Pseudocapacitive kinetics in rationally engineered nanostructures can deliver higher energy and power densities simultaneously. The present report reveals a high-performance all-solid-state flexible symmetric supercapacitor (FSSC) based on MoS-MoN nanowires deposited directly on stainless steel mesh (MoS-MoN/SSM) employing DC reactive magnetron co-sputtering technology. The abundance of synergistically coupled interfaces and junctions between MoS nanosheets and MoN nanostructures across the nanocomposite results in greater porosity, increased ionic conductivity, and superior electrical conductivity. Consequently, the FSSC device utilizing poly(vinyl alcohol)-sodium sulfate (PVA-NaSO) hydrogel electrolyte renders an outstanding cell capacitance of 252.09 F·g (44.12 mF·cm) at 0.25 mA·cm and high rate performance within a wide 1.3 V window. Dunn's and -value analysis reveals significant energy storage by surface-controlled capacitive and pseudocapacitive mechanisms. Remarkably, the symmetric device boosts tremendous energy density ∼10.36 μWh·cm (59.17 Wh·kg), superb power density ∼6.5 mW·cm (37.14 kW·kg), ultrastable long cyclability (∼93.7% after 10,000 galvanostatic charge-discharge cycles), and impressive mechanical flexibility at 60°, 90°, and 120° bending angles.
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http://dx.doi.org/10.1021/acsami.4c00067 | DOI Listing |
J Colloid Interface Sci
January 2025
School of Chemistry and Chemical Engineering, Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, Guangxi University (GXU), 100 Daxuedong Road, Xixiangtang District, Nanning 530004 China. Electronic address:
Porous carbons with large surface area (>3000 m/g) and heteroatom dopants have shown great promise as electrode materials for zinc ion hybrid capacitors. Centralized mesopores are effective to accelerate kinetics, and edge nitrogen can efficiently enhance pseudocapacitive capability. It is a great challenge to engineer centralized mesopores and edge nitrogen in large-surface-area porous carbons.
View Article and Find Full Text PDFSci Rep
January 2025
UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria, South Africa.
This research successfully synthesized semiconductive magnesioferrite (MgFeO) nanomaterials using a green chemistry method that utilizes the natural extract of Moringa olefeira serving as both a reducing and oxidizing agent. The optical characteristics and crystalline structure of the MgFeO nanomaterials were analysed using photoluminescence, diffuse reflectance spectroscopy, and X-ray diffraction. Additionally, Fourier transform infrared spectroscopy provided valuable insights into the chemical bonding and composition.
View Article and Find Full Text PDFHeliyon
January 2025
Sharif Institute of Energy, Water and Environment, Sharif University of Technology, Azadi Avenue, P.O.Box11365-9465, Tehran, Iran.
Manganese dioxide (MnO) is a well-known pseudocapacitive material that has been extensively studied and highly regarded, especially in supercapacitors, due to its remarkable surface redox behavior, leading to a high specific capacitance. However, its full potential is impeded by inherent characteristics such as its low electrical conductivity, dense morphology, and hindered ionic diffusion, resulting in limited rate capability in supercapacitors. Addressing this issue often requires complicated strategies and procedures, such as designing sophisticated composite architectures.
View Article and Find Full Text PDFAdv Sci (Weinh)
January 2025
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, Shaanxi Key Laboratory for Advanced Energy Devices, Shaanxi Engineering Lab for Advanced Energy Technology, School of Materials Science and Engineering, Shaanxi Normal University, Xi'an, 710119, P. R. China.
Understanding the oxygen evolution reaction (OER) mechanism is pivotal for improving the overall efficiency of water electrolysis. Despite methylammonium lead halide perovskites (MAPbX) have shown promising OER performance due to their soft-lattice nature that allows lattice-oxygen oxidation of active α-PbO layer surface, the role of A-site MA or X-site elements in the electrochemical reconstruction and OER mechanisms has yet to be explored. Here, it is demonstrated that the OER mechanism of perovskite@zeolite composites is intrinsically dominated by the A-site group of lead-halide perovskites, while the type of X-site halogen is crucial for the reconstruction kinetics of the composites.
View Article and Find Full Text PDFAdv Mater
January 2025
Center for Renewable Energy and Storage Technologies (CREST), Physical Science and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Kingdom of Saudi Arabia.
The sluggish anodic oxygen evolution reaction (OER) in proton exchange membrane (PEM) electrolysis necessitates applied bias to facilitate electron transfer as well as bond cleavage and formation. Traditional electrocatalysis focuses on analyzing the effects of electron transfer, while the role of charge accumulation induced by the applied overpotential has not been thoroughly investigated. To explore the influence mechanism of bias-driven charge accumulation, capacitive Mn is incorporated into IrO to regulate the local electronic structure and the adsorption behavior.
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