基于SCA波形采样读出电子学的CSNS Back-n中子飞行时间测量

中国散裂中子源(CSNS)反角白光中子束线(Back-n)对中子核数据测量和核技术应用等多个领域均有重要意义。为监测其中子束斑轮廓、束流密度及束流能量，研制了由镀硼微网格气体(Micromegas)探测器构成的束流剖面监测装置，并通过测量中子的飞行时间(TOF)来获得能量信息。采用基于开关电容阵列(SCA)专用集成电路(ASIC)的波形采样电子学系统，实现了128路Micromegas探测器阳极条信号的低噪声放大、成形和波形数字化，在现场可编程逻辑门阵列(FPGA)芯片中实现了对信号过阈时间的实时测量，其量程为650 ns～10 ms，电子学时间分辨好于10 ns。在CSNS Back-n上开展实验，成功获得了中子束流剖面及10.65 μs～10 ms范围的飞行时间谱，对应的中子能量范围约为0.16 eV～0.14 MeV。利用钽、钴等吸收体进行了中子共振吸收峰的检验，验证了读出电子学系统的功能及飞行时间测量的正确性。     

Formation of Uniform Water Microdroplets on Wrinkled Graphene for Ultrafast Humidity Sensing

Portable humidity sensors with ultrafast responses fabricated in wearable devices have promising application prospects in disease diagnostics, health status monitoring, and personal healthcare data collecting. However, prolonged exposures to high‐humidity environments usually cause device degradation or failure due to excessive water adsorbed on the sensor surface. In the present work, a graphene film based humidity sensor with a hydrophobic surface and uniformly distributed ring‐like wrinkles is designed and fabricated that exhibits excellent performance in breath sensing. The wrinkled morphology of the graphene sensor is able to effectively prevent the aggregation of water microdroplets and thus maximize the evaporation rate. The as‐fabricated sensor responds to and recovers from humidity in 12.5 ms, the fastest response of humidity sensors reported so far, yet in a very stable manner. The sensor is fabricated into a mask and successfully applied to monitoring sudden changes in respiratory rate and depth, such as breathing disorder or arrest, as well as subtle changes in humidity level caused by talking, cough and skin evaporation. The sensor can potentially enable long‐term daily monitoring of breath and skin evaporation with its ultrafast response and high sensitivity, as well as excellent stability in high‐humidity environments.     

Matrilin-3-Primed Adipose-Derived Mesenchymal Stromal Cell Spheroids Prevent Mesenchymal Stromal-Cell-Derived Chondrocyte Hypertrophy

Adipose-derived mesenchymal stromal cells (Ad-MSCs) are a promising tool for articular cartilage repair and regeneration. However, the terminal hypertrophic differentiation of Ad-MSC-derived cartilage is a critical barrier during hyaline cartilage regeneration. In this study, we investigated the role of matrilin-3 in preventing Ad-MSC-derived chondrocyte hypertrophy in vitro and in an osteoarthritis (OA) destabilization of the medial meniscus (DMM) model. Methacrylated hyaluron (MAHA) (1%) was used to encapsulate and make scaffolds containing Ad-MSCs and matrilin-3. Subsequently, the encapsulated cells in the scaffolds were differentiated in chondrogenic medium (TGF-β, 1–14 days) and thyroid hormone hypertrophic medium (T3, 15–28 days). The presence of matrilin-3 with Ad-MSCs in the MAHA scaffold significantly increased the chondrogenic marker and decreased the hypertrophy marker mRNA and protein expression. Furthermore, matrilin-3 significantly modified the expression of TGF-β2, BMP-2, and BMP-4. Next, we prepared the OA model and transplanted Ad-MSCs primed with matrilin-3, either as a single-cell suspension or in spheroid form. Safranin-O staining and the OA score suggested that the regenerated cartilage morphology in the matrilin-3-primed Ad-MSC spheroids was similar to the positive control. Furthermore, matrilin-3-primed Ad-MSC spheroids prevented subchondral bone sclerosis in the mouse model. Here, we show that matrilin-3 plays a major role in modulating Ad-MSCs’ therapeutic effect on cartilage regeneration and hypertrophy suppression.     

