Mesoporous carbons synthesized via a soft-templating approach have attracted much attention due to their easy synthesis and facile control over the derived pore structure. In analogy to soft-templating approaches for mesoporous metal oxides, their synthesis is based on a sequence of forming supramolecular arrangements of precursor molecules with the soft templates, stabilization of the precursor framework by polymerization and finally the removal of the templates. Using micelles of amphiphilic block-copolymers as templates, facile control over the morphology and size of mesopores can be achieved by e.g. controlling size, composition, and concentration of the template polymers or composition and degree of polymerization of the precursor. Moreover, soft templating approaches can be extended to obtain also carbon materials with hierarchical meso- and macroporosity. The additional macroporosity either can result from templating by polymer latex or is induced via macrophase separation. In this review, we describe recent progress and examples in the synthesis and application of mesoporous carbon materials based on soft-templating approaches. Moreover, we reiterate fundamental principles of self-aggregation, highlight proposed synthesis mechanisms and present means of controlling pore size, also in hierarchical meso–macroporous carbon materials.

A hierarchical system of highly porous nanofibers has been prepared by electrospinning MOF (metal–organic framework) nanoparticles with suitable carrier polymers. Nitrogen adsorption proved the MOF nanoparticles to be fully accessible inside the polymeric fibers.

The novel material class of high entropy oxides with their unique and unexpected physicochemical properties is a candidate for energy applications. Herein, it is reported for the first time about the physico‐ and (photo‐) electrochemical properties of ordered mesoporous (CoNiCuZnMg)Fe₂O₄ thin films synthesized by a soft‐templating and dip‐coating approach. The A‐site high entropy ferrites (HEF) are composed of periodically ordered mesopores building a highly accessible inorganic nanoarchitecture with large specific surface areas. The mesoporous spinel HEF thin films are found to be phase‐pure and crack‐free on the meso‐ and macroscale. The formation of the spinel structure hosting six distinct cations is verified by X‐ray‐based characterization techniques. Photoelectron spectroscopy gives insight into the chemical state of the implemented transition metals supporting the structural characterization data. Applied as photoanode for photoelectrochemical water splitting, the HEFs are photostable over several hours but show only low photoconductivity owing to fast surface recombination, as evidenced by intensity‐modulated photocurrent spectroscopy. When applied as oxygen evolution reaction electrocatalyst, the HEF thin films possess overpotentials of 420 mV at 10 mA cm⁻² in 1 m KOH. The results imply that the increase of the compositional disorder enhances the electronic transport properties, which are beneficial for both energy applications.