Regulating Li-Ion Transport through Ultrathin Molecular Membrane to Enable High-Performance All-Solid-State–Battery

Solid-state lithium metal batteries with garnet-type electrolyte provide several advantages over conventional lithium-ion batteries, especially for safety and energy density. However, a few grand challenges such as the propagation of Li dendrites, poor interfacial contact between the solid electrolyte and the electrodes, and formation of lithium carbonate during ambient exposure over the solid-state electrolyte prevent the viability of such batteries. Herein, an ultrathin sub-nanometer porous carbon nanomembrane (CNM) is employed on the surface of solid-state electrolyte (SSE) that increases the adhesion of SSE with electrodes, prevents lithium carbonate formation over the surface, regulates the flow of Li-ions, and blocks any electronic leakage. The sub-nanometer scale pores in CNM allow rapid permeation of Li-ions across the electrode–electrolyte interface without the presence of any liquid medium. Additionally, CNM suppresses the propagation of Li dendrites by over sevenfold up to a current density of 0.7 mA cm⁻² and enables the cycling of all-solid-state batteries at low stack pressure of 2 MPa using LiFePO₄ cathode and Li metal anode. The CNM provides chemical stability to the solid electrolyte for over 4 weeks of ambient exposure with less than a 4% increase in surface impurities.     

Chemical Stability and Hydrogen Reaction Behavior of SmCo 2:17-Type Permanent Magnets

Herein, the reaction behavior and chemical stability of two commercially available SmCo 2:17-type sintered magnets with nominal composition of Sm_23.75Co_48.67Fe_balCu_4.91Zr_2.37 and Sm_24.95Co_48.80Fe_balCu_4.46Zr_2.68 (wt%) are investigated. The magnets are placed in a hydrogen atmosphere with systematically varied pressure, exposure time, and temperature ranging from 1–11 bar, 2–10 d, and 25–500 °C, respectively. Hydrogen content, magnetic properties, microstructure, and lattice constants are characterized in detail. It is found that for short exposure times like 2 d an activation temperature of 120 °C is necessary to initiate the reaction and to increase the amount of hydrogen in the Sm–Co material. Hydrogen absorption starts at lower temperatures with longer exposure times. An increase in exposure time, temperature, or pressure leads to a higher hydrogen content and a decrease in remanence B_r, energy product (BH)_max, and coercivity H_cB. Lattice expansion, estimated by X-ray diffraction analysis, correlates with the increasing amount of hydrogen in the Sm–Co magnets. With respect to all varied parameters under investigation, the exposure temperature has the highest impact on the observed property changes followed by reaction time and H₂ pressure.     

Six-layer lamination of a new dry film negative-tone photoresist for fabricating complex 3D microfluidic devices

We present a new epoxy-based negative-tone dry film photoresist (DFR) for fabricating multilayer microfluidic devices using a lamination process combined with a standard photolithography technology. As proof-of-concept, a complex 3D-hydrodynamic focusing device was produced via a six-layer lamination process of 33 µm-thick DFR layers. The bonding strength of the new DFR was tested on silicon, glass, and titanium substrates, respectively. A maximum bonding strength of 37 MPa was obtained for the dry film photoresist laminated on glass. No leakage was found, and burst tests proved excellent robustness and sealing reliability of the microchannels.     

Surface‐Mounted Metal–Organic Frameworks: Crystalline and Porous Molecular Assemblies for Fundamental Insights and Advanced Applications

Metal–organic frameworks (MOFs) are crystalline coordination polymers, assembled from inorganic nodes connected by organic linker molecules. An enormous surface area, huge compositional variety, regular structure, and favorable mechanical properties are among their outstanding properties. Monolithic MOF thin films, i.e., surface‐mounted metal–organic frameworks (SURMOFs), with high degree of structural order and adjustable defect density, can be prepared on solid substrates using layer‐by‐layer techniques. Recent studies where SURMOFs served as model systems for quantitative studies of molecular interactions in porous media, including diffusion, are reviewed. Moreover, SURMOFs are ideally suited for the incorporation of photoactive molecules as well as to study electrical transport through crystalline molecular assemblies. Recent work has demonstrated that the realization of crystalline chromophore assemblies via the SURMOF approach allows the study of fundamental aspects of exciton transport, exciton channeling, and photon upconversion at internal interfaces in organic semiconductor materials. Due to their crystalline nature, MOF materials are well suited for quantitative comparisons with theoretical results; especially, since defect densities and types can be characterized and varied in a straightforward fashion. The active role of these nanoporous films in advanced applications, like for remote‐controlled release of molecules, membranes with photoswitchable selectivity, and ion‐conductors with adjustable conductivity, are also emphasized.     

