Novel N-doped porous carbon enables high energy density zinc ion hybrid capacitor (120.75 Wh kg⁻¹) and superior energy density supercapacitor (29.41 Wh kg⁻¹), offering efficient electrode materials for advanced energy storage.

A protocol for visible light-mediated selective C–Cl activation of chlorides for the polychlorination of alkenes has been developed. This strategy allows for the installation of multiple chlorine atoms into double bonds under mild conditions.

A novel metal organic framework (MOF)-derived porous copper/zinc bimetallic oxide catalyst was developed for the photoreduction of CO₂ to methanol at a very fast rate of 3.71 mmol g_cat⁻¹ h⁻¹. This kind of photocatalyst with high activity, selectivity and a simple preparation catalyst provides promising photocatalyst candidates for reducing CO₂ to methanol.

Solid–liquid interfacial phenomena play an essential role in our everyday lives and are often regarded as the outcome of interactions at the solid–liquid interface. However, the intricately intrinsic mechanism underlying interfacial interactions renders in situ simulations and direct measurements challenging. As an effective analytic method for studying solid–liquid interfacial interactions, microcalorimetry can provide the most basic thermodynamic information (including changes in enthalpy, entropy, and Gibbs free energy during solid–liquid binding/separation processes), which is extremely crucial for understanding interaction directionality and limitation. This review is dedicated to highlighting the pivotal role of microcalorimetry in studying solid–liquid immersion and adsorption processes. Specifically, we provide an overview of the commonly employed microcalorimetric methods, including differential scanning calorimetry (DSC), isothermal titration calorimetry (ITC), and immersion microcalorimetry (IM), and delve into the influence factors of enthalpy change, and finally discuss the specific applications of microcalorimetry in studying various solid–liquid binding processes. There remains a vast expanse of thermodynamic information regarding solid–liquid interactions that await exploration via calorimetry.

The interaction between clay minerals and electrolyte solutions critically affects waterflooding efficiency in enhanced oil recovery (EOR). This study systematically investigated the adsorption and thermodynamic properties of montmorillonite, illite, and kaolinite in different cationic solutions (K⁺, Na⁺, Ca²⁺, Mg²⁺), integrating adsorption isotherm analysis with immersion calorimetry for the first time. Montmorillonite showed the highest adsorption capacity, with the cation affinity following K⁺ > Na⁺ > Ca²⁺ > Mg²⁺. The highest immersion enthalpy was observed in KCl solution, indicating the dominant roles of ionic radius and solvation energy. Cation adsorption induced deformation of clay lamellae and modification of Si-O and Al-OH groups. These findings suggest that optimizing injected ion composition can enhance reservoir stability and waterflood performance, providing thermodynamic insights for EOR process optimization.