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At least 19 records

Unusual stoichiometry control in the atomic layer deposition of manganese borate films from manganese bis(tris(pyrazolyl)borate) and ozone

The atomic layer deposition (ALD) of films with the approximate compositions Mn{sub 3}(BO{sub 3}){sub 2} and CoB{sub 2}O{sub 4} is described using MnTp{sub 2} or CoTp{sub 2} [Tp = tris(pyrazolyl)borate] with ozone. The solid state decomposition temperatures of MnTp{sub 2} and CoTp{sub 2} are ∼370 and ∼340 °C, respectively. Preparative-scale sublimations of MnTp{sub 2} and CoTp{sub 2} at 210 °C/0.05 Torr afforded >99% recoveries with <0.1% nonvolatile residues. Self-limited ALD growth was demonstrated at 325 °C for MnTp{sub 2} or CoTp{sub 2} with ozone as the coreactant. The growth rate for the manganese borate process was 0.19 Å/cycle within the ALD window of 300–350 °C. The growth rate for the cobalt borate process was 0.39–0.42 Å/cycle at 325 °C. X-ray diffraction of the as-deposited films indicated that they were amorphous. Atomic force microscopy of 35–36 nm thick manganese borate films grown within the 300–350 °C ALD window showed root mean square surface roughnesses of 0.4–0.6 nm. Film stoichiometries were assessed by x-ray photoelectron spectroscopy and time of flight-elastic recoil detection analysis. The differing film stoichiometries obtained from the very similar precursors MnTp{sub 2} and CoTp{sub 2} are proposed to arise from the oxidizing ability of the intermediate high valent manganese oxide layers and lack thereof for cobalt.

36 MATERIALS SCIENCE↗

Oxidative Deboronation of Boronic Acids by Hydrogen Peroxide in Planta Generates Borate for Cross-Linking of Rhamnogalacturonan II

Vascular plants require boron to cross-link the rhamnogalacturonan-II (RG-II) domain of pectin to form functional cell walls. Boronic acids, which form reversible esters with cis-diols like borate, have been proposed to influence RG-II cross-linking, though the mechanism remains unclear. We used suspension-cultured rose cells adapted to grow without boron to investigate the effect of boronic acids on RG-II dimerization. When grown with phenylboronic acid (PBA) as the sole boron source, nearly all RG-II was crosslinked, whereas methylboronic acid (MBA) only partially restored cross-linking. In contrast, in vitro assays showed that homogeneous RG-II monomers did not dimerize with alkyl or aryl boronic acids unless supplemented with hydrogen peroxide (H2O2), which oxidatively converts boronic acids to boric acid. Real-time NMR spectroscopy and density functional theory calculations provided insight into the reaction mechanism and energetics of oxidation respectively. Together, our data show that exogenous boronic acids are a source of boric acid for plants, and that the deboronation reaction generates aryl or alkyl alcohol byproducts that can undergo further chemical modification in planta. The fate and potential roles of these byproducts in planta remain to be determined.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Simultaneous Stabilization of LiNi 0.76 Mn 0.14 Co 0.10 O 2 Cathode and Lithium Metal Anode by Lithium Bis(oxalato)borate as Additive

Abstract The long‐term cycling performance, rate capability, and voltage stability of lithium (Li) metal batteries with LiNi 0.76 Mn 0.14 Co 0.10 O 2 (NMC76) cathodes is greatly enhanced by lithium bis(oxalato)borate (LiBOB) additive in the LiPF 6 ‐based electrolyte. With 2 % LiBOB in the electrolyte, a Li∥NMC76 cell is able to achieve a high capacity retention of 96.8 % after 200 cycles at C/3 rate (1 C=200 mA g −1 ), which is the best result reported for a Ni‐rich NMC cathode coupled with Li metal anode. The significantly enhanced electrochemical performance can be ascribed to the stabilization of both the NMC76 cathode/electrolyte and Li‐metal‐anode/electrolyte interfaces. The LiBOB‐containing electrolyte not only facilitates the formation of a more compact solid–electrolyte interphase on the Li metal surface, it also forms a enhanced cathode electrolyte interface layer, which efficiently prevents the corrosion of the cathode interface and mitigates the formation of the disordered rock‐salt phase after cycling. The fundamental findings of this work highlight the importance of recognizing the dual effects of electrolyte additives in simultaneously stabilizing both cathode and anode interfaces, so as to enhance the long‐term cycle life of high‐energy‐density battery systems.

