Correction: 5D total scattering computed tomography reveals the full reaction mechanism of a bismuth vanadate lithium ion battery anode.

Correction for '5D total scattering computed tomography reveals the full reaction mechanism of a bismuth vanadate lithium ion battery anode' by Jonas Sottmann et al., Phys. Chem. Chem. Phys., 2022, 24, 27075-27085, https://doi.org/10.1039/D2CP03892G.

5D total scattering computed tomography reveals the full reaction mechanism of a bismuth vanadate lithium ion battery anode.

We have used operando 5D synchrotron total scattering computed tomography (TSCT) to understand the cycling and possible long term deactivation mechanisms of the lithium-ion battery anode bismuth vanadate. This anode material functions via a combined conversion/alloying mechanism in which nanocrystals of lithium-bismuth alloy are protected by an amorphous matrix of lithium vanadate. This composite is formed in situ during the first lithiation of the anode. The operando TSCT data were analyzed and mapped using both pair distribution function and Rietveld methods. We can follow the lithium-bismuth alloying reaction at all stages, gaining real structural insight including variations in nanoparticle sizes, lattice parameters and bond lengths, even when the material is completely amorphous. We also observe for the first time structural changes related to the cycling of lithium ions in the lithium vanadate matrix, which displays no interactions beyond the first shell of V-O bonds. The first 3D operando mapping of the distribution of different materials in an amorphous anode reveals a decline in coverage caused by either agglomeration or partial dissolution of the active material, hinting at the mechanism of long term deactivation. The observations from the operando experiment are backed up by post mortem transmission electron microscope (TEM) studies and theoretical calculations to provide a complete picture of an exceptionally complex cycling mechanism across a range of length scales.

Pseudo-ternary LiBH4·LiCl·P2S5 system as structurally disordered bulk electrolyte for all-solid-state lithium batteries.

The properties of the mixed system LiBH4-LiCl-P2S5 are studied with respect to all-solid-state batteries. The studied material undergoes an amorphization upon heating above 60 °C, accompanied with increased Li+ conductivity beneficial for battery electrolyte applications. The measured ionic conductivity is ∼10-3 S cm-1 at room temperature with an activation energy of 0.40(2) eV after amorphization. Structural analysis and characterization of the material suggest that BH4 groups and PS4 may belong to the same molecular structure, where Cl ions interplay to accommodate the structural unit. Thanks to its conductivity, ductility and electrochemical stability (up to 5 V, Au vs. Li+/Li), this new electrolyte is successfully tested in battery cells operated with a cathode material (layered TiS2, theo. capacity 239 mA h g-1) and Li anode resulting in 93% capacity retention (10 cycles) and notable cycling stability under the current density ∼12 mA g-1 (0.05C-rate) at 50 °C. Further advanced characterisation by means of operando synchrotron X-ray diffraction in transmission mode contributes explicitly to a better understanding of the (de)lithiation processes of solid-state battery electrodes operated at moderate temperatures.

Operando investigations of lithiation and delithiation processes in a BiVO4 anode material.

BiVO4 undergoes a series of conversion and alloying reactions as an anode material in lithium ion batteries. The current work demonstrates a charge capacity of 485 mA h g-1 after 50 cycles in a voltage range of 0-2.00 V (graphite has a capacity of 372 mA h g-1 theoretically). An exceptionally high volumetric capacity makes BiVO4 suitable for compact applications (volumetric capacity of 3984 mA h cm-3 for BiVO4 in comparison to 756 mA h cm-3 for graphite theoretically). Reaction steps and electronic transformations have been identified by operando quasi simultaneous synchrotron X-ray diffraction and absorption spectroscopy studies. An irreversible reaction step occurs for the Bi3+/Bi0 redox pair, whereas reversible mechanisms are found for the V5+/V3+ and Bi0/Bi3- redox pairs. The proposed mechanisms are supported by density functional theory (DFT) calculations.

Zirconia dental implants; the relationship between design and clinical outcome: A systematic review.

OBJECTIVE: To evaluate the clinical outcome of different designs of zirconia dental implants. DATA: This systematic review adhered to the PRISMA checklist and followed the PICO framework. The protocol is registered in PROSPERO (CRD42022337228). SOURCES: The search was conducted in March 2023 through four databases (PubMed, Web of Science, Cochrane Library, and Google Scholar) along with a search of references in the related reviews. Three authors reviewed on title, and abstract level and analysed the risk of bias, and all authors reviewed on a full-text level. STUDY SELECTION: Clinical studies excluding case reports for patients treated with different designs of zirconia dental implants were included. From a total of 2728 titles, 71 full-text studies were screened, and 27 studies were included to assess the risk of bias (ROBINS-I tool) and data extraction. After quality assessment, four studies were included, and the remaining 23 excluded studies were narratively described. RESULT: The included prospective studies with moderate risk of bias reported success and survival rates of one-piece implants that ranged between 95 and 98.4 % with no difference between different lengths and diameters. The acid-etched roughened surface showed higher clinical outcomes compared to other surface roughness designs. CONCLUSION: Promising 5-year clinical outcomes were found for one-piece zirconia implants with no difference between different diameters and lengths. Concerning surface roughness, better outcomes were found when using the acid-etched implant surface. However, due to the limited available studies, further high-quality clinical studies comparing zirconia one-piece and two-piece implants with different diameters, lengths, and surface roughness are needed. CLINICAL SIGNIFICANCE: Based on this systematic review, under suitable clinical situations, the one-piece zirconia implants with diameters of 4.0 mm, 4.5 mm, or 5.5 mm and lengths of 8 mm, 10 mm, 12 mm, or 14 mm have similar promising clinical outcomes. Additionally, the acid-etched roughened implant surface may be preferable.

