Search

This work describes the development and performance of a symmetric micro-supercapacitor made of nanostructured electrodes based on silicon nanowires (SiNWs) deposited using chemical vapor deposition (CVD) on silicon substrates. The performance of the SiNWs micro-supercapacitor employing an aprotic ionic liquid (N-methyl-N-propylpyrrolidinium bis(trifluoromethylsulfonyl)imide) (PYR 13 TFSI) as an electrolyte was able to deliver a maximal power density of 182 mW cm −2 and a specific energy of 190 μJ cm −2 operating at a wide cell voltage of 4 V with a quasi-ideal capacitive behavior. The lifetime of the device exhibited a remarkable electrochemical stability retaining 75% of the initial capacitance after several million galvanostatic charge–discharge cycles at a high current density of 1 mA cm −2 . Furthermore, a coulombic efficiency of approximately 99% was obtained after galvanostatic cycling test without structural degradation on the morphology of SiNWs. [ABSTRACT FROM AUTHOR]

Developing flexible solid-state micro-supercapacitors with large potential window is crucial for many technologies. The present study focuses on the synthesis and elaboration of quasi-solid-state (QSS) electrolytes with an electrochemical stability greater than 3.0 V based on functionalized polysiloxane. Their electrochemical behavior was studied with silicon nanowires electrodes. The polysiloxane was functionalized with both ammonium and cross-linkable functions. The nanostructured electrodes were impregnated with a mixture of ionic liquid and functionalized polysiloxane. The crosslinking of the polymer electrolyte was then performed by thermal curing directly within the nanostructured electrodes. The quasi-solid system exhibits very high stability upon galvanostatic cycling i.e. during 100 000 cycles with a cell potential of 3.0 V only a capacitance loss of 2.10−5% per cycle was registered. The performance of this QSS with safe electrolyte is remarkable. [Display omitted] [ABSTRACT FROM AUTHOR]

Silicon nanotrees (SiNTrs) have been grown by Chemical Vapor Deposition (CVD) via gold catalysis and a three steps process: trunks and branches growth are separated by a new gold catalyst deposition. The influence of growth conditions and the second gold catalyst deposition method on SiNTrs morphology are investigated. SiNTrs based electrodes show a capacitive behavior and better capacitance than the corresponding silicon nanowires (SiNWs) electrode. Electrode capacitance is increased up to 900 µF cm-2, i.e. 150 fold higher than for bulk silicon. Micro-supercapacitors with SiNTrs electrodes have a remarkable stability (only 1.2% loses of their initial capacitance after more than one million cycles). The use of an ionic liquid based electrolyte leads to a high maximum power density (around 225 mW cm-2) which is competitive with Onion Like Carbon based micro-supercapacitors. [ABSTRACT FROM AUTHOR]

Dielectric materials have been used for decades for energy applications where their insulation and polarizability properties are critical. In the energy storage field, most material scientists envision high-k dielectric layers in contact with an active material only as an insulating passivation layer. In microelectronics, this concept has been modified with the study of dielectrics at nanoscale level revealing interesting properties scarcely known by other fields. We propose to reconsider the vision of high-k dielectric materials for energy at nanoscale specifically. Based on microelectronic measurement techniques and nanometric control of dielectric thickness by Atomic Layer Deposition (ALD), an ultra-thin pinhole-free alumina (Al 2 O 3) layer on a silicon nanowire (SiNW) is shown to display thickness dependent tunneling electrical conduction. This result brings a new light on this material class in the energy field and allows original approaches toward achieving scientific leaps. As an illustrative application, a silicon based micro-supercapacitor (MSC) protected by 3 nm of alumina dielectric layer exhibits Electrical Double Layer Capacitance (EDLC) by means of tunneling current in aqueous electrolyte, an unprecedented result for this material, with outstanding lifetime capacity retaining 99% of its initial capacitance after 2 million cycles. Extended to multiple energy materials, such method could lead to notable progress. [Display omitted] [ABSTRACT FROM AUTHOR]