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Supramolecular aggregateʼs self-assembling approach has derived diverse mesostructured inorganic solids. Recent progresses involve ordered mesoporous carbonaceous frameworks. This review paper summarizes the synthesis of ordered mesoporous polymers and carbons based on the supramolecular aggregates as templates. Block copolymers are mainly introduced here. Both the aggregates of block copolymers themselves and the assembling with thermosetting resins have the abilities to organize ordered mesostructures. The understanding of the synthesis is on the formation of supramolecular arrangement of molecules, templating, cross-linking, removal of templates, and carbonization. In addition, the morphological control and the functionalization of ordered mesoporous carbonaceous materials are briefly summarized. The attractive mesoporous carbonaceous materials offer great opportunities in catalysis, water purification, electrodes, adsorbents, gas storage, aero-space, etc. [ABSTRACT FROM AUTHOR]

A facile dual-templating approach is demonstrated to prepare hierarchically ordered macro-/mesoporous carbons. Monodispersed silica colloidal crystals are used as a hard template, amphiphilic triblock copolymer PEO−PPO−PEO as a soft template, and soluble resols as a carbon source. The procedure involves packing and aging of silica microspheres, evaporation-induced organic−organic assembly of mesostructures in the void of microspheres, thermosetting and carbonization of phenolic formaldehyde (PF), and removal of silica scaffolds by HF. The obtained porous carbons have a highly ordered face-centered cubic macrostructure with tunable pore sizes of 230−430 nm and interconnected windows with a size of 30−65 nm. The rigid silica hard templates can prevent the shrinkage of the mesostructure during the thermosetting and carbonization process, resulting in large cell parameters (∼18 nm) and pore sizes (∼11 nm). The bimodal porous carbon materials have large BET surface areas (up to 760 m2/g), large pore volumes (∼1.25 cm3/g), and partially graphitized frameworks. With the increase in the silica sphere diameter, the BET surface areas and the window sizes increase. The hierarchically ordered carbon structures show strong diffraction at wavelengths of 500−690 nm depending on the treatment used. [ABSTRACT FROM AUTHOR]