Communication—Microscopic View of the Ethylene Carbonate Based Lithium-Ion Battery Electrolyte by X-ray Scattering

2019 ◽  
Vol 166 (2) ◽  
pp. A47-A49 ◽  
Author(s):  
Zhange Feng ◽  
Erik Sarnello ◽  
Tao Li ◽  
Lei Cheng
ACS Nano ◽  
2017 ◽  
Vol 11 (2) ◽  
pp. 1443-1454 ◽  
Author(s):  
Sarang M. Bhaway ◽  
Zhe Qiang ◽  
Yanfeng Xia ◽  
Xuhui Xia ◽  
Byeongdu Lee ◽  
...  

2001 ◽  
Vol 3 (3) ◽  
pp. 136-141 ◽  
Author(s):  
Artur Braun ◽  
Soenke Seifert ◽  
Pappannan Thiyagarajan ◽  
Stephen P. Cramer ◽  
Elton J. Cairns

2021 ◽  
Vol 12 ◽  
pp. 100076
Author(s):  
M. Kodama ◽  
A. Takeuchi ◽  
M. Uesugi ◽  
T. Miyuki ◽  
H. Yasuda ◽  
...  

Langmuir ◽  
2015 ◽  
Vol 31 (6) ◽  
pp. 2028-2035 ◽  
Author(s):  
Katharine E. Silberstein ◽  
Michael A. Lowe ◽  
Benjamin Richards ◽  
Jie Gao ◽  
Tobias Hanrath ◽  
...  

2018 ◽  
Vol 25 (2) ◽  
pp. 537-542 ◽  
Author(s):  
Didem Ketenoglu ◽  
Georg Spiekermann ◽  
Manuel Harder ◽  
Erdinc Oz ◽  
Cevriye Koz ◽  
...  

The effects of varying LiPF6salt concentration and the presence of lithium bis(oxalate)borate additive on the electronic structure of commonly used lithium-ion battery electrolyte solvents (ethylene carbonate–dimethyl carbonate and propylene carbonate) have been investigated. X-ray Raman scattering spectroscopy (a non-resonant inelastic X-ray scattering method) was utilized together with a closed-circle flow cell. Carbon and oxygenK-edges provide characteristic information on the electronic structure of the electrolyte solutions, which are sensitive to local chemistry. Higher Li+ion concentration in the solvent manifests itself as a blue-shift of both the π* feature in the carbon edge and the carbonyl π* feature in the oxygen edge. While these oxygenK-edge results agree with previous soft X-ray absorption studies on LiBF4salt concentration in propylene carbonate, carbonK-edge spectra reveal a shift in energy, which can be explained with differing ionic conductivities of the electrolyte solutions.


Author(s):  
Eva-Maria Mandelkow ◽  
Eckhard Mandelkow ◽  
Joan Bordas

When a solution of microtubule protein is changed from non-polymerising to polymerising conditions (e.g. by temperature jump or mixing with GTP) there is a series of structural transitions preceding microtubule growth. These have been detected by time-resolved X-ray scattering using synchrotron radiation, and they may be classified into pre-nucleation and nucleation events. X-ray patterns are good indicators for the average behavior of the particles in solution, but they are difficult to interpret unless additional information on their structure is available. We therefore studied the assembly process by electron microscopy under conditions approaching those of the X-ray experiment. There are two difficulties in the EM approach: One is that the particles important for assembly are usually small and not very regular and therefore tend to be overlooked. Secondly EM specimens require low concentrations which favor disassembly of the particles one wants to observe since there is a dynamic equilibrium between polymers and subunits.


Author(s):  
Eva-Maria Mandelkow ◽  
Ron Milligan

Microtubules form part of the cytoskeleton of eukaryotic cells. They are hollow libers of about 25 nm diameter made up of 13 protofilaments, each of which consists of a chain of heterodimers of α-and β-tubulin. Microtubules can be assembled in vitro at 37°C in the presence of GTP which is hydrolyzed during the reaction, and they are disassembled at 4°C. In contrast to most other polymers microtubules show the behavior of “dynamic instability”, i.e. they can switch between phases of growth and phases of shrinkage, even at an overall steady state [1]. In certain conditions an entire solution can be synchronized, leading to autonomous oscillations in the degree of assembly which can be observed by X-ray scattering (Fig. 1), light scattering, or electron microscopy [2-5]. In addition such solutions are capable of generating spontaneous spatial patterns [6].In an earlier study we have analyzed the structure of microtubules and their cold-induced disassembly by cryo-EM [7]. One result was that disassembly takes place by loss of protofilament fragments (tubulin oligomers) which fray apart at the microtubule ends. We also looked at microtubule oscillations by time-resolved X-ray scattering and proposed a reaction scheme [4] which involves a cyclic interconversion of tubulin, microtubules, and oligomers (Fig. 2). The present study was undertaken to answer two questions: (a) What is the nature of the oscillations as seen by time-resolved cryo-EM? (b) Do microtubules disassemble by fraying protofilament fragments during oscillations at 37°C?


1992 ◽  
Vol 2 (6) ◽  
pp. 899-913 ◽  
Author(s):  
Patrick Davidson ◽  
Elisabeth Dubois-Violette ◽  
Anne-Marie Levelut ◽  
Brigitte Pansu

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