The Electrochemical Cycling of Pasted Sb and Ca/Sn Lead Electrodes (Positives)

1983 ◽  
Vol 130 (9) ◽  
pp. 1800-1803 ◽  
Author(s):  
J. A. Bialacki ◽  
N. A. Hampson ◽  
K. Peters
Keyword(s):  
Electrochemical Cycling ◽  
Lead Electrodes

Electrochemical cycling of pasted antimonial lead electrodes (positives)

1981 ◽  
Vol 11 (5) ◽  
pp. 595-600 ◽  
Author(s):  
S. Kelly ◽  
N. A. Hampson ◽  
K. Peters
Keyword(s):  
Electrochemical Cycling ◽  
Lead Electrodes ◽  
Antimonial Lead

Anionic and Cationic Redox Processes in β-Li2IrO3 and Their Structural Implications on Electrochemical Cycling in Li-Ion Cell

2019 ◽  
Author(s):  
Paul Pearce ◽  
Gaurav Assat ◽  
Antonella Iadecola ◽  
François Fauth ◽  
Rémi Dedryvère ◽  
...  
Keyword(s):  
Analytical Techniques ◽  
Charge Compensation ◽  
Coupling Mechanism ◽  
Redox Processes ◽  
Positive Electrodes ◽  
X Ray ◽  
Electrochemical Cycling ◽  
Li Ion ◽  
Electrochemical Instability ◽  
High Degree

The recent discovery of anionic redox as a means to increase the energy density of transition metal oxide positive electrodes is now a well established approach in the Li-ion battery field. However, the science behind this new phenomenon pertaining to various Li-rich materials is still debated. Thus, it is of paramount importance to develop a robust set of analytical techniques to address this issue. Herein, we use a suite of synchrotron-based X-ray spectroscopies as well as diffraction techniques to thoroughly characterize the different redox processes taking place in a model Li-rich compound, the tridimentional hyperhoneycomb β-Li2IrO3. We clearly establish that the reversible removal of Li+ from this compound is associated to a previously described reductive coupling mechanism and the formation of the M-(O-O) and M-(O-O)* states. We further show that the respective contributions to these states determine the spectroscopic response for both Ir L3-edge X-ray absorption spectroscopy (XAS) and X-ray photoemissions spectroscopy (XPS). Although the high covalency and the robust tridimentional structure of this compound enable a high degree of reversibile delithiation, we found that pushing the limits of this charge compensation mechanism has significant effects on the local as well as average structure, leading to electrochemical instability over cycling and voltage decay. Overall, this work highlights the practical limits to which anionic redox can be exploited and sheds some light on the nature of the oxidized species formed in certain lithium-rich compounds.<br>

Anionic and Cationic Redox Processes in β-Li2IrO3 and Their Structural Implications on Electrochemical Cycling in Li-Ion Cell

2019 ◽  
Author(s):  
Paul Pearce ◽  
Gaurav Assat ◽  
Antonella Iadecola ◽  
François Fauth ◽  
Rémi Dedryvère ◽  
...  
Keyword(s):  
Analytical Techniques ◽  
Charge Compensation ◽  
Coupling Mechanism ◽  
Redox Processes ◽  
Positive Electrodes ◽  
X Ray ◽  
Electrochemical Cycling ◽  
Li Ion ◽  
Electrochemical Instability ◽  
High Degree

The recent discovery of anionic redox as a means to increase the energy density of transition metal oxide positive electrodes is now a well established approach in the Li-ion battery field. However, the science behind this new phenomenon pertaining to various Li-rich materials is still debated. Thus, it is of paramount importance to develop a robust set of analytical techniques to address this issue. Herein, we use a suite of synchrotron-based X-ray spectroscopies as well as diffraction techniques to thoroughly characterize the different redox processes taking place in a model Li-rich compound, the tridimentional hyperhoneycomb β-Li2IrO3. We clearly establish that the reversible removal of Li+ from this compound is associated to a previously described reductive coupling mechanism and the formation of the M-(O-O) and M-(O-O)* states. We further show that the respective contributions to these states determine the spectroscopic response for both Ir L3-edge X-ray absorption spectroscopy (XAS) and X-ray photoemissions spectroscopy (XPS). Although the high covalency and the robust tridimentional structure of this compound enable a high degree of reversibile delithiation, we found that pushing the limits of this charge compensation mechanism has significant effects on the local as well as average structure, leading to electrochemical instability over cycling and voltage decay. Overall, this work highlights the practical limits to which anionic redox can be exploited and sheds some light on the nature of the oxidized species formed in certain lithium-rich compounds.<br>

Obtaining of lead (II) sulfate by polarization of bipolar lead electrodes with alternating current

2019 ◽  
Vol 96 (4) ◽  
pp. 83-91
Author(s):  
A.K. Bayeshova ◽  
◽  
A.M. Kongyratbay ◽  
F.M. Zhumabay ◽  
A. Bayeshov ◽  
...  
Keyword(s):  
Alternating Current ◽  
Lead Electrodes

scholarly journals In situ XRD and operando spectra-electrochemical investigation of tetragonal WO3-x nanowire networks for electrochromic supercapacitors

