Disentangling the Li-Ion transport and Boundary Phase Transition Processes in Li10 GeP2 S12 Electrolyte by In-Operando High-Pressure and High-Resolution NMR Spectroscopy.

Li-ion transport and phase transition of solid electrolytes are critical and fundamental issues governing the rate and cycling performances of solid-state batteries. In this work, in-operando high-pressure nuclear magnetic resonance (NMR) spectroscopy for the solid-state battery is developed and applied, in combination with 6 Li-tracer NMR and high-resolution NMR spectroscopy, to investigate the Li10 GeP2 S12 electrolyte under true-to-life operation conditions. The results reveal that the Li10 GeP2 S12 phase may become more disordered and a large amount of conductive metastable ß-Li3 PS4 as the glassy matrix in the electrolyte transforms into less conductive phases, mainly γ-Li3 PS4 , when high current densities (e.g., ≥0.5 mA cm-2 ) are applied to the electrolyte. The overall Li-transport also varies and shows a tendency of boundary phases and Li10 GeP2 S12 synergistic dominant conduction at high currents. Accordingly, a mechanism of structural change induced by stress variation due to the drastic morphological change during Li-In alloying at high currents, and the local Li+ diffusion coefficient discrepancy is proposed. These new findings of Li-ion transport and boundary phase transition in Li10 GeP2 S12 solid electrolyte under high-pressure and high current density are first reported and will help provide previously lacking insights into the relationship of structure and performance of Li10 GeP2 S12 .

Transfer Hydrogenation with a Carbon-Nitride-Supported Palladium Single-Atom Photocatalyst and Water as a Proton Source.

Solar-driven transfer hydrogenation of unsaturated bonds has received considerable attention in the research area of sustainable organic synthesis; however, water, the ultimate green source of hydrogen, has rarely been investigated due to the high barrier associated with splitting of water molecules. We report a carbon-nitride-supported palladium single-atom heterogeneous catalyst with unparalleled performance in photocatalytic water-donating transfer hydrogenation compared to its nanoparticle counterparts. Isotopic-labeling experiments and operando nuclear magnetic resonance measurements confirm the direct hydrogenation mechanism using in situ-generated protons from water splitting under visible-light irradiation. Density functional theory calculations attribute the high activity to lower barriers for hydrogenation, facilitated desorption of ethylbenzene, and facile hydrogen replenishment from water on the atomic palladium sites.

Clarifying the Temperature-Dependent Lithium Deposition/Stripping Process and the Evolution of Inactive Li in Lithium Metal Batteries.

The deposition/stripping behavior of lithium metal is intriguing, and the associated formation of inactive lithium at various temperatures remains elusive, which hinders the practical application of lithium metal batteries. Here, utilizing the variable-temperature operando solid-state nuclear magnetic resonance (SS NMR) technique, we reveal the temperature effects on the lithium microstructure evolution in a carbonate-based electrolyte system. In addition, the mass spectrometry titration (MST) method is used to quantify the evolution of inactive lithium components, including dead lithium, solid electrolyte interface (SEI), and lithium hydride (LiH). Combined SS NMR and MST results show that the morphology of lithium metal is reasonably correlated to the amount of inactive Li formed. At low/ambient temperature, the lithium microstructure has a similar evolution pattern, and its poor morphology leads to a large amount of dead lithium, which dominates capacity loss; however, at high temperature large and dense lithium deposits form with less dead Li detected, and the intensified electrolyte consumption in SEI formation is the major cause for capacity loss. Our phase-field simulation results reveal that the compact lithium deposition formed at higher temperature is due to the more uniformly distributed electric field and Li+ concentration. Lastly, two strategies in forming a dense Li deposit are proposed and tested that show performance-enhancing results.

Operando benchtop NMR reveals reaction intermediates and crossover in redox flow batteries.

