Volatile organic compounds (VOCs), as a significant contributor to atmospheric pollution such as ozone pollution and PM2.5, bring serious harm to the environment and human health. Catalytic oxidation is one...

As a typical class of man‐made nanoreactors, metal‐loaded hollow carbon nanostructures (MHC nanoreactors) exhibit competitive potentials in the heterogeneous catalysis due to their tailorable microenvironment effects, in which the void‐confinement effect is one of the most fundamental functions in boosting the catalytic performance. Herein this paper, Ru‐loaded hollow carbon spheres are employed as nanoreactors with a crucial biomass hydrogenation process, levulinic acid (LA) hydrogenation into γ‐valerolactone, as the probe reaction to further recognize the forming mechanism of this pivotal effect. We demonstrated that the void‐confinement effect of the selected MHC nanoreactors is essentially driven by an integrating action of electronic metal‐support interaction, reactant enrichment and diffusion, which are mainly ascribed to peculiar properties of hollow nanoreactors both in electronic and structural aspects, respectively. This work offers a distinct case for interpreting the catalytic behaviour of MHC nanoreactors, which could potentially promise broader insights into the microenvironment engineering strategies of hollow nanostructures.

Valerate esters (VAEs) commonly derived from levulinic acid (LA), which is deemed as one of the most promising biomass platform molecules, have been hailed as “valeric biofuels” in recent years. The cascade transformation of LA to VAEs consists of a series of acid‐ and metal‐catalyzed processes alternately, in which heterogeneous bifunctional catalysts are required for better catalytic performance. The transformation pathway from LA to VAEs is presented, and bifunctional catalytic systems for the cascade transformation of LA into valeric acid (VA) and its esters, as well as one‐pot conversion processes, are reviewed. Additionally, effects of metal and acid sites on the catalytic performance are discussed in detail. Impacts of and improvements to coke deposition, which is determined to be the primary reason for the reduction in catalytic activity, are also analyzed. Finally, feasible suggestions are proposed for enhanced catalytic performance and a reduction in overall costs.

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As a novel class of catalytic materials, hollow nanoreactors offer new opportunities for improving catalytic performance owing to their higher controllability on molecular kinetic behavior. Nevertheless, to achieve controllable catalysis with specific purposes, the catalytic mechanism occurring inside hollow nanoreactors remains to be further understood. In this context, this Review presents a focused discussion about the basic concept of hollow nanoreactors, the underlying theory for hollow nanoreactor-driven kinetics, and the intrinsic correlation between key structural parameters of hollow nanoreactors and molecular kinetic behaviors. We aim to provide in-depth insights into understanding kinetics occurred within typical hollow nanoreactors. The perspectives proposed in this paper may contribute to the development of the fundamental theoretical framework of hollow nanoreactor-driven catalysis.