Bimetal-oxide (Fe/Co) modified bagasse-waste carbon coated on lead oxide-battery electrode for metronidazole removal.

Current study covers the preparation and application of a commercial modified lead oxide battery electrode (LBE) in electrochemical oxidation (ECO) of metronidazole (MNZ) in an aqueous phase. Modified electrode is prepared by doping of bimetal-oxide (Fe and Zn) nanoparticles (NPs) & single metal-oxide (Fe/Zn) on bagasse-waste carbon (bwc) which is further coated on LBE. The modified LBE electrode surface was examined for metal-oxide NPs through X-ray diffraction analysis (XRD). Different electrodes are prepared by varying combinations of two metal-oxide based on molar ratio and tested for electrochemical characterization and MNZ removal test. Based on large oxygen evolution potential in a linear sweep volumetry (LSV) analysis and high MNZ removal rate, the best electrode has been represented as Fe1:Co2-bwc/LBE which contains Fe & Co molar ratio of 1:2. Moreover, equilibrium attained at faster rate in degradation process of MNZ, where pseudo first order kinetics of 2.29 × 10-2 min-1 was obtained under optimized condition of (MNZ:100 mg/L, pH:7, CD: 30 mA/cm2 and electrolyte: 0.05 M Na2SO4). Maximum MNZ removal, total organic carbon removal (TOC), mineralization current efficiency (MCE) & energy consumption (EC) of 98.7%, 85.3%, 62.2% & 96.143 kW h/kg-TOC removed are found in 180 min of treatment time for Fe1:Co2-bwc/LBE electrode. Accelerated service life test confirms that the stability of modified electrode is enhanced by 1.5 times compared to pristine LBE. Repeatability test confirms that modified LBE (Fe1:Co2-bwc/LBE) can be utilized up to 3 times.

Degradation of polyvinyl alcohol (PVA) in neutral conditions based on copper-manganese bimetallic catalyst.

There have been many studies on the degradation of polyvinyl alcohol (PVA) by the Fenton-like method, but the narrow acid-base (pH) range, poor degradation effect, and time-consuming of the Fenton-like method limit its development. Therefore, to improve the shortcomings of the Fenton-like method, the study aimed to synthesize copper-manganese bimetal oxide loaded catalysts (MnCuO@γ-Al2O3) through the impregnation calcination method, and its potential to activate hydrogen peroxide (H2O2) for the degradation of PVA was evaluated. The X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer Emmett Teller (BET), energy dispersive spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS) characterizations revealed the chemical composition, structure and morphology of the prepared MnCuO@γ-Al2O3, furthermore the synergistic mechanism was proposed. Results indicated that copper and manganese could successfully attach to γ-Al2O3 and reduce the specific surface area of γ-Al2O3, promoting the transformation of multivalent metals and the generation of oxygen vacancies. In addition, comparative experiments demonstrated that the PVA removal efficiency was significantly improved at the catalyst calcination temperature of 500 °C, reaction temperature of 70 °C, H2O2 dosage of 125 [Formula: see text], and catalyst dosage of 625 [Formula: see text] and more than 96% of PVA was removed within 20 min in neutral conditions. Lastly, four catalyst cycle degradation experiments of PVA were carried out, and the degradation effect could reach more than 96% in a certain time.

Phosphate interactions with iron-titanium oxide composites: Implications for phosphorus removal/recovery from wastewater.

Understanding the interactions between phosphate (P) and mineral adsorbents is critical for removing and recovering P from wastewater, especially in the presence of both cationic and organic components. To this end, we investigated the surface interactions of P with an iron-titanium coprecipitated oxide composite in the presence of Ca (0.5-3.0 mM) and acetate (1-5 mM), and quantified the molecular complexes and tested the possible removal and recovery of P from real wastewater. A quantitative analysis of P K-edge X-ray absorption near edge structure (XANES) confirmed the inner-sphere surface complexation of P with both Fe and Ti, whose contribution to P adsorption relies on their surface charge determined by pH conditions. The effects of Ca and acetate on P removal were highly pH-dependent. At pH 7, Ca (0.5-3.0 mM) in solution significantly increased P removal by 13-30% by precipitating the surface-adsorbed P, forming hydroxyapatite (14-26%). The presence of acetate had no obvious influence on P removal capacity and molecular mechanisms at pH 7. At pH 4, the removal amount of P was not obviously affected by the presence of Ca and acetate. However, acetate and high Ca concentration jointly facilitated the formation of amorphous FePO4 precipitate, complicating the interactions of P with Fe-Ti composite. In comparison with ferrihydrite, the Fe-Ti composite significantly decreased the formation of amorphous FePO4 probably by decreasing Fe dissolution due to the coprecipitated Ti component, facilitating further P recovery. An understanding of these microscopic mechanisms can lead to the successful use and simple regeneration of the adsorbent to recover P from real wastewater.

Porous Lanthanum-Zirconium phosphate with superior adsorption capability of fluorine for water treatment.

Bimetal oxide is a popular defluorinating material. Hexadecyl trimethyl ammonium bromide (CTAB) as a surfactant successfully synthesizes a novel lanthanum-zirconium phosphate to remove fluorine from groundwater. Lanthanum-zirconium phosphate at a Zr/La molar ratio of 2 exhibited a specific surface area of 455.14 m2/g with a wide pore size, which was achieved by incorporating lanthanum into materials and removing CTAB through calcination. The maximum fluoride adsorption capacity is 109.17 mg/g, which is tenfold that of mesostructured zirconium phosphate. Specifically, analysis revealed that mZrP and LamZrP2-1 were amorphous, which is consistent with HAADF-STEM. The fluoride adsorption fitted well with the pseudo-second-order equation model and Langmuir isotherm mode. LamZrP2-1 had potent anti-interference ability without PO43-. Moreover, LamZrP2-1 was reusable for at least six cycles of adsorption-desorption with little influence. The adsorption mechanism of fluoride was discussed by X-ray photoelectron spectroscopy (XPS), nuclear magnetic resonance spectroscopy (NMR) analysis, and Fourier transform infrared (FTIR) spectroscopy. Fluoride was captured by LamZrP2-1 via charge attraction, ligand exchange of different bond strengths, and ion exchange. Lanthanum-zirconium phosphate is important not only in the research and development of bimetal oxides but also in the treatment of groundwater for fluoride removal.

Hybrid structures of cobalt-molybdenum bimetallic oxide embedded in flower-like molybdenum disulfide for sensitive detection of the antibiotic drug nitrofurantoin.

Excessive residues of nitrofurantoin (NFT) can cause serious contamination of water bodies and food, and potential harm to ecosystems and food safety. Given that, rapid and efficient detection of NFT in real samples is of particular importance. MoS2 is a promising electrochemical material for this application. Here, MoS2 was modulated by Metal-organic framework through the interfacial microenvironment to enhance the catalytic activity and carbonized to form Co2Mo3O8 nanosheets with high electrical activity. The resulting Co2Mo3O8/MoS2 hybrid structure can be used to prepare highly sensitive NFT electrochemical sensor. The Co2Mo3O8/MoS2@CC electrochemical sensor exhibits strong electrochemical properties due to its fast electron transfer, excellent electrical conductivity, abundant defect sites, and high redox response. Based on this, this electrochemical sensor exhibited excellent electrocatalytic activity for NFT with a wide linear detection range, low detection limit, and high sensitivity. Moreover, the electrode was successfully applied to detect NFT in milk, honey, and tap water, strongly confirming its potential in real samples. This work could furnish the evidence for interfacial microenvironmental regulation of MoS2, and also offer a novel candidate material for NFT sensing.

Fabrication of a New Electrochemical Sensor Based on Bimetal Oxide for the Detection of Furazolidone in Biological Samples.

