Potassium-ion batteries (PIBs) have received much attention as next-generation energy storage systems because of their abundance, low cost, and slightly lower standard redox potential than lithium-ion batteries (LIBs). Nevertheless, they still face great challenges in the design of the best electrode materials for applications. Herein, we have successfully synthesized nano-sized CoSe encapsulated by N-doped reduced graphene oxide (denoted as CoSe@N-rGO) by a direct one-step hydrothermal method, including both orthorhombic and cubic CoSe phases. The CoSe@N-rGO anodes exhibit a high reversible capacity of 599.3 mA h g at 0.05 A g in the initial cycle, and in particular, they also exhibit a cycling stability of 421 mA h g after 100 cycles at 0.2 A g. Density functional theory (DFT) calculations show that CoSe with N-doped carbon can greatly accelerate electron transfer and enhance the rate performance. In addition, the intrinsic causes of the higher electrochemical performance of orthorhombic CoSe than that of cubic CoSe are also discussed.
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http://dx.doi.org/10.1039/d2ra03608h | DOI Listing |
Nat Commun
December 2024
Department of Chemical Engineering, Electrochemical Innovation Lab, University College London, London, UK.
High-temperature proton exchange membrane fuel cells (HT-PEMFCs) offer solutions to challenges intrinsic to low-temperature PEMFCs, such as complex water management, fuel inflexibility, and thermal integration. However, they are hindered by phosphoric acid (PA) leaching and catalyst migration, which destabilize the critical three-phase interface within the membrane electrode assembly (MEA). This study presents an innovative approach to enhance HT-PEMFC performance through membrane modification using picosecond laser scribing, which optimises the three-phase interface by forming a graphene-like structure that mitigates PA leaching.
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December 2024
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Nanjing Forestry University, Nanjing, 210037, China.
Carbon nanomaterials show outstanding promise as electrocatalysts for hydrogen peroxide (HO) synthesis via the two-electron oxygen reduction reaction. However, carbon-based electrocatalysts that are capable of generating HO at industrial-level current densities (>300 mA cm) with high selectivity and long-term stability remain to be discovered. Herein, few-layer boron nanosheets are in-situ introduced into a porous carbon matrix, creating a metal-free electrocatalyst (B-C) with HO production rates of industrial relevance in neutral or alkaline media.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
Department of Chemistry and Research Institute of Molecular Alchemy, Gyeongsang National University, Jinju, 52828, South Korea.
To address the ongoing demand for high-performance energy storage devices, it is crucial to identify new electrode materials. Lithium-ion batteries (LIBs) store energy via the electrochemical redox process, so their electrode materials should have reversible redox properties for rechargeability. On that note, redox-active metal complexes are explored as innovative electrode materials for LIBs.
View Article and Find Full Text PDFSmall
December 2024
Songshan Lake Materials Laboratory (SLAB), Dongguan, 523808, P. R. China.
Aqueous zinc-ion batteries (AZIBs) stand out among many energy storage systems due to their many merits, and it's expected to become an alternative to the prevailing alkali metal ion batteries. Nevertheless, the cumbersome manufacturing process and the high cost of conventional separators make them unfavorable for large-scale applications. Herein, inspired by the unique nature of cellulose and ZrO, a Janus cellulose fiber (CF)/polyvinyl alcohol (PVA)/ZrO separator is prepared via the vacuum filtration method.
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December 2024
National Local Joint Engineering Laboratory for Key Materials of New Energy Storage Battery, Hunan Province Key Laboratory for Electrochemical Energy Storage and Conversion, School of Chemistry, Xiangtan University, Xiangtan, 411105, China.
The rapid catalytic conversion toward polysulfides is considered to be an advantageous approach to boost the reaction kinetics and inhibit the shuttle effect in lithium-sulfur (Li─S) batteries. However, the prediction of high catalytic activity Li─S catalysts has become challenging given the carelessness in the relationship between important electronic characteristics of catalysts and catalytic activity. Herein, the relationships between the D-band regulation of catalysts with reaction kinetics toward polysulfides are described.
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