Zhao, Wengao↗

Two-Dimensional Uranyl Borates: From Conventional to Extreme Synthetic Conditions: Two-Dimensional Uranyl Borates: From Conventional to Extreme Synthetic Conditions

A systematic investigation of uranyl borates under different synthetic conditions resulted in five new 2D compounds, namely, (H 3 O)[(UO 2 )(BO 3 )], Li[(UO 2 )(BO 3 )] · (H 2 O), α-K 4 [(UO 2 ) 5 (BO 3 ) 2 O 4 ], β-K 4 [(UO 2 ) 5 (BO 3 ) 2 O 4 ] and K 2.5 [(UO 2 ) 5 (BO 3 ) 2 O 2.5 (OH) 1.5 ] · (H 2 O) 2.5 . (H 3 O)[(UO 2 )(BO 3 )] and Li[(UO 2 )(BO 3 )] · (H 2 O) were obtained from hydrothermal reactions at 220 °C using the same mineralizer. Both materials possess the uranophane sheet topology with different symmetry of the unit cells. In the structure of (H 3 O)[(UO 2 )(BO 3 )] and Li[(UO 2 )(BO 3 )] · (H 2 O), UO 7 pentagonal bipyramids share edges and vertexes with four BO 3 planar triangles. α-K 4 [(UO 2 ) 5 (BO 3 ) 2 O 4 ] and β-K 4 [(UO 2 ) 5 (BO 3 ) 2 O 4 ] are polytypes. α-K 4 [(UO 2 ) 5 (BO 3 ) 2 O 4 ] was synthesized from a high-temperature solid-state reaction under ambient pressure; whereas β-K 4 [(UO 2 ) 5 (BO 3 ) 2 O 4 ] was obtained from a high-temperature/high-pressure (HT/HP) reaction. Both structures have an identical anion topology, but β-K 4 [(UO 2 ) 5 (BO 3 ) 2 O 4 ] crystallizes in space group with higher symmetry. In K 2.5 [(UO 2 ) 5 (BO 3 ) 2 O 2.5 (OH) 1.5 ] · (H 2 O) 2.5 , which was obtained from a hydrothermal reaction, UO 7 polyhedra share vertexes and edges with two independent BO 3 triangles, forming the most complex uranyl borate layers among all five compounds. The different synthetic routes, novel topologies, thermal behavior and Raman spectra are discussed.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Formation mechanisms of boron oxide films fabricated by large-area electron beam-induced deposition of trimethyl borate [Formation Mechanisms of Boron Oxide Fillms Fabricated by Large Area Electron Beam-Induced Deposition of Trimethyl Borate]

Boron-containing materials are increasingly drawing interest for the use in electronics, optics, laser targets, neutron absorbers, and high-temperature and chemically resistant ceramics. In this article, the first investigation into the deposition of boron-based material via electron beam-induced deposition (EBID) is reported. Thin films were deposited using a novel, large-area EBID system that is shown to deposit material at rates comparable to conventional techniques such as laser-induced chemical vapor deposition. The deposition rate and stoichiometry of boron oxide fabricated by EBID using trimethyl borate (TMB) as precursor is found to be critically dependent on the substrate temperature. By comparing the deposition mechanisms of TMB to the conventional, alkoxide-based precursor tetraethyl orthosilicate it is revealed that ligand chemistry does not precisely predict the pathways leading to deposition of material via EBID. Lastly, the results demonstrate the first boron-containing material deposited by the EBID process and the potential for EBID as a scalable fabrication technique that could have a transformative effect on the athermal deposition of materials.

36 MATERIALS SCIENCE↗

Fundamental Study on Effects of Borate on the Sorption of Cesium ions to Calcium Silicate Hydrate - 18068

The effects of borate on the formation of calcium silicate hydrate (C-S-H) and the Cs sorption behavior were examined by the sorption experiments without drying process. C-S-H was prepared by mixing calcium oxide, fumed silica, and sodium-borate solution in a glove bag filled with nitrogen gas. The volume of sodium borate solution was 30 mL, in order to adjust the liquid/solid weight ratio to 20. The Ca/Si molar ratio of C-S-H was adjusted so as to be 0.4, 0.8, 1.2, and 1.6. The concentration of sodium borate was set to the range from 0 to 600 mM in the sample solution. The solution of cesium chloride was added to the each sample for setting the initial concentration of Cs ions to 1 mM. The samples were cured in a shaking chamber at 298 K and 120 strokes/min during 7 days. In addition, for estimating the curing-period dependencies, the curing period was set to the range from 0.5 to 28 days for the condition of 0 M or 400 M sodium borate. In the results, under the conditions of the borate concentration up to 200 mM, the sorption behavior of Cs ions to C-S-H was hardly different from those without borate, while the sorption ratio of Cs ions for the borate concentration of 400 mM or more decreased by down to 46% compared with the blank samples. However, the sorption ratio of Cs ions in the case of 400 mM borate increased and reached as much as that for the blank sample until 28 days. Besides, the Raman spectra of solid phase showed that the peak derived from boric acid or borate (calcium borate or calcium borosilicate hydrate) appeared under the high concentration conditions of borate, and the peak of the silica chain of C-S-H was weakened. Considering the practical concentration of borate and much longer period for the performance assessment of the solidified wastes, the immobilization properties for Cs ions of cementitious materials contained borate will be kept appropriately in the disposal system for low-level wastes. (authors)

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Combined effects of lithium and borate ions on the hydration of calcium sulfoaluminate cement

This work investigates the combined influence of borate and lithium ions on the hydration of two calcium sulfoaluminate (CSA) cements containing 0 or 10 wt% gypsum. On the one hand, borates are known to retard CSA cement hydration due to the rapid precipitation of ulexite. On the other hand, lithium ions accelerate CSA cement hydration thanks to the fast precipitation of Li-containing aluminum hydroxide. When borates and lithium are present simultaneously, these two mechanisms are superimposed. With a gypsum-free cement, a third process is additionally observed: lithium promotes the initial precipitation of a borated AFm phase which is later converted into a borated AFt phase when hydration accelerates. Lithium salts can counteract the retardation by sodium borate. However, their influence is limited once a sufficient amount of Li-containing Al(OH){sub 3} seeds is formed. For the CSA cements under investigation, the threshold lithium concentration is close to 0.03 mmol/g of cement and similar with or without borate.

36 MATERIALS SCIENCE↗

Influence of Borate on Sorption of Strontium and Barium to Calcium Silicate Hydrate - 20148

Radioactive waste with the decommissioning process at the Fukushima Daiichi Nuclear Power Plant (FDNPP), contains borate with relatively high concentration. As with general low-level wastes, such waste is also assumed the solidification with cementitious materials which calcium silicate hydrate (C-S-H) is one of the main components. In this study, the sorption behavior of strontium (Sr) ions and barium (Ba) ions to C-S-H in the presence of borate was examined by the sorption experiments without drying process. In the sorption experiments, C-S-H was synthesized by the mixture of calcium oxide, fumed silica and a solution with setting the Ca/Si molar ratios to 0.4, 0.8, 1.2 and 1.6. The total amount of a solid phase was 1.5 g, and the total volume of the solution containing borate and adsorbed ions (Sr or Ba) was 30 mL. The concentration of borate was set to 0 M or 0.6 M and the sodium/boron (Na/B) ratios was set to 0.2 or 1.0 by mixing boric acid and sodium hydroxide. The concentration of Sr ions or Ba ions was adjusted to 1 mM. The sorption period was set to 7 days. In the results, the sorption ratios of Sr ions and Ba ions for C-S-H exceeded 80% under all experimental conditions, although the sorption competition of cations with Na ions and the inhibition of the C-S-H formation with generating borate compounds observed by Raman spectroscopy might slightly reduce the sorption of them. These suggest that cationic radionuclides will be immobilized by C-S-H contained in the cements even in the presence of borate. (authors)

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Borate-assisted alkaline extraction of hemicellulose from switchgrass with enhanced structural stability and purity

Valorization of non-cellulosic polysaccharides is crucial for enhancing the economic competitiveness of biorefinery processes. In this study, a mixture of boric acid and sodium hydroxide was employed to efficiently extract hemicellulose from holocellulose switchgrass. Borate-assisted alkaline extraction resulted in a higher xylan content (59.5 %) compared to conventional alkaline extraction. Here, the hemicellulose fractions derived from the borate-alkaline treatment exhibited a higher molecular weight (M w = 51.2 kDa) and a relatively lower degree of polydispersity (1.28), indicating improved structural stability. The presence of borate had a protective effect against chain scission, preserving glucuronic acid residues and increasing galactose content. Additionally, borate improved hemicellulose purity, with up to 74.1 % of the extracted hemicellulose being suitable for further enzymatic applications. Extended extraction time further enhanced hemicellulose recovery, reaching 97.9 % under NaOH/boric acid conditions while maintaining structural integrity, as confirmed by SEM, FTIR and 2D HSQC NMR analyses. These findings provide insights into the role of borate in optimizing hemicellulose extraction and improving its potential for bioconversion processes.

Borate alkaline↗

A vibrational spectroscopic study of kernite to 25 GPa: Implications for the high-pressure stability of borate polyhedra

The Raman and infrared spectra of kernite [Na 2 B 4 O 6 (OH) 2 ·3H 2 O] have been characterized up to ~25 and 23 GPa, respectively, to explore pressure-induced changes in a structurally novel mineral that contains mixed coordination borate groups (threefold and fourfold), as well as both hydroxyl groups and water molecules. BO 3 and BO 4 vibrational modes are characterized in both the Raman and infrared spectra of kernite, and reassignments of some modes are made based on observed pressure shifts. Under compression to ~25 GPa, kernite undergoes three phase transitions: one initiates near ~2.5 GPa, the second occurs at ~7.0 GPa, and the third near 11.0 GPa. The first transition is characterized by a loss of both a subset of the Na-associated modes and a sharp OH peak, and it is fully reversible. The second transition is characterized by the loss of most of the BO 3 modes, some of the BO 4 modes at ~7 GPa, and further broadening of the H 2 O and OH peaks. This transition is partially reversible on decompression, but the Raman spectra indicate that the high-pressure structure and its reversion products are likely disordered. The third transition is characterized by the loss of most of the Raman and infrared modes, and it is not reversible on decompression. The decompression products from ~25 GPa have markedly different infrared and Raman spectra from the starting material, and appear to involve different bonding environments of boron than are present in the starting materials: thus, pressure treatment of boron-rich materials may generate novel quenchable structures. Notably, the BO 3 groups in kernite are destabilized under compression, with the BO 4 groups appearing to be more stable under compression. This shift in coordination may be endemic among borate glasses and crystalline borates under compression. The coordination conversion (and its products on decompression) is likely to highly depend on the detailed topology of the starting materials. Commonalities and differences between the threefold to fourfold transitions in borate systems relative to those in carbonate systems are presented. Lastly our results, combined with prior shock data, indicate that kernite, which may be representative of low-temperature borate minerals, can persist during impact events with peak shock pressures less than ~33 GPa, and the primary polyborate structural units involved in early ribose stabilization would thus survive most impact conditions.

36 MATERIALS SCIENCE↗

Luminescence of alkali rare earth borates A 3 Ln(BO 3 ) 2 (A = Na, K; Ln = Eu, Tb)

Single crystals of a series of rare earth borates, A 3 Ln (BO 3 ) (A = Na, K; Ln = Eu, Tb), were synthesized using a boric acid/hydroxide melt. The Na 3 Ln (BO 3 ) 2 borates crystallized in the monoclinic system with space group P2 1 /n, and the K 3 Ln (BO 3 ) 2 borates crystallized in the orthorhombic system with space group Pnma. Here, the luminescence of these borates was investigated under ultraviolet and X-ray excitations for the first time. Radioluminescence (RL) measurements showed K 3 Tb(BO 3 ) 2 to be the brightest compound, with an integral intensity equal to 55% of the integral emission of Bi 4 Ge 3 O 12 (BGO) powder.

