Electrochemical oxidation stability of anions for modern battery electrolytes: a CBS and DFT study

The electrochemical stability vs. oxidation is a crucial property of anions in order to be suitable as components in lithium-ion batteries. Here the applicability of a number of computational approaches and methods to assess this property, employing a wide selection of DFT functionals, has been studied using the CCSD(T)/CBS method as the reference. In all, the vertical anion oxidation potential, Delta E-v, is a fair way to calculate the stability vs. oxidation, however, a functional of at least hybrid quality is recommended. In addition, the chemical hardness, eta, is identified as a novel approach to calculate the stability vs. oxidation

Natural abundance solid-state 33S NMR study of NbS3: applications for battery conversion electrodes.

We report ultra-wideline, high-field natural abundance solid-state 33S NMR spectra of the Li-ion battery conversion electrode NbS3, the first 33S NMR study of a compound containing disulfide (S22-) units. The large quadrupolar coupling parameters (CQ ≈ 31 MHz) are consistent with values obtained from DFT calculations, and the spectra provide evidence for the linear Peierls distortion that doubles the number of 33S sites

Molecular simulation study of CO2 and N2 absorption in a phosphonium based organic ionic plastic crystal

 An organic ionic plastic crystal (OIPC), methyl(diethyl)isobutylphosphonium hexafluorophosphate [P122i4][PF6], was investigated for CO2 and N2 absorption using molecular simulations. Ab initio calculations showed that both the cation and anion exhibit larger binding energy for CO2 compared with N2. The CO2 absorption, as calculated from classical molecular dynamics simulations, increased by a factor of 7.5 from 275 K to 325 K, while that of N2 showed low absorption at both temperatures. The simulations suggest that the significant increase in CO2 absorption at 325 K is attributed to a higher degree of disorder and increase in the free volume due to the gas/solid interfaces. While the ab initio calculations were helpful in identifying specific interaction sites on the constituent ions, the classical MD simulations elucidated the importance of interfaces in gas absorption studies in this material. The results show that the OIPC can be a promising material for CO2 separations from CO2/N2 mixture

Blurring the boundary between homogenous and heterogeneous catalysis using palladium nanoclusters with dynamic surfaces.

Using a magnetron sputtering approach that allows size-controlled formation of nanoclusters, we have created palladium nanoclusters that combine the features of both heterogeneous and homogeneous catalysts. Here we report the atomic structures and electronic environments of a series of metal nanoclusters in ionic liquids at different stages of formation, leading to the discovery of Pd nanoclusters with a core of ca. 2 nm surrounded by a diffuse dynamic shell of atoms in [C4C1Im][NTf2]. Comparison of the catalytic activity of Pd nanoclusters in alkene cyclopropanation reveals that the atomically dynamic surface is critically important, increasing the activity by a factor of ca. 2 when compared to compact nanoclusters of similar size. Catalyst poisoning tests using mercury and dibenzo[a,e]cyclooctene show that dynamic Pd nanoclusters maintain their catalytic activity, which demonstrate their combined features of homogeneous and heterogeneous catalysts within the same material. Additionally, kinetic studies of cyclopropanation of alkenes mediated by the dynamic Pd nanoclusters reveal an observed catalyst order of 1, underpinning the pseudo-homogeneous character of the dynamic Pd nanoclusters

Ab initio REMPI spectra of HCl and HF

HCl sameindin er vinsæl í rannsóknum með litrófsgreiningu. Sameindin hefur verið rannsökuð í nokkurn tíma við Raunvísindastofnun Háskólans með REMPI aðferðinni (Resonance Enhanced Multiphoton Ionization). Þessi aðferð gerir kleift að rannsaka áður óþekkt örvuð ástönd sameindarinnar. Samhliða þessum rannsóknum eru ab-initio útreikningar, þar sem hægt er að reikna mættisferla örvuðu ástandanna. Út frá þessum mættisferlum er hægt að reikna litrófsfasta hvers ástands fyrir sig. Nokkur örvuð ástönd HCl sameindarinnar hafa verið reiknuð. Einhverjir útreikningar voru einnig keyrðir fyrir HF sameindina. Getan til að beita útreikningum einfaldlega á örvuð ástönd sameinda er fremur nýleg. Aðferðinni sem hér er beitt er equations of motion (EOM), sem er stækkun á coupled cluster (CC) aðferðinni

Novel pseudo-delocalized anions for lithium battery electrolytes

A novel anion concept of pseudo-delocalized anions, anions with distinct positive and negative charge regions, has been studied by a computer aided synthesis using DFT calculations. With the aim to find safer and better performing lithium salts for lithium battery electrolytes two factors have been evaluated: the cation-anion interaction strength via the dissociation reaction LiAn (sic) Li+ + An(-) and the anion oxidative stability via a vertical ionisation from anion to radical. Based on our computational results some of these anions have shown promise to perform well as lithium salts for modern lithium batteries and should be interesting synthetic targets for future research

NMR Methodology for Measuring Dissolved O₂ and Transport in Lithium-Air Batteries.

