Une approche client introduite dans les relations avec les usagers d'un service médicosocial améliore-t-elle nos pratiques ? Est-elle perceptible par nos parties prenantes (proches, autorités de tarification, etc.) ? Apporte-t-elle une forme de réponse aux demandes actuelles de personnalisation, de continuité de parcours, d'inclusion, de désinstitutionnalisation ? Pour y répondre, un outil original d'analyse du parcours des usagers-clients issu du marketing des services est présenté, testé dans un service pour enfants déficients visuels et discuté.
The electronic structure of the TiO2 (110)-(1 × 2) surface has been studied by means of angular resolved ultraviolet photoemission spectroscopy (ARUPS). The valence band dispersion along the high symmetry surface directions, [001] and [1–10], has been recorded. The experimental data show no dispersion of the band-gap Ti 3d states. However, the existence of dispersive bands along the [001] direction located at about 7 eV below the Fermi level is reported. The existence of two different contributions in the emission from the defects-related state located in the gap of the surface is univocally shown for the first time. ; This work has been supported by the Spanish CYCIT (MAT2011-26534) and the Ministry of Science and Innovation (CSD2007-41 NANOSELECT). C.S.S. gratefully acknowledges Ministerio de Educación for the financial support inside the "FPU programme" under the AP2005-0433 grant. M.G. G. and P.A. are grateful for the support by the Fonds National Suisse pour la Recherche Scientifique through Div. II and the Swiss National Center of Competence in Research MaNEP. M.B.-R. acknowledges financial support from the Gipuzkoako Foru Aldundia and the European Union 7th Framework Programme (FP7/2007–2013) under grant agreement no. FP7-PEOPLE-2010-RG276921. ; Peer reviewed
[EN] On-surface synthesis, complementary to wet chemistry, has been demonstrated to be a valid approach for the synthesis of tailored graphenic nanostructures with atomic precision. Among the different existing strategies used to tune the optoelectronic and magnetic properties of these nanostructures, the introduction of non-hexagonal rings inducing out-of-plane distortions is a promising pathway that has been scarcely explored on surfaces. Here, we demonstrate that non-hexagonal rings, in the form of tropone (cycloheptatrienone) moieties, are thermally transformed into phenyl or cyclopentadienone moieties upon an unprecedented surface-mediated retro–Buchner-type reaction involving a decarbonylation or an intramolecular rearrangement of the CO unit, respectively. ; We acknowledge the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (ERC-2015-STG-677023 and ERC-2013-SYG-610256 NANOCOSMOS) and the innovation program under grant agreement No. 696656 (GrapheneCore1-Graphene-based disruptive technologies) and grant agreement No. 785219 (GrapheneCore2-Graphenebased disruptive technologies) for financial support. Grants PGC2018-101181-B-I00 and MAT2017- 85089-C2-1-R funded by MCIN/AEI/10.13039/501100011033 and "ERDF A way of making Europe" by the "European Union", and grant PID2020-113142RB-C21 funded by MCIN/AEI/ 10.13039/501100 011033 also provided financial support. We also acknowledge Comunidad de Madrid via Programade Investigación Tecnologías 2018 (FOTOART-CM S2018/NMT-4367), the Swiss National Science Foundation (grant number 200020-182015), the NCCR MARVEL funded by the Swiss National Science Foundation (grant number 51NF40-182892) and FEDER/Junta de Andalucía-Consejería de Economía y Conocimiento (B-FQM-428-UGR20). C. S. S. and N. R. A. acknowledge Grants RYC2018-024364-I and BES-2015-072642, respectively, funded by MCIN/AEI/ 10.13039/501100011033 and "ESF Investing in your future". I. R. M. acknowledges the University of Granada for her postdoctoral contract (Contrato Puente-Plan Propio UGR). F.V. thanks Ministerio de Universidades for the FPU grant (FPU18/05938). ; Peer reviewed
