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The synthesis, transformation, and application in catalysis of triphenyllead hydroperoxide, the first dioxygen lead complex, are described. Triphenyllead hydroperoxide is characterized by

Novel peroxosolvates of tetraalkylammonium halides Et4N+Cl–•2(H2O2) (1), Et4N+Br–•2(H2O2) (2), Me3(ClCH2CH2)N+Cl–•H2O2 (3) and Me3PhN+Cl–•H2O2 (4) were prepared from concentrated hydrogen peroxide and the corresponding structures were determined by X-ray crystallography. Structures 1 and 2 are formed by globose Et4N+ cations and are the first examples of layers containing H-bonded peroxide molecules. By contrast, 3 and 4 are formed by sufficiently aspherical Me3(ClCH2CH2)N+ and Me3PhN+ units and contain infinitely long hydrogen-bonded peroxide-halide chains.

Abstract Sodium and potassium tert-butyl peroxide hydrates 2Na+·2C4H9$${\text{O}}_{2}^{ - }$$·7H2O (I) and 2K+· 2C4H9$${\text{O}}_{2}^{ - }$$·4H2O (II) were prepared. According to X-ray diffraction data (CIF files CCDC no. 2081025 (I) and no. 2081024 (II)), the compounds are coordination polymers in which alkali metal atoms have C.N.(Na) of 6 or C.N.(K) of 6 and 8. The crystal packings comprise layers with clearly defined hydrophobic surfaces consisting of hydrocarbon groups and hydrophilic inner areas including water molecules, alkali metal cations, and peroxy groups of the tert-butyl peroxide anions. Compounds were characterized by vibrational spectroscopy, 1H, 13C NMR spectroscopy, thermogravimetry, and differential scanning calorimetry.

Hydrogen peroxide assisted sol–gel coating of core-shell microcapsules of phase change materials (PCMs) is reported. A doubly coated paraffin core with an inner poly(melamine-formaldehyde) shell and an outer coating of peroxostannate, peroxoantimonate, their mixture or the respective metal oxides are reported. Triple coating of the paraffin core with a poly(melamine-formaldehyde) inner shell, tin oxide middle layer and graphene oxide outer coating is also achieved by hydrogen peroxide sol–gel processing. The latent heats of the microencapsulated PCMs ranged between 122 and 192 J g−1. The sol–gel process involves stabilization of the peroxostannate or peroxoantimonate sol in basic aqueous hydrogen peroxide and subsequent destabilization and deposition of the sol by addition of an antisolvent. Transformation to the metal oxide coating is conducted by chemical reduction with sodium sulfite or by mild heat treatment without leakage of the paraffin core.

Microencapsulation of a carbon nanotube (CNT)-loaded paraffin phase change material, PCM in a poly(melamine-formaldehyde) shell, and the respective CNT-PCM gypsum composites is explored. Although a very low level (0.001-0.1 wt %) of intramicrocapsule loading of CNT dopant does not change the thermal conductivity of the solid, it increases the measured effusivity and thermal buffering performance during phase transition. The observed effusivity of 0.05 wt % CNT-doped PCM reaches 4000 W s

We introduce a green synthesis approach for high-performance sodium-ion battery anodes that does not involve hydrothermal treatment or excessive energy use. Wet chemistry involving ammonium peroxostannate intermediate coating of reduced graphene oxide can be done at low temperature without excessive use of solvents. The process is practically waste-free and does not involve acid waste. Thermal treatment is required only for the solid material. The electrode exhibited very high stability and the charging capacity was reduced from 320 to 310 mA h g–1 after 2000 cycles at 3 A g–1. Moreover, the synthesis protocol demonstrated here is highly versatile with different, alternative pathways that provide many degrees of freedom in the process sheet design and in material composition.

