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101.
Muhammad Khurram Tufail Niaz Ahmad Le Yang Lei Zhou Muhammad Adnan Naseer Renjie Chen Wen Yang 《中国化学工程学报》2021,39(11):16-36
The development of an inorganic electrochemical stable solid-state electrolyte is essentially responsible for future state-of-the-art all-solid-state lithium batteries (ASSLBs). Because of their advantages in safety, working temperature, high energy density, and packaging, ASSLBs can develop an ideal energy storage system for modern electric vehicles (EVs). A solid electrolyte (SE) model must have an economical synthesis approach, exhibit electrochemical and chemical stability, high ionic conductivity, and low interfacial resistance. Owing to its highest conductivity of 17 mS·cm-1, and deformability, the sulfide-based Li7P3S11 solid electrolyte is a promising contender for the high-performance bulk type of ASSLBs. Herein, we present a current glimpse of the progress of synthetic procedures, structural aspects, and ionic conductivity improvement strategies. Structural elucidation and mechanistic approaches have been extensively discussed by using various characterization techniques. The chemical stability of Li7P3S11 could be enhanced via oxide doping, and hard and soft acid/base (HSAB) concepts are also discussed. The issues to be undertaken for designing the ideal solid electrolytes, interfacial challenges, and high energy density have been discoursed. This review aims to provide a bird's eye view of the recent development of Li7P3S11-based solid-state electrolyte applications and explore the strategies for designing new solid electrolytes with a target-oriented approach to enhance the efficiency of high energy density all-solid-state lithium batteries. 相似文献
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Chi Nguyen Quynh Ho Minh Thi Tran Chung Chinh Doan Son Nghia Hoang Diem Hong Tran Long Thanh Le 《International journal of molecular sciences》2021,22(9)
Simulated microgravity (SMG) induced the changes in cell proliferation and cytoskeleton organization, which plays an important factor in various cellular processes. The inhibition in cell cycle progression has been considered to be one of the main causes of proliferation inhibition in cells under SMG, but their mechanisms are still not fully understood. This study aimed to evaluate the effects of SMG on the proliferative ability and cytoskeleton changes of Chang Liver Cells (CCL-13). CCL-13 cells were induced SMG by 3D clinostat for 72 h, while the control group were treated in normal gravity at the same time. The results showed that SMG reduced CCL-13 cell proliferation by an increase in the number of CCL-13 cells in G0/G1 phase. This cell cycle phase arrest of CCL-13 cells was due to a downregulation of cell cycle-related proteins, such as cyclin A1 and A2, cyclin D1, and cyclin-dependent kinase 6 (Cdk6). SMG-exposed CCL-13 cells also exhibited a downregulation of α-tubulin 3 and β-actin which induced the cytoskeleton reorganization. These results suggested that the inhibited proliferation of SMG-exposed CCL-13 cells could be associate with the attenuation of major cell cycle regulators and main cytoskeletal proteins. 相似文献
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双滑移取向Cu单晶的循环形变行为──Ⅱ.滑移带和形变带SCIEI 总被引:2,自引:0,他引:2
用光学显微镜和扫描电镜研究了双滑移取向([034],[117])Cu单晶循环饱和后的表面形貌,塑性分切应变幅(γpl)低于10^(-3)时,[034]晶体表面上要为主滑移系的驻留滑移带(PSBs)占据,次滑移只在边缘区域启动,其PSBs细窄(<1μm),体积百分数在1%以下.γpl>10^(-3)时,次滑移开始在试样的中部启动,同时,表面出现二种贯穿晶体的宏观形变带(DBI,DBII),滑移带在形变带内集中.[117]晶体在γpl=4.4×10^(-4)时,双滑移现象已十分明显.γpl>10^(-3)时,表面也形成与前者相似的形变带.DBI的惯习面与主滑移面平行([034]晶体)或接近([117]晶体),DBII的惯习面则与前者垂直,文章讨论了形变带形成的可能原因. 相似文献
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1 INTRODUCTIONAlumina(Al2 O3)ceramicsareoftenconsideredforstructuralapplications,duetotheirpropertiesofhighhardness ,chemicalandwearresistanceandgoodmechanicalpropertiesatroomandhightemperature .Thewellknownlimitationfortheseceramics ,how ever ,istheverylowtoughness .Recentstudieshaveshownsignificantimprovementsinmechanicalprop erties ,includingtoughness ,byaddingductilesecondphaseparticles ,suchasNi,Al,MoandCu[14 ] .Anincreaseof 80 % 333%inthefracturetoughnesshasbeenreportedforAl2 O3… 相似文献
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