Ammonia Uptake from Ambient Air by Protonic Layered Metal Oxide as a Cause of the Gradual Degradation of Its Swelling Reactivity.

Protonic layered transition metal oxides readily undergo significant swelling and exfoliation into unilamellar nanosheets upon contact with aqueous solutions of amines and other basic compounds. Despite the crucial importance of this reactivity, it often degrades over time, leading to a loss of swelling and exfoliation capabilities. However, the cause of this degradation has remained unclear.

Supported Platinum Nanoparticles Catalyzed Carbon-Carbon Bond Cleavage of Polyolefins: Role of the Oxide Support Acidity.

Supported platinum nanoparticle catalysts are known to convert polyolefins to high-quality liquid hydrocarbons using hydrogen under relatively mild conditions. To date, few studies using platinum grafted onto various metal oxide (MO) supports have been undertaken to understand the role of the acidity of the oxide support in the carbon-carbon bond cleavage of polyethylene under consistent catalytic conditions. Specifically, two Pt/MO catalysts (MO = SrTiO and SiO-AlO; Al = 3.

Stabilization of Dinuclear Rhodium and Iridium Clusters on Layered Titanate and Niobate Supports.

Atomically dispersed organometallic clusters can provide well-defined nuclearity of active sites for both fundamental studies as well as new regimes of activity and selectivity in chemical transformations. More recently, dinuclear clusters adsorbed onto solid surfaces have shown novel catalytic properties resulting from the synergistic effect of two metal centers to anchor different reactant species. Difficulty in synthesizing, stabilizing, and characterizing isolated atoms and clusters without agglomeration challenges allocating catalytic performance to atomic structure.

Probing the Reactivity of the Active Material of a Li-Ion Silicon Anode with Common Battery Solvents.

Calculations and modeling have shown that replacing the traditional graphite anode with silicon can greatly improve the energy density of lithium-ion batteries. However, the large volume change of silicon particles and high reactivity of lithiated silicon when in contact with the electrolyte lead to rapid capacity fading during charging/discharging processes. In this report, we use specific lithium silicides (LS) as model compounds to systematically study the reaction between lithiated Si and different electrolyte solvents, which provides a powerful platform to deconvolute and evaluate the degradation of various organic solvents in contact with the active lithiated Si-electrode surface after lithiation.

Silver Adsorption on Calcium Niobate(001) Nanosheets: Calorimetric Energies That Explain Sinter-Resistant Support.

Metal nanoparticles deposited on oxide supports are essential to many technologies, including catalysts, fuel cells, and electronics. Therefore, understanding the chemical bonding strength between metal nanoparticles and oxide surfaces is of great interest. The adsorption energetics, adhesion energy, and adsorbate structure of Ag on dehydrated HCaNbO(001) nanosheets at 300 K have been studied using metal adsorption calorimetry and surface spectroscopies.

Competing Polar and Antipolar Structures in the Ruddlesden-Popper Layered Perovskite LiSrNbO.

Over the past few years, several studies have reported the existence of polar phases in Ruddlesden-Popper layer perovskites by trilinear coupling of oxygen octahedral rotations (OOR) and polar distortions, a phenomenon termed as hybrid improper ferroelectricity. This phenomenon has opened an avenue to expand the available compositions of ferroelectric and piezoelectric layered oxides. In this study, we report a new polar Ruddlesden-Popper layered niobate, LiSrNbO, which undergoes a structural transformation to an antipolar phase when cooled to 90 K.

Soft chemistry of ion-exchangeable layered metal oxides.

Soft chemical reactions such as ion-exchange and acid-base reactions have been extensively investigated to synthesize novel metastable layered inorganic solids, to exfoliate them into individual nanosheets, and to re-assemble them as thin films and nanocomposite materials. These reactions proceed at relatively low temperature and enable the synthesis of a rich variety of structures by stepwise reactions. In recent years, the toolbox of soft chemical reactions has been utilized to rationally design and tailor the properties of functional layered transition metal oxides.