This study utilized a simple hydrothermal method to synthesize nickel molybdenum oxide (NMO) for the detection of furazolidone (FZE). Our synthesized NMO was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), field emission scanning electron spectroscopy (FE-SEM), and energy dispersive X-ray spectroscopy (EDX). The cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used to detect the FZE. Under optimized conditions, the obtained results showed that the NMO had an excellent electrocatalytic property towards FZE. As a result, NMO/GCE showed a good linear range of 0.001-1765 µM, an excellent detection limit (LOD) of 0.02 µM, and sensitivity of 0.2042 µA µM-1 cm-2.

A novel molybdenum disulfide nanosheet loaded Titanium/Zirconium bimetal oxide affinity probe for efficient enrichment of phosphopeptides in A549 cells.

In this paper, we developed a facile route for the preparation of a novel bimetal oxide affinity chromatography (MOAC) material. The TiO2/ZrO2@MoS2 was constructed by the electrostatic interaction between titanium oxide/zirconia (w:w, 10:1) and molybdenum disulfide nanosheet. The nanocomposite has the large specific surface area (186.30 m2⋅g-1) and pore volume (0.37 cm3⋅g-1). Compared with single-metal probes, the combination of bimetallic oxides probe (TiO2/ZrO2) and hydrophilicity MoS2 support offered multitudinous affinity sites for phosphopeptides capturing from tryptic digests of protein samples under 50% acetonitrile-1% trifluoroacetate conditions. Singnificant feasibility of the TiO2/ZrO2@MoS2 nanomaterial for the enrichment of phosphopeptides under optimal conditions was proved via the bovine serum albumin (BSA) and the mixtures of ß-casein. The phosphopeptide expression was identified using ultra-performance liquid chromatography (uHPLC) separation and-linear ion trap mass spectrometry (MSn). With these affinity characters of TiO2/ZrO2@MoS2, it exhibited higher binding capacity (25 mg⋅g-1), better selectivity for phosphopeptides from ß-casein/BSA (1:2000) tryptic digests, high sensitivity (1 fmol⋅µL-1) towards phosphopeptides from ß-casein tryptic digests, and great reusability of 8 cycles test for capturing phosphopeptides. In addition, the TiO2/ZrO2@MoS2 with high sensitivity and selectivity was successfully applied to enriching phosphopeptides from nonfat milk and human serum samples. More importantly, the TiO2/ZrO2@MoS2 was further successfully applied to multi-phosphopeptides enrichment, 1779 serine, threonine and tyrosine phosphosites can be identified in A549 cell protein tryptic digest. Compared with commercial TiO2 from enrichening 416 phosphopeptide from A549 cell lysates, the successful locating of 44 phosphosites were overlapped.

Fe-Ti bimetal oxide adsorbent for removing low concentration H2S at room temperature.

ABSTRACTHerein, a series of Fe-Ti bimetal oxide adsorbents were prepared by reduction-co-precipitation method, and their performance in removing low concentration H2S at room temperature was investigated. The adsorbents were characterized by X-Ray diffraction (XRD), Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), Ultraviolet Visible diffuse reflectance spectroscopy (UV-Vis-DRS), X-Ray photoelectron spectroscopy (XPS) and N2 adsorption-desorption. The results showed that the addition of Ti increased the specific surface area, pore volume and small oligomeric Fe2O3 of ferrihydrite. When the Fe/Ti molar ratio was 8:1, Fe-Ti bimetal oxide formed a large amount of oligomeric Fe2O3, and its specific surface area and pore volume reached 344.99 m2/g and 0.34 cm3/g, respectively. At this time, Fe-Ti bimetal oxide exhibited the highest breakthrough sulfur capacity of 222.8 mg/g. High temperature calcination caused Fe-Ti bimetal oxide to form small specific surface area and pore volume, and produced crystalline α-Fe2O3. And the breakthrough sulfur capacity of Fe-Ti bimetal oxide decreased with the increasing calcination temperature. In addition, the desulfurization process conformed to the unreacted shrinking nucleus model.

Enhanced degradation of bisphenol A by mixed ZIF derived CoZn oxide encapsulated N-doped carbon via peroxymonosulfate activation: The importance of N doping amount.