Poly(1,4‐Diethynylbenzene) Gradient Homojunction with Enhanced Charge Carrier Separation for Photoelectrochemical Water Reduction

As appealing photoelectrode materials for photoeletrochemical hydrogen evolution reaction (PEC HER), conjugated polymers still show poor PEC HER performance as a result of their serious recombination of photogenerated electrons and holes. Herein, a novel design of gradient homojunction is demonstrated by controlled copolymerization of 1,4‐diethynylbenzene (DEB) and 1,3,5‐triethynylbenzene (TEB). The as‐built gradient distribution of TEB monomer in poly(1,4‐diethynylbenzene) (pDEB) leads to continuous band bending engineering, which constitutes a gradient homojunction. Under AM 1.5G irradiation and in 0.1 m Na₂SO₄ aqueous solution, the as‐fabricated pDEB gradient homojunction exhibits a charge separation efficiency of 0.27% at 0.3 V versus reversible hydrogen electrode (RHE), which is 3.4 and 1.7 times higher than those for pure pDEB and the traditionally designed pDEB homojunction. As a result, the photocurrent of the pDEB gradient homojunction unprecedentedly reaches 55 µA cm^?2 at 0.3 V versus RHE, which is much higher than 19 µA cm^?2 for pure pDEB, 32 µA cm^?2 for the pDEB homojunction, and state‐of‐the‐art organic photocathodes, e.g., g‐C₃N₄ (≈1?32 µA cm^?2). This work opens up a new window for the design of gradient homojunctions and will advance the exploration of high‐performance organic photoelectrodes.     

Maximizing the SDMA Mobile Radio Capacity Increase by DOA Sensitive Channel Allocation

In a cellular mobile radio system an SDMA (Space Division Multiple Access) component can be implemented for the reuse of radio channels physically incorporated by time, frequency or code slots. Since SDMA is based on the spatial separation of different users operating in the same channel, a DOA (Direction of arrival) sensitive channel allocation scheme is essential for maximizing system capacity. In this paper we present the Eigenvector method, a computationally efficient algorithm to do this job. We also present simulation results on the Eigenvector method operating in a typical urban mobile radio cell. The simulated blocking probabilities are then used to predict the capacity increase which can be expected after adding an SDMA component to a conventional mobile radio system.     

Long‐range wireless sensor networks with transmit‐only nodes and software‐defined receivers

Wireless sensor networks for environmental monitoring and agricultural applications often face Long‐range requirements at low bit rates together with a large numbers of nodes. This paper presents the design and test of a novel wireless sensor network that combines a large radio range with very low power consumption and cost. Our asymmetric sensor network uses ultra‐low‐cost 40‐MHz transmitters and a sensitive software‐defined radio receiver with multi‐channel capability. Experimental radio range measurements in two different outdoor environments demonstrate a single‐hop range of up to 1.8 km. A theoretical model for radio propagation at 40 MHz in outdoor environments is proposed and validated with the experimental measurements. The reliability and fidelity of network communication over longer periods is evaluated with a deployment for distributed temperature measurements. Our results demonstrate the feasibility of the transmit‐only low‐frequency system design approach for future environmental sensor networks. Although there have been several papers proposing the theoretical benefits of this approach, to the best of our knowledge, this is the first paper to provide experimental validation of such claims. Copyright © 2011 John Wiley & Sons, Ltd.     

Abnormalities of auditory evoked magnetic fields and structural changes in the left hemisphere of male schizophrenics--a magnetoencephalographic-magnetic resonance imaging study

Functional and structural changes in 10 DSM-III-R male schizophrenics and 10 healthy volunteers were investigated using magnetoencephalographically (MEG) detected long-latency (N100 m) auditory evoked fields (AEFs) and magnetic resonance imaging (MRI). The AEFs were characterized by single moving equivalent dipoles, which were superimposed on MRIs. There were significant differences in dipole orientations and in AEF latencies in the left hemisphere of schizophrenics, when compared to the controls. The MEG-detected alterations were found to be associated with a bilateral volume reduction of the posterior superior temporal gyrus (pSTG), which was more pronounced in the left hemisphere. Separate analysis of white and gray matter has shown that the pSTG volume reduction resulted from decreased gray matter volumes without white matter changes. Both the functional and the morphological data indicate a left-hemispheric disturbance in our patients.