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  • 1.
    Aili, Daniel
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Sensor Science and Molecular Physics . Linköping University, The Institute of Technology.
    Tai, Feng-I
    Linköping University, Department of Physics, Chemistry and Biology. Linköping University, The Institute of Technology.
    Enander, Karin
    Linköping University, Department of Physics, Chemistry and Biology, Sensor Science and Molecular Physics . Linköping University, The Institute of Technology.
    Baltzer, Lars
    Department of Biochemistry andOrganic Chemistry Uppsala University, BMC, Box 576, 75123 Uppsala, Sweden.
    Liedberg, Bo
    Linköping University, Department of Physics, Chemistry and Biology, Sensor Science and Molecular Physics . Linköping University, The Institute of Technology.
    Self-Assembly of Fibers and Nanorings from Disulfide-Linked Helix–Loop–Helix Polypeptides2008In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 47, no 30, p. 5554-5556Article in journal (Refereed)
  • 2.
    Bally, Marta
    et al.
    Chalmers, Sweden .
    Rydell, Gustaf E.
    Institute Curie, France .
    Zahn, Raphael
    University of Zurich, Switzerland Swiss Federal Institute Technology, Switzerland .
    Nasir, Waqas
    University of Gothenburg, Sweden .
    Eggeling, Christian
    Max Planck Institute Biophys Chemistry, Germany .
    Breimer, Michael E.
    University of Gothenburg, Sweden .
    Svensson, Lennart
    Linköping University, Department of Clinical and Experimental Medicine, Molecular Virology. Linköping University, Faculty of Health Sciences.
    Hook, Fredrik
    Chalmers, Sweden .
    Larson, Gran
    University of Gothenburg, Sweden .
    Norovirus GII.4 Virus-like Particles Recognize Galactosylceramides in Domains of Planar Supported Lipid Bilayers2012In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 51, no 48, p. 12020-12024Article in journal (Refereed)
    Abstract [en]

    n/a

  • 3.
    Comina, German
    et al.
    Linköping University, Department of Physics, Chemistry and Biology. Linköping University, Faculty of Science & Engineering.
    Suska, Anke
    Linköping University, Department of Physics, Chemistry and Biology, Chemical and Optical Sensor Systems. Linköping University, Faculty of Science & Engineering.
    Filippini, Daniel
    Linköping University, Department of Physics, Chemistry and Biology, Chemical and Optical Sensor Systems. Linköping University, Faculty of Science & Engineering.
    Autonomous Chemical Sensing Interface for Universal Cell Phone Readout2015In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 54, no 30, p. 8708-8712Article in journal (Refereed)
    Abstract [en]

    Exploiting the ubiquity of cell phones for quantitative chemical sensing imposes strong demands on interfacing devices. They should be autonomous, disposable, and integrate all necessary calibration and actuation elements. In addition, a single design should couple universally to a variety of cell phones, and operate in their default configuration. Here, we demonstrate such a concept and its implementation as a quantitative glucose meter that integrates finger pumps, unidirectional valves, calibration references, and focusing optics on a disposable device configured for universal video acquisition.

  • 4.
    Herland, Anna
    et al.
    Cell and Molecular Biology, Karolinska Institute, Stockholm.
    Persson, Kristin M
    Linköping University, Department of Science and Technology, Physics and Electronics. Linköping University, The Institute of Technology.
    Lundin, Vanessa
    Cell and Molecular Biology, Karolinska Institute, Stockholm.
    Fahlman, Mats
    Linköping University, Department of Physics, Chemistry and Biology, Surface Physics and Chemistry. Linköping University, The Institute of Technology.
    Berggren, Magnus
    Linköping University, Department of Science and Technology, Physics and Electronics. Linköping University, The Institute of Technology.
    Jager, Edwin W H
    Linköping University, Department of Science and Technology, Physics and Electronics. Linköping University, The Institute of Technology.
    Teixeira, Ana I
    Cell and Molecular Biology, Karolinska Institute, Stockholm.
    Electrochemical Control of Growth Factor Presentation To Steer Neural Stem Cell Differentiation2011In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 50, no 52, p. 12529-12533Article in journal (Refereed)
    Abstract [en]

