All Inorganic Halide Perovskites Nanosystem: Synthesis,Structural Features,Optical Properties and Optoelectronic Applications

The recent success of organometallic halide perovskites (OHPs) in photovoltaic devices has triggered lots of corresponding research and many perovskite analogues have been developed to look for devices with comparable performance but better stability. Upon the preparation of all inorganic halide perovskite nanocrystals (IHP NCs), research activities have soared due to their better stability, ultrahigh photoluminescence quantum yield (PL QY), and composition dependent luminescence covering the whole visible region with narrow line‐width. They are expected to be promising materials for next generation lighting and display, and many other applications. Within two years, a lot of interesting results have been observed. Here, the synthesis of IHPs is reviewed, and their progresses in optoelectronic devices and optical applications, such as light‐emitting diodes (LEDs), photodetectors (PDs), solar cells (SCs), and lasing, is presented. Information and recent understanding of their crystal structures and morphology modulations are addressed. Finally, a brief outlook is given, highlighting the presently main problems and their possible solutions and future development directions.     

Cesium lead halide perovskite triangular nanorods as high-gain medium and effective cavities for multiphoton-pumped lasing

High-performance multiphoton-pumped lasers based on cesium lead halide perovskite nanostructures are promising for nonlinear optics and practical frequency upconversion devices in integrated photonics.However,the performance of such lasers is highly dependent on the quality of the material and cavity,which makes their fabrication challenging.Herein,we demonstrate that cesium lead halide perovskite triangular nanorods fabricated via vapor methods can serve as gain media and effective cavities for multiphoton-pumped lasers.We observed blue-shifts of the lasing modes in the excitation fluence-dependent lasing spectra at increased excitation powers,which fits well with the dynamics of Burstein-Moss shifts caused by the band filling effect.Moreover,efficient multiphoton lasing in CsPbBr3 nanorods can be realized in a wide excitation wavelength range (700-1,400 nm).The dynamics of multiphoton lasing were investigated by time-resolved photoluminescence spectroscopy,which indicated that an electron-hole plasma is responsible for the multiphoton-pumped lasing.This work could lead to new opportunities and applications for cesium lead halide perovskite nanostructures in frequency upconversion lasing devices and optical interconnect systems.     

脉冲电磁场作用下碳纤维增强聚乳酸复合材料的体外降解特性

碳纤维增强聚乳酸(C/PLA)复合材料是较为理想的可降解骨折内固定材料,但由于其降解特性与人体骨骼愈合速度的不匹配,很难达到最佳治疗效果。文中将脉冲电磁场(PEF)引入C/PLA的体外降解过程,并研究了该条件下复合材料的降解特性。结果表明,PEF处理对C/PLA试样的吸水率、质量保持率、弯曲强度和剪切强度均有不同程度的影响;扫描电镜观察发现,PEF处理使界面处的PLA基体出现降解洞穴;差示扫描量热分析说明经不同降解时间的PLA基体的玻璃化转变温度没有明显变化。模型分析表明PEF处理影响降解溶液中正负离子的扩散行为,使得界面处的PLA基体出现局域降解加速区,进而影响C/PLA复合材料的体外降解行为。这一研究将为研究可降解骨折内固定装置的外部辅助治疗器械提供途径。     

DNA电化学传感器对金属离子检测的研究进展

由于DNAzyme、T-T和C-C之间错配以及G-四链体等能与金属离子特异性结合,基于DNA与金属离子相互作用来检测金属离子的DNA电化学传感器逐渐发展起来。介绍了几种DNA电化学传感器检测金属离子的新方法,并对DNA电化学传感器对金属离子检测的发展趋势和研究方向进行了展望。     

以玉米衣为模板生物遗态ZnO的制备及Pb2+吸附性能

以玉米衣为模板,利用生物模板法制备了生物遗态多孔ZnO。经过预处理的玉米衣在醋酸锌前驱体溶液中浸渍24h,烘干,800℃煅烧3h得到最终的产物。利用X射线衍射(X-ray)、扫描电镜(SEM)和透射电镜(TEM)对其进行表征,并研究了对铅离子的吸附性能。结果表明:通过原位生长技术,结晶度良好的ZnO晶粒自组装形成表面多孔的类卷叶状生物遗态ZnO;生物遗态ZnO对铅离子有良好的吸附性能,吸附量为49.9mg/g,在120min可基本达到吸附平衡,吸附过程符合准二级动力学模型,吸附等温线拟合结果较为符合Langmuir模型,且升温有利于吸附的进行。     

Facile synthesis of CsPbBr3/PbSe composite clusters

In this work, CsPbBr₃ and PbSe nanocomposites were synthesized to protect perovskite material from self-enlargement during reaction. UV absorption and photoluminescence (PL) spectra indicate that the addition of Se into CsPbBr₃ quantum dots modified the electronic structure of CsPbBr₃, increasing the band gap from 2.38 to 2.48 eV as the Cs:Se ratio increased to 1:3. Thus, the emission color of CsPbBr₃ perovskite quantum dots was modified from green to blue by increasing the Se ratio in composites. According to X-ray diffraction patterns, the structure of CsPbBr₃ quantum dots changed from cubic to orthorhombic due to the introduction of PbSe at the surface. Transmission electron microscopy and X-ray photoemission spectroscopy confirmed that the atomic distribution in CsPbBr₃/PbSe composite clusters is uniform and the composite materials were well formed. The PL intensity of a CsPbBr₃/PbSe sample with a 1:1 Cs:Se ratio maintained 50% of its initial intensity after keeping the sample for 81 h in air, while the PL intensity of CsPbBr₃ reduced to 20% of its initial intensity. Therefore, it is considered that low amounts of Se could improve the stability of CsPbBr₃ quantum dots.     

Triethylenetetramine/hydroxyethyl cellulose-functionalized graphene oxide monoliths for the removal of copper and arsenate ions

Nitrogen-doped graphene oxide monoliths (GOMs) were readily constructed by crosslinking graphene oxide (GO) using triethylenetetramine (TETA) and hydroxyethyl cellulose (HEC). The addition of HEC was beneficial to the formation of a network structure compared to that in the absence of HEC. The generated monoliths have shown various morphologies with different d spacing, layer thickness, and micropore size. Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) analyses provided evidences for the formation of covalent C–N bonds and some nitrogen-containing heterocyclic composition inside the graphene oxide sheet, indicating that the interaction of GO with the amine crosslinker involved the crosslinking reaction between GO epoxides and amine groups. HEC was also involved in the N-doping reaction via the partial reduction of oxygen in HEC molecules. Analysis of X-ray diffraction (XRD) results indicated that the lattice distance between GO sheets increased after TETA/HEC crosslinking. Thermogravimetric analysis (TGA) confirmed the successful incorporation of crosslinker moieties on the surface of GO sheets. The fabricated GOMs could be used to efficiently adsorb metal ions and arsenate by the introduced polar functional groups on GO sheets and porous structures based on hydrogen bonds, whose morphologies and compositions were confirmed via XRD, scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS).