The accelerated evolution of communication platforms including Internet of Things (IoT) and the fifth generation (5G) wireless communication network makes it possible to build intelligent gas sensor networks for real-time monitoring chemical safety and personal health. However, this application scenario requires a challenging combination of characteristics of gas sensors including small formfactor, low cost, ultralow power consumption, superior sensitivity, and high intelligence. Herein, self-powered integrated nanostructured-gas-sensor (SINGOR) systems and a wirelessly connected SINGOR network are demonstrated here. The room-temperature operated SINGOR system can be self-driven by indoor light with a Si solar cell, and it features ultrahigh sensitivity to H2, formaldehyde, toluene, and acetone with the record low limits of detection (LOD) of 10, 2, 1, and 1 ppb, respectively. Each SINGOR consisting of an array of nanostructured sensors has the capability of gas pattern recognition and classification. Furthermore, multiple SINGOR systems are wirelessly connected as a sensor network, which has successfully demonstrated flammable gas leakage detection and alarm function. They can also achieve gas leakage localization with satisfactory precision when deployed in one single room. These successes promote the development of using nanostructured-gas-sensor network for wide range applications including smart home/building and future smart city.

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Phase-change materials (PCMs), possessing thermo-optic and thermo-electric properties, have constantly enabled the rewritable optical data storage and the commercialized phase-change memory devices. In particular, Ge2Sb2Te5 (GST) has been considered for configurable photonics applications, such as active dielectric metasurface. In this paper, we report an active absorber with metal-insulator-metal (MIM) scheme with GST in the infrared region. The absorber consists of Al disk and reflective Al film with a GST spacer layer. Extraordinary absorption with peaks of more than 90% can be achieved over a broad bandwidth, attributing to highly confined gap surface plasmon resonance. In addition, the absorption can be tuned via adjusting the proportion of GST crystallization, which is a unique advantage to design active device. Meanwhile, the absorption is polarization-independent owing to its structural symmetry. Furthermore, we introduce the designed absorber to the application of sensing. This nearly perfect absorbing strategy offers great potential in sensing applications due to its flexibility and polarization-independence.

Ni-doped Co(HPO)(OH) with different morphologies was directly grown on Ni foam hydro(solvo)thermally under different synthetic conditions. The optimum condition is solvothermal reaction for 6 h in an ethanol/water (EW) mixed solution, the molar ratio of NaHPO/Co(NO) being 0.5:0.1, and the obtained S0.5-6 h-EW shows three-dimensional (3D) porous nanowire bundles. Whereas in the water-only solution, microrods are obtained, suggesting that the nanowires in bundles are aggregated together via the lateral (400) direction. Long reaction time and low molar ratio of reactants are all beneficial for the lateral growth of the nanowires, and the possible formation mechanism is proposed. All the obtained Ni-doped Co(HPO)(OH)/Ni foam samples are directly used as supercapacitor electrodes, and S0.5-6 h-EW shows the best electrochemical performance with a specific capacity of 159 mAh g at 0.5 A g, which is close to the theoretical value of 212 mAh g for Co(HPO)(OH), and it is the largest reported value so far. The excellent capacitive behavior of S0.5-6 h-EW is ascribed to the 3D porous nanowire bundles directly grown on a Ni foam collector without an additive and a binder, as well as to the doping of Ni into the cobalt phosphite. The S0.5-6 h-EW//activated carbon asymmetrical supercapacitor shows a maximum energy density of 58.7 Wh kg at a power density of 532 W kg and good cycling stability with the capacity retention of 90.5% after 10 000 charging-discharging cycles at 5.5 A g.

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Plants are typically exposed to a variety of potential pests and pathogens throughout their lifespan. During the course of evolution, plants have developed numerous defensive mechanisms against infection by pathogens. Defensive responses at infection sites are initiated by recognition of pathogen-associated molecular patterns (PAMPs) that are conserved in pathogenic microbes; such responses are collectively termed PAMP-triggered immunity (PTI) (Zhang et al., 2018). In a typical case of plant-pathogen co-evolution, microbes have developed effector proteins that they release inside host cells and which interfere with PTI. Plants detect such effector proteins through resistance (R) genes and activate a more robust and faster type of defensive response, termed effector-triggered immunity (ETI)

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