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Shen Wang ◽  
Hongbo Xu ◽  
Tingting Hao ◽  
Peiyuan Wang ◽  
Xiang Zhang ◽  
...  
Keyword(s):  
Reaction Mechanism ◽  
Electronic Device ◽  
High Capacity ◽  
Optical Modulation ◽  
Function Evaluation ◽  
Dual Function ◽  
Electrochemical Performances ◽  
Electrochemical Cycling ◽  
Nanowire Networks

AbstractElectrochromic supercapacitors (ESCs) are appealing for smart electronic device applications due to their advantages of dual-function integration. Unfortunately, the synchronous dual-function evaluation and the essential reaction mechanism are ambiguous. Herein, we constructed a 3D WO3-x nanowire networks/fluorine-doped tin oxide (WO3-x NWNs/FTO) bifunctional electrode for ESCs by a solvothermal self-crystal seeding method. The synchronous correspondence relationship between the optical and electrochemical performances of the WO3-x NWNs/FTO electrode was explored using an operando spectra-electrochemical characterization method. It reveals an excellent areal capacity of 57.57 mF cm−2 with a high corresponding optical modulation (ΔT) of 85.05% and high optical-electrochemical cycling stability. Furthermore, the synergistic reaction mechanism between the Al3+ ion intercalation behavior and the surface pseudocapacitance reaction during electrochemical cycling is revealed utilizing in situ X-ray diffraction. Based on these results, an ESC device was constructed by pairing WO3-x/FTO as the cathode with V2O5 nanoflowers/FTO (V2O5 NFs/FTO) as the anode, which simultaneously deliver high capacity and large optical modulation. Moreover, the energy storage level of the ESC device could be visually monitored by rapid and reversible color transitions in real time. This work provides a promising pathway to developing multi-functional integrated smart supercapacitors.

The AMPIX electrochemical cell: a versatile apparatus forin situX-ray scattering and spectroscopic measurements

2012 ◽  
Vol 45 (6) ◽  
pp. 1261-1269 ◽  
Author(s):  
Olaf J. Borkiewicz ◽  
Badri Shyam ◽  
Kamila M. Wiaderek ◽  
Charles Kurtz ◽  
Peter J. Chupas ◽  
...  
Keyword(s):  
Electrochemical Cell ◽  
Function Analysis ◽  
Kinetic Studies ◽  
Spectroscopic Measurements ◽  
Battery Materials ◽  
X Ray ◽  
Complex Processes ◽  
Electrochemical Cycling ◽  
Ray Scattering

This article presents a versatile easy-to-use electrochemical cell suitable forin operando,in situmeasurements of battery materials during electrochemical cycling using a variety of X-ray techniques. Argonne's multi-purposein situX-ray (AMPIX) cell provides reliable electrochemical cycling over extended periods owing to the uniform stack pressure applied by rigid X-ray windows and the formation of a high-fidelity hermetic seal. The suitability of the AMPIX cell for a broad range of synchrotron-based X-ray scattering and spectroscopic measurements has been demonstrated with studies at eight Advanced Photon Source beamlines to date. Compatible techniques include pair distribution function analysis, high-resolution powder diffraction, small-angle scattering and X-ray absorption spectroscopy. These techniques probe a broad range of electronic, structural and morphological features relevant to battery materials. The AMPIX cell enables experiments providing greater insight into the complex processes that occur in operating batteries by allowing the electrochemical reactions to be probed at fine reaction intervals with greater consistency (within the charge–discharge cycle and between different methodologies) with potential for new time-dependent kinetic studies or studies of transient species. Representative X-ray and electrochemical data to demonstrate the functionality of the AMPIX cell are presented.

Real-time monitoring of stress development during electrochemical cycling of electrode materials for Li-ion batteries: overview and perspectives

2019 ◽  
Vol 7 (41) ◽  
pp. 23679-23726 ◽  
Author(s):  
Manoj K. Jangid ◽  
Amartya Mukhopadhyay
Keyword(s):  
Real Time ◽  
Electrode Materials ◽  
Electrochemical Potential ◽  
Li Ion Batteries ◽  
Stress Development ◽  
Electrochemical Cycling ◽  
Li Ion ◽  
Real Time Information ◽  
Time Information

Monitoring stress development in electrodes in-situ provides a host of real-time information on electro-chemo-mechanical aspects as functions of SOC and electrochemical potential.

scholarly journals The effect of electrochemical cycling on the strength of LiCoO2

2018 ◽  
Vol 102 (1) ◽  
pp. 372-381 ◽  
Author(s):  
Lin Feng ◽  
Xuefeng Lu ◽  
Tingting Zhao ◽  
Shen Dillon
Keyword(s):  
Electrochemical Cycling

Highly Sensitive and Wide Range Non-Enzymatic Electrochemical Detection of Cholesterol using Pencil Lead Electrodes

2021 ◽  
Author(s):  
Navaneeth Punnakkal ◽  
Jeethu Raveendran ◽  
Suneesh Punathil Vasu ◽  
Bipin G Nair ◽  
T G Satheesh Babu
Keyword(s):  
Electrochemical Detection ◽  
Highly Sensitive ◽  
Wide Range ◽  
Lead Electrodes ◽  
Pencil Lead
Sign in / Sign up

Export Citation Format

Share Document