Investigation of Pseudocapacitive Charge-Storage Reaction of MnO[sub 2]⋅nH[sub 2]O Supercapacitors in Aqueous Electrolytes

2006 ◽  
Vol 153 (7) ◽  
pp. A1317 ◽  
Author(s):  
Shin-Liang Kuo ◽  
Nae-Lih Wu
Keyword(s):  
Charge Storage ◽  
Aqueous Electrolytes

scholarly journals The Role of Al3+-Based Aqueous Electrolytes in the Charge Storage Mechanism of MnOx Cathodes

2020 ◽  
Author(s):  
Véronique Balland ◽  
Mickaël Mateos ◽  
Kenneth D. Harris ◽  
Benoit Limoges
Keyword(s):  
Manganese Oxide ◽  
Critical Analysis ◽  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Storage Mechanism ◽  
Main Charge ◽  
Charge Storage Mechanism ◽  
The Subject

<p>Rechargeable aqueous aluminium batteries are the subject of growing interest, but the charge storage mechanisms at manganese oxide-based cathodes remain poorly understood with as many mechanisms as studies. Here, we use an original <i>in situ</i> spectroelectrochemical methodology to unambiguously demonstrate that the reversible proton-coupled MnO<sub>2</sub>-to-Mn<sup>2+</sup> conversion is the main charge storage mechanism occurring at MnO<sub>2</sub> cathodes over a range of slightly acidic Al<sup>3+</sup>-based aqueous electrolytes. In Zn/MnO<sub>2</sub> assemblies, this mechanism is associated with high gravimetric capacity and discharge potentials, up to 560 mAh·g<sup>-1</sup> and 1.76 V respectively, attractive efficiencies (<i>CE</i> > 98.5 % and <i>EE</i> > 80%) and excellent cyclability (> 750 cycles at 10 A·g<sup>-1</sup>). Finally, we conducted a critical analysis of the data previously published on MnO<sub>x</sub> cathodes in Al<sup>3+</sup>-based aqueous electrolytes to conclude on a universal charge storage mechanism, <i>i.e.</i>, the reversible electrodissolution/electrodeposition of MnO<sub>2</sub>.<i></i></p>

The Charge Storage Mechanism of MnCO 3 in Aqueous Electrolytes

2020 ◽  
Vol 5 (17) ◽  
pp. 5316-5322
Author(s):  
Vishnu Vardhan Palem ◽  
Mustapha Balarabe Idris ◽  
Thiruvenkatam Subramaniam ◽  
Devaraj Sappani
Keyword(s):  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Storage Mechanism ◽  
Charge Storage Mechanism

scholarly journals On the unsuspected role of multivalent metal ions on the charge storage of a metal oxide electrode in mild aqueous electrolytes

2019 ◽  
Vol 10 (38) ◽  
pp. 8752-8763 ◽  
Author(s):  
Yee-Seul Kim ◽  
Kenneth D. Harris ◽  
Benoît Limoges ◽  
Véronique Balland
Keyword(s):  
Metal Oxide ◽  
Metal Ions ◽  
Metal Ion ◽  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Electron Charge ◽  
Oxide Electrode ◽  
Metal Ion Complexes ◽  
Multivalent Metal

The hidden role of hexaaquo metal ion complexes in the proton-coupled electron charge storage at a metal oxide electrode.