Herein we describe a distorted ribbon-shaped nanographene exhibiting unprecedented combination of optical properties in graphene-related materials, namely upconversion based on two-photon absorption (TPA-UC) together with circularly polarized luminescence (CPL). The compound is a graphene molecule of ca. 2 nm length and 1 nm width with edge defects that promote the distortion of the otherwise planar lattice. The edge defects are an aromatic saddle-shaped ketone unit and a [5]carbohelicene moiety. This system is shown to combine two-photon absorption and circularly polarized luminescence and a remarkably long emission lifetime of 21.5 ns. The [5]helicene is responsible for the chiroptical activity while the push–pull geometry and the extended network of sp2 carbons are factors favoring the nonlinear absorption. Electronic structure theoretical calculations support the interpretation of the results. ; This project has received funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (ERC-2015-STG-677023). We also thank the Ministerio de Economía y Competitividad (MINECO, Spain) (CTQ2015-70283-P, CTQ2014-53598-R, MAT2014-54231-C4-1P, FIS2016-77578-R) and the "Unidad de Excelencia Química Aplicada a Biomedicina y Medioambiente (UGR)". A. G. C., C. S. S. and C. M. C. acknowledge funding from MINECO (Spain) for RyC-2013-12943, IJCI-2014-19291 and BES-2016-076371 contracts, respectively. I. R. M. thanks UGR (Spain) for a postdoctoral scholarship. I. M. and E. M. thank the Fundação para a Ciência e a Tecnologia for financial support (IF/00759/2013 and post-doc grant SFRH/BPD/75782/2011). We thank the CSIRC-Alhambra for supercomputing facilities.
Technologically useful and robust graphene-based interfaces for devices require the introduction of highly selective, stable, and covalently bonded functionalities on the graphene surface, whilst essentially retaining the electronic properties of the pristine layer. This work demonstrates that highly controlled, ultrahigh vacuum covalent chemical functionalization of graphene sheets with a thiol-terminated molecule provides a robust and tunable platform for the development of hybrid nanostructures in different environments. We employ this facile strategy to covalently couple two representative systems of broad interest: metal nanoparticles, via S–metal bonds, and thiol-modified DNA aptamers, via disulfide bridges. Both systems, which have been characterized by a multitechnique approach, remain firmly anchored to the graphene surface even after several washing cycles. Atomic force microscopy images demonstrate that the conjugated aptamer retains the functionality required to recognize a target protein. This methodology opens a new route to the integration of high-quality graphene layers into diverse technological platforms, including plasmonics, optoelectronics, or biosensing. With respect to the latter, the viability of a thiol-functionalized chemical vapor deposition graphene-based solution-gated field-effect transistor array was assessed. ; This work was supported by the European Union's Horizon 2020 research and innovation programme under grant agreement No 696656 (Graphene Flagship-core 1) and no 785219 (Graphene Flagship −core 2); UE FP7 ideas: ERC (grant ERC-2013-SYG-610256 Nanocosmos) and Spanish MINECO grants MAT2014-54231-C4-1-P, MAT2014-54231-C4-4-P, MAT2017-85089-C2-1-R, MAT2014-59772-C2-2-P, and BIO2016-79618-R (funded by EU under the FEDER programme), as well as the Nanoavansens program from the Community of Madrid (S2013/MIT-3029). This work has made use of the Spanish ICTS Network MICRONANOFABS partially supported by MINECO and also the ICTS NANBIOSIS, more specifically the Micro-Nano Technology Unit of the CIBER in Bioengineering, Biomaterials & Nanomedicine (CIBER-BBN) at the IMB-CNM. We are grateful to Matthias Muntwiler for his assistance with experiments in the PEARL beamline in the SLS facility. Finally, we acknowledge the TEM and ICP services at the CNB and ICMM institutes, respectively. CSS acknowledges the MINECO for a Juan de la Cierva Incorporación grant (IJCI-2014-19291). M. Marciello is grateful to the Comunidad de Madrid (CM) and European Social Fund (ESF) for supporting her research work through the I+D Collaborative Programme in Biomedicine NIETO-CM (B2017-BMD3731). ; Peer reviewed
