Nanomaterials Physicochemistry Department, Faculty of Chemical Technology and Engineering, West Pomeranian University of Technology, Szczecin, Piastów Ave. 42, 71-065 Szczecin, Poland; State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, China.
Faculty of Chemistry, Department of Polymer and Carbonaceous Materials, Wroclaw University of Technology, Wroclaw, Poland.
Waste Manag. 2019 Mar 15;87:691-700. doi: 10.1016/j.wasman.2019.03.006. Epub 2019 Mar 11.
Recently, sustainable development and serious energy crisis called for appropriate managements for the large number of municipal and industrial waste plastics as well as the development of low-cost, advanced materials for energy storage. However, the complexity of waste plastics significantly hampers the application of ever used methods, and little attention is paid to the utilization of waste plastics-derived carbon in energy storage. Herein, porous carbon nanosheets (PCNSs) was produced by catalytic carbonization of "real-world" mixed waste plastics on organically-modified montmorillonite (OMMT) and the subsequent KOH activation. PCNSs was featured on hierarchically micro-/mesoporous structures with the pore size distribution centered on 0.57, 1.42 and 3.63 nm and partially exfoliated graphitic layers, and showed a high specific surface area of 2198 m g and a large pore volume of 3.026 cm g. Benefiting from these extraordinary properties, PCNSs displayed a superior performance for supercapacitors with high specific capacitances approaching 207 and 120 F g at a current density of 0.2 A g in aqueous and organic electrolytes, respectively. Importantly, when the current density increased to 10 A g, the specific capacitances remained at 150 F g (72.5%) and 95 F g (79.2%) in aqueous and organic electrolytes, respectively. The outstanding rate capability of PCNSs was in sharp contrast to the performance of traditional activated carbons. This work not only provides a potential way to recycle mixed waste plastics, but also puts forward a facile sustainable approach for the large-scale production of PCNSs as a promising candidate for supercapacitors.
最近,可持续发展和严重的能源危机要求对大量的城市和工业废塑料进行适当的管理,同时开发低成本、先进的储能材料。然而,废塑料的复杂性极大地阻碍了以往方法的应用,而对废塑料衍生碳在储能中的利用则关注甚少。在此,通过在有机改性蒙脱石(OMMT)上催化碳化“真实世界”混合废塑料,并随后进行 KOH 活化,制备了多孔碳纳米片(PCNSs)。PCNSs 具有分级的微孔/介孔结构,孔径分布集中在 0.57、1.42 和 3.63nm,部分剥离的石墨层,比表面积高达 2198m²/g,孔体积为 3.026cm³/g。得益于这些非凡的特性,PCNSs 在超级电容器中表现出优异的性能,在水相和有机电解液中的比电容分别在 0.2A/g 的电流密度下接近 207 和 120F/g。重要的是,当电流密度增加到 10A/g 时,在水相和有机电解液中的比电容分别保持在 150F/g(72.5%)和 95F/g(79.2%)。PCNSs 的出色倍率性能与传统活性炭的性能形成鲜明对比。这项工作不仅为回收混合废塑料提供了一种潜在的途径,而且还提出了一种简单可持续的方法来大规模生产 PCNSs,使其成为超级电容器的有前途的候选材料。