, security, and quality control, among others. Inkjet printing is a powerful digital tool for the deposition of smart and functional materials on various substrates, allowing the development of electronic devices such as PDs on various substrates. In this work, inkjet-printed PD arrays, based on the organic thin-film transistor architecture, have been developed and applied for the indirect detection of X-ray radiation using a scintillator ink as an X-ray absorber. The >90% increase of the photocurrent of the PDs under X-ray radiation, from about 53 nA without the scintillator film to about 102 nA with the scintillator located on top of the PD, proves the suitability of the developed printed device for X-ray detection applications, The authors thank FEDER funds through the COMPETE 2020 Programme and National Funds through FCT-Portuguese Foundation for Science and Technology under Strategic Funding UID/FIS/04650/2013 and projects PTDC/EEI-SII/5582/2014, PTDC/CTM-ENE/5387/2014 and in the framework of EuroNanoMed 2016 call, Project LungChek ENMed/0049/2016. J.O. and V.C. thank the FCT for the SFRH/BD/98219/2013 and SFRH/BPD/97739/2013 grants, respectively. The authors acknowledge funding by the Spanish Ministry of Economy and Competitiveness (MINECO) through the project MAT2016-76039-C4-3-R. Financial support from the Basque Government Industry Department under the ELKARTEK program is also acknowledged. The authors thank Iain McCulloch and Martin Heeney from Flexink for providing the OSC. Dirk Rittrich (Department Layer Deposition at Fraunhofer ENAS) is acknowledged for the FIB/SEM analysis and the sample preparation. R.D.R acknowledges the DFG Unit FOR1317 SMINT, the Cluster of Excellence, and the Tomsk Polytechnic University Competitiveness Enhancement Program grant TPU CEP_IHTP_73\2017. This work was performed in the context of the European COST Action MP1302 Nanospectroscopy., info:eu-repo/semantics/publishedVersion