The redox mediators help prevent cathode passivation and promote the formation and decomposition of LiO within the electrolyte of the battery. Understanding the mechanistic properties of the soluble catalyst from an atomic level is crucial for developing an all-in-one multifunctional soluble catalyst for Li-O batteries. With the help of density functional theory and atom-centered density matrix propagation molecular dynamics simulations, we report how butylated hydroxytoluene (BHT), an experimentally reported soluble catalyst, mediates the stabilization of reactive intermediates and the mechanism behind the formation and decomposition of LiO. The hydroxy group in BHT facilitates the stabilization of O via hydrogen bonding and the solvation of Li, LiO, and LiO. This characteristic of BHT helps to promote the solution-phase mechanism and suppress parasitic reactions induced by O. During the charging process, the reversibility of BHT and BHT happens and the disappearance of the hydrogen bonding interaction facilitates the delithiation process. The Mulliken charge distribution analysis shows that the reversibility of BHT and BHT is due to the electron delocalization between the oxygen atom and benzene ring of BHT. We observe the two benefits of the hydrogen bond: the presence and absence of hydrogen bonding enhance the formation and decomposition of LiO respectively. We find that tetraethylene glycol dimethyl ether solvent plays a significant role in stabilizing lithium-oxygen-containing species such as LiO and LiO. However, the presence of BHT further improves the results. This finding highlights the cooperative activity of BHT in conjugation with the tetraethylene glycol dimethyl ether solvent. The atom-centered density matrix propagation method reveals that BHT facilitates LiO decomposition through protonation, whereas BHT induces LiO decomposition by promoting the formation of LiO and the BHT:Li complex without transferring the proton.
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http://dx.doi.org/10.1021/acs.jpca.4c08558 | DOI Listing |
Nano Lett
March 2025
Department of Chemical Sciences and Bernal Institute, University of Limerick, V94 T9PX Limerick, Ireland.
The development of sustainable and tunable materials is crucial for advancing modern technologies. We present a controlled synthesis of colloidal Na-Cu-S nanostructures. To overcome the reactivity difference between Na and Cu precursors toward chalcogens in a colloidal synthesis and to achieve metastable phase formation, we designed a single-source precursor for Cu and S.
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March 2025
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan, Shanxi 030001, China.
Electrosynthesis of hydrogen peroxide (HO) through the two-electron oxygen reduction reaction (2e-ORR) is environmentally friendly and sustainable. Transition-metal single-atom catalysts (SACs) have gained attention for this application due to their low cost, high atom utilization, adjustable coordination, and geometric isolation of active metal sites. Although various synthetic methods of SACs have been reported, the specific mechanism of the formation of active sites is still less studied.
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March 2025
Kidney Institute of New Mexico, University of New Mexico Health Sciences Center, Albuquerque, NM, USA; New Mexico VA Health Care System, Albuquerque, NM, USA. Electronic address:
The formation of gadolinium-rich nanoparticles in multiple tissues from intravenous magnetic resonance imaging contrast agents may be the initial step in rare earth metallosis. The mechanism of gadolinium-induced diseases is poorly understood, as is how these characteristic nanoparticles are formed. Gadolinium deposition has been observed with all magnetic resonance imaging contrast agent brands.
View Article and Find Full Text PDFDalton Trans
March 2025
State Key Laboratory of Coal Combustion, School of Energy and Power Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
Herein, the relationship between the selective catalytic activity of CO in the reduction of NO and the active site of LaFeO perovskite was established through the combination of density functional theory and microkinetic studies. A reaction network consisting of various possible elementary reactions was built to reveal the pathway of CO, N and NO formation during CO-SCR on LaFeO. The results indicated that the Fe site was active for reactant adsorption, which followed a chemisorption mechanism.
View Article and Find Full Text PDFACS Omega
March 2025
Department of Chemical Engineering, Indian Institute of Technology Guwahati, Guwahati, Assam 781039, India.
Waste flowers constitute a significant portion of organic waste, offering the potential for sustainable waste management through pyrolysis. This study explores the pyrolysis behavior, kinetic parameters, and biochar production from waste flowers. Thermogravimetric analysis (TGA) was employed to examine thermal degradation characteristics under varying heating rates (10, 20, and 50 °C min).
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