    Graphical Abstract

    Let it grow: The conjugated polymer poly(3,4-ethylenedioxythiophene) (PEDOT) was synthesized with heparin as the counterion to form a cell culture substrate. The surface of PEDOT:heparin in the neutral state associated biologically active growth factors (see picture). Electrochemical in situ oxidation of PEDOT during live cell culture decreased the bioavailability of the growth factor and created an exact onset of neural stem cell differentiation.

  • 5.
    Jianhao, Bai
    et al.
    Division of Bioengineering, National University of Singapore, Singapore.
    Sebastian, Beyer
    Division of Bioengineering, National University of Singapore, Singapore.
    Wing Cheung, Mak
    Department of Chemistry, Hong Kong University of Science and Technology, Hong Kong SAR, P.R. China.
    Raj, Rajagopalan
    Department of Chemical & Biomolecular Engineering, National University of Singapore, Singapore.
    Dieter, Trau
    Department of Chemical & Biomolecular Engineering, National University of Singapore, Singapore and .
    Inwards buildup of concentric polymer layers: A method for biomolecule encapsulation and microcapsule encoding2010In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 49, no 330, p. 5189-5193Article in journal (Refereed)
    Abstract [en]

    Encoding by encapsulation: A polymeric shell fabrication approach combines biomolecule encapsulation with encoding. Striated polymeric shells, fabricated through an inwards diffusion of poly(allylamine) into the matrices of agarose microbeads, serves to encapsulate the biomolecules within the microcapsule. Encoding is performed through the color and/or thickness permutation of the striated polymeric shells (see picture).

  • 6.
    Lukatskaya, Maria R.
    et al.
    Engineering Department, Drexel University, Philadelphia, USA.
    Halim, Joseph
    Engineering Department, Drexel University, Philadelphia, USA.
    Dyatkin, Boris
    Engineering Department, Drexel University, Philadelphia, USA.
    Naguib, Michael
    Engineering Department, Drexel University, Philadelphia, USA.
    Buranova, Yulia S.
    Engineering Department, Drexel University, Philadelphia, USA.
    Barsoum, Michel W.
    Engineering Department, Drexel University, Philadelphia, USA.
    Gogotsi, Yury
    Engineering Department, Drexel University, Philadelphia, USA.
    Room-Temperature Carbide-Derived Carbon Synthesis by Electrochemical Etching of MAX Phases2014In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 126, no 19, p. 4977-4980Article in journal (Refereed)
    Abstract [en]

    Porous carbons are widely used in energy storage and gas separation applications, but their synthesis always involves high temperatures. Herein we electrochemically selectively extract, at ambient temperature, the metal atoms from the ternary layered carbides, Ti3AlC2, Ti2AlC and Ti3SiC2 (MAX phases). The result is a predominantly amorphous carbide-derived carbon, with a narrow distribution of micropores. The latter is produced by placing the carbides in HF, HCl or NaCl solutions and applying anodic potentials. The pores that form when Ti3AlC2 is etched in dilute HF are around 0.5 nm in diameter. This approach forgoes energy-intensive thermal treatments and presents a novel method for developing carbons with finely tuned pores for a variety of applications, such as supercapacitor, battery electrodes or CO2 capture.

  • 7.
    Lundqvist, Martin
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Molecular Biotechnology. Linköping University, The Institute of Technology.
    Nygren, Patrik
    Linköping University, Department of Physics, Chemistry and Biology, Molecular Biotechnology. Linköping University, The Institute of Technology.
    Jonsson, Bengt-Harald
    Linköping University, Department of Physics, Chemistry and Biology, Molecular Biotechnology. Linköping University, The Institute of Technology.
    Broo, Klas
    Linköping University, Department of Physics, Chemistry and Biology, Applied Optics . Linköping University, The Institute of Technology.
    Induction of structure and function in a designed peptide upon adsorption on a silica nanoparticle2006In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 45, no 48, p. 8169-8173Article in journal (Refereed)
    Abstract [en]

    No abstrack available.

