scholarly journals Stratigraphic analysis of intercalated graphite electrodes in aqueous inorganic acid solutions

Nano Research ◽  
2021 ◽  
Author(s):  
Stefania De Rosa ◽  
Paolo Branchini ◽  
Valentina Spampinato ◽  
Alexis Franquet ◽  
Rossella Yivlialin ◽  
...  

AbstractA detailed stratigraphic investigation of the intercalation mechanism when graphite electrodes are immersed inside diluted perchloric (HClO4) and sulfuric (H2SO4) electrolytes is obtained by comparing results when graphite crystals are simply immersed in the same acid solutions. By combining time-of-flight secondary ion mass spectrometry (ToF-SIMS) and in-situ atomic force microscopy (AFM), we provide a picture of the chemical species involved in the intercalation reaction. The depth intensity profile of the ion signals along the electrode crystal clearly shows a more complex mechanism for the intercalation process, where the local morphology of the basal plane plays a crucial role. Solvated anions are mostly located within the first tens of nanometers of graphite, but electrolytes also diffuse inside the buried layers for hundreds of nanometers, the latter process is also aided by the presence of mesoscopic crystal defects. Residual material from the electrolyte solution was found localized in well-defined circular spots, which represent preferential interaction areas. Interestingly, blister-like micro-structures similar to those observed on the highly oriented pyrolytic graphite (HOPG) surface were found in the buried layers, confirming the equivalence of the chemical condition on the graphite surface and in the underneath layers.

Langmuir ◽  
1998 ◽  
Vol 14 (9) ◽  
pp. 2508-2514 ◽  
Author(s):  
X. W. Cai ◽  
J. S. Gao ◽  
Z. X. Xie ◽  
Y. Xie ◽  
Z. Q. Tian ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ayse N. Koyun ◽  
Julia Zakel ◽  
Sven Kayser ◽  
Hartmut Stadler ◽  
Frank N. Keutsch ◽  
...  

AbstractSurface microstructures of bitumen are key sites in atmospheric photo-oxidation leading to changes in the mechanical properties and finally resulting in cracking and rutting of the material. Investigations at the nanoscale remain challenging. Conventional combination of optical microscopy and spectroscopy cannot resolve the submicrostructures due to the Abbe restriction. For the first time, we report here respective surface domains, namely catana, peri and para phases, correlated to distinct molecules using combinations of atomic force microscopy with infrared spectroscopy and with correlative time of flight—secondary ion mass spectrometry. Chemical heterogeneities on the surface lead to selective oxidation due to their varying susceptibility to photo-oxidation. It was found, that highly oxidized compounds, are preferentially situated in the para phase, which are mainly asphaltenes, emphasising their high oxidizability. This is an impressive example how chemical visualization allows elucidation of the submicrostructures and explains their response to reactive oxygen species from the atmosphere.


2018 ◽  
Vol 2018 ◽  
pp. 1-5 ◽  
Author(s):  
Hee-Youb Song ◽  
Soon-Ki Jeong

Interfacial reactions strongly influence the performance of lithium-ion batteries, with the main interfacial reaction between graphite and propylene carbonate- (PC-) based electrolytes corresponding to solvent cointercalation. Herein, the redox reactions of solvated lithium ions occurring at the graphite interface in 1 M·LiClO4/PC were probed by chronopotentiometry, in situ atomic force microscopy (AFM), and in situ Raman spectroscopy. The obtained results revealed that high coulombic efficiency (97.5%) can be achieved at high current density, additionally showing the strong influence of charge capacity on the above redox reactions. Moreover, AFM imaging indicated the occurrence of solvent cointercalation during the first reduction, as reflected by the presence of hills and blisters on the basal plane of highly oriented pyrolytic graphite subjected to the above process.


1997 ◽  
Vol 12 (8) ◽  
pp. 1942-1945 ◽  
Author(s):  
H. J. Gao ◽  
H. X. Zhang ◽  
Z. Q. Xue ◽  
S. J. Pang

Scanning tunneling microscopy (STM) and atomic force microscopy (AFM) investigation of tetracyanoquinodimethane (TCNQ) and the related C60-TCNQ thin films is presented. Periodic molecular chains of the TCNQ on highly oriented pyrolytic graphite (HOPG) substrates were imaged, which demonstrated that the crystalline (001) plane was parallel to the substrate. For the C60-TCNQ thin films, we found that there were grains on the film surface. STM images within the grain revealed that the well-ordered rows and terraces, and the parallel rows in different grains were generally not in the same orientation. Moreover, the grain boundary was also observed. In addition, AFM was employed to modify the organic TCNQ film surface for the application of this type of materials to information recording and storage at the nanometer scale. The nanometer holes were successfully created on the TCNQ thin film by the AFM.


1996 ◽  
Vol 11 (1) ◽  
pp. 63-71 ◽  
Author(s):  
A. Ureña ◽  
J. M. Gómez de Salazar ◽  
J. J. Martín ◽  
J. Quiñones

This paper describes a new application of two complementary surface characterization techniques to study solid-state bonding in an Al–Li alloy. Through the two mentioned techniques, Atomic Force Microscopy (AFM) and Secondary Ion Mass Spectrometry (SIMS), important findings about what takes place in the bond interface have been determined. These findings enclose both the formation of discontinuous mixed oxides and the evolution of Li through the bond line and into theadjacent diffusion affected zones. Homogenization of Li and Cu alloyelements has been detected even in those cases where a metallic interlayer was used to favor the union.


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