Design and Synthesis of Cubic K Ba SbSe Solid Electrolytes for K-O Batteries.

Developing K-ion conducting solid-state electrolytes (SSEs) plays a critical role in the safe implementation of potassium batteries. In this work, a chalcogenide-based potassium ion SSE is reported, K SbSe , which adopts a trigonal structure at room temperature. Single-crystal structural analysis reveals a trigonal-to-cubic phase transition at the low temperature of 50 °C, which is the lowest among similar compounds and thus provides easy access to the cubic phase.

Multifunctional Composite Binder for Thick High-Voltage Cathodes in Lithium-Ion Batteries.

High-voltage LiNiMnO (LNMO) spinel offers high specific energy and good rate capability with relatively low raw-material cost due to cobalt-free and manganese-rich chemical compositions. Also, increasing mass loading (mg/cm) by thickening cathodes has been one of the focused areas to greatly improve the energy density of lithium-ion batteries (LIBs) at the cell level. The LNMO cathode made with a polyvinylidene fluoride (PVdF) binder, however, suffers from an oxidative decomposition of liquid electrolytes and cathode delamination from a current collector.

Deactivation-free ethanol steam reforming at nickel-tipped carbon filaments.

Ni based catalysts have been widely studied for H2 production due to the ability of Ni to break C-C and C-H bonds. In this work, we study inverse catalysts prepared by well-controlled sub-monolayer deposition of CeO2 nanocubes onto Ni thin films for ethanol steam reforming (ESR). Results show that controlling the coverage of CeO2 nanocubes on Ni enhances H2 production by more than an order of magnitude compared to pure Ni.

Ambient Pressure X-ray Photoelectron Spectroscopy Investigation of Thermally Stable Halide Perovskite Solar Cells via Post-Treatment.

Long-term thermal stability is one limiting factor that impedes the commercialization of the perovskite solar cell. Inspired by our prior results from machine learning, we discover that coating a thin layer of 4,4'-dibromotriphenylamine (DBTPA) on top of a CHNHPbI layer can improve the stability of resultant solar cells. The passivated devices kept 96% of the original power conversion efficiency for 1000 h at 85 °C in a N atmosphere without encapsulation.

Mass Transfer Thermodynamics through a Gas-Liquid Interface.

Molecular level information about thermodynamic variations (enthalpy, entropy, and free energy) of a gas molecule as it crosses a gas-liquid interface is strongly lacking from an experimental perspective under equilibrium conditions. Herein, we perform in situ measurements of water interacting with the ionic liquid (IL) 1-butyl-3-methylimidazolium acetate, [Cmim][Ace], using ambient pressure X-ray photoelectron spectroscopy in order to assess the interfacial uptake of water quantitatively as a function of temperature, pressure, and water mole fraction ( x). The surface spectroscopy results are compared to existing bulk water absorption experiments, showing that the amount of water in the interfacial region is consistently greater than that in the bulk.

Surface enhancement of water at the ionic liquid-gas interface of [HMIM][Cl] under ambient water vapor.

The ionic liquid-gas interface of 1-hexyl-3-methyl-imidazolium chloride, [HMIM][Cl], was examined in the presence of water vapor using lab-based ambient pressure x-ray photoelectron spectroscopy (APXPS) at room temperature. The interfacial water uptake was measured quantitatively in the pressure range of high vacuum up to a maximum of 5 Torr (27% RH) and back to high vacuum in a systematic manner. Water mole fractions in the interface determined from APXPS were compared to previously published tandem differential mobility analysis results on [HMIM][Cl] nanodroplets.

ZnO(101̅0) Surface Hydroxylation under Ambient Water Vapor.

The interaction of water vapor with a single crystal ZnO(101̅0) surface was investigated using synchrotron-based ambient pressure X-ray photoelectron spectroscopy (APXPS). Two isobaric experiments were performed at 0.3 and 0.

A lab-based ambient pressure x-ray photoelectron spectrometer with exchangeable analysis chambers.

Ambient pressure X-ray photoelectron spectroscopy (APXPS) is a powerful spectroscopy tool that is inherently surface sensitive, elemental, and chemical specific, with the ability to probe sample surfaces under Torr level pressures. Herein, we describe the design of a new lab-based APXPS system with the ability to swap small volume analysis chambers. Ag 3d(5/2) analyses of a silver foil were carried out at room temperature to determine the optimal sample-to-aperture distance, x-ray photoelectron spectroscopy analysis spot size, relative peak intensities, and peak full width at half maximum of three different electrostatic lens modes: acceleration, transmission, and angular.