A hierarchical porous carbon prepared via direct carbonization of Ni-MOF-74 loaded with furfuryl alcohol at 450 8C displays high specific capacitance in comparison with other MOF-derived carbons as a result of the formation of micropores smaller than 1 nm. Thus, the catalytic activity of the template can be finely tuned by a suitable choice of the metal, or combination of metals, in the porous scaffold to control the crystallinity and porosity of the resulting carbon. Furthermore, previous reports suggest a linear correlation between the M/C ratio in zinc MOFs acting as sacrificial precursors and the surface area of the resulting carbons. 13 Carbon poor organic linkers might be thus better fitted to produce a bigger number of metal particles, which can be then removed for overall increase in porosity. Ni-MOF-74 features a ratio of 0.25, well above those displayed by Al-PCP, Fe-BTC, ZIF-8, MOF-5, MIL-100 or HKUST-1 between 0.08 and 0.17. A delicate control over these features is the key to maximizing the performance of MOF-derived carbons as electrodes in EDLCs. Ni-MOF-74 was prepared by a solvothermal reaction of Ni(NO 3 ) 2 and dhtp and pre-treated at reduced pressure for solvent removal. The activated solid was then soaked in furfuryl alcohol. The mixture was heated at 60 1C for 12 hours with soft stirring for favouring the diffusion of FA into the pores of the MOF, followed by thorough washing with ethanol to remove non-infiltrated FA molecules stuck to the surface of the crystals (synthetic details in SI2, ESI †). The phase purity and morphology of Ni-MOF-74/FA was studied using powder X-ray diffraction (PXRD) and Scanning Electron Microscopy (SEM) to rule out structural changes upon solvent removal or guest loading ( Fig. SI3 and SI4, ESI †). The solid is isolated as yellowish, micrometric crystals featuring a rose-like morphology. Indexing of the PXRD pattern agrees well with a pure MOF-74 phase.
Research in Metal-