  • 8.
    Preechaburana, Pakorn
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Applied Physics. Linköping University, Faculty of Science & Engineering.
    Gonzalez, Marcos
    Linköping University, Department of Physics, Chemistry and Biology, Applied Physics. Linköping University, The Institute of Technology.
    Suska, Anke
    Linköping University, Department of Physics, Chemistry and Biology, Applied Physics. Linköping University, The Institute of Technology.
    Filippini, Daniel
    Linköping University, Department of Physics, Chemistry and Biology, Applied Physics. Linköping University, The Institute of Technology.
    Surface Plasmon Resonance Chemical Sensing on Cell Phones2012In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 51, no 46, p. 11585-11588Article in journal (Refereed)
    Abstract [en]

    Chemosensing based on angle-resolved surface plasmon resonance is demonstrated on intact cell phones using a disposable optical coupler and software to configure illumination and acquisition. This coupler operates on different cell phones and is applied for classical affinity assays with commercial chips and custom-made tests with embedded calibration. Measured performance (2.14x10−6 refractive index units) is comparable with compact SPR systems.

  • 9.
    Rastgoo-Lahrood, Atena
    et al.
    Technical University of Munich, Germany; Deutsch Museum, Germany; Nanosyst Initiat Munich, Germany; Centre Nanosci, Germany.
    Björk, Jonas
    Linköping University, Department of Physics, Chemistry and Biology, Theoretical Physics. Linköping University, Faculty of Science & Engineering.
    Lischka, Matthias
    Technical University of Munich, Germany; Deutsch Museum, Germany; Nanosyst Initiat Munich, Germany; Centre Nanosci, Germany.
    Eichhorn, Johanna
    Technical University of Munich, Germany; Deutsch Museum, Germany; Nanosyst Initiat Munich, Germany; Centre Nanosci, Germany.
    Kloft, Stephan
    Technical University of Munich, Germany; Deutsch Museum, Germany; Nanosyst Initiat Munich, Germany; Centre Nanosci, Germany.
    Fritton, Massimo
    Technical University of Munich, Germany; Deutsch Museum, Germany; Nanosyst Initiat Munich, Germany; Centre Nanosci, Germany.
    Strunskus, Thomas
    University of Kiel, Germany.
    Samanta, Debabrata
    University of Siegen, Germany.
    Schmittel, Michael
    University of Siegen, Germany.
    Heckl, Wolfgang M.
    Technical University of Munich, Germany; Deutsch Museum, Germany; Nanosyst Initiat Munich, Germany; Centre Nanosci, Germany.
    Lackinger, Markus
    Technical University of Munich, Germany; Deutsch Museum, Germany; Nanosyst Initiat Munich, Germany; Centre Nanosci, Germany.
    Post-Synthetic Decoupling of On-Surface-Synthesized Covalent Nanostructures from Ag(111)2016In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 55, no 27, p. 7650-7654Article in journal (Refereed)
    Abstract [en]

    The on-surface synthesis of covalent organic nanosheets driven by reactive metal surfaces leads to strongly adsorbed organic nanostructures, which conceals their intrinsic properties. Hence, reducing the electronic coupling between the organic networks and commonly used metal surfaces is an important step towards characterization of the true material. We demonstrate that post-synthetic exposure to iodine vapor leads to the intercalation of an iodine monolayer between covalent polyphenylene networks and Ag(111) surfaces. The experimentally observed changes from surface-bound to detached nanosheets are reproduced by DFT simulations. These findings suggest that the intercalation of iodine provides a material that shows geometric and electronic properties substantially closer to those of the freestanding network.

  • 10.
    Ulrich, Christian
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Applied Physics . Linköping University, The Institute of Technology.
    Andersson, Olof
    Linköping University, Department of Physics, Chemistry and Biology, Sensor Science and Molecular Physics . Linköping University, The Institute of Technology.
    Nyholm, Leif
    Department of Materials Chemistry, Uppsala University, P.O. Box 538, 75121 Uppsala, Sweden.
    Björefors, Fredrik
    Linköping University, Department of Physics, Chemistry and Biology, Sensor Science and Molecular Physics . Linköping University, The Institute of Technology.
    Formation of Molecular Gradients on Bipolar Electrodes2008In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 47, no 16, p. 3034-3036Article in journal (Refereed)
  • 11.
    Zhang, Xuanjun
    et al.
    Linköping University, Department of Physics, Chemistry and Biology, Molecular Surface Physics and Nano Science. Linköping University, Faculty of Science & Engineering.
    Ballem, Mohamed
    Linköping University, Department of Physics, Chemistry and Biology, Nanostructured Materials. Linköping University, The Institute of Technology.
    Hu, Zhang-Jun
    Linköping University, Department of Physics, Chemistry and Biology, Molecular Surface Physics and Nano Science. Linköping University, Faculty of Science & Engineering.
    Bergman, J Peder
    Linköping University, Department of Physics, Chemistry and Biology, Semiconductor Materials. Linköping University, The Institute of Technology.
    Uvdal, Kajsa
    Linköping University, Department of Physics, Chemistry and Biology, Molecular Surface Physics and Nano Science. Linköping University, Faculty of Science & Engineering.
    Nanoscale Light-Harvesting Metal-Organic Frameworks2011In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 50, no 25, p. 5728-5732Article in journal (Refereed)
    Abstract [en]

    n/a

  • 12.
    Zhang, Xuanjun
    et al.
    Department of Chemistry and Multidisciplinary Research Center Shantou University, China.
    Li, Dan
    Department of Chemistry and Multidisciplinary Research Center Shantou University, China.
    Metal-Compound-Induced Vesicles as Efficient Directors for Rapid Synthesis of Hollow Alloy Spheres2006In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 45, no 36, p. 5971-5974Article in journal (Refereed)
    Abstract [en]

    Hollow alloy: Vesicles formed from tetrabutylammonium bromide and metal compounds act as efficient directors for the rapid synthesis of a variety of binary, ternary, and quaternary intermetallic materials with hollow structures. In this way, different metals were co-alloyed on the vesicle surface to produce hollow alloy spheres containing more than two kinds of metals.

  • 13.
    Zhou, Jie
    et al.
    Chinese Academic Science, Peoples R China.
    Zha, Xianhu
    Chinese Academic Science, Peoples R China.
    Chen, Fan Y.
    Chinese Academic Science, Peoples R China.
    Ye, Qun
    Chinese Academic Science, Peoples R China.
    Eklund, Per
    Linköping University, Department of Physics, Chemistry and Biology, Thin Film Physics. Linköping University, Faculty of Science & Engineering.
    Du, Shiyu
    Chinese Academic Science, Peoples R China.
    Huang, Qing
    Chinese Academic Science, Peoples R China.
    A Two-Dimensional Zirconium Carbide by Selective Etching of Al3C3 from Nanolaminated Zr3Al3C52016In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 55, no 16, p. 5008-5013Article in journal (Refereed)
    Abstract [en]

    The room-temperature synthesis of a new two-dimensional (2D) zirconium-containing carbide, Zr3C2Tz MXene is presented. In contrast to traditional preparation of MXene, the layered ternary Zr3Al3C5 material instead of MAX phases is used as source under hydrofluoric acid treatment. The structural, mechanical, and electronic properties of the synthesized 2D carbide are investigated, combined with first-principles density functional calculations. A comparative study on the structrual stability of our obtained 2D Zr3C2Tz and Ti3C2Tz MXenes at elevated temperatures is performed. The obtained 2D Zr3C2Tz exhibits relatively better ability to maintain 2D nature and strucural integrity compared to Ti-based Mxene. The difference in structural stability under high temperature condition is explained by a theoretical investigation on binding energy.

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