Electrochemical capacitors, also called supercapacitors, store energy using either ion adsorption (electrochemical double layer capacitors) or fast surface redox reactions (pseudo-capacitors). They can complement or replace batteries in electrical energy storage and harvesting applications, when high power delivery or uptake is needed. A notable improvement in performance has been achieved through recent advances in understanding charge storage mechanisms and the development of advanced nanostructured materials. The discovery that ion desolvation occurs in pores smaller than the solvated ions has led to higher capacitance for electrochemical double layer capacitors using carbon electrodes with subnanometre pores, and opened the door to designing high-energy density devices using a variety of electrolytes. Combination of pseudo-capacitive nanomaterials, including oxides, nitrides and polymers, with the latest generation of nanostructured lithium electrodes has brought the energy density of electrochemical capacitors closer to that of batteries. The use of carbon nanotubes has further advanced micro-electrochemical capacitors, enabling flexible and adaptable devices to be made. Mathematical modelling and simulation will be the key to success in designing tomorrow's high-energy and high-power devices.

https://hal.archives-ouvertes.fr/hal-02417326/document

Materials for electrochemical capacitors

In this critical review, metal oxides-based materials for electrochemical supercapacitor (ES) electrodes are reviewed in detail together with a brief review of carbon materials and conducting polymers. Their advantages, disadvantages, and performance in ES electrodes are discussed through extensive analysis of the literature, and new trends in material development are also reviewed. Two important future research directions are indicated and summarized, based on results published in the literature: the development of composite and nanostructured ES materials to overcome the major challenge posed by the low energy density of ES (476 references).

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A review of electrode materials for electrochemical supercapacitors

The interest in nanoscale materials stems from the fact that new properties are acquired at this length scale and, equally important, that these properties * To whom correspondence should be addressed. Phone, 404-8940292; fax, 404-894-0294; e-mail, mostafa.el-sayed@ chemistry.gatech.edu. † Case Western Reserve UniversitysMillis 2258. ‡ Phone, 216-368-5918; fax, 216-368-3006; e-mail, burda@case.edu. § Georgia Institute of Technology. 1025 Chem. Rev. 2005, 105, 1025−1102

Chemistry and properties of nanocrystals of different shapes.

Electrochemical energy storage technology is based on devices capable of exhibiting high energy density (batteries) or high power density (electrochemical capacitors). There is a growing need, for current and near-future applications, where both high energy and high power densities are required in the same material. Pseudocapacitance, a faradaic process involving surface or near surface redox reactions, offers a means of achieving high energy density at high charge–discharge rates. Here, we focus on the pseudocapacitive properties of transition metal oxides. First, we introduce pseudocapacitance and describe its electrochemical features. Then, we review the most relevant pseudocapacitive materials in aqueous and non-aqueous electrolytes. The major challenges for pseudocapacitive materials along with a future outlook are detailed at the end.

https://hal.archives-ouvertes.fr/hal-01171774/document

Pseudocapacitive oxide materials for high-rate electrochemical energy storage

Since the discovery of mechanically exfoliated graphene in 2004, research on ultrathin two-dimensional (2D) nanomaterials has grown exponentially in the fields of condensed matter physics, material science, chemistry, and nanotechnology. Highlighting their compelling physical, chemical, electronic, and optical properties, as well as their various potential applications, in this Review, we summarize the state-of-art progress on the ultrathin 2D nanomaterials with a particular emphasis on their recent advances. First, we introduce the unique advances on ultrathin 2D nanomaterials, followed by the description of their composition and crystal structures. The assortments of their synthetic methods are then summarized, including insights on their advantages and limitations, alongside some recommendations on suitable characterization techniques. We also discuss in detail the utilization of these ultrathin 2D nanomaterials for wide ranges of potential applications among the electronics/optoelectronics, electrocat...

Recent Advances in Ultrathin Two-Dimensional Nanomaterials

Preparation of Ruthenic Acid Nanosheets and Utilization of Its Interlayer Surface for Electrochemical Energy Storage

Electrochemical impedance spectroscopy was conducted on a series of hydrous ruthenium oxides, RuO(2).xH(2)O, (x = 0.5, 0.3, 0) and a layered ruthenic acid hydrate (H(0.2)RuO(2.1).nH(2)O) in order to evaluate their protonic and electronic conduction. The capacitor response frequency was observed at lower frequency for RuO(2).xH(2)O with higher water content, which was suggested to be due to electrolyte exhaustion within the film and/or utilization of hydrated interparticle micropores that have high ionic resistance. Analysis of the impedance data indicated that the charge-transfer resistance through the film is not significantly affected by the water content in RuO(2).xH(2)O, and the capacitor frequency response is dominated by the protonic conduction. The capacitor response frequency of layered H(0.2)RuO(2.1).nH(2)O was comparable to RuO(2).0.5H(2)O. The high specific capacitance at low frequency for layered H(0.2)RuO(2.1).nH(2)O is attributed to the utilization of the expandable hydrous interlayer, which accounts for the ionic conduction. The present results demonstrate the importance of hydrous regions (either interparticle or interlayer) to allow appreciable protonic conduction for high energy and high power electrochemical capacitors.

Proton and electron conductivity in hydrous ruthenium oxides evaluated by electrochemical impedance spectroscopy: the origin of large capacitance.

Size effects of platinum particles on the electroreduction of oxygen

Charge storage mechanism of nanostructured anhydrous and hydrous ruthenium-based oxides

Carbon‐supported binary PtRu electrocatalysts were prepared by coimpregnation using ethanolic solutions of as the Pt source, various Ru sources [, , and ], and carbon black by thermal decomposition under reducing conditions, and their structure, morphology, and electrocatalytic properties were investigated. X‐ray diffraction analysis and high resolution scanning electron microscopy indicated that the use of Cl‐free Ru sources, i.e., or afforded highly dispersed and uniform PtRu nanoparticles. Surface area measurements conducted by electro‐oxidation of preadsorbed carbon monoxide indicated that the use of as the Ru source yielded high surface area catalysts. In terms of the surface‐area specific current density (current density normalized by the specific surface area of PtRu metal obtained from preadsorbed CO electro‐oxidation measurements), the electrocatalytic activity of and were equal. PtRu/C electrocatalysts prepared from ethanolic solutions of resulted in high mass‐specific activity toward methanol oxidation, with mass‐specific current density as high as at 500 mV. The efficiency of PtRu/C electrodes is discussed based on the significance of the use of Cl‐free Ru sources. © 2000 The Electrochemical Society. All rights reserved.

https://iopscience.iop.org/article/10.1149/1.1394080/pdf

Yasushi Murakami

Papers

Preparation of Ruthenic Acid Nanosheets and Utilization of Its Interlayer Surface for Electrochemical Energy Storage

Proton and electron conductivity in hydrous ruthenium oxides evaluated by electrochemical impedance spectroscopy: the origin of large capacitance.

Size effects of platinum particles on the electroreduction of oxygen

Charge storage mechanism of nanostructured anhydrous and hydrous ruthenium-based oxides

Effect of Structure of Carbon‐Supported PtRu Electrocatalysts on the Electrochemical Oxidation of Methanol