A novel all-solid-state, hybrid solar cell based on organic-inorganic metal halide perovskite (CH 3 NH 3 PbX 3 ) materials has attracted great attention from the researchers all over the world and is considered to be one of the top 10 scientific breakthroughs in 2013. The perovskite materials can be used not only as light-absorbing layer, but also as an electron/hole transport layer due to the advantages of its high extinction coefficient, high charge mobility, long carrier lifetime, and long carrier diffusion distance. The photoelectric power conversion efficiency of the perovskite solar cells has increased from 3.8% in 2009 to 22.1% in 2016, making perovskite solar cells the best potential candidate for the new generation of solar cells to replace traditional silicon solar cells in the future. In this paper, we introduce the development and mechanism of perovskite solar cells, describe the specific function of each layer, and focus on the improvement in the function of such layers and its influence on the cell performance. Next, the synthesis methods of the perovskite light-absorbing layer and the performance characteristics are discussed. Finally, the challenges and prospects for the development of perovskite solar cells are also briefly presented.

[001]-Oriented α-MoO3 nanoribbons were synthesized via hydrothermal method at temperature from 120 to 200 °C and following assembled a membrane on interdigital electrodes to form sensors. The sensitivity, response speed, and recovery speed of the sensor improve with the increasing hydrothermal temperature. Among them, the sample obtained at 200 °C exhibits a room-temperature response time of 14.1 s toward 1000 ppm of H2. The nanoribbons also show good selectivity against CO, ethanol, and acetone, as well as high sensitivity to H2 with a concentration as low as 500 ppb. The hydrogen sensing behavior is dependent on the redox reaction between the H2 and chemisorbed oxygen species. Higher hydrothermal temperature creates larger specific surface area and higher Mo(5+) content, leading to increased chemisorbed oxygen species on the nanoribbon surface.

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ABSTRACT:In order to seek the balance point between liquid crystalline and high efficiency emission, two novel aggregation-induced emission-based (AIE) liquid crystal materials of TPE-PBN and TPE-2PBN, which contains tetraphenylethene derivative as the emission core and 4-cynobiphenyl moiety as the mesogenic unit, were designed and prepared. Both simple molecules showed a mesophase at high temperature evidenced by polarised optical microscopy (POM), differential scanning calorimetry (DSC) and temperature-dependent X-ray diffraction (XRD).Simultaneously, TPE-PBN and TPE-2PBN presented clearly AIE characteristics in the blueishgreen region and achieved the high emission quantum efficiency of 71% and 83% in solid state, respectively. Due to the self-assembly property of thermotropic liquid crystals, both compounds showed higher hole mobilities in the annealed films than in pristine films. Employing TPE-PBN and TPE-2PBN as the emitting materials, both non-doped devices and doped devices were fabricated. The TPE-PBN-based doped OLEDs showed a better device performance with an external quantum efficiency (EQE) of 4.1% which is among the highest EQE of the blue AIE fluorescent OLEDs.

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The development of micro-/nano-scaled energy harvesters and the self-powered sensor system has attracted great attention due to the miniaturization and integration of the micro-device. In this work, lead-free NaNbO3 piezoelectric nanofibers with a monoclinic perovskite structure were synthesized by the far-field electrospinning method. The flexible active humidity sensors were fabricated by transferring the nanofibers from silicon to a soft polymer substrate. The sensors exhibited outstanding piezoelectric energy-harvesting performance with output voltage up to 2 V during the vibration process. The output voltage generated by the NaNbO3 sensors exhibited a negative correlation with the environmental humidity varying from 5% to 80%, where the peak-to-peak value of the output voltage generated by the sensors decreased from 0.40 to 0.07 V. The sensor also exhibited a short response time, good selectively against ethanol steam, and great temperature stability. The piezoelectric active humidity sensing property could be attributed to the increased leakage current in the NaNbO3 nanofibers, which was generated due to proton hopping among the H3O+ groups in the absorbed H2O layers under the driving force of the piezoelectric potential.

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