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Highly porous carbide-derived carbon (CDC) mesofoams (DUT-70) are prepared by nanocasting of mesocellular silica foams with a polycarbosilane precursor. Ceramic conversion followed by silica removal and high-temperature chlorine treatment yields CDCs with a hierarchical micro-mesopore arrangement. This new type of polymer-based CDC is characterized by specific surface areas as high as 2700 m2 g−1, coupled with ultrahigh micro- and mesopore volumes up to 2.6 cm3 g−1. The relationship between synthesis conditions and the properties of the resulting carbon materials is described in detail, allowing precise control of the properties of DUT-70. Since the hierarchical pore system ensures both efficient mass transfer and high capacities, the novel CDC shows outstanding performance as an electrode material in electrochemical double-layer capacitors (EDLCs) with specific capacities above 240 F g−1 when measured in a symmetrical two-electrode configuration. Remarkable capacities of 175 F g−1 can be retained even at high current densities of 20 A g−1 as a result of the enhanced ion-transport pathways provided by the cellular mesostructure. Moreover, DUT-70 can be infiltrated with sulfur and host the active material in lithium-sulfur battery cathodes. Reversible capacities of 790 mAh g−1 are achieved at a current rate of C/10 after 100 cycles, which renders DUT-70 an ideal support material for electrochemical energy-storage applications. [ABSTRACT FROM AUTHOR]

We report on the successful application of porous hollow carbon nanospheres consisting of graphitic shells with a hierarchical porosity that were obtained by carbonizing an iron-containing commercially available metal-organic framework, as active material for supercapacitors. The influence of basic key parameters, such as the degree of graphitization and the accessible surface area of the carbons obtained at different temperatures, on the electrochemical performance is discussed in-depth. A high specific capacitance of 91 F g −1 in an aqueous electrolyte and 156 F g −1 using an ionic liquid is achieved. Furthermore a very steady specific capacitance over the course of 10,000 charge-discharge cycles is demonstrated. In addition, electrochemical impedance spectroscopy studies revealed that these carbons can feature a stable performance over several orders of magnitude of frequency, which render them interesting candidates for future electrochemical energy storage systems. [ABSTRACT FROM AUTHOR]