36 MATERIALS SCIENCE↗

Towards Elucidating Structure–Spectra Relationships in Rhamnogalacturonan II: Computational Protocols for Accurate 13C and 1H Shifts for Apiose and Its Borate Esters

Apiose is a naturally occurring, uncommon branched-chain pentose found in plant cell walls as part of the complex polysaccharide Rhamnogalacturonan II (RG-II). The structural elucidation of the three-dimensional structure of RG-II by nuclear magnetic resonance (NMR) spectroscopy is significantly complicated by the ability of apiose to cross-link via borate ester linkages to form RG-II dimers. Here, we developed a computational approach to gain insight into the structure–spectra relationships of apio–borate complexes in an effort to complement experimental assignments of NMR signals in RG-II. Our protocol involved structure optimizations using density functional theory (DFT) followed by isotropic magnetic shielding constant calculations using the gauge-invariant atomic orbital (GIAO) approach to predict chemical shifts. We evaluated the accuracy of 23 different functional–basis set (FBS) combinations with and without implicit solvation for predicting the experimental 1 H and 13 C shifts of a methyl apioside and its three borate derivatives. The computed NMR predictions were evaluated on the basis of the overall shift accuracy, relative shift ordering, and the ability to distinguish between dimers and monomers. We demonstrate that the consideration of implicit solvation during geometry optimizations in addition to the magnetic shielding constant calculations greatly increases the accuracy of NMR chemical shift predictions and can correctly reproduce the ordering of the 13 C shifts and yield predictions that are, on average, within 1.50 ppm for 13 C and 0.12 ppm for 1 H shifts for apio–borate compounds.

BASIC BIOLOGICAL SCIENCES,BIOMASS FUELS↗

Impact of Lithium‐Free Borate Additives on the Cycle Life and Calendar Aging of Silicon‐Based Lithium‐Ion Batteries

Silicon-anode lithium-ion batteries (LIBs) suffer from limited cycle life and poor calendar life, constraining their large-scale commercialization. Integrating additives into electrolytes is a simple and cost-effective strategy to improve these aspects. The effects of lithium-free boron-based additives on cycling and calendar performance of high-loading Si-anode LIBs remain largely unexplored. In this work, the influence of five Li-free borate additives, each with distinct molecular structures and elemental compositions, is systematically investigated. All additives enhance cycle life to varying extents. Notably, the addition of 1 v/v% tri(2,2,2-trifluoroethyl) borate to the baseline electrolyte nearly doubles the cycle life at 50% state of health. This enhancement is attributed to three key factors. Specifically, borate additives 1) improve electrochemical activity, 2) act as anion receptors that interact with [PF6]- anions and carbonate solvents to reduce electrolyte decomposition, and 3) promote the formation of a stable and polymeric solid electrolyte interphase layer. Furthermore, these additives exhibited negligible impact in mitigating leakage current during a 180 h voltage-hold calendar-aging test, indicating their limited effect in calendar life. These findings provide insight into the role of Li-free borate additives in improving cycle life while addressing the knowledge gap regarding their influence on calendar aging.

Li, Defu↗

Gas phase fragmentation of adducts between dioxygen and closo-borate radical anions

The icosahedral closo-borate anions, [closo-B12X12]2- (B12) and [1-H-closo-1-CB11X11]- (CB11) with X=H or halogen are exceptionally stable weakly coordinating anions. Recent studies, which focused on the gas phase ion chemistry of this class of anions, revealed several unusual ion-molecule and unimolecular dissociation pathways. Herein, we demonstrate that collisional activation of highly iodinated closo-borate anions results in a loss of an iodine atom followed by a spontaneous addition of O2 present in a mass spectrometer background producing B12-O2 and CB11-O2 species. We examined the electronic structure of a representative O2 adduct using photoelectron spectroscopy and explored collision-induced dissociation (CID) pathways of a series of iodinated B12-O2 and CB11-O2 anions with different substituents. A systematic study of the gas phase dissociation pathways of the B12-O2 and CB11-O2 anions revealed several unusual dissociation pathways characteristic of this class of species. Abundant fragment ions are formed by neutral loss of BOX2• (X=boron bound substituent), Y2H• (Y=boron bound halogen, if any H is present in the molecular ion) and BO2•. Loss of BO2 was observed for CB11-O2 but not for B12-O2 anions. Substantial differences in stability of the corresponding fragments is responsible for the observed differences in dissociation of B12-O2 and CB11-O2 species. Furthermore, we show that in addition to O2 other molecules with a radical character (e.g. •SCH3) can form adducts with closo-borate anions after iodine abstraction. The boron cage fragmentation observed for the O2 adducts is untypical for highly iodinated closo-borates and is attributed to the strength of B-O bonds which dominate the thermochemistry of B12-O2 and CB11-O2 fragmentation reactions.

Warneke, Jonas↗