In this study, mixed metal cobalt zinc oxide embedded nitrogen enriched porous carbon composites (CoZnO-PC) were prepared via pyrolyzing polyvinylpyrrolidone (PVP) encapsulated Co, Zn-bimetal centered zeolitic imidazolate frameworks (ZIF). The prepared composites were then used to activate peroxymonosulfate (PMS) for bisphenol A (BPA) removal in water. When mole ratio of Co/Zn was 2/1, the resulted Co2Zn1O-PC possessed spinel structure with prominent degradation capability, in which the introduction of Zn accelerated the PMS activation performance of Co through establishing bimetal synergistic interactions. Both radical and non-radical activation pathways were existed in the Co2Zn1O-PC/PMS system, in which Co2Zn1O dominated the radical pathway whereas PC dominated the non-radical way. Since PVP contained abundant nitrogen atoms and could form strong coordination interactions with the ZIF precursor, the introduction of PVP in the ZIF precursor prevented pore collapsing during pyrolysis process, as well as enhancing the nitrogen content in the pyrolzed composites, which significantly promoted the generation of singlet oxygen. With combined pathways, the Co2Zn1O-PC/PMS system showed a wide pH application range with promising mineralization rate. Meanwhile, the spinel-structured Co2Zn1O-PC was magnetically separable with desirable recyclability. This study presents a novel composite with remarkable performance for the removal of refractory organic pollutants in municipal wastewater.

Synthesis of Two-Dimensional Sr-Doped LaNiO3 Nanosheets with Improved Electrochemical Performance for Energy Storage.

Designing a novel, efficient, and cost-effective nanostructure with the advantage of robust morphology and outstanding conductivity is highly promising for the electrode materials of high-performance electrochemical storage device. In this paper, a series of honeycombed perovskite-type Sr-doped LaNiO3 nanosheets with abundant porous structure were successfully synthesized by accurately controlling the Sr-doped content. The study showed that the optimal LSNO-0.4 (La0.6Sr0.4NiO3-δ) electrode exhibited excellent electrochemical performance, which showed a high capacity of 115.88 mAh g-1 at 0.6 A g-1. Furthermore, a hybrid supercapacitor device (LSNO//AC) based on LSNO-0.4 composites and activated carbon (AC) showed a high energy density of 17.94 W h kg-1, a high power density of 1600 W kg-1, and an outstanding long-term stability with 104.4% capacity retention after 16,000 cycles, showing an excellent electrochemical performance and a promising application as an electrode for energy storage.

Bimetal oxide CuO/Co3O4 derived from Cu ions partly-substituted framework of ZIF-67 for toluene catalytic oxidation.

A MOF-templated method is developed to prepare bimetal oxide CuO/Co3O4 by in situ pyrolysis of Cu2+ partly-substituted ZIF-67 precursor. The physicochemical properties of CuO/Co3O4 are studied by various characterizations such as X-ray diffraction, Raman analysis, transmission electron microscope, scanning electron microscope, N2 adsorption-desorption measurement, X-ray photoelectron spectroscope, O2 temperature-programmed desorption, H2 temperature-programmed reduction, etc. Comparison with CuO, Co3O4 and Mix-CuO/Co3O4, 90 % of both toluene conversion and mineralization over CuO/Co3O4 are fulfilled at around 229 °C under the condition of 1000 ppm toluene and weight hour space velocity =20,000 mL/(g h), which is promoted more than 40 °C. The better catalytic performance of CuO/Co3O4 attributes to high mutual dispersion of two oxides, porous structure, lower temperature reducibility, abundant lattice defects, more active oxygen species, higher Co3+/Co2+ and Olatt/Oads molar ratios. Meanwhile, CuO/Co3O4 exhibits a better catalytic stability at different conversions and a good tolerance to 10 vol.% of water vapour. The investigation of temperature-dependent active oxygen species and in-situ DRIFTS results reveal that toluene oxidation on CuO/Co3O4 obeys Mars van Krevelen mechanism.

Ultrasonic-assisted preparation and characterization of magnetic ZnFe2O4/g-C3N4 nanomaterial and their applications towards electrocatalytic reduction of 4-nitrophenol.

Nanoball-structured ferromagnetic zinc ferrite nanocrystals (ZnFe2O4 NPs) entrapped with graphitic-carbon nitride (g-C3N4) was produced via straightforward and facile sonochemical synthetical technique (titanium probe; 100 W/cm2 and 50 KHz). The morphological (SEM), elemental (EDS), diffraction (XRD), XPS, and electrochemical studies (CV) have been carry out to verify the nanostructure and shape of the materials. The ZnFe2O4 NPs/g-C3N4 electrode (GCE) was constructed which displayed outstanding electrochemical ability towards toxic 4-nitrophenol (NTP). A sensitive, selective, reproducible, and durable electrochemical NTP sensor was developed by ZnFe2O4 NPs/g-C3N4 modified electrode. The modified sensor exhibited a high sensitivity and 4.17 nanomolars of LOD. It's greater than the LOD of previously reported NTP modified sensors. The real-time experiments of the modified electrochemical (ZnFe2O4 NPs/g-C3N4 electrode) sensor were successfully explained in various water (river and drinking) samples and its showed high standard recoveries. Therefore, sonochemical synthetical method and fabrication of modified electrode were developed this work based on environmental analysis of NTP sensor.

Sonochemical synthesis of graphitic carbon nitrides-wrapped bimetal oxide nanoparticles hybrid materials and their electrocatalytic activity for xanthine electro-oxidation.

A novel network-like magnetic nanoparticle was fabricated on a graphitic carbon nitride through a facile sonochemical route at frequency 20 kHz and power 70 W. To enhance the electrocatalytic activity of the modified materials, the graphitic carbon nitrides (g-C3N4) was prepared from melamine. Monitoring of xanthine concentration level in biological fluids is more important for clinical diagnosis and medical applications. As modified CuFe2O4/g-C3N4 nanocomposite exhibits better electrochemical activity towards the oxidation of xanthine with higher anodic current compared to other modified and unmodified electrode for the detection of xanthine with larger linear range (0.03-695 µM) and lower limit of detection (13.2 nM). To compare with these methods, the electrochemical techniques may be an alternative high sensitive method due to their simplicity and rapid detection time. In addition, the practical feasibility of the sensor was inspected with biological samples, reveals the acceptable recovery of the sensor in real samples.

A simple sonochemical assisted synthesis of NiMoO4/chitosan nanocomposite for electrochemical sensing of amlodipine in pharmaceutical and serum samples.

In this investigation, a facile sonochemical route has been developed for the preparation of porous nickel molybdate nanosheets/chitosan nanocomposite (NiMoO4/CHIT) by using ammonium molybdate and nickel(II) acetate tetrahydrate and as nickel and molybdate precursor, respectively (ultrasonic power 60 W/cm2 and frequency 20 kHz). The ultrasonic based materials preparation as a fast, convenient and economical approach has been widely used to generate novel nanomaterials. Herein, we report an efficient voltammetric sensor for amlodipine drug by using porous nickel molybdate nanosheets/chitosan nanocomposite (NiMoO4/CHIT). Its structure and properties were characterized by x-ray diffraction pattern, scanning electron microscope, transmission electron microscope, elemental analysis and mapping. The electrochemical studies are indicated the NiMoO4/CHIT modified glassy carbon electrode (GCE) exhibited the good performance towards electrocatalytic sensing of amlodipine drug. Consequently, a linear correlation between the anodic peak current with sensor concentration 0.025-373.6 µM with a detection limit and sensitivity of 4.62 nM and 4.753 µA·µM-1·cm-2, respectively. A voltammetry based drug analysis was found to be high sensitive and reproducible, which able to detect nanomolar concentration. Furthermore, the fabricated electrochemical sensor was applied in drug and biological samples.

Cu(I)-doped Fe3O4 nanoparticles/porous C composite for enhanced H2O2 oxidation of carbamazepine.

Cu(I) doped nano-Fe3O4 were synthesized and loaded on ordered porous carbon materials using a facile co-precipitated. The synthesized catalysts were characterized by XRD, XPS, HRTEM, FESEM-EDX mapping and N2 adsorption-desorption. The results showed that the crystal unit cell of Fe3O4 was enlarged due to the implantation of small amount of Cu(I) into the Fe3O4 structure (Fe2.85Cu0.15O4). With increased Cu content, the catalyst was dominated with Cu2O and the Fe3O4 phase disappeared, the catalytic performance of Fe-Cu bimetal oxide became worse. The Cu(I)-Fe3O4/C composite was enriched with Fe(II), Fe(III) and Cu(I) sites. The prepared Cu-Fe bimetal oxide/C composite exhibited higher specific TOF and oxidation efficiency E on carbamazepine oxidation than Fe2.85Cu0.15O4 and Fe3O4. The enhanced catalytic reactivity was attributed to the synergetic effect of surface Fe and Cu species on the H2O2 activation. The dissolved metals induced catalytic reaction at pH 4.5-8.1 was ignorable. Thus, the catalytic decomposition of H2O2 by Cu-Fe3O4/C at near neutral pH was controlled by interface reactions. The CBZ in the close proximity to the interface was attacked by the generated ROS and formed urea, 2-hydroxybenzyl alcohol and other oxidative products.

A hollow CuOx/NiOy nanocomposite for amperometric and non-enzymatic sensing of glucose and hydrogen peroxide.

The authors report that CuOx/NiOy hollow nanocomposites are an effective bifunctional catalyst capable of oxidizing glucose and reducing hydrogen peroxide. Synthesis is based on a solvothermal process and subsequent thermal treatment. The structure can be controlled by adjusting the amounts of added NiCl2 during the solvothermal etching process, and core-shell, yolk-shell or hollow structures can be obtained. The porous hollow structure composite of type CuO30/NiO90 was used to modify a glassy carbon electrode. It exhibits excellent electrocatalytic activity towards glucose oxidation in solution of pH 13, typically at a working potential of +0.60 V (vs. Ag/AgCl). This enables voltammetric sensing of glucose with (a) a low limit of detection (0.08 µM, at S/N = 3), (b) over a wide linear range (0.20 µM - 2.5 mM), and (c) high sensitivity (2043 µA·mM-1·cm-2). The sensor is reproducible, selective and stable. It can be used to detect glucose in spiked human serum. The CuO30/NiO90 composite also displays good electrocatalytic activity towards reduction of H2O2 in neutral aqueous medium, typically at an applied potential of -0.35 V. It has a detection limit of 90 nM, a sensitivity of 271.1 µA·mM-1·cm-2, and a linear detection range that extends from 0.30 µM to 9.0 mM. Graphical abstract CuOx/NiOy nanocomposites with three different structures were synthesized by coordinated etching precipitation method. The hollow structure CuO30/NiO90 was coated on the surface of glassy carbon electrode for the amperometric determination of glucose and hydrogen peroxide.

Fe-Ti/Fe (II)-loading on ceramic filter materials for residual chlorine removal from drinking water.

Ceramic filter material was prepared with silicon dioxide (SiO2), which was recovered from red mud and then modified with Fe (II) and Fe-Ti bimetal oxide. Ceramic filter material can be used to reduce the content of residual chlorine from drinking water. The results showed that after a two-step leaching process with 3 M hydrochloric acid (HCl) and 90% sulfuric acid (H2SO4), the recovery of SiO2 exceeded 80%. Fe (II)/Fe-Ti bimetal oxide, with a high adsorption capacity of residual chlorine, was prepared using a 3:1 M ratio of Fe/Ti and a concentration of 0.4 mol/L Fe2+. According to the zeta-potential, scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) analysis, Fe (II) and Fe-Ti bimetal oxide altered the zeta potential and structural properties of the ceramic filter material. There was a synergistic interaction between Fe and Ti in which FeOTi bonds on the material surface and hydroxyl groups provided the active sites for adsorption. Through a redox reaction, Fe (II) transfers hypochlorite to chloride, and FeOTiCl bonds were formed after adsorption.

Nature-Inspired 2D-Mosaic 3D-Gradient Mesoporous Framework: Bimetal Oxide Dual-Composite Strategy toward Ultrastable and High-Capacity Lithium Storage.

In allusion to traditional transition-metal oxide (TMO) anodes for lithium-ion batteries, which face severe volume variation and poor conductivity, herein a bimetal oxide dual-composite strategy based on two-dimensional (2D)-mosaic three-dimensional (3D)-gradient design is proposed. Inspired by natural mosaic dominance phenomena, Zn1-xCoxO/ZnCo2O4 2D-mosaic-hybrid mesoporous ultrathin nanosheets serve as building blocks to assemble into a 3D Zn-Co hierarchical framework. Moreover, a series of derivative frameworks with high evolution are controllably synthesized, based on which a facile one-pot synthesis process can be developed. From a component-composite perspective, both Zn1-xCoxO and ZnCo2O4 provide superior conductivity due to bimetal doping effect, which is verified by density functional theory calculations. From a structure-composite perspective, 2D-mosaic-hybrid mode gives rise to ladder-type buffering and electrochemical synergistic effect, thus realizing mutual stabilization and activation between the mosaic pair, especially for Zn1-xCoxO with higher capacity yet higher expansion. Moreover, the inside-out Zn-Co concentration gradient in 3D framework and rich oxygen vacancies further greatly enhance Li storage capability and stability. As a result, a high reversible capacity (1010 mA h g-1) and areal capacity (1.48 mA h cm-2) are attained, while ultrastable cyclability is obtained during high-rate and long-term cycles, rending great potential of our 2D-mosaic 3D-gradient design together with facile synthesis.

CaO-Based CO2 Sorbents Effectively Stabilized by Metal Oxides.

Calcium looping (i.e., CO2 capture by CaO) is a promising second-generation CO2 capture technology. CaO, derived from naturally occurring limestone, offers an inexpensive solution, but due to the harsh operating conditions of the process, limestone-derived sorbents undergo a rapid capacity decay induced by the sintering of CaCO3 . Here, we report a Pechini method to synthesize cyclically stable, CaO-based CO2 sorbents with a high CO2 uptake capacity. The sorbents synthesized feature compositional homogeneity in combination with a nanostructured and highly porous morphology. The presence of a single (Al2 O3 or Y2 O3 ) or bimetal oxide (Al2 O3 -Y2 O3 ) provides cyclic stability, except for MgO which undergoes a significant increase in its particle size with the cycle number. We also demonstrate a direct relationship between the CO2 uptake and the morphology of the synthesized sorbents. After 30 cycles of calcination and carbonation, the best performing sorbent, containing an equimolar mixture of Al2 O3 and Y2 O3 , exhibits a CO2 uptake capacity of 8.7 mmol CO2 g-1 sorbent, which is approximately 360 % higher than that of the reference limestone.

Facile and Mild Strategy to Construct Mesoporous CeO2-CuO Nanorods with Enhanced Catalytic Activity toward CO Oxidation.

CeO2-CuO nanorods with mesoporous structure were synthesized by a facile and mild strategy, which involves an interfacial reaction between Ce2(SO4)3 precursor and NaOH ethanol solution at room temperature to obtain mesoporous CeO2 nanorods, followed by a solvothermal treatment of as-prepared CeO2 and Cu(CH3COO)2. Upon solvothermal treatment, CuO species is highly dispersed onto the CeO2 nanorod surface to form CeO2-CuO composites, which still maintain the mesoporous feature. A preliminary CO catalytic oxidation study demonstrated that the CeO2-CuO samples exhibited strikingly high catalytic activity, and a high CO conversion rate was observed without obvious loss in activity even after thermal treatment at a high temperature of 500 °C. Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and hydrogen temperature-programmed reduction (H2-TPR) analysis revealed that there is a strong interaction between CeO2 and CuO. Moreover, it was found that the introduction of CuO species into CeO2 generates oxygen vacancies, which is highly likely to be responsible for high catalytic activity toward CO oxidation of the mesoporous CeO2-CuO nanorods.