Similar to fuel cells, poor mass transport of redox active species, such as dissolved oxygen gas, is one of the challenges faced by lithium-air batteries (LABs). Capitalizing on the paramagnetic properties of O2, we used nuclear magnetic resonance (NMR) spectroscopy to measure oxygen concentration and transport in LAB electrolytes. Lithium bis(trifluoromethane) sulfonylimide (LiTFSI) in glymes or dimethyl sulfoxide (DMSO) solvents were investigated with 1H, 13C, 7Li, and 19F NMR spectroscopy, with the results showing that both the 1H, 13C, 7Li, and 19F bulk magnetic susceptibility shifts and the change in 19F relaxation times were accurate measures of dissolved O2 concentration. O2 saturation concentrations and diffusion coefficients were extracted that are comparable to values measured by electrochemical or pressure methods reported in the literature, highlighting the validity of this new methodology. This method also provides experimental evidence of the local O2 solvation environment, with results again comparable to previous literature and supported by our molecular dynamics simulations. A preliminary in situ application of our NMR methodology is demonstrated by measuring O2 evolution during LAB charging using LiTFSI in the glyme electrolyte. While the in situ LAB cell showed poor coulombic efficiency, since no additives were used, the O2 evolution was successfully quantified. Our work demonstrates the first usage of this NMR methodology to quantify O2 in LAB electrolytes, experimentally demonstrate solvation environments of O2, and detect O2 evolution in situ in a LAB flow cell

NMR Methodology for Measuring Dissolved O₂ and Transport in Lithium–Air Batteries

Similar to fuel cells, poor mass transport of redox active species, such as dissolved oxygen gas, is one of the challenges faced by lithium–air batteries (LABs). Capitalizing on the paramagnetic properties of O2, we used nuclear magnetic resonance (NMR) spectroscopy to measure oxygen concentration and transport in LAB electrolytes. Lithium bis­(trifluoromethane) sulfonylimide (LiTFSI) in glymes or dimethyl sulfoxide (DMSO) solvents were investigated with 1H, 13C, 7Li, and 19F NMR spectroscopy, with the results showing that both the 1H, 13C, 7Li, and 19F bulk magnetic susceptibility shifts and the change in 19F relaxation times were accurate measures of dissolved O2 concentration. O2 saturation concentrations and diffusion coefficients were extracted that are comparable to values measured by electrochemical or pressure methods reported in the literature, highlighting the validity of this new methodology. This method also provides experimental evidence of the local O2 solvation environment, with results again comparable to previous literature and supported by our molecular dynamics simulations. A preliminary in situ application of our NMR methodology is demonstrated by measuring O2 evolution during LAB charging using LiTFSI in the glyme electrolyte. While the in situ LAB cell showed poor coulombic efficiency, since no additives were used, the O2 evolution was successfully quantified. Our work demonstrates the first usage of this NMR methodology to quantify O2 in LAB electrolytes, experimentally demonstrate solvation environments of O2, and detect O2 evolution in situ in a LAB flow cell

NMR Methodology for Measuring Dissolved O2 and Transport in Lithium-Air Batteries.

Similar to fuel cells, poor mass transport of redox active species, such as dissolved oxygen gas, is one of the challenges faced by lithium-air batteries (LABs). Capitalizing on the paramagnetic properties of O2, we used nuclear magnetic resonance (NMR) spectroscopy to measure oxygen concentration and transport in LAB electrolytes. Lithium bis(trifluoromethane) sulfonylimide (LiTFSI) in glymes or dimethyl sulfoxide (DMSO) solvents were investigated with 1H, 13C, 7Li, and 19F NMR spectroscopy, with the results showing that both the 1H, 13C, 7Li, and 19F bulk magnetic susceptibility shifts and the change in 19F relaxation times were accurate measures of dissolved O2 concentration. O2 saturation concentrations and diffusion coefficients were extracted that are comparable to values measured by electrochemical or pressure methods reported in the literature, highlighting the validity of this new methodology. This method also provides experimental evidence of the local O2 solvation environment, with results again comparable to previous literature and supported by our molecular dynamics simulations. A preliminary in situ application of our NMR methodology is demonstrated by measuring O2 evolution during LAB charging using LiTFSI in the glyme electrolyte. While the in situ LAB cell showed poor coulombic efficiency, since no additives were used, the O2 evolution was successfully quantified. Our work demonstrates the first usage of this NMR methodology to quantify O2 in LAB electrolytes, experimentally demonstrate solvation environments of O2, and detect O2 evolution in situ in a LAB flow cell.The authors thank EPSRC-EP/M009521/1 and the Cambridge Trust (E.W.) for research funding. C.P.G. acknowledge support from Centre of Advanced Materials for Integrated Energy Systems (CAM-IES), via EPSRC grant no. EP/P007767/1. E.J. and C.P.G. acknowledge support from the ERC grant BATNMR no 835073. The authors thank Fikile R. Brushett (MIT) for sharing the design of the flow battery that is compatible with non-aqueous solvents