Displays are basic building blocks of modern electronics 1,2. Integrating displays into textiles 17 offers exciting opportunities for smart electronic textiles-the ultimate form of wearables 18 poised to change the way we interact with electronic devices 3-6. Display textiles serve to bridge human-machine interactions 7-9 , offering for instance, a real-time communication tool for individuals with voice or speech disorders. Electronic textiles capable of communicating 10 , sensing 11,12 and supplying electricity 13,14 have been reported previously. However, textiles 22 with functional, large-area displays have not been achieved so far because obtaining small illuminating units that are both durable and easy to assemble over a wide area is challenging. Here, we report a 6 m (L) × 25 cm (W) display textile containing 5×10 5 electroluminescent (EL) units narrowly spaced to ~800 μm. Weaving conductive weft and luminescent warp fibres forms micron-scale EL units at the weft-warp contact points. Brightness between EL units deviates by < 6.3% and remains stable even when the textile is bent, stretched or pressed. We attribute this uniform and stable lighting to the smooth luminescent coating around the 2 warp fibres and homogenous electric field distribution at the contact points. Our display textile is flexible and breathable and withstands repeatable machine-washing, making them suitable for practical applications. We show an integrated textile system consisting of display, 32 keyboard and power supply can serve as a communication tool, which could potentially drive 33 the Internet of Things in various areas including healthcare. Our approach unifies the 34 fabrication and function of electronic devices with textiles, and we expect weaving fibre 35 materials to shape the next-generation electronics.

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B3LYP is by far the most popular density functional in chemistry. Nevertheless, there is growing evidence, showing that B3LYP (1) degrades as the system becomes larger, (2) underestimates reaction barrier heights, (3) yields too low bond dissociation enthalpies, (4) gives improper isomer energy differences, and (5) fails to bind van der Waals systems, etc.

We propose the X1 method which combines the density functional theory method with a neural network (NN) correction for an accurate yet efficient prediction of heats of formation. It calculates the final energy by using B3LYP6-311+G(3df,2p) at the B3LYP6-311+G(d,p) optimized geometry to obtain the B3LYP standard heats of formation at 298 K with the unscaled zero-point energy and thermal corrections at the latter basis set. The NN parameters cover 15 elements of H, Li, Be, B, C, N, O, F, Na, Mg, Al, Si, P, S, and Cl. The performance of X1 is close to the Gn theories, giving a mean absolute deviation of 1.43 kcalmol for the G399 set of 223 molecules up to 10 nonhydrogen atoms and 1.48 kcal/mol for the X107 set of 393 molecules up to 32 nonhydrogen atoms.

Nitrogen-doping represents a general and effective method in adjusting the physical and chemical properties of carbon nanomaterials. The recent progress in the synthesis of nitrogen-doped carbon nanomaterials and their applications in batteries are carefully discussed with a focus on their electrochemical properties.

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Recently, we proposed the X1 method which combines density functional theory method (B3LYP) with a neural network correction for an accurate yet efficient prediction of heats of formation [J. M. Wu and X. Xu, J. Chem. Phys. 127, 214105 (2007)]. In the present work, we examine the X1 performance to calculate bond energies. We use 32 radicals and 115 molecules to set up 142 bond dissociation reactions. For the total of 147 heats of formations and 142 bond energies, B3LYP leads to mean absolute deviations of 4.54 and 6.26 kcal/mol, respectively, while X1 reduces the corresponding errors to 1.41 and 2.45 kcal/mol.

Photocatalyzed self-cleaning cotton fabrics with TiO2 nanoparticles covalently immobilized are obtained by cograft polymerization of 2-hydroxyethyl acrylate (HEA) together with the surface functionalized TiO2 nanoparticles under γ-ray irradiation. The covalent bonds between the TiO2 nanoparticles and cotton fabrics bridged by poly(2-hydroxyethyl acrylate) (PHEA) graft chains is strong enough to survive 30 accelerated laundering circles, equivalent to 150 commercial or domestic launderings.