Morphological, Microstructural, and In Situ Chemical Characteristics of Siderite Produced by Iron-Reducing Bacteria.

Dissimilatory iron-reducing bacteria (DIRB) oxidize organic matter or hydrogen and reduce ferric iron to form Fe(II)-bearing minerals, such as magnetite and siderite. However, compared with magnetite, which was extensively studied, the mineralization process and mechanisms of siderite remain unclear. Here, with the combination of advanced electron microscopy and synchrotron-based scanning transmission X-ray microscopy (STXM) approaches, we studied in detail the morphological, structural, and chemical features of biogenic siderite via a growth experiment with Shewanella oneidensis MR-4. Results showed that along with the growth of cells, Fe(II) ions were increasingly released into solution and reacted with CO32- to form micrometer-sized siderite minerals with spindle, rod, peanut, dumbbell, and sphere shapes. They are composed of many single-crystal siderite plates that are fanned out from the center of the particles. Additionally, STXM revealed Fh and organic molecules inside siderite. This suggests that the siderite crystals might assemble around a Fh-organic molecule core and then continue to grow radially. This study illustrates the biomineralization and assembly of siderite by a successive multistep growth process induced by DIRB, also provides evidences that the distinctive shapes and the presence of organic molecules inside might be morphological and chemical features for biogenic siderite.

Direct Electrocatalytic Methanol Oxidation on MoO3/Ni(OH)2: Exploiting Synergetic Effect of Adjacent Mo and Ni.

Ni-based materials have been widely investigated as methanol oxidation reaction (MOR) catalysts. The formation of NiOOH and its reduction to Ni(OH)2 are generally regarded as essential steps for methanol oxidation. However, in such an indirect route, the efficiency of proton coupled electron transfer is fundamentally limited by the rate of transition from Ni(OH)2 to NiOOH back and forth. Herein we demonstrate a direct MOR pathway on MoO3/Ni(OH)2 without the formation of a NiOOH mediator. The MoO3/Ni(OH)2 exhibits a benchmark electrocatalytic MOR current density of 1000 mA cm-2 at 1.52 V vs. RHE with a nearly 100% faradic efficiency, outperforming all the state of art MOR electrocatalysts. In-situ Raman spectroscopy confirms that NiOOH is not formed during the electrocatalytic MOR process on the MoO3/Ni(OH)2. Density functional theory calculations suggest that Ni2+ in MoO3/Ni(OH)2 serves as the methanol adsorption site while the doped Mo6+ plays a key role in capturing the deprotonated H·. Benefiting from the Mo-Ni synergistic effect, the energy barrier of the CH2O* → CHO* + H* process is significantly reduced, avoiding the NiOOH formation and leading to the direct MOR. Our research unravels a direct electrochemical MOR pathway that does not rely on NiOOH formation and provides a facile strategy of regulating the intermediate process barrier for MOR.

Ultrathin CuBi2O4 on a bipolar Bi2O3 nano-scaffold: a self-powered broadband photoelectrochemical photodetector with improved responsivity and response speed.

CuBi2O4 is a promising photoactive material for photoelectrochemical (PEC) broadband photodetectors due to its suitable band structure, but its photo-responsivity is severely limited by the short carrier diffusion length and long light penetration depth. To address the trade-off between light absorption and charge separation, a nano-structured bipolar Bi2O3 host scaffold was coupled with an ultrathin CuBi2O4 light absorbing layer to construct a host-guest Bi2O3/CuBi2O4 photocathode. The work function of the bipolar Bi2O3 scaffold lies in between FTO and CuBi2O4, making Bi2O3 a suitable back contact layer for hole transport. Compared with the flat CuBi2O4 and Bi2O3 scaffold counterpart, the nanostructured Bi2O3/CuBi2O4 exhibits significantly improved light absorption and enhanced charge separation efficiency. The Bi2O3/CuBi2O4 PEC photodetector can be self-powered and demonstrates a broad photo-response ranging from ultraