SnO₂/graphitic carbon nitride (g-C₃N₄) composites were synthesized via a facile solid-state method by using SnCl₄·5H₂O and urea as the precursor. The structure and morphology of the as-synthesized composites were characterized by the techniques of X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), energy dispersive spectrometer (EDS), thermogravimetry-differential thermal analysis (TG-DTA), X-ray photoelectron spectroscopy (XPS), and N₂ sorption. The results indicated that the composites possessed a two-dimensional (2-D) structure, and the SnO₂ nanoparticles were highly dispersed on the surface of the g-C₃N₄ nanosheets. The gas-sensing performance of the samples to ethanol was tested, and the SnO₂/g-C₃N₄ nanocomposite-based sensor exhibited admirable properties. The response value (Ra/Rg) of the SnO₂/g-C₃N₄ nanocomposite with 10 wt % 2-D g-C₃N₄ content-based sensor to 500 ppm of ethanol was 550 at 300 °C. However, the response value of pure SnO₂ was only 320. The high surface area of SnO₂/g-C₃N₄-10 (140 m²·g⁻¹) and the interaction between 2-D g-C₃N₄ and SnO₂ could strongly affect the gas-sensing property.

Dual‐atom site catalysts (DASCs) provide more advantages than single‐atom systems in improving energy conversions, owing to their unique features. For example, the coupling effect may align the spin of two adjacent dual‐atom active centers in parallel or antiparallel via electron exchange interactions, thereby altering reaction mechanisms and overall efficiency. While numerous reviews have explored spin‐dependent electrocatalysis, there remains a lack of a comprehensive, spin‐focused framework for understanding the catalytic behavior of DASCs. This review emphasizes the role of spin in dual‐atom site centers for electrocatalysis research. First, spin fundamentals in electrocatalysts, including spin‐selective orbital occupation, spin ordering, and spin coupling, are comprehensively summarized to provide a solid foundation for subsequent discussions. Then, spin engineering strategies of DASCs are reviewed, including manipulating the spin configuration of the central atoms, modulating coordination environments, and tuning metal–support interactions. Next, recent developments in spin engineering of DASCs are reviewed, with a focus on structure–performance relationships. Furthermore, high‐throughput screening techniques integrated with machine learning are discussed for developing highly efficient DASCs based on spin engineering. The challenges and opportunities of DASCs and spin engineering are thoroughly discussed to promote the advancement of new energy applications.

Most gas hydrates on the earth are in sediments and permafrost areas, and porous media are often used industrially as additives to improve gas hydrate formation. For further understanding its exploration and exploitation under natural conditions and its application in industry, it is necessary to study the effect of porous media on hydrate formation. The results show that the stacked porous media affects the phase equilibrium of hydrate formation depending on the competition water activity and large specific surface areas, while integrated porous media, such as metal foam, can transfer the hydration heat rapidly and moderate the hydrate phase equilibrium. A supersaturated metal-organic framework is able to significantly improve gas storage performance and can be used as a new material to promote hydrate formation. However, the critical particle size should be studied further for approaching the best promotion effect. In addition, together with the kinetic accelerators, porous media has a synergistic effect on gas hydrate formation. The carboxyl and hydroxyl groups on the surface of porous media can stabilize hydrate crystals through hydrogen bonding. However, the hydroxyl radicals on the silica surface inhibit the combination of CH₄ and free water, making the phase equilibrium conditions more demanding.

Red mud modified by an acid digestion and alkali reprecipitation approach was employed as support for the preparation of Ni/MRM catalysts using the homogeneous precipitation method. The textural and structural properties of the as-received red mud (RM), the modified red mud (MRM) and the as-prepared Ni/MRM catalysts were characterized by X-ray diffraction (XRD), energy dispersive X-ray fluorescence (EDXRF), thermogravimetry-differential scanning calorimetry analysis (TG-DSC), Fourier transform infrared spectra (FT-IR), transmission electron microscopy (TEM) combined with energy-dispersive X-ray spectroscopy (EDX) and N₂ sorption techniques. The analysis results revealed a mesoporous nanocatalyst system with high surface area and uniform pore-size distribution. The results of the catalytic activity measurements showed that these mesoporous nanostructured Ni/MRM catalysts were very active for ammonia decomposition. The catalyst with 15% Ni loading and calcined at 600 °C exhibited the highest catalytic activity. Due to its unique properties and the feature of resource utilization of industrial solid waste, MRM holds great promise for developing catalysts and catalyst supports for applications in various catalytic reactions including catalytic ammonia decomposition.