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Despite being the major cause of battery safety issues and detrimental performance, a comprehensive growth mechanism for metallic lithium deposited at electrode surfaces in lithium metal batteries remains elusive. While lithium surface morphology is often derived indirectly, here, detailed information is directly obtained using in situ small and ultra-small angle neutron scattering, in bulk and non-destructively. Features of 1-10 um and 100-300 nm are identified; the latter contribute to most of the surface area and their size inversely correlates to applied current density. Surface area per unit volume increases continuously during charging from 1-4 h at 2 mA/cm2 but more slowly during discharge. Comparatively higher values are reached after just 1 h at 20 mA/cm2 which remain constant in subsequent cycles. Such quantitative insight into the processes of metallic lithium growth within batteries may enable the development of safer high performance lithium metal batteries., Comment: Main article: 23 pages, 9 figures, 1 table. Supplementary information: 14 pages, 11 figures, 6 tables, 3 technical notes. To be published in a peer-reviewed journal. Please forward a copy of email requests to drchristophedidier@gmail.com

Small angle neutron scattering (SANS) responses of particulate silica as disordered and ordered porous and non-porous powders were obtained. Each classification provided distinct scattering patterns which were fitted and analysed using Guinier-Porod and mass-surface fractal (msf) models. The resulting particle dimensions showed good agreement with the same from nitrogen gas adsorption analyses. Additionally, the excellent fit of the msf model to the non-porous silica scattering response resulted in an agreement between the mass and surface fractal dimension values for it and similar analyses and results published previously for fumed silica. The msf fitting gave additional insight into particle and cluster scattering dimensions with particle dimensions being consistent with those from the G-P analyses. Refereed/Peer-reviewed

In this study, we explore the overall structural ensembles and transitions of a biomimetic, multi-stimuli-responsive, intrinsically disordered protein (IDP), Rec1-resilin. The structural transition of Rec1-resilin with change in molecular crowding and environment is evaluated using small-angle neutron scattering and small-angle X-ray scattering. The quantitative analyses of the experimental scattering data using a combination of computational models allowed comprehensive description of the structural evolution, organization, and conformational ensembles of Rec1-resilin in response to the changes in concentration, pH, and temperature. Rec1-resilin in uncrowded solutions demonstrates the equilibrium intrinsic structure quality of an IDP with radius of gyration Rg ∼ 5 nm, and a scattering function for the triaxial ellipsoidal model best fit the experimental dataset. On crowding (increase in concentration >10 wt %), Rec1-resilin molecules exert intermolecular repulsive force of interaction, the Rg value reduces with a progressive increase in concentration, and molecular chains transform from a Gaussian coil to a fully swollen coil. It is also revealed that the structural organization of Rec1-resilin dynamically transforms from a rod (pH 2) to coil (pH 4.8) and to globular (pH 12) as a function of pH. The findings further support the temperature-triggered dual-phase-transition behavior of Rec1-resilin, exhibiting rod-shaped structural organization below the upper critical solution temperature (∼4 °C) and a large but compact structure above the lower critical solution temperature (∼75 °C). This work attempted to correlate unusual responsiveness of Rec1-resilin to the evolution of conformational ensembles. Refereed/Peer-reviewed