Redox flow batteries (RFBs) provide a promising battery technology for grid-scale energy storage. High-field operando NMR analyses of RFBs have yielded useful insight into their working mechanisms and helped improve battery performance. Nevertheless, the high cost and large footprint of a high-field NMR system limit its implementation by a wider electrochemistry community. Here, we demonstrate an operando NMR study of an anthraquinone/ferrocyanide-based RFB on a low-cost and compact 43 MHz benchtop system. The chemical shifts induced by bulk magnetic susceptibility effects differ remarkably from those obtained in high-field NMR experiments, due to the different orientations of the sample relative to the external magnetic field. We apply Evans method to estimate the concentrations of paramagnetic anthraquinone radical and ferricyanide anions. The degradation of 2,6-dihydroxy-anthraquinone (DHAQ) to 2,6-dihydroxy-anthrone and 2,6-dihydroxy-anthranol has been quantified. We further identified the impurities commonly present in the DHAQ solution to be acetone, methanol and formamide. The crossover of DHAQ and impurity molecules through the sseparation Nafion® membrane was captured and quantified, and a negative correlation between the molecular size and crossover rate was established. We show that a benchtop NMR system has sufficient spectral and temporal resolution and sensitivity for the operando study of RFBs, and anticipate a broad application of operando benchtop NMR methods for studying flow electrochemistry targeted for different applications.

Operando nuclear magnetic resonance spectroscopy: Detection of the onset of metallic lithium deposition on graphite at low temperature and fast charge in a full Li-ion battery.

Lithium-ion batteries are at the core of the democratisation of electric transportation and portative electronic devices. However, fast and/or low temperature charge induce performance loss, mainly through lithium plating, a degrading mechanism. In this report, 7Li operando Nuclear Magnetic Resonance spectroscopy is used to detect the onset of metastable lithium deposits in an NMC622/graphite cell at 0 °C and fast charge. An operando setup, compatible with low temperatures, was developed with special attention to the pressure applied on the electrodes/separator stack and noise reduction to enable early detection and good time-resolution. Direct detection of metallic lithium enables drawing correlations between lithium plating and electrochemical data.

Nuclear magnetic resonance studies of carbon dioxide capture.

Carbon dioxide capture is an important greenhouse gas mitigation technology that can help limit climate change. The design of improved capture materials requires a detailed understanding of the mechanisms by which carbon dioxide is bound. Nuclear magnetic resonance (NMR) spectroscopy methods have emerged as a powerful probe of CO2 sorption and diffusion in carbon capture materials. In this article, we first review the practical considerations for carrying out NMR measurements on capture materials dosed with CO2 and we then present three case studies that review our recent work on NMR studies of CO2 binding in metal-organic framework materials. We show that simple 13C NMR experiments are often inadequate to determine CO2 binding modes, but that more advanced experiments such as multidimensional NMR experiments and 17O NMR experiments can lead to more conclusive structural assignments. We further discuss how pulsed field gradient (PFG) NMR can be used to explore diffusion of adsorbed CO2 through the porous framework. Finally, we provide an outlook on the challenges and opportunities for the further development of NMR methodologies that can improve our understanding of carbon capture.

Anion Redox in an Amorphous Titanium Polysulfide.

Amorphous transition-metal polysulfides are promising positive electrode materials for next-generation rechargeable lithium-ion batteries because of their high theoretical capacities. In this study, sulfur anion redox during lithiation of amorphous TiS4 (a-TiS4) was investigated by using experimental and theoretical methods. It was found that a-TiS4 has a variety of sulfur valence states such as S2-, S-, and Sδ-. The S2- species became the main component in the Li4TiS4 composition, indicating that sulfur is a redox-active element up to this composition. The simulated a-TiS4 structure changed gradually by lithium accommodation to form a-Li4TiS4: S-S bonds in the disulfide units and polysulfide chains were broken. Bader charge analysis suggested that the average S valency decreased drastically. Moreover, deep lithiation of a-TiS4 provided a conversion reaction to metallic Ti and Li2S, with a high practical capacity of ∼1000 mAh g-1 when a lower cutoff voltage was applied.