Preparation and Characterization of High-Strength Geopolymer Based on BH-1 Lunar Soil Simulant with Low Alkali Content

The construction of a lunar base and habitation on the Moon has always been on researchers’ minds. Building materials used in in situ lunar resources are of great significance for saving expensive space freight. In this study, a new type of lunar soil simulant named Beihang (BH)-1 was developed. The chemical mineral composition and microstructure of BH-1 closely resemble those of real lunar soil, as verified by X-ray fluorescence spectroscopy (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and reflectance spectra. This research also synthesized a geopolymer based on BH-1 cured at simulated lunar atmospheric conditions. We also investigated the effect of supplementing aluminum (Al) sources on the enhancement of geopolymer strength based on BH-1. The rheological behavior of alkali-activated BH-1 pastes was determined for workability. XRF, XRD, Fourier transform infrared spectroscopy, SEM coupled with energy dispersive spectroscopy, and ²⁷Al magic angle spinning-nuclear magnetic resonance were used to characterize resulting geopolymers. Rheological test findings showed that the rheology of BH-1 pastes fits the Herschel–Bulkley model, and they behaved like a shear-thinning fluid. The results showed that the 28-day compressive strength of the BH-1 geopolymer was improved by up to 100.8%. Meanwhile, the weight of additives required to produce per unit strength decreased, significantly reducing the mass of materials transported from the Earth for the construction of lunar infrastructure and saving space transportation costs. Microscopic analyses showed that the mechanism to improve the mechanical properties of the BH-1 geopolymer by adding an additional Al source enhances the replacement of silicon atoms by Al atoms in the silicon–oxygen group and generates a more complete and dense amorphous gel structure.     

Polyoxometalate‐Based Organic–Inorganic Hybrids as Antitumor Drugs

Polyoxometalates (POMs) have shown encouraging antitumor activity. However, their cytotoxicity in normal cells and unspecific interactions with biomolecules are two major obstacles that impede the practical applications of POMs in clinical cancer treatment. Derivatization of POMs with more biocompatible organic ligands is expected to cause a synergetic effect and achieve improved bioactivity and biospecificity. Herein, the synthesis of an amphiphilic organic–inorganic hybrid is reported by grafting a long‐chain organoalkoxysilane lipid onto a POM. The amphiphilic POM hybrid could spontaneously assemble into the vesicles and exhibits enhanced antitumor activity for human colorectal cancer cell lines (HT29) compared to that of parent POMs. This detailed study reveals that the amphiphilic nature of POM hybrids enables the as‐formed vesicles to easily bind to the cell membranes and then be uptaken by the cells, thus leading to a substantial increase in antitumor activity. Such prominent antitumor action is mostly accomplished via cell apoptosis, which ultimately results in cell death. Our finding demonstrates that novel POM hybrids‐based drugs with increased bioactivity could be obtained by decorating POMs with selective organic ligands.     

Hybrid Perovskite Light‐Emitting Diodes Based on Perovskite Nanocrystals with Organic–Inorganic Mixed Cations

Organic–inorganic hybrid perovskite materials with mixed cations have demonstrated tremendous advances in photovoltaics recently, by showing a significant enhancement of power conversion efficiency and improved perovskite stability. Inspired by this development, this study presents the facile synthesis of mixed‐cation perovskite nanocrystals based on FA_{(1?x )}Cs_x PbBr₃ (FA = CH(NH₂)₂). By detailed characterization of their morphological, optical, and physicochemical properties, it is found that the emission property of the perovskite, FA_{(1?x )}Cs_x PbBr₃, is significantly dependent on the substitution content of the Cs cations in the perovskite composition. These mixed‐cation perovskites are employed as light emitters in light‐emitting diodes (LEDs). With an optimized composition of FA_0.8Cs_0.2PbBr₃, the LEDs exhibit encouraging performance with a highest reported luminance of 55 005 cd m^?2 and a current efficiency of 10.09 cd A^?1. This work provides important instructions on the future compositional optimization of mixed‐cation perovskite for obtaining high‐performance LEDs. The authors believe this work is a new milestone in the development of bright and efficient perovskite LEDs.     

Self‐Assembly of Ferromagnetic Organic–Inorganic Perovskite‐Like Films

Perovskite‐based organic–inorganic hybrids hold great potential as active layers in electronics or optoelectronics or as components of biosensors. However, many of these applications require thin films grown with good control over structure and thickness—a major challenge that needs to be addressed. The work presented here is an effort towards this goal and concerns the layer‐by‐layer deposition at ambient conditions of ferromagnetic organic–inorganic hybrids consisting of alternating CuCl₄‐octahedra and organic layers. The Langmuir‐Blodgett technique used to assemble these structures provides intrinsic control over the molecular organization and film thickness down to the molecular level. Magnetic characterization reveals that the coercive field for these thin films is larger than that for solution‐grown layered bulk crystals. The strategy presented here suggests a promising cost effective route to facilitate the excellently controlled growth of sophisticated materials on a wide variety of substrates that have properties relevant for the high density storage media and spintronic devices.     

Hybrid Organic–Inorganic Perovskite Photodetectors

Hybrid organic–inorganic perovskite materials garner enormous attention for a wide range of optoelectronic devices. Due to their attractive optical and electrical properties including high optical absorption coefficient, high carrier mobility, and long carrier diffusion length, perovskites have opened up a great opportunity for high performance photodetectors. This review aims to give a comprehensive summary of the significant results on perovskite‐based photodetectors, focusing on the relationship among the perovskite structures, device configurations, and photodetecting performances. An introduction of recent progress in various perovskite structure‐based photodetectors is provided. The emphasis is placed on the correlation between the perovskite structure and the device performance. Next, recent developments of bandgap‐tunable perovskite and hybrid photodetectors built from perovskite heterostructures are highlighted. Then, effective approaches to enhance the stability of perovskite photodetector are presented, followed by the introduction of flexible and self‐powered perovskite photodetectors. Finally, a summary of the previous results is given, and the major challenges that need to be addressed in the future are outlined. A comprehensive summary of the research status on perovskite photodetectors is hoped to push forward the development of this field.     

基于虚拟样机技术月球机器人运动仿真

采用“虚拟样机”技术,建立一个集三维实体设计,动力学建模,控制,可视化仿真于一体的虚拟月面计算机仿真环境,对月球机器人的静力学,运动学以及动力学进行仿真研究,为月球机器人结构参数,动力学参数及控制算法的优化提供了设计参数和验证场所。     

Efficient Room‐Temperature Phosphorescence from Organic–Inorganic Hybrid Perovskites by Molecular Engineering

Solution‐processed organic–inorganic hybrid perovskites are promising emitters for next‐generation optoelectronic devices. Multiple‐colored, bright light emission is achieved by tuning their composition and structures. However, there is very little research on exploring optically active organic cations for hybrid perovskites. Here, unique room‐temperature phosphorescence from hybrid perovskites is reported by employing novel organic cations. Efficient room‐temperature phosphorescence is activated by designing a mixed‐cation perovskite system to suppress nonradiative recombination. Multiple‐colored phosphorescence is achieved by molecular design. Moreover, the emission lifetime can be tuned by varying the perovskite composition to achieve persistent luminescence. Efficient room‐temperature phosphorescence is demonstrated in hybrid perovskites that originates from the triplet states of the organic cations, opening a new dimension to the further development of perovskite emitters with novel functional organic cations for versatile display applications.