海水淡化用空心锥喷嘴喷淋性能理论及实验研究

设计开发一种具有高通量、低流阻特征的空心锥喷嘴,并通过理论与实验方法研究空心锥喷嘴的喷淋性能,基于准自由涡理论建立空心锥喷嘴内部流体流动的数学模型,阐明流量系数、喷淋锥角、喷嘴流量与喷嘴结构参数之间的定量关系,并利用多效蒸馏海水淡化喷淋实验台对理论计算结果进行实验测试和验证。研究结果表明:正常工作状态下喷嘴流量系数、喷淋锥角、喷淋流量等参数理论值与测量值之间的误差小于5%,验证了设计模型的准确性。同时根据实验测试数据,拟合得到该类型空心锥喷嘴喷淋锥角与雷诺数之间的经验公式,可为蒸馏海水淡化用大流量空心锥喷嘴的结构设计、工艺选型提供理论指导和数据支持。     

Low Li ion diffusion barrier on low-crystalline FeOOH nanosheets and high performance of energy storage

Nano Research - To obtain symmetric supercapacitors (SCs) with high energy density, it is critical to fabricate an electrode with wide potential window and excellent capacitive performance. Herein,...     

Microwave dielectric properties of SrLa[Ga1−x(Mg0.5Ti0.5)x]O4 and SrLa[Ga1−x(Zn0.5Ti0.5)x]O4 (x = 0.2-0.8) ceramics

SrLa[Ga_1−x(R_0.5Ti_0.5)_x]O₄ (R = Mg, Zn) ceramics were prepared by a standard solid state sintering method. The single-phase ceramics with K₂NiF₄-type layered perovskite structure and I4/mmm space group were obtained, indicating that SrLa(R_0.5Ti_0.5) and SrLaGaO₄ can form the unlimited solid solutions. With increasing x for R = Mg and Zn, ε_r increases monotonously, the Qf value first increases and then decreases, while τ_f increases from a negative to a positive value. The optimized microwave dielectric properties were obtained as following: ε_r = 23.3, Qf = 89 400 GHz, τ_f = −0.8 ppm/°C for SrLa[Ga_0.6(Mg_0.5Ti_0.5)_0.4]O₄ and ε_r = 23.3, Qf = 76 200 GHz, τ_f = 0.2 ppm/°C for SrLa[Ga_0.7(Zn_0.5Ti_0.5)_0.3]O₄, indicating that the present solid solution ceramics are the promising candidates as microwave resonator materials for the telecommunication applications.     

Sequence-Dependent Nanofiber Structures of Phenylalanine and Isoleucine Tripeptides

The molecular design of short peptides to achieve a tailor-made functional architecture has attracted attention during the past decade but remains challenging as a result of insufficient understanding of the relationship between peptide sequence and assembled supramolecular structures. We report a hybrid-resolution model to computationally explore the sequence–structure relationship of self-assembly for tripeptides containing only phenylalanine and isoleucine. We found that all these tripeptides have a tendency to assemble into nanofibers composed of laterally associated filaments. Molecular arrangements within the assemblies are diverse and vary depending on the sequences. This structural diversity originates from (1) distinct conformations of peptide building blocks that lead to different surface geometries of the filaments and (2) unique sidechain arrangements at the filament interfaces for each sequence. Many conformations are available for tripeptides in solution, but only an extended β-strand and another resembling a right-handed turn are observed in assemblies. It was found that the sequence dependence of these conformations and the packing of resulting filaments are determined by multiple competing noncovalent forces, with hydrophobic interactions involving Phe being particularly important. The sequence pattern for each type of assembly conformation and packing has been identified. These results highlight the importance of the interplay between conformation, molecular packing, and sequences for determining detailed nanostructures of peptides and provide a detailed insight to support a more precise design of peptide-based nanomaterials.