SO 3 H-Containing Functional Carbon Materials: Synthesis, Structure, and Acid Catalysis

The “sulfonated carbons” are a new class of metal-free solid protonic acids characterized by their unique carbon structure and Brønsted acidity (− H 0 = 8–11) on par to concentrated H 2 SO 4 . These carbon materials covalently functionalized with SO 3 H groups via C–PhSO 3 H or C–SO 3 H linkages can act as versatile water-tolerant solid acids. Due to their low production costs, unique surface chemistry, high chemical and thermal stability, as well as tailorable pore structures they are regarded as potential substitutes to liquid H 2 SO 4 . Catalysis, in particular, biomass and large molecule catalysis, is one of the important areas in which acidic carbons have demonstrated exceptional activity and selectivity, outperforming traditional solid acid catalysts (cation-exchange resins, sulfated oxides, and acidic zeolites). In this review we address developments in the different types SO 3 H- and PhSO 3 H-functionalized acidic carbon materials, their structure, active sites, and surface properties, applications in catalysis, as well as activation and deactivation characteristics covering important literature since 2004. In particular, we aim to provide a systematic discussion on the specific merits and demerits of such materials obtained from different carbon precursors and functionalization methods which directly influence the structure–stability–acidic properties and catalytic performance.