A proton-hopping charge storage mechanism of ionic one-dimensional coordination polymers for high-performance supercapacitors

2017 ◽  
Vol 53 (86) ◽  
pp. 11786-11789 ◽  
Author(s):  
Nutthaphon Phattharasupakun ◽  
Juthaporn Wutthiprom ◽  
Surasak Kaenket ◽  
Thana Maihom ◽  
Jumras Limtrakul ◽  
...  
Keyword(s):  
Coordination Polymer ◽  
Coordination Polymers ◽  
High Performance ◽  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Proton Conducting ◽  
One Dimensional ◽  
Storage Mechanism ◽  
Charge Storage Mechanism

A proton-conducting coordination polymer of Zn2+ phosphate and protonated imidazole has been used as a novel supercapacitor material in aqueous electrolytes.

scholarly journals On the Unsuspected Role of Multivalent Metal Ions on the Charge Storage of a Metal Oxide Electrode in Mild Aqueous Electrolytes

2019 ◽  
Author(s):  
Yee-Seul Kim ◽  
Kenneth D. Harris ◽  
Benoit Limoges ◽  
Véronique Balland
Keyword(s):  
Metal Oxide ◽  
Metal Ions ◽  
Chemical Nature ◽  
Aqueous Electrolyte ◽  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Oxide Electrode ◽  
Multivalent Metal

<p>The main objective of the work is to elucidate and rationalize the role played by an Al<sup>3+</sup>-based aqueous electrolyte on the charge accumulated in model mesoporous TiO<sub>2</sub> electrodes and to decipher the chemical nature of the inserting cation.<br></p>

scholarly journals The Role of Al3+-Based Aqueous Electrolytes in the Charge Storage Mechanism of MnOx Cathodes

2020 ◽  
Author(s):  
Véronique Balland ◽  
Mickaël Mateos ◽  
Kenneth D. Harris ◽  
Benoit Limoges
Keyword(s):  
Manganese Oxide ◽  
Critical Analysis ◽  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Storage Mechanism ◽  
Main Charge ◽  
Charge Storage Mechanism ◽  
The Subject

<p>Rechargeable aqueous aluminium batteries are the subject of growing interest, but the charge storage mechanisms at manganese oxide-based cathodes remain poorly understood with as many mechanisms as studies. Here, we use an original <i>in situ</i> spectroelectrochemical methodology to unambiguously demonstrate that the reversible proton-coupled MnO<sub>2</sub>-to-Mn<sup>2+</sup> conversion is the main charge storage mechanism occurring at MnO<sub>2</sub> cathodes over a range of slightly acidic Al<sup>3+</sup>-based aqueous electrolytes. In Zn/MnO<sub>2</sub> assemblies, this mechanism is associated with high gravimetric capacity and discharge potentials, up to 560 mAh·g<sup>-1</sup> and 1.76 V respectively, attractive efficiencies (<i>CE</i> > 98.5 % and <i>EE</i> > 80%) and excellent cyclability (> 750 cycles at 10 A·g<sup>-1</sup>). Finally, we conducted a critical analysis of the data previously published on MnO<sub>x</sub> cathodes in Al<sup>3+</sup>-based aqueous electrolytes to conclude on a universal charge storage mechanism, <i>i.e.</i>, the reversible electrodissolution/electrodeposition of MnO<sub>2</sub>.<i></i></p>

scholarly journals Accessing the Two-Electron Charge Storage Capacity of MnO2 in Mild Aqueous Electrolytes

2020 ◽  
Author(s):  
Mickaël Mateos ◽  
Nikolina Makivic ◽  
Yee-Seul Kim ◽  
Benoit Limoges ◽  
Véronique Balland
Keyword(s):  
High Performance ◽  
Coulombic Efficiency ◽  
Rechargeable Batteries ◽  
Water Soluble ◽  
High Rate ◽  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Energy Storage Devices ◽  
Common View ◽  
Wide Range

