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A strategy for creating potent and pan-genotypic stimulator of interferon genes (STING) agonists is described. Locking a bioactive U-shaped conformation of cyclic dinucleotides by introducing a transannular macrocyclic bridge between the nucleic acid bases leads to a topologically novel macrocycle-bridged STING agonist (MBSA). In addition to substantially enhanced potency, the newly designed MBSAs, exemplified by clinical candidate E7766 , exhibit broad pan-genotypic activity in all major human STING variants. E7766 is shown to have potent antitumor activity with long lasting immune memory response in a mouse liver metastatic tumor model. Two complementary stereoselective synthetic routes to E7766 are also described.  相似文献   
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本文介绍了光纤光栅技术在测力锚杆上的应用,并且基于常用托盘的力学结构,增大了托盘内部的空间、设计了与之相连接的金属保护套筒使之成为一体式结构,从而有效地保护了光纤测力锚杆的主体结构。  相似文献   
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Qi  Shuang  Xiang  WenXin  Cai  LiXun  Liu  XiaoKun  Shao  ChunBing  Ning  FangMao  Shi  JinHua  Yu  WeiWei 《中国科学:技术科学(英文版)》2021,64(12):2577-2585
Science China Technological Sciences - Mixed-mode I-II crack-based fatigue crack propagation (FCPI-II) usually occurs in engineering structures; however, no theoretical formula or effective...  相似文献   
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The electrode materials with high pseudocapacitance can enhance the rate capability and cycling stabil-ity of lithium-ion storage devices.Herein,we fabricated MoS2 nanoflowers with ultra-large interlayer spacing on N-doped hollow multi-nanochannel carbon nanofibers(F2-MoS2/NHMCFs)as freestanding binder-free anodes for lithium-ion batteries(LIBs).The ultra-large interlayer spacing(0.78~1.11 nm)of MoS2 nanoflowers can not only reduce the internal resistance,but also increase accessible active sur-face area,which ensures the fast Li+intercalation and deintercalation.The NHMCFs with hollow and multi-nanochannel structure can accommodate the large internal strain and volume change during lithi-ation/delithiation process,it is beneficial to improving the cycling stability of LIBs.Benefiting from the above combined structure merits,the F2-MoS2/NHMCFs electrodes deliver a high rate capability 832 mA h g-1 at 10 A g-1 and ultralong cycling stability with 99.29 and 91.60%capacity retention at 10 A g-1 after 1000 and 2000 cycles,respectively.It is one of the largest capacities and best cycling stability at 10 A g-1 ever reported to date,indicating the freestanding F2-MoS2/NHMCFs electrodes have potential applications in high power density LIBs.  相似文献   
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运用往复线性摩擦试验方法,搭配自制的摩擦试验夹具,模拟织造过程中氧化铝纤维束-筘齿的摩擦行为,研究加载力、预加张力和摩擦频率对悬空状态下氧化铝纤维束摩擦磨损性能的影响.结果表明:随着加载力的增加,氧化铝纤维束所受摩擦力及长丝断裂根数增加,摩擦系数减小;在预加张力为0.40 N时,氧化铝纤维束所受摩擦力和摩擦系数出现最小值,磨损程度也最小;在摩擦稳定阶段,摩擦频率增加,则氧化铝纤维束所受摩擦力先下降,后略有上升,当摩擦频率增加至5 Hz时,氧化铝纤维束的摩擦系数较1 Hz时增加18.7%,磨损程度也最为严重.  相似文献   
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Srx(Zr0.9Y0.05Yb0.05)O1.95+x (x=1.0, 0.9, 0.8, 0.7) ceramics were prepared by solid state reaction sintering. The sintered Sr1.0(Zr0.9Y0.05Yb0.05)O2.95 is a single-phase solid solution while the sintered Srx(Zr0.9Y0.05Yb0.05)O1.95+x (x=0.9?0.7) are composites, and a significant grain growth inhibition is observed in the sintered Srx(Zr0.9Y0.05Yb0.05)O1.95+x (x=1.0, 0.9). Rare-earth elements distribution in the bulk materials indicates that Yb and Y preferentially substitute Zr-sites in SrZrO3, and the highest solubility of RE2O3 in pure SrZrO3 is ~0.8 mol%. The sintered Srx(Zr0.9Y0.05Yb0.05)O1.95+x have high thermal expansion coefficients up to ~11.0×10?6 K-1 (1200°C). Sr0.8(Zr0.9Y0.05Yb0.05)O2.75 has the lowest thermal conductivity of 1.38 W·m-1·K-1 at 800°C. Srx(Zr0.9Y0.05Yb0.05)O1.95+x (x=1.0, 0.9, 0.8) show no phase transition from 600 to 1400°C, whereas Srx(Zr0.9Y0.05Yb0.05)O1.95+x (x=0.9, 0.8) have excellent high-temperature phase stability over the whole investigated temperature range. Therefore, Srx(Zr0.9Y0.05Yb0.05)O1.95+x (x=1.0, 0.9, 0.8) are considered as promising TBCs materials that might be operated at higher temperatures compared to YSZ.  相似文献   
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Electroreduction of small molecules such as H2O, CO2, and N2 for producing clean fuels or valuable chemicals provides a sustainable approach to meet the increasing global energy demands and to alleviate the concern on climate change resulting from fossil fuel consumption. On the path to implement this purpose, however, several scientific hurdles remain, one of which is the low energy efficiency due to the sluggish kinetics of the paired oxygen evolution reaction (OER). In response, it is highly desirable to synthesize high-performance and cost-effective OER electrocatalysts. Recent advances have witnessed surface reconstruction engineering as a salient tool to significantly improve the catalytic performance of OER electrocatalysts. In this review, recent progress on the reconstructed OER electrocatalysts and future opportunities are discussed. A brief introduction of the fundamentals of OER and the experimental approaches for generating and characterizing the reconstructed active sites in OER nanocatalysts are given first, followed by an expanded discussion of recent advances on the reconstructed OER electrocatalysts with improved activities, with a particular emphasis on understanding the correlation between surface dynamics and activities. Finally, a prospect for clean future energy communities harnessing surface reconstruction-promoted electrochemical water oxidation will be provided.  相似文献   
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Pulsed laser deposition (PLD) was used to prepare tungsten trioxide (WO3) films on ITO substrates with a varying laser power density of 4.0–5.5 W/cm2. XPS indicated that when the laser power density decreased, the peak positions of the W 4f and O 1s orbits shifted slightly to low energy due to the difference in oxygen vacancies. As the laser power density decreased, W6+ gradually replaced the lattice position of O2?, increasing oxygen vacancies in the lattice. The transmittance modulated values (ΔT) were over 44% at 830 nm, indicating strong absorption by the WO3 thin films in the near-infrared ray. The switching time of the WO3 thin films between bleached states and coloured states decreased as the laser power density increased due to the amorphous structure, morphology, and lower oxygen deficiency at a high power density. The high ΔT and very fast switching time of tb (1.09 s) and tc (6.01 s) demonstrated the excellent electrochromic (EC) properties of the WO3 films prepared by PLD.  相似文献   
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