Deterioration of direct restorative materials under erosive conditions with impact of abrasion and attrition in vitro.

Objective: To compare the cumulative impact of sequential wear on mechanical properties and appearance of a composite resin (CR), Filtek Z250®, a glass ionomer GI, Fuji IX GP®, and a glass hybrid (GH), Equia Forte®. Material and Methods: Six equally sized specimens of each material were subjected to wear tests, i.e., simulation of brushing, chewing and acidic liquid exposure, mimicking at least 6 months of clinical exposure. Surface roughness, hardness, substance loss and degree of shade lightness were determined. Results: Following wear tests, significant increase in surface roughness and decrease in hardness values were observed for all materials (p < .05). Significantly larger substance loss was found in Equia Forte® specimens compared to Filtek Z250® (p < .05), while that of Fuji IX® exceeded the measurement capacity of the instrument. Opposite to the two other materials, the shade of Filtek Z250® became darker. Conclusions: Sequential wear exposure mimicking abrasion, erosion and attrition to products representing CR, GI and GH, caused weakening and change in appearance of the materials. The composite resin was the most mechanically resistant to the sequential wear.

Wear particle release at the interface of dental implant components: Effects of different material combinations. An in vitro study.

OBJECTIVES: Particle generation from implant components caused by frictional wear affect the surrounding peri-implant tissues. The objective of this study was to evaluate the effect of combining implant and abutment materials on wear and particle release in a dynamical loading setup. METHODS: A customized dynamical loading machine was used to subject two implant materials (Titanium and Titanium- Zirconium alloy) paired with two different abutment materials (Titanium and Zirconia) to a cyclic loading set of 240.000 cycles (simulating 1 year of clinical use). The implant and abutment complex was immersed in corrosive liquid to collect particle debris and measure the release of corroded ions. Scanning electron microscopy was used to analyze signs of wear on the components after testing and evaluate the size and composition of particle debris. RESULTS: Wear signs were evident in all material couplings. Particle debris was found on top, inside the implants, and on the abutment heads. The particle size ranged between 0.6 and 16.9 µm, with larger particles composed of Ti. Smaller-sized particles were found in the container liquid ranging from 0.253 to 1.7 µm compared to inside the implants ranging from 3.25 to 95.3 µm. Larger particles were found inside Tizr implants compared to Ti implants. Low levels of ions released due to corrosion were found when measuring content in surrounding liquid. SIGNIFICANCE: Particle generation is evident when subjecting dental implant and abutment couplings in a dynamic loading setup. Internally connected implants hinder the release of larger particles to surrounding container liquid.

Pre-cementation procedures' effect on dental zirconias with different yttria content.

OBJECTVE: Several pre-cementation procedures have been advocated to enhance adhesion between zirconia and resin-based cement. There is, however, limited documentation on how these pre-treatments affect the strength of zirconia crowns as most tests are performed on discs or bars. The aim was to assess the effect of pre-cementation procedures on fracture mode, fracture strength and cement retention on zirconia. METHODS: Two dental zirconia materials with different yttria content were assessed (<4 and>5 mol%). Both discs (n = 45) and crown-shaped specimens (n = 30) of the two materials were pretreated with either air-abrasion or hot-etching with KHF2 and compared with untreated controls with regards to surface roughness, crystallography, wettability, cement adhesion and fracture strength. RESULTS AND SIGNIFICANCE: Air-abrasion improves adhesion and strength of zirconia with moderate yttria content (<4 mol%). Acid etching with heated KHF2 showed the best effect on strength and cement retention on zirconia with higher yttria content (>5 mol%). Application of KHF2 was, however, complicated on crown-shaped specimens. Pre-treatment and cementation protocols should be optimized for different dental zirconias to improve both strength and retention.

A novel polytype - the stacking fault based γ-MoO3 nanobelts.

γ-MoO3 nanobelts prepared by hydrothermal synthesis were studied by synchrotron radiation powder diffraction, scanning electron microscopy, transmission electron microscopy and selected area electron diffraction. Their nm dimensions, in particular in two crystallographic directions, have a profound influence on electrochemical properties during cycling as the cathode material in lithium-ion batteries (LIBs). The diffraction analysis shows clearly that the crystal structure for the γ-MoO3 nanobelts differs significantly from that of bulk α-MoO3. The observed powder diffraction pattern, with asymmetric peaks, extremely broad peaks, as well as additional or absent diffraction peaks, is fully described by means of a model based on stacking disorder of MoO3 slabs.