CONSPECTUS: Mesoporous materials with various structures have attracted considerable attention due to their distinctive properties such as large pore sizes, high surface areas, tunable pore structures, and controllable framework compositions. Among them, spherical mesoporous materials (SMMs) are of great interest owing to the unique spherical shape, which show the closed packing nature and lowest surface energy. The open mesopores and short channels of SMMs not only increase the density of high accessible active sites but also facilitate the mass diffusion with short length. These characteristics are particularly useful for applications in catalysis, adsorption, energy storage and conversion, biomedicine, and so on. In addition, the creation of a spherical shape is conformable to the law of natural selection because objects in nature tend to minimize energy, while the sphere is one of the most perfect matter structures. Therefore, the design and synthesis of SMMs are very important from both fundamental and technological viewpoints. Compared to the simple single-level, SMMs with more complex multilevel structures inevitably bring unusual mechanical, electrical, and optical properties, which are highly desired for practical applications. For example, the construction of core−shell structured SMMs has inspired great attention as they can combine multiple components into one functional unit, exhibiting ameliorated or new physicochemical properties, which cannot be obtained from the isolated one. The presence of a hollow cavity in the yolk−shell structure allows sufficient exposure of the core while maintaining the protective ability of the shell, which is conducive to retaining the distance-dependent properties of the core. Multishelled hollow structures consisting of two or more mesoporous shells are expected to show superior activities in various applications compared to their bulk counterparts because more active interfaces and unique compartmentation environments can be provided. Therefore, SMMs from single to multilevel structure represent a class of advanced nanostructured materials with unique structures and fascinating properties. In this Account, we highlight the progresses on the synthesis and applications of SMMs from single to multilevel architectures. The synthetic strategies have been summarized and categorized into (i) the modified Stober method, (ii) the hydrothermal strategy, (iii) the biphase stratification approach, (iv) the nanoemulsion assembly method, (v) the evaporation induced aggregating assembly (EIAA) method, and (vi) the confined self-assembly strategy. Special emphasis is placed on the synthetic principles and underlying mechanisms for precise control of SMMs over the particle sizes, pore sizes, pore structures and functionalities as well as different levels of architectures. Moreover, the implementation performances in catalysis, drug delivery, and energy related fields have been highlighted. Finally, the opportunities and challenges for the future development of SMMs in terms of synthe...

Heterogeneous sonocatalysis, as an emerging advanced oxidation process (AOP), has shown immense potential in water treatment and been widely demonstrated to remove persistent organic compounds in the past decade. The present article aims to provide a comprehensive review on the development of a heterogeneous catalyst for enhancing the ultrasonic degradation rate of organic pollutants from a viewpoint of sonocatalytic mechanism. The rational design and fundamentals for preparing sonocatalysts are presented in the context of facilitating the heterogeneous nucleation and photo-thermal-catalytic effects as well as considering the mechanical stability and separation capacity of the heterogeneous catalyst. In addition, some new trends, ongoing challenges and possible methods to overcome these challenges are also highlighted and proposed.

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Recent efforts have observed nanoscaled chemical short‐range order in bulk high‐entropy alloys (HEAs). Simultaneously inspired with the nanostructuring technology, HEA nanoparticles (NPs) with complete chemical order may be achieved. Herein, structurally ordered HEA (OHEA) NPs are constructed on a novel 2D nitrogen‐rich mesoporous carbon sandwich framework (OHEA‐mNC) by combining a ligand‐assisted interfacial assembly with NH3 annealing. Characterization results show that the resultant materials possess an ultrathin 2D nanosheet structure with large mesopores (≈10 nm), where structurally ordered HEA NPs with an L12 phase are homogeneously dispersed. The atom‐resolved chemical analyses explicitly determine the location of each atomic site. When being evaluated for the oxygen reduction reaction, the OHEA‐mNC NPs afford a greatly enhanced catalytic performance, including a large half‐wave potential (0.90 eV) and a high durability (0.01 V decay after 10 000 cycles) compared with the disordered HEA and commercial Pt/C catalysts. The excellent performance is attributed to the enhanced mass transfer rate, improved electron conductivity, and the presence of the stable chemically ordered HEA phase, as revealed by both the experimental results and theoretical calculation. This study suggests a highly feasible process to achieve structurally ordered HEA NPs with advanced mesoporous function in the electrochemical field.