The Effect of Crystallinity on the Rapid Pseudocapacitive Response of Nb2O5

Capacitive energy storage offers several attractive properties compared to batteries, including higher power, faster charging, and a longer cycle life. A key limitation to this electrochemical energy‐storage approach is its low energy density and, for this reason, there is considerable interest in identifying pseudocapacitor materials where faradaic reactions are used to achieve greater charge storage. This paper reports on the electrochemical properties of Nb₂O₅ and establishes that crystalline phases of the material undergo fast faradaic reactions that lead to high specific capacitance in short charging times. In particular, the specific capacitance for the orthorhombic phase at infinite sweep rate reaches ≈400 F g^?1, which exceeds that of birnessite MnO₂ in nonaqueous electrolyte and is comparable to RuO₂ at the same extrapolated rate. The specific capacitances of the orthorhombic and pseudohexagonal phases are much greater than that of the amorphous phase, suggesting that the faradaic reactions which lead to additional capacitive energy storage are associated with Li⁺ insertion along preferred crystallographic pathways. The ability for Nb₂O₅ to store charge at high rates despite its wide bandgap and low electronic conductivity is very different from what is observed with other transition metal oxides.     

Quantifying the Role of Nanotubes in Nano:Nano Composite Supercapacitor Electrodes

Many promising supercapacitor electrode materials have high resistivity and require conductive additives to function effectively. However, the detailed role of the additive is not understood. Here, this question is resolved by applying a quantitative model for resistance‐limited supercapacitor electrodes to Co(OH)₂‐nanosheet/carbon nanotube composites. Without nanotubes, theory predicts and experiments show that while the low‐rate capacitance increases linearly with electrode thickness, the high rate capacitance decreases with thickness due to slow charging. Experiments supported by theory show that nanotube addition has two effects. First, the nanotube network effectively distributes charge, increasing the intrinsic electrode performance to the limit associated with its accessible surface area. Second, at high‐rate, the increased electrode conductivity shifts the rate‐limiting resistance from electrode to electrolyte, thus removing the thickness‐dependent capacitance falloff. Furthermore, the analysis quantifies the out‐of‐plane conductivity of the nanotube network, identifies the cross‐over from resistance‐limited to diffusion‐limited behavior, and allows full electrode modeling, facilitating rational design.     

Controlled Synthesis and Energy Applications of One‐Dimensional Conducting Polymer Nanostructures: An Overview

The past decade has witnessed increasing attention in the synthesis, properties, and applications of one‐dimensional (1D) conducting polymer nanostructures. This overview first summarizes the synthetic strategies for various 1D nanostructures of conjugated polypyrrole (PPy), polyaniline (PANI), polythiophene (PTh), poly(p‐phenylenevinylene) (PPV) and derivatives thereof. By using template‐directed or template‐free methods, nanoscale rods, wires/fibers, belts/ribbons, tubes, arrays, or composites have been successfully synthesized. With their unique structures and advantageous characteristics (e.g., high conductivity, high carrier mobility, good electrochemical activity, large specific surface area, short and direct path for charge/ion transportation, good mechanical properties), 1D conducting polymer nanostructures are demonstrated to be very useful for energy applications. Next, their applications in solar cells, fuel cells, rechargeable lithium batteries, and electrochemical supercapacitors are highlighted, with a strong emphasis on recent literature examples. Finally, this review ends with a summary and some perspectives on the challenges and opportunities in this emerging area of research.     

Stretchable Supercapacitors as Emergent Energy Storage Units for Health Monitoring Bioelectronics

Emerging health monitoring bioelectronics require energy storage units with improved stretchability, biocompatibility, and self‐charging capability. Stretchable supercapacitors hold great potential for such systems due to their superior specific capacitances, power densities, and tissue‐conforming properties, as compared to both batteries and conventional capacitors. Despite the rapid progress that has been made in supercapacitor research, practical applications in health monitoring bioelectronics have yet to be achieved, requiring innovations in materials, device configurations, and fabrications tailored for such applications. In this review, the progress in stretchable supercapacitor‐powered health monitoring bioelectronics is summarized and the required specifications of supercapacitors for different types of application settings with varying demands on biocompatibility are discussed, including nontouching wearables, skin‐touching wearables, skin‐conforming wearables, and implantables. The perspective of this review is then broadened to focus on integration of stretchable supercapacitors in bioelectronics and aspects of energy harvesting and sensing. Finally further insights on the existing challenges in this developing field and potential solutions are provided.     

Manganese Oxide/Carbon Aerogel Composite: an Outstanding Supercapacitor Electrode Material

Manganese oxide/carbon aerogel composite electrodes are prepared by a self‐limiting anodic‐electrochemical deposition of manganese oxide into a binder‐enriched carbon aerogel layer, drop‐cast on a graphite substrate, using 0.1 M Mn(CH₃COO)₂·4H₂O as the electrolyte. Manganese oxide grows in the form of thin nanofibers along the backbone of the carbon aerogel, leaving adequate working space for the electrolyte and enabling a fuller extent of the utilization of the manganese oxide to make the composite an outstanding supercapacitor electrode material. The manganese oxide is determined to be Mn₃O₄ with the Raman spectroscopy and high‐resolution transmission electron microscopy. The rectangularity of the cyclic‐voltammogram loops of the composite electrode is excellent and remains that way for scan rates up to a very‐high value of 500 mV s^?1, indicating extremely good redox reversibility and cycle efficiency. At a scan rate of 25 mV s^?1, the specific capacitance, as measured in 0.5 M Na₂SO₄ for a potential window of 0.1–0.9 V vs. Ag/AgCl, reaches a maximum value of 503 F g^?1 and experiences only a negligible decay of less than 1% at the 6000th cycle, implying an extraordinary cycling stability. The cycling efficiency is as high as 98% at a current density of 8 A g^?1 cm^?2, showing an almost‐ideal capacitive behavior. The power density reaches 48.5 kW kg^?1 and the energy density 21.6 W h kg^?1 at a scan rate of 500 mV s^?1, well above the specifications of current state‐of‐the‐art supercapacitors.