Triphenyl silicon hydroperoxide and its isostructural germanium complex were characterized by single crystal X-ray analysis revealing H-bonding of two triphenylhydroperoxocomplexes, with each hydroperoxo ligand acting as a hydrogen donor and a hydrogen acceptor. Only two other structures with localized protons of hydroperoxo complexes' main group elements (boron and tin) are known (compared to 130 p-block element peroxo compounds) and both exhibit the same hydroperoxo double hydrogen bonding motif. The reaction of the hydroperoxo complexes with triphenylgermanium chloride to give the dinuclear peroxobridged germanium complex demonstrates the higher reactivity of the hydroperoxo moieties compared to the peroxo moiety. DFT calculations provide an estimate of the hydroperoxo double hydrogen bond energies: 62.8 and 63.6 kJ mol−1 for triphenyl silicon, 63.6 and 65 kJ mol−1 for the germanium complex.

Potassium-ion batteries are attracting considerable attention as a viable type of high voltage battery. Among available anode materials, composites containing Sb2S3are some of the most interesting high capacity candidates. A nanostructured Sb2S3-reduced graphene oxide composite anode material is evaluated in this study and compared with a structurally similar SnS2-reduced graphene oxide material reported previously by this team. The behaviour of the Sb2S3-based electrodes is assessed in both 1 M KPF6in ethylene carbonate-diethyl carbonate and 1 M KPF6in 1,2-dimethoxyethane electrolytes. Depotassiation capacities in excess of 650 mA h g−1are recorded for the composite electrodes, superior not only to SnS2-based electrodes but also to all previously reported Sb2S3-containing electrode materials for potassium-ion batteries. In order to establish insights into the reaction mechanism of the Sb2S3phase with potassium, post-cycling X-ray diffraction andin situtransmission electron microscopy are utilised. The recorded data suggest the presence of antimony alloys and potassium polysulphides as reaction products and intermediates; a possible conversion-alloying reaction mechanism is discussed. The results indicate that a capacity higher than previously believed is achievable in the Sb2S3active component of potassium-ion battery electrodes.

2-Aminobenzimidazole hemiperoxosolvate 2(C7H7N3)·H2O2 was synthesized and studied by single crystal X-ray analysis and periodic (solid-state) DFT calculations. The obtained compound, after urea and melamine peroxosolvates, is the third example of an H2O2 crystalline adduct stabilized with the maximum possible number of hydrogen bonds formed by one hydrogen peroxide molecule – 2 H-bonds as proton donors and 4 as acceptors. Due to the small size of the hydrogen peroxide molecule, its hydrogen bonding energy contributes the maximal impact and determines the relative value of the hydrogen bonding energy of the peroxosolvate crystal and can be suggested as an energetic criterion of perhydrate stability. The total energy of the 6 hydrogen bonds formed by one hydrogen peroxide molecule in all three compounds (∼140–∼170 kJ mol−1) was calculated and compared to the corresponding values for crystalline hydrogen peroxide and L-serine peroxosolvate. The total energy of the 4 hydrogen bonds of hydrogen peroxide molecule in crystalline H2O2 and L-serine peroxosolvate (150 and 113 kJ mol−1, respectively) was evaluated by solid-state DFT calculations.

Two new peroxosolvates of drug-like compounds were synthesized and studied by a combination of X-ray crystallographic, Raman spectroscopic methods, and periodic DFT computations. The enthalpies of H-bonds formed by hydrogen peroxide (H

Tellurates have attracted the attention of researchers over the past decade due to their properties and as less toxic forms of tellurium derivatives. However, the speciation of Te(VI) in aqueous solutions has not been comprehensively studied. We present a study of the equilibrium speciation of tellurates in aqueous solutions at a wide pH range, 2.5–15 by 17O, 123Te, and 125Te NMR spectroscopy. The coexistence of monomeric, dimeric, and trimeric oxidotellurate species in chemical equilibrium at a wide pH range has been shown. NMR spectroscopy, DFT computations, and single-crystal X-ray diffraction studies confirmed the formation and coexistence of trimeric tellurate anions with linear and triangular structures. Two cesium tellurates, Cs2[Te4O8(OH)10] and Cs2[Te2O4(OH)6], were isolated from the solution at pH 5.5 and 9.2, respectively, and studied by single-crystal X-ray diffractometry, revealing dimeric and tetrameric tellurate anions in corresponding crystal structures.

Nanocrystalline zinc peroxide is passivated against further oxidation by the addition of minute, substoichiometric amounts of potassium permanganate, which also endows it with increased thermal sta...

Vanadium oxides (V3O7) have been used as electrode materials for supercapacitor applications because of its multiple oxidation states. V3O7 nanoparticles were coated on reduced graphene oxide (rGO) from a peroxovanadate-rGO composite by thermal microexplosive decomposition method. These V3O7 decorated rGO were made composite with the flexible multi redox conducting polymer (Polyaniline). The performance of the composite materials as electrode for supercapacitors was analyzed in a 3-electrode cell, obtaining a specific capacitance of about 579 F g−1 at 0.2 A g−1 specific current. Cycling stability is one of the main barriers noticed in V3O7, which limits the practical performance of supercapacitors. This is overcome by modifying V3O7 with rGO and polyaniline composites which produces good electrical contact resulting in higher capacitances and enhanced cycling stability when compared to pristine V3O7. A superior electrochemical performance and ultra-long cyclic stability of 94% over 2500 cycles was obtained through these developed electrodes.

High, nearly 100%, yield synthesis of ammonium peroxogermanate (APG), (NH4)6[Ge6(μ-OO)6(μ-O)6(OH)6]·6H2O, is presented, and its crystal structure is determined by single crystal X-ray study. It comprises centrosymmetric hexanuclear peroxogermanate anions [Ge6(μ-OO)6(μ-O)6(OH)6]6- with six μ-oxo- and six μ-peroxo groups forming negatively charged layers. The space between these layers is filled by ammonium cations and water molecules, forming a highly stable structure due to hydrogen bonding. Highly soluble macroporous amorphous germanium oxide (HSGO) is then synthesized by mild treatment of APG. The compound forms highly oversaturated metastable germanium oxide solution with a solubility of 100 g/L, over 20 times higher than the solubility of amorphous germanium oxide. HSGO solution is a versatile reagent that can react with basic and acidic reagents to give a diverse range of salts including, e.g., germanium sulfide, germanium hydrophosphate, and potassium germanate. In the absence of acid or base, the aqueous HSGO solution yields hexagonal germanium oxide under ambient conditions.

Herein, peroxosolvates of the cyclic dipeptides disarcosine (C6H10N2O2·H2O2), dialanine (C6H10N2O2·2(H2O2)), diglycine (C4H6N2O2·2(H2O2) and C4H6N2O2·1.786(H2O2)·0.214(H2O)) were synthesized and studied by single crystal X-ray analysis and periodic DFT calculations. The hydrogen bonding networks of cyclic diglycine peroxosolvate and isomorphous hydrate were characterized using Bader analysis of periodic electron density and empirical correlations between enthalpy and metric and spectroscopic parameters of the H-bond. The obtained data for the peroxosolvate of cyclic dipeptides provided a molecular-level insight into the non-redox interaction of hydrogen peroxide with the peptide backbone in aqueous systems. In all structures, H2O2 acts as a proton donor in two hydrogen bonds. The carbonyl oxygen atom of the peptide (–CO–NH–) forms a relatively stronger hydrogen bond with the hydrogen peroxide molecule (32–34 kJ mol−1) as compared to that with water in the isomorphous hydrate of cyclic diglycine (26–28 kJ mol−1). The hydrogen atom of the peptide group (–CO–NH–) can form a moderate H-bond with hydrogen peroxide (25 kJ mol−1). The total hydrogen bonding energy of the peroxosolvate is higher than that of the corresponding hydrate (91 vs. 82 kJ mol−1). The stronger hydrogen bonding in peroxosolvates as compared to that in the hydrate and the fact that the intermolecular H-bonds C(O)NH⋯OCNH between cyclic dipeptides are not found in peroxosolvates, despite being prevalent in the structure of nonsolvated dipeptides, imply that hydrogen peroxide can interfere with the secondary structure of proteins via a mechanism that can lead to reversible inhibition or signaling in living systems.

Energy/enthalpy of intermolecular hydrogen bonds (H-bonds) in crystals have been calculated in many papers. Most of the theoretical works used non-periodic models. Their applicability for describing intermolecular H-bonds in solids is not obvious since the crystal environment can strongly change H-bond geometry and energy in comparison with non-periodic models. Periodic DFT computations provide a reasonable description of a number of relevant properties of molecular crystals. However, these methods are quite cumbersome and time-consuming compared to non-periodic calculations. Here, we present a fast quantum approach for estimating the energy/enthalpy of intermolecular H-bonds in crystals. It has been tested on a family of crystalline peroxosolvates in which the H∙∙∙O bond set fills evenly (i.e., without significant gaps) the range of H∙∙∙O distances from ~1.5 to ~2.1 Å typical for strong, moderate, and weak H-bonds. Four of these two-component crystals (peroxosolvates of macrocyclic ethers and creatine) were obtained and structurally characterized for the first time. A critical comparison of the approaches for estimating the energy of intermolecular H-bonds in organic crystals is carried out, and various sources of errors are clarified.

A breakthrough "superoxide colloidal solution route" for low-temperature synthesis of barium and strontium stannate perovskites and their doped analogues was recently introduced. The synthesis starts from hydrogen peroxide-rich stannate solutions and yields a so-called "crystalline superoxide molecular cluster" that is converted by low temperature (300 °C) to the respective perovskites. In this paper, the so-called "crystalline superoxide molecular cluster" is identified as a superoxide-free, barium trihydroxo(hydroperoxo)peroxostannate, BaSn(OH)

A combined procedure of zinc peroxide granulation and encapsulation in one technological stage has been developed, which ensures the stabilization of ZnO2 by forming a coating on the surface of the product granules. It is shown that the use of sodium polyphosphate in a combined process of granulation and encapsulation as encapsulating agents with the concentration in the initial solution of 1% allows obtaining a capsular product, which is significantly more resistant to the action of wet carbon dioxide than a nonencapsulated analogue.

The review addresses synthetic approaches to composite materials based on graphene oxide and nano tin dioxide and their electrochemical properties as anodes for lithium- and sodiumion batteries. The introduction of a carbon matrix into the composite material improves the electrochemical characteristics of the anodes. In most methods, the synthesis of graphene oxide–tin dioxide composites is based on the use of tin(II,IV) chlorides as the starting compounds, and the most efficient electrode materials were obtained by the hydrothermal or solvothermal routes. Thermal processing is much more economic than the gas phase deposition protocols but requires heating of a large volume of dilute tin oxide dispersions in an autoclave. Mechanochemistry (ball milling) is also economically unfavorable for the synthesis of composite materials. In addition, large volumes of acidic wastes that should be neutralized and safely discarded are formed when tin chlorides are used. An alternative environmentally friendly technique based on the use of aqueous peroxide solutions can be applied for the production of efficient anode materials based on graphene oxide and tin dioxide. This process does not involve acidic wastes, uses hydrogen peroxide and ethanol as reagents, and accomplishes film deposition (coating) at room temperature. Final thermal treatment is required only for the active material, which minimizes energy expenses and equipment costs.

Formation of vanadium oxide nanofilm-coated graphene oxide (GO) is achieved by thermally induced explosive disintegration of a microcrystalline ammonium peroxovanadate-GO composite. GO sheets isolate the microcrystalline grains and capture and contain the microexplosion products, resulting in the deposition of the nanoscale products on the GO. Thermal treatment of the supported nanofilm yields a sequence of nanocrystalline phases of vanadium oxide (V3O7, VO2) as a function of temperature. This is the first demonstration of microexplosive disintegration of a crystalline peroxo compound to yield a nanocoating. The large number of recently reported peroxide-rich crystalline materials suggests that the process can be a useful general route for nanofilm formation. The V3O7@GO composite product was tested as a sodium ion battery anode and showed high charge capacity at high rate charge-discharge cycling (150 mAh g-1 at 3000 mA g-1 vs 300 mAh g-1 at 100 mA g-1) due to the nanomorphology of the vanadium oxide. NRF (Natl Research Foundation, S’pore)

High-charge-capacity sodium-ion battery anodes made of Sb2Te3@reduced graphene oxide are reported for the first time. Uniform nano-coating of graphene oxide is carried out from common sol of peroxotellurate and peroxoantimonate under room temperature processing. Reduction by hydrazine under glycerol reflux yields Sb2Te3@reduced graphene oxide. The electrodes exhibit exceptionally high volumetric charge capacity, above 2300mAhcm-3 at 100mAg-1 current density, showing very good rate capabilities and retaining 60% of this capacity even at 2000mAg-1. A comparison of sodiation and lithiation shows that lithiation exhibits better volumetric charge capacity, but surprisingly only marginally better relative rate capability retention at 2000mAg-1. Tellurium-based electrodes are attractive due to the high volumetric charge capacity of Te, its very high electric conductivity, and the low relative expansion upon lithiation/sodiation.

A composite based on sodium germanate and reduced graphene oxide was obtained for the first time by precipitating the initial peroxogermanate on a graphene oxide followed by heat treatment in vacuum. According to powder X-ray diffraction, sodium germanate crystallizes during the heat treatment in vacuum at 500°C. Scanning transmission electron microscopy examination showed that sodium peroxogermanate nanoparticles form a thin film on the surface of graphene oxide flakes. The electrochemical characteristics of composites obtained with different heat treatment conditions were studied as the anodes of lithium ion batteries.

High‐charge‐capacity sodium‐ and lithium‐ion battery anodes based on tin telluride are reported for the first time. Graphene oxide/cubic β‐SnTe electrodes exhibit exceptionally high reversible volumetric charge capacities above 3000 and 1300 mAh cm−3 at 100 mA g−1 charging rate for lithium and sodium ion batteries, respectively, and they show very good rate capabilities retaining 68 and 60 % of the respective capacities even at 2000 mA g−1 charging rate. The reversible charge capacity for lithiation is approximately equal to the theoretical value of the active material. The superior electrode performance is attributed to the high conductivity of tellurium, the mechanical buffering of volume changes by the large row‐V host elements, the elasticity of the reduced graphene oxide support, and the very low specific equivalent volumes involved in sodiation and lithiation of SnTe. NRF (Natl Research Foundation, S’pore)

We report the first attempt to study the behavior of the [AlO4Al12(OH)25(H2O)11]6+ (Al13) Keggin cation (KC) in water–peroxide solutions. Addition of hydrogen peroxide into an aqueous solution containing the Al13 KC reduces pH due to the acidity of hydrogen peroxide. According to the 27Al NMR studies of water–peroxide solutions prepared just before the NMR experiment, with their pH adjusted to the initial value of 5.5 with aqueous NaOH, the Al13 KC concentration decreases immediately once hydrogen peroxide is added to the initial system. Addition of 18.2 wt % hydrogen peroxide to the initial 0.88 mM Al13 solution gives rise to a fourfold decline in Al13 polyoxo cation concentration to 0.22 mM. Then, the KC concentration in the test system remains unchanged for 1 week. Large hydrogen peroxide amounts (27.9 wt % or higher) added to the initial system almost completely degrade the KC. Sodium sulfate added to the initial water–peroxide solution of Al13 chloride where the hydrogen peroxide concentration is 5.5 wt % precipitates the earlier described Al13 sulfate [AlO4Al12(OH)25(H2O)11](SO4)3 · 16H2O, where the aluminum polyoxo cation does not contain coordinated hydrogen peroxide molecules, peroxo or hydroperoxo groups as shown by X-ray diffraction.

The title adduct, C14H13NO·H2O2, consists of (Z)-N-benzylidene-1-phenylmethanamine oxide and hydrogen peroxide molecules in a 1:1 ratio. The organic coformer adopts a skew geometry with an inter-aryl-ring dihedral angle of 81.9 (2)°. In the crystal, the organic and peroxide molecules are linked through both peroxide O—H donor groups to oxide O-atom acceptors, giving one-dimensional chains extending along thebaxis. Present also are weak intermolecular C—H...O hydrogen-bonding interactions.

Peroxosolvates of 2-aminonicotinic acid (I) and lidocaine N-oxide (II) including the largest insular hydrogen peroxide clusters were isolated and their crystal structures were determined by single-crystal X-ray diffraction. An unprecedented dodecameric hydrogen peroxide insular cluster was found in I. An unusual cross-like pentameric cluster was observed in the structure of II. The topology of the (H2 O2 )12 assembly was never observed for small-molecule clusters. In I and II new double and triple cross-orientational disorders of H2 O2 were found. Cluster II is the first example of a peroxosolvate crystal structure containing H2 O2 molecules with a homoleptic hydrogen peroxide environment. In II, a hydrogen bond between an H2 O2 molecule and a peptide group -CONH⋅⋅⋅O2 H2 was observed for the first time.

A combined granulation and encapsulation procedure in the production of sodium percarbonate (SPC) has been developed that enables the stabilization of SPC to form a coating on the surface of product granules in one technological stage. The separation of the granulating and encapsulating agents during the drying process and formation of an encapsulating coating are performed due to large differences in the solubility of the components of initial solution. Sodium polyphosphate or oxyethylidenediphosphonic acid used as encapsulating agents with an initial solution concentration (1%) in the combined granulation and encapsulation process enables the preparation of encapsulated SPC, which is significantly more resistant to wet carbon dioxide than unencapsulated product.

A peroxogermanate thin film was deposited in high yield at room temperature on graphene oxide (GO) from peroxogermanate sols. The deposition of the peroxo-precursor onto GO and the transformations to amorphous GeO2, crystalline tetragonal GeO2, and then to cubic elemental germanium were followed by electron microscopy, XRD, and XPS. All of these transformations are influenced by the GO support. The initial deposition is explained in view of the sol composition and the presence of GO, and the different thermal transformations are explained by reactions with the graphene support acting as a reducing agent. As a test case, the evaluation of the different materials as lithium ion battery anodes was carried out revealing that the best performance is obtained by amorphous germanium oxide@GO with >1000 mAh g–1 at 250 mA g–1 (between 0 and 2.5 V vs Li/Li+ cathode), despite the fact that the material contained only 51 wt % germanium. This is the first demonstration of the peroxide route to produce peroxogermanate ...

Sodium peroxostannate nanoparticles with graded composition were produced from aqueous hydrogen peroxide–sodium hydroxostannate solution. The uniform particles were converted to composition graded sodium stannate by mild thermal treatment for peroxide decomposition and yielded yolk–shell tin dioxide particles by dilute acid treatment. The mechanism of formation of the graded sodium concentration is explained in view of the solubility of peroxostannate in H2O2–H2O solution and based on 119Sn NMR, XRD, dynamic light scattering (DLS) and electron microscopy studies. Initial studies illuminating sensitive hydrogen sensing by yolk–shell tin oxide particles are presented.

An anode material incorporating a sulfide is reported. SnS2 nanoparticles anchored onto reduced graphene oxide are produced via a chemical route and demonstrate an impressive capacity of 350 mA h g−1, exceeding the capacity of graphite. These results open the door for a new class of high capacity anode materials (based on sulfide chemistry) for potassium-ion batteries.

The Cambridge Structural Database has been used to investigate the detailed environment of H2O2 molecules and hydrogen-bond patterns within “true” peroxosolvates in which the H2O2 molecules do not interact directly with the metal atoms. A study of 65 crystal structures and over 260 hydrogen bonds reveals that H2O2 always forms two H-bonds as proton donors and up to four H-bonds as a proton acceptor, but the latter can be absent altogether. The necessary features of peroxosolvate coformers are clarified. (1) Coformers should not participate in redox reactions with H2O2 and should not catalyze its decomposition. (2) Coformers should be Bronsted bases or exhibit amphoteric properties. The efficiency of the proposed criteria for peroxosolvate formation is illustrated by the synthesis and characterization of several new crystals. Conditions preventing the H2O2/H2O isomorphous substitution are essential for peroxosolvate stability: (1) Every H2O2 in the peroxosolvate has to participate in five or six hydrogen b...

Using peroxostannate as a precursor, a composite material based on tin dioxide and carbon black was obtained, in which tin dioxide forms a coating on the surface of carbon black nanoparticles. The synthesized material was characterized by electron microscopy and X-ray powder diffraction analysis, and also the electrochemical characteristics of this material as an anode material for lithium-ion batteries were studied. The material demonstrates good stability and rate performance, which is indicative of the efficiency of the peroxide method for producing promising inexpensive anode materials based on tin dioxide and carbon black.

A tin dioxide–sodium stannate composite has been obtained by the thermal treatment of sodium peroxostannate nanoparticles at 500°C in air. X-ray powder diffraction study has revealed that the composite includes crystalline phases of cassiterite SnO2, sodium stannate Na2Sn2O5, and sodium hexahydroxostannate Na2Sn(OH)6. Scanning electron microscopy has shown that material morphology does not change considerably as compared with the initial tin peroxo compound. Electrochemical characteristics have been compared for the anodes of lithium-ion batteries based on tin dioxide–sodium stannate composite and anodes based on a material manufactured by the thermal treatment of graphene oxide–tin dioxide–sodium stannate composite at 500°C in air.

A novel composite material for the encapsulation of redox enzymes was prepared. Reduced graphene oxide film with adsorbed phenothiazone was used as a highly efficient composite for electron transfer between flavin adenine dinucleotide (FAD)-dependent glucose dehydrogenase and electrodes. Measured redox potential for glucose oxidation was lower than 0 V vs Ag/AgCl electrode. The fabricated biosensor showed high sensitivity of 42 mA M(-1) cm(-2), a linear range of glucose detection of 0.5-12 mM, and good reproducibility and stability as well as high selectivity for different interfering compounds. In a semibiofuel cell configuration, the hybrid film generated high power output of 345 μW cm(-2). These results demonstrate a promising potential for this composition in various bioelectronic applications.

Potassium (K6[Ge6(μ-OO)6(μ-O)6(OH)6]·14H2O, 1), cesium ammonium (Cs4.2(NH4)1.8[Ge6(μ-OO)6(μ-O)6(OH)6]·8H2O, 2), and potassium ammonium (K2.4(NH4)3.6[Ge6(μ-OO)6(μ-O)6(OH)6]·6H2O, 3) peroxogermanates were isolated from 3% hydrogen peroxide aqueous solutions of the corresponding hydroxogermanates and characterized by single crystal and powder X-ray diffraction studies and by Raman spectroscopy and thermal analysis. The crystal structure of all three compounds consists of cations of potassium and/or ammonium and cesium, water molecules, and centrosymmetric hexanuclear peroxogermanate anion [Ge6(μ-OO)6(μ-O)6(OH)6](6-) with six μ-oxo- and six μ-peroxo groups. Peroxogermanates demonstrate relatively high thermal stability: the peroxide remains in the structure even after water release after heating to 100-120 °C. DFT calculations of the peroxogermanate [Ge6(μ-OO)6(μ-O)6(OH)6](6-) anion confirm its higher thermodynamic stability compared to the hydroperoxo- and oxogermanate analogues.

The limited applicability of the dimeric heterosynthon concept to a two-component urea–H2O2 crystal is reported. It is due to the absence of the relatively short O–H⋯O bonds, i.e. primary interactions, in the urea–H2O2 1 : 1 complex. The target O–H⋯O bonds do exists in trimeric heterosynthons, i.e. the urea–2(H2O2) and 2(urea)–H2O2 complexes. The mutual orientation of the H2O2 molecules in the gas-phase complexes differs from the one in the crystalline structure due to the existence of additional N–H⋯O bonds which are absent in the crystal. Implicitly accounting for the polar environment does not change the molecule conformations in the considered complexes. It is found that the DFT computations with/without accounting for polar solvent are not sufficient for the deduction of such a heterosynthon. The results of the database analysis should be used for unambiguous identification of the molecules' conformations in the target trimeric heterosynthon. An approach for deducing the trimeric heterosynthon structure for molecules with equivalent binding sites is developed. It includes three steps. (i) Identification of structural motifs formed by the considered molecules in the two-component crystals using database analysis. (ii) Establishing a hierarchy of the intermolecular interactions in the crystals by solid-state DFT followed by Bader analysis of the periodic electronic density. (iii) Evaluation of the structure and relative stability of the trimeric heterosynthons by DFT methods with/without accounting for environmental effects.

Since there has been a notable improvement in the performance of graphene-supported tin-based lithium ion battery anodes, they have become a viable alternative to state of the art graphite anodes. However, currently these anodes are produced by energy-demanding thermal processes and generate lithium chloride or other wastes. In this research, we demonstrate the formation of efficient and stable lithium ion battery anodes based on sodium stannate-coated reduced graphene oxide. Coating is performed at low temperatures and when a sodium peroxostannate precursor is used, the process can be carried out with zero waste discharge. Thermal treatment is required only for the solid material. The anode exhibited a charge capacity of 610 mA h g−1 after 140 cycles at 100 mA g−1. This is the first characterization of a sodium stannate-based anode for LIBs.

The crystal structure of previously unknown ammonium succinate peroxosolvate is studied. It is shown that it represents a rare example of the structure where H2O2 molecule forms two donor hydrogen bonds and does participate in any acceptor hydrogen bonds, despite the presence of substantial quantity of nonperoxide active hydrogen atoms.

Sodium peroxostannate nanoparticles with graded composition were produced from aqueous hydrogen peroxide-sodium hydroxostannate solution. The uniform particles were converted to composition graded sodium stannate by mild thermal treatment for peroxide decomposition and yielded yolk-shell tin dioxide particles by dilute acid treatment. The mechanism of formation of the graded sodium concentration is explained in view of the solubility of peroxostannate in H

The title structure consists of a (Z)-N-benzyl­idene-1-phenyl­methanamine oxide and a hydrogen peroxide mol­ecule linked through both O—H groups into a one-dimensional chain structure., The title adduct, C14H13NO·H2O2, consists of (Z)-N-benzyl­idene-1-phenyl­methanamine oxide and hydrogen peroxide mol­ecules in a 1:1 ratio. The organic coformer adopts a skew geometry with an inter-aryl-ring dihedral angle of 81.9 (2)°. In the crystal, the organic and peroxide mol­ecules are linked through both peroxide O—H donor groups to oxide O-atom acceptors, giving one-dimensional chains extending along the b axis. Present also are weak inter­molecular C—H⋯O hydrogen-bonding inter­actions.

An anode material incorporating a sulfide is reported. SnS

A peroxogermanate thin film was deposited in high yield at room temperature on graphene oxide (GO) from peroxogermanate sols. The deposition of the peroxo-precursor onto GO and the transformations to amorphous GeO

Nanoparticles of zinc peroxide, a well known and convenient solid source of hydrogen peroxide, oxygen or active oxygen species, can be readily regenerated by exposure of zinc oxide to slightly basic hydrogen peroxide solutions after being depleted of their active oxygen peroxide content, and these charge–discharge cycles can be repeated many times. We demonstrate the renewability of zinc peroxide coated mica and neat zinc peroxide powders by permanganometric titration, powder X-ray studies, thermal analysis and Raman spectroscopy, all showing good recovery with a rather small change of properties upon repeated cycling. We believe that renewable zinc peroxide can be useful for rechargeable antibiofouling or antifungal paints, clothing additive, floor coverings and other applications where hydrogen peroxide is slowly depleted and should be reloaded to regain its favorable activity.