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Oxidative-polymerization and deoxygenation of mixed phenols to faradaic-oxygen modified mesoporous carbon and its supercapacitive performances

机译:混合酚对法拉第 - 氧改性介孔碳的氧化聚合和脱氧,其超级电容性能

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摘要

To find the effect of phenols type on the physical/chemical characteristics and their supercapacitor performances of the derived carbons. Herein, three types of diphenol isomers (catechol, resorcinol and hydroquinone) mixed with phenol (molar ratio of 1:1) were employed as precursors to prepared porous carbon by oxidation polymerization and deoxygenation method. Systematically investigation shows that the derived three carbons all ahcieves a disordered mesoporous structure, while, hydroquinone mixed with phenol derived carbon (HPMC973) owns higher surface area of 1758 m(2)/g than that of catechol mixed with phenol derived CPMC973 of 1303 m(2)/g and resorcinol mixed with phenol derived RPMC973 of 1452 m(2)/g, larger pore volume of 1.94 cm(3)/g (vs. CPMC973 of 1.09 and RPMC973 of 1.25 cm(3)/g) and more open structure with larger mesoporosity of 97.3% vs. CPMC973 (86.1%) and RPMC973 (96.1%) resulted from its unique spatial structure enabling the formation of highly cross-linked structure. The residual oxygen species in the three carbons mainly exist in the forms of -C = O and -COO-. Benefited from the highly open-accessed mesoporosity and rich electroactive oxygenic species, the HPMC973 electrode exhibits a high capacitance of 418 F/g@0.5 A/g (vs 306 F/g for CPMC973 and 302 F/g for RPMC973) in 1.0 M H2SO4, the capacitance can be maintianed at 325 F/g@20 A/g, showing a superior rate capability with the retention of 77.8%. The fabricated symmetric supercapacitor based on HPMC973 in 1.0 M Li2SO4 delivers a ultrahigh specific energy of 27.9 Wh/kg@895 W/kg (vs. 16.9 Wh/kg for RPMC973 and 15.8 Wh/kg for CPMC973) and achieves an excellent cycling stablity with near 100% capacitance retention after 10 000 cylces at large current density of 20 A/g, offering a great potential for energy storage application. The current research provides a facile method for the fabrication of mesoporous carbon without using the harmful formaldehyde thus affords a promissing candidate for wide application in sorption, catalysis, energy storage, and etc.
机译:寻找酚类对衍生碳的物理/化学特性及其超级电容器性能的影响。这里,与苯酚(摩尔比为1:1)混合的三种二酚异构体(儿茶酚,间苯二酚和氢醌)作为通过氧化聚合和脱氧方法制备多孔碳的前体。系统调查表明,衍生的三个碳全部Ahcieves无序的介孔结构,而氢醌与酚衍生的碳(HPMC973)混合的含量高于1758米(2)/ g的表面积,而比儿茶酚与酚衍生的CPMC973为1303米(2)/ g和间苯二酚与酚衍生的RPMC973为1452米(2)/ g,孔体积的1.94cm(3)/ g(与1.09的CPMC973为1.25cm(3)/ g的rpmc973)和更大的开放结构具有97.3%的较大型与CPMC973(86.1%)和RPMC973(96.1%)由其独特的空间结构产生,从而形成高度交联结构。三种碳中的残留氧物种主要存在于-C = O和-COO-的形式中。受益于高度开放的介或富含电活性含氧物质,HPMC973电极在1.0米中显示出418 f / g的高电容为418 f / g至3.0.5 a / g(用于CPMC973和302 f / g的VS 306 F / g) H2SO4,电容可在325 f / g @ 20a / g处维持,显示出优异的速率能力,保持77.8%。基于HPMC973的基于HPMC973,在1.0M Li2SO4中的制造对称超级电容器提供了27.9WH / kg @ 895W / kg(用于rpmc973和15.8WH / kg的vs.16.9wh / kg for cpmc973)的超高特定能量,并实现了出色的循环稳定性在电流密度为20 A / g的10 000个圆柱之后接近100%电容保留,为能量存储应用提供了很大的潜力。目前的研究提供了用于在不使用有害甲醛的情况下制造介孔碳的容纳方法,从而为吸附,催化,能量储存等宽申请提供了较广泛的应用。

著录项

  • 来源
    《Journal of Energy Storage》 |2021年第2期|102198.1-102198.8|共8页
  • 作者单位

    Lianyungang Tech Coll Dept Med & Chem Engn Lianyungang 222006 Jiangsu Peoples R China;

    Huanggang Normal Univ Hubei Key Lab Proc & Applicat Catalyt Mat Huanggang 438000 Peoples R China;

    Huanggang Normal Univ Hubei Key Lab Proc & Applicat Catalyt Mat Huanggang 438000 Peoples R China;

    Huanggang Normal Univ Hubei Key Lab Proc & Applicat Catalyt Mat Huanggang 438000 Peoples R China;

    Huanggang Normal Univ Hubei Key Lab Proc & Applicat Catalyt Mat Huanggang 438000 Peoples R China;

    Huanggang Normal Univ Hubei Key Lab Proc & Applicat Catalyt Mat Huanggang 438000 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Diphenol isomers; Oxidation polymerization; Deoxygenation; Mesoporous carbon; Aqueous supercapacitor;

    机译:二酚异构体;氧化聚合;脱氧;中孔碳;水性超级电容器;

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