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A universal model for nanoporous carbon supercapacitors applicable to diverse pore regimes, carbon materials, and electrolytes

机译:纳米多孔碳超级电容器的通用模型,适用于各种孔隙状况,碳材料和电解质

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摘要

Supercapacitors, commonly called electric double-layer capacitors (EDLCs), are emerging as a novel type of energy-storage device with the potential to substitute batteries in applications that require high power densities. In response to the latest experimental breakthrough in nanoporous carbon supercapacitors, we propose a heuristic theoretical model that takes pore curvature into account as a replacement for the EDLC model, which is based on a traditional parallel-plate capacitor. When the pore size is in the mesopofe regime (2-50 nm), counterions enter mesoporous carbon materials and approach the pore wall to form an electric double-cylinder capacitor (EDCC); in the micropore regime (<2 nm), solvated/desolvated counterions line up along the pore axis to form an electric wire-in-cylinder capacitor (EWCC). In the macropore regime (>50 nm) at which pores are large enough so that pore curvature is no longer significant, the EDCC model can be reduced naturally to the EDLC model. We present density functional theory calculations and detailed analyses of available experimental data in various pore regimes, which show the significant effects of pore curvature on the supercapacitor properties of nanoporous carbon materials. It is shown that the EDCC/EWCC model is universal for carbon supercapacitors with diverse carbon materials, including activated carbon materials, template carbon materials, and novel carbide-derived carbon materials, and with diverse electrolytes, including organic electrolytes, such as tetraethylammonium tetrafluoroborate (TEABF(4)) and tetraethylammonium methylsulfonate (TEAMS) in acetonitrile, aqueous H2SO4 and KOH electrolytes, and even an ionic liquid electrolyte, such as 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (EMI-TFSI). The EDCC/EWCC model allows the supercapacitor properties to be correlated with pore size, specific surface area, Debye length, electrolyte concentration and dielectric constant, and solute ion size It may lend support for the systematic optimization of the properties of carbon supercapacitors through experiments. On the basis of the insight obtained from the new model, we also discuss the effects of the kinetic solvation/desolvation process, multimodal (versus unimodal) pore size distribution, and exohedral (versus endohedral) capacitors on the electrochemical properties of supercapacitors.
机译:超级电容器,通常称为双电层电容器(EDLC),正在作为一种新型的能量存储设备而出现,在需要高功率密度的应用中,它有可能替代电池。为了响应纳米多孔碳超级电容器的最新实验突破,我们提出了一种启发式理论模型,该模型考虑了孔隙曲率,以代替基于传统平行板电容器的EDLC模型。当孔尺寸处于介孔结构(2-50 nm)时,抗衡离子进入中孔碳材料并接近孔壁,从而形成双圆柱电容器(EDCC);在微孔状态(<2 nm)中,溶剂化/去溶剂化的抗衡离子沿着孔轴排列,形成一个圆筒内电线电容器(EWCC)。在大孔状态(> 50 nm)下,孔足够大,以致孔曲率不再明显,可以将EDCC模型自然还原为EDLC模型。我们提供了密度泛函理论计算和各种孔隙状态下可用实验数据的详细分析,这些结果表明了孔隙曲率对纳米多孔碳材料的超级电容器性能的显着影响。结果表明,EDCC / EWCC模型对于具有多种碳材料(包括活性炭材料,模板碳材料和新型碳化物衍生的碳材料)以及具有多种电解质(包括有机电解质,例如四乙基四氟硼酸铵)的碳超级电容器通用。乙腈,H2SO4和KOH水溶液中的TEABF(4))和四乙基甲基磺酸铵(TEAMS),甚至是离子液体电解质,例如1-乙基-3-甲基咪唑鎓双(三氟甲磺酰基)酰亚胺(EMI-TFSI)。 EDCC / EWCC模型可以使超级电容器的性能与孔径,比表面积,德拜长度,电解质浓度和介电常数以及溶质离子的大小相关联。这可以为通过实验对碳超级电容器的性能进行系统优化提供支持。在从新模型获得的见解的基础上,我们还讨论了动力学溶剂化/去溶剂化过程,多峰(相对于单峰)孔径分布和外面(相对于内面)电容器对超级电容器电化学性能的影响。

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