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Rechargeable aqueous zinc-ion batteries (AZIBs) have become a viable option in electrochemical energy storage systems (EESS) owing to their inherent safety features and economic friendliness. Nonetheless, creating suitable cathode materials for AZIBs with high structural stability, good rate performance, and great capacity remains a significant challenge. Polyoxometalate (POM)-based nanohybrid materials have shown promising results in high cycling stability and great specific capacity. However, POMs susceptible to electrolyte dissolution and the sluggish Zn-ion (Zn) kinetics have significantly hampered their electrochemical performance as cathodes for AZIBs. Herein, we present a Keggin POM, K[PWO]·HO (KPW), anchored on hydroxyl (OH)-functionalized single-walled carbon nanotubes (SWOH) that were fabricated via a facile ultrasonication procedure. Employed as cathodes for AZIBs, the optimal KPW/SWOH feature exhibited remarkable electrochemical performance. The system satisfied the Zn storage, achieving a reversible discharge capacity of 183 mAh g at a high current density of 5C with a flat and long discharge plateau after 160 cycles. The perfect synergistic contribution of the pseudocapacitive nature of the super-reduced state of KPW and the electron-conductive network of SWOH was attributed to this exceptional electrochemical performance. Furthermore, the presence of oxygen in SWOH enhanced the transfer kinetics of electrons and smooth Zn diffusion while lowering the Zn migration energy barrier by providing more accessible active sites. This demonstrates remarkable promise in fabricating robust electrode materials optimized for integration within aqueous battery systems that pave the way for further research into POM-based materials for EESS.
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http://dx.doi.org/10.1021/acsomega.5c05213 | DOI Listing |
Chem Commun (Camb)
September 2025
Department of Applied Chemistry, School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China.
Herein, 1,3,5-benzenetricarboxylate (BTC) intercalation and oxygen vacancy engineering are proposed to enhance the electrochemical performance of layered double hydroxide (LDH) nanosheets. The optimized LDH exhibits a remarkable capacity of 426 mAh g at 3 A g and 70% capacity retention after 15 000 cycles, attributed to improved ion transport, abundant active sites, and structural stability.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Key Laboratory of Special Functional Materials for Ecological Environment and Information (Ministry of Education), School of Material Science and Engineering, Hebei University of Technology, Tianjin 300130, P. R. China.
High-performance, low-cost electrocatalysts are essential for freshwater-independent seawater electrolysis. We design a SWCNT-supported (FeCoNiMnCr)O high-entropy spinel oxide by a hydrothermal method and air-firing, where the conductive network enhances charge transfer and active site exposure. The catalyst achieves 282 mV@10 mA cm with 100 h stability in alkaline seawater.
View Article and Find Full Text PDFiScience
September 2025
State Key Laboratory of Advanced Marine Materials, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China.
Super austenitic stainless steels (SASS) face challenges like galvanic corrosion and antibacterial performance when welded to carbon steel (Q235) in marine environments. This study demonstrates that adding 1.0 wt% cerium (Ce) to SASS refines the heat-affected zone (HAZ) grain structure (from 7 μm to 2 μm), suppresses detrimental σ-phase precipitation, and forms a dense oxide film.
View Article and Find Full Text PDFNatl Sci Rev
September 2025
College of Chemistry, Huazhong Agricultural University, Wuhan 430070, China.
The stress distribution in Li metal strongly affects the interfacial Li-ion diffusion, thereby influencing the morphology of plated Li and the performance of the battery. Here, we report a mechano-electrochemical coupling strategy that utilizes an arched structured carbon aerogel to achieve stable Li-plating/stripping electrochemistry. The arch-structured carbon aerogel can actively regulate stress distributions in response to the compressive stresses induced by Li deposition, generating the transition of stress from compressive on the convex surface to tensile on the concave surface, which can effectively promote the Li-migration kinetics and thus suppress the non-uniform deposition of Li.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Chemical Resource Engineering, Beijing Key Laboratory of Electrochemical Process and Technology of Materials, Beijing University of Chemical Technology, Beijing, 10029, P.R. China.
Lithium metal batteries (LMBs) have emerged as the most promising candidate for next-generation high-energy-density energy storage systems. However, their practical implementation is hindered by the inability of conventional carbonate electrolytes to simultaneously stabilize the lithium metal anode and LiNiCoMnO (NCM811) cathode interfaces, particularly under extreme operating conditions. Herein, we present a transformative molecular design using 3,5-difluorophenylboronic acid neopentyl glycol ester (DNE), which uniquely integrates dual interfacial stabilization mechanisms in a single molecule.
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