Rational interface control of porous carbon electrode materials is of significance for achieving efficient supercapacitors. Herein, biomass-derived carbon microspheres with a highly graphitized porous surface and amorphous subsurface were well constructed a flexible coupled catalysis-activation process. The unique structure not only endows the carbon microspheres with rapid electron transfer but also an ultra-high specific surface area. Owing to the optimized graphitized/amorphous structure, the obtained graphitized and activated starch-derived carbon microspheres display obviously impressive energy storage capability among the reported starch-derived carbon materials, even though they were evaluated in a narrow voltage window. The assembled symmetrical supercapacitor based on the optimized carbon microspheres exhibits a high capacitance of 198 F g at 1 A g, a high energy density of 14.67 W h kg at a power density of 4142.80 W kg, robust cycle performance, and good rate performance in alkaline aqueous electrolyte. This work provides a strategy for flexible construction of biomass-derived carbon electrode materials, with an optimized graphitized/amorphous and porous structure, for boosted energy storage in supercapacitor applications.
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http://dx.doi.org/10.1039/d1na00262g | DOI Listing |
ACS Appl Mater Interfaces
December 2024
School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, P. R. China.
Developing hybrid fluorescence (FL)/room-temperature phosphorescent (RTP) materials in dry-state, aqueous, and organic solvents holds paramount importance in broadening their applications. However, it is extremely challenging due to dissolved oxygen and solvent-assisted relaxation causing RTP quenching in an aqueous environment and great dependence on SiO-based materials. Herein, an efficient endogenetic carbon dot (CD) strategy within melamine-formaldehyde (MF) microspheres to activate RTP of CDs has been proposed through the pyrolysis of isophthalic acid (IPA) molecules and branched-chain intra-microspheres.
View Article and Find Full Text PDFNanoscale
December 2024
Key Laboratory of Advanced Energy Storage and Conversion of Wenzhou, Key Laboratory of Carbon Materials of Zhejiang Province, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, P. R. China.
Lead oxides (PbO, 1 ≤ ≤ 2) are promising high-capacity and low-cost anodes for lithium ion batteries (LIBs). However, the huge lithiation-induced volume expansion of conventional large-sized PbO particles leads to severe electrode pulverization with poor cycling stability. Herein, a rare mixed-valence PbO with a unique hierarchical architecture of nanoparticle-assembled interconnected hollow spheres (denoted PbO NAHSs) is crafted by introducing polyvinylpyrrolidone (PVP) into the solution of generating β-PbO microspheres (MSs), which is exploited for the first time as a potential advanced anode material for LIBs.
View Article and Find Full Text PDFHeavy metal wastewater is a direct threat to the ecological environment and human health because it is highly toxic at low concentrations. Therefore, it is very important to explore and develop efficient wastewater treatment agents. MnFeO-loaded bamboo pulp carbon-based aerogel (MCA) is prepared by directional freeze-drying and carbonization.
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
December 2024
Department of Organic Chemistry, Faculty of Chemistry, Alzahra University, Tehran, Iran.
The efficient utilization of light and the prolonged lifetime of photo-induced charge carriers are essential elements that contribute to superior photocatalytic activity. Yolk-shell nanostructures with porous shells and mobile cores offer significant structural advantages in achieving these goals. However, designing yolk-shell multicomponent nanocomposites with diverse architectures remains a persistent challenge.
View Article and Find Full Text PDFMaterials (Basel)
November 2024
Department of Chemistry, Dong-A University, Busan 49315, Republic of Korea.
Cobalt (II, III) oxide (CoO) has recently gained attention as an alternative anode material to commercial graphite in lithium-ion batteries (LIBs) due to its superior safety and large theoretical capacity of about 890 mAh g. However, its practical application is limited by poor electrical conductivity and rapid capacity degradation because of significant volume increases and structural strain during repeated lithiation/delithiation cycles. To address these issues, this work presents a novel approach to synthesizing carbon-composited CoO microspheres (CoO@C), using abietic acid (AA) as a carbon source to increase conductivity and structural stability.
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