<p>Rechargeable batteries based on MnO2 cathodes, able to operate in mild aqueous electrolytes, have attracted remarkable attention due to their appealing features for the design of low-cost stationary energy storage devices. However, the charge/discharge mechanism of MnO2 in such media is still unclear and a matter of debate. Here, an in-depth quantitative spectroelectrochemical analysis of MnO2 thin-films provides a set of important new mechanistic insights. A major finding is that charge storage occurs through the reversible two electron faradaic conversion of MnO2 into water-soluble Mn2+ in the presence of a wide range of weak Brønsted acids, including the [Zn(H2O)6]2+ or [Mn(H2O)6]2+ complexes commonly present in aqueous Zn/MnO2 batteries. Furthermore, it is evidenced that buffered electrolytes loaded with Mn2+ are ideal to achieve highly reversible conversion of MnO2 with both high gravimetric capacity and remarkably stable charging/discharging potentials. In the most favorable case, a record gravimetric capacity of 450 mA·h·g-1 was obtained at a high rate of 1.6 A·g-1, with a coulombic efficiency close to 100% and a MnO2 utilization of 84%. Overall, the present results challenge the common view on MnO2 charge storage mechanism in mild aqueous electrolytes and underline the benefit of buffered electrolytes for high-performance rechargeable aqueous batteries.<br></p>

scholarly journals Accessing the Two-Electron Charge Storage Capacity of MnO2 in Mild Aqueous Electrolytes

2020 ◽  
Author(s):  
Mickaël Mateos ◽  
Nikolina Makivic ◽  
Yee-Seul Kim ◽  
Benoit Limoges ◽  
Véronique Balland
Keyword(s):  
High Performance ◽  
Coulombic Efficiency ◽  
Rechargeable Batteries ◽  
Water Soluble ◽  
High Rate ◽  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Energy Storage Devices ◽  
Common View ◽  
Wide Range

<p>Rechargeable batteries based on MnO2 cathodes, able to operate in mild aqueous electrolytes, have attracted remarkable attention due to their appealing features for the design of low-cost stationary energy storage devices. However, the charge/discharge mechanism of MnO2 in such media is still unclear and a matter of debate. Here, an in-depth quantitative spectroelectrochemical analysis of MnO2 thin-films provides a set of important new mechanistic insights. A major finding is that charge storage occurs through the reversible two electron faradaic conversion of MnO2 into water-soluble Mn2+ in the presence of a wide range of weak Brønsted acids, including the [Zn(H2O)6]2+ or [Mn(H2O)6]2+ complexes commonly present in aqueous Zn/MnO2 batteries. Furthermore, it is evidenced that buffered electrolytes loaded with Mn2+ are ideal to achieve highly reversible conversion of MnO2 with both high gravimetric capacity and remarkably stable charging/discharging potentials. In the most favorable case, a record gravimetric capacity of 450 mA·h·g-1 was obtained at a high rate of 1.6 A·g-1, with a coulombic efficiency close to 100% and a MnO2 utilization of 84%. Overall, the present results challenge the common view on MnO2 charge storage mechanism in mild aqueous electrolytes and underline the benefit of buffered electrolytes for high-performance rechargeable aqueous batteries.<br></p>

Charge storage mechanism and degradation of P2-type sodium transition metal oxides in aqueous electrolytes

2018 ◽  
Vol 6 (44) ◽  
pp. 22266-22276 ◽  
Author(s):  
Shelby Boyd ◽  
Rohan Dhall ◽  
James M. LeBeau ◽  
Veronica Augustyn
Keyword(s):  
Transition Metal ◽  
Metal Oxides ◽  
Transition Metal Oxides ◽  
Structural Changes ◽  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Storage Mechanism ◽  
Charge Storage Mechanism

P2-type sodium transition metal oxides undergo water-driven structural changes that strongly affect electrochemical charge storage in aqueous electrolytes.

scholarly journals Accessing the Two‐Electron Charge Storage Capacity of MnO 2 in Mild Aqueous Electrolytes

2020 ◽  
Vol 10 (23) ◽  
pp. 2000332 ◽  
Author(s):  
Mickaël Mateos ◽  
Nikolina Makivic ◽  
Yee‐Seul Kim ◽  
Benoît Limoges ◽  
Véronique Balland
Keyword(s):  
Storage Capacity ◽  
Charge Storage ◽  
Aqueous Electrolytes ◽  
Electron Charge
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