烧焦
材料科学
化学工程
超级电容器
沥青
原材料
碳化
沥青质
重量分析
电解质
碳纤维
电容
热解
水溶液
活性炭
比表面积
产量(工程)
石油
电极
结块
柴油
渗透(战争)
多孔性
纳米技术
复合材料
作者
Dian Yang,Zhongxing Geng,Xinran Liu,Wei Sun
出处
期刊:Langmuir
[American Chemical Society]
日期:2026-07-29
卷期号:42 (31): 22890-22906
标识
DOI:10.1021/acs.langmuir.6c02708
摘要
Direct conversion of raw petroleum asphalt into activated carbons (ACs) ignores its compositional heterogeneity and results in poor carbonization efficiency. Here we separate asphalt into saturates (SAT), asphaltenes (ASP), and an aromatics-resins blend (AR-R). SAT fully volatilizes below 400 °C and contributes no solid carbon. ASP, although accounting for only 8.9 wt % of the raw material, gives a precarbonization yield of 51.7 wt % - more than three times that of whole asphalt (16.4 wt %). The ASP-derived char is fragmented and accessible, enabling deep, uniform KOH etching. The resulting AC has a specific surface area of 2593 m2 g-1 with a hierarchical pore network. In contrast, AR-R char is dense and monolithic, restricting activator penetration and giving poorly developed porosity. The optimal ASP-based carbon delivers a competitive gravimetric capacitance of 357 F g-1, a volumetric capacitance of 180 F cm-3 in aqueous electrolyte, and an energy density of 40.18 Wh kg-1 in organic electrolyte for supercapacitors (SCs). This work demonstrates that precursor chemistry, specifically the H/C ratio and thermal stability, dictates char morphology and final carbon architecture. The component-targeted strategy identifies ASP as the active ingredient, turning a low-value byproduct into a high-performance SC electrode with clear scalability advantages over conventional one-step processing.
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