Crystal engineering--the planning and construction of crystalline supramolecular architectures from modular building blocks--permits the rational design of functional molecular materials that exhibit technologically useful behaviour such as conductivity and superconductivity, ferromagnetism and nonlinear optical properties. Because the presence of two cooperative properties in the same crystal lattice might result in new physical phenomena and novel applications, a particularly attractive goal is the design of molecular materials with two properties that are difficult or impossible to combine in a conventional inorganic solid with a continuous lattice. A promising strategy for creating this type of 'bi-functionality' targets hybrid organic/inorganic crystals comprising two functional sub-lattices exhibiting distinct properties. In this way, the organic pi-electron donor bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) and its derivatives, which form the basis of most known molecular conductors and superconductors, have been combined with molecular magnetic anions, yielding predominantly materials with conventional semiconducting or conducting properties, but also systems that are both superconducting and paramagnetic. But interesting bulk magnetic properties fail to develop, owing to the discrete nature of the inorganic anions. Another strategy for achieving cooperative magnetism involves insertion of functional bulky cations into a polymeric magnetic anion, such as the bimetallic oxalato complex [MnIICrIII(C2O4)3]-, but only insoluble powders have been obtained in most cases. Here we report the synthesis of single crystals formed by infinite sheets of this magnetic coordination polymer interleaved with layers of conducting BEDT-TTF cations, and show that this molecule-based compound displays ferromagnetism and metallic conductivity.

The magnetic exchange between epitaxial thin films of the multiferroic (antiferromagnetic and ferroelectric) hexagonal YMnO 3 oxide and a soft ferromagnetic (FM) layer is used to couple the magnetic response of the FM layer to the magnetic state of the antiferromagnetic one. We will show that biasing the ferroelectric YMnO 3 layer by an electric field allows control of the magnetic exchange bias and subsequently the magnetotransport properties of the FM layer. This finding may contribute to paving the way towards a new generation of electric-field controlled spintronic devices. DOI: 10.1103/PhysRevLett.97.227201 PACS numbers: 75.70.Cn, 85.80.Jm Multiferroic materials have been proposed for building a new generation of devices in spintronics, eventually allowing us to overcoming critical limitations in technology [1]. Much effort has been directed to searching for materials displaying the elusive coexistence of ferroelectricity (FE) and ferromagnetism (FM) [2,3], which is thought to be essential for progress in this direction. In contrast, materials displaying coupled FE and antiferromagnetic (AF) behavior have received much less attention. To exploit the multiferroic character of a material, it is essential that the ferroic properties (magnetic and electric, in the present context) are coupled. Hexagonal YMnO 3 (YMO), in bulk form, is ferroelectric up to 900 K and exhibits an antiferromagnetic character at low temperature (T N 90 K). It has been shown that in YMO single crystals, both order parameters are coupled [4], and this observation has triggered a renewed attention to this oxide [5,6]. The electric polarization axis of YMO is along the c axis; the Mn atomic spins lie in a perpendicular plane, forming a two dimensional, frustrated antiferromagnetic, triangular network [7,8]. Hence, in principle, one could use AF YMO to pin the magnetic state of a FM material and subsequently exploit its ferroelectric character and the coupling between FE and AF order parameters to tailor the properties of the FM layer. As a first step, it has been recently shown that indeed it is possible to exchange-bias NiFe (Permalloy-Py) with AF epitaxial (0001) YMO films which display a remanent electric polarization [5].Attempts towards electric-field control of exchange bias have been recently reported by Borisov et al. using magnetoelectric, but not multiferroic (AF) Cr 2 O 3 single crystals as pinning layers [9]. Here, we will show that it is possible to grow heterostructures that, exploiting the AF and FE character of YMO, allow us to control the magnetic state of a FM layer by an electric field. For that purpose, an epitaxial layer of YMO has been sandwiched between metallic electrodes (Pt and Py), and the exchange bias between YMO and Py has been monitored as a function of a biasing electric field applied across the YMO layer [ Fig. 1(b)].When a magnetic field is applied parallel to the interface between FM and AF materials, the magnetization of the FM layer does not follow (neglecting the anisotropy of the FM layer) the ex...

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Understanding the compatibility between spider silk and conducting materials is essential to advance the use of spider silk in electronic applications. Spider silk is tough, but becomes soft when exposed to water. Here we report a strong affinity of amine-functionalised multi-walled carbon nanotubes for spider silk, with coating assisted by a water and mechanical shear method. The nanotubes adhere uniformly and bond to the silk fibre surface to produce tough, custom-shaped, flexible and electrically conducting fibres after drying and contraction. The conductivity of coated silk fibres is reversibly sensitive to strain and humidity, leading to proof-of-concept sensor and actuator demonstrations.

Doped and wired: The organization of the π functional units in amide‐functionalized tetrathiafulvalene in a gel by hydrogen‐bonding interactions has given rise to nanofibers. Doping with iodine generates a conducting material, which upon annealing gives rise to nanowires with metal‐like conductivity (see current‐sensing AFM image).

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Solution prepared single crystal organic field-effect transistors (OFETs) combine low-cost with high performance due to structural ordering of molecules. However, in organic crystals polymorphism is a known phenomenon, which can have a crucial influence on charge transport. Here, the performance of solution-prepared single crystal OFETs based on two different polymorphs of dithiophene-tetrathiafulvalene, which were investigated by confocal Raman spectroscopy and X-ray diffraction, are reported. OFET devices prepared using different configurations show that both polymorphs exhibited excellent device performance, although the -phase revealed charge carrier mobility between two and ten times higher in accordance to the closer stacking of the molecules.