This study investigates methods to enhance the efficiency of CO₂ capture using organic amine absorption and compares the performance of traditional and novel amine solvents. It reviews various single-component and mixed amine absorbents, as well as catalysts used in these methods, highlighting the superiority of mixed amine absorbents over single-component amine absorbents in CO₂ absorption and desorption. Additionally, the study explores the catalytic mechanisms and effects of catalysts in the CO₂ absorption/desorption process with amine solvents and provides an outlook on future research directions. The aim is to promote the widespread adoption of organic amine absorption technology in industrial applications and to contribute to the development of more sustainable and efficient CO₂ capture technologies.

Transition metal sulfides are widely used in supercapacitor electrode materials and exhibit excellent performance because of their rich variety, low price, and high theoretical specific capacity. At present, the main methods to prepare transition metal sulfides include the hydrothermal method and the electrochemical method. In order to further improve their electrochemical performance, two aspects can be addressed. Firstly, by controllable synthesis of nanomaterials, porous structures and large surface areas can be achieved, thereby improving ion transport efficiency. Secondly, by combining transition metal sulfides with other energy storage materials, such as carbon materials and metal oxides, the synergy between different materials can be fully utilized. However, future research still needs to address some challenges. In order to guide further in-depth research, it is necessary to combine the current research-derived knowledge and propose a direction for future development of transition metal sulfide electrode materials.

3d transition metal oxides composed of Mn, Fe, Co, and Ni have emerged as promising candidates for supercapacitor electrode materials due to their high theoretical specific capacitance, abundant redox-active sites, variable oxidation states, environmental friendliness, and low cost. Various synthesis strategies have been developed to fabricate these nanostructures, including hydrothermal/solvothermal methods, sol–gel processing, and microwave-assisted synthesis. Among them, microwave irradiation technology, with its rapid heating characteristics and unique thermal/non-thermal effects, offers significant advantages in controlling crystallinity and particle size distribution, suppressing particle agglomeration, and enhancing material purity. Furthermore, microwave effects facilitate the self-assembly and morphological evolution of transition metal oxides, promote the formation of crystal defects, and strengthen interfacial interactions. These effects enable precise microstructural tuning, leading to an increased specific surface area and a higher density of active sites, ultimately enhancing specific capacitance, rate capability, and cycling stability. In recent years, microwave-assisted synthesis has made significant progress in constructing 3d transition metal oxides and their composites, particularly in the development of single-metal and binary-metal oxides, as well as their hybrids with carbon-based materials (e.g., graphene and carbon nanotubes) and other metal oxides. This review systematically summarizes the research progress on microwave-assisted techniques for 3d transition metal oxide-based nanomaterials, with a particular focus on the role of microwave effects in morphology control, interfacial optimization, and electrochemical performance enhancement. Additionally, key challenges in current research are critically analyzed, and potential optimization strategies are proposed. This review aims to provide new insights and perspectives for advancing microwave-assisted synthesis of 3d transition metal oxides in energy storage applications.

Microwave-assisted interfacial oxygen-bridge confined MnO₂/CNT heterostructures effectively enhance performance.

High-performance electrode materials are fundamental to improving supercapacitor performance, serving as key factors in developing devices with high energy density, high power density, and excellent cyclic stability. Non-stoichiometric spinels with phase deficiencies can achieve electrochemical performance that surpasses that of stoichiometric materials, owing to their unique structural characteristics. In this study, we used a microwave-assisted method to synthesize a high-performance non-stoichiometric spinel material with phase deficiencies, Mn_0.5Co_2.5O₄, which displayed a wide potential window (1.13 V in a traditional aqueous three-electrode system) and high specific capacitance (716.9 F g⁻¹ at 1 A g⁻¹). More critically, through microwave-assisted doping engineering, nickel was successfully doped into the phase-deficient Mn_0.5Co_2.5O₄, resulting in a spinel material, Ni−Mn_0.5Co_2.5O₄, with significant lattice defects and a mixed 1D/2D morphology. The doping of nickel effectively promoted the high-state conversion of manganese valence states within the manganese cobaltite material, substantially increasing the quantity of highly active Co³⁺ ions. These changes led to an increase in the density of reactive sites, effectively promoting synergistic interactions, thereby significantly enhancing the material’s conductivity and energy storage performance. The specific capacitance of Ni−Mn_0.5Co_2.5O₄ reached 1180.6 F g⁻¹ at 1 A g⁻¹, a 64.7% improvement over the original Mn_0.5Co_2.5O₄; at a high current density of 10 A g⁻¹, the capacitance increased by 14.3%. Notably, the charge transfer resistance was reduced by a factor of 41.6. After 5000 cycles of testing, the capacity retention stood at 79.2%. This work reveals the effectiveness of microwave-assisted doping engineering in constructing high-performance non-stoichiometric spinel-type bimetallic oxide materials, offering advanced strategies for the development of high-performance electrode materials.

This study investigated the temporal appearance of CO₂-derived signals and qualitative spectral differences between rich and lean phases in a diethylenetriamine (DETA)/dimethyl sulfoxide (DMSO)/H₂O (DTSO) biphasic absorbent using FTIR, time-series and phase-separated ¹³C NMR, and DFT calculations. CO₂ reacted mainly with DETA, forming carbamate-related species. The earliest detectable CO₂-derived carbonyl signal appeared at 10 min and was tentatively assigned to a terminal mono-carbamate-related environment. Additional overlapping resonances attributable to candidate carbamate environments appeared as absorption progressed. Phase-separated ¹³C NMR showed carbonyl signals in both phases. Preliminary internal-standard estimates indicated a higher amount associated with the selected DETA-related signal in the analyzed rich-phase aliquot and a slightly higher amount associated with the selected DMSO-related signal in the lean-phase aliquot. However, these estimates do not establish a complete mass balance or quantitative partition coefficients. At the original B3LYP/SMD(H₂O) level, terminal-site candidates had lower calculated relative Gibbs free energies than corresponding central-site candidates. Representative ion-associated structures exhibited N–H···O contacts geometrically consistent with hydrogen bonding, although the relative electronic-energy ordering of the ion-pair models was sensitive to D3(BJ) dispersion treatment. Therefore, the calculations provide a model-dependent comparison of candidate-structure stability, not definitive predictions of solution-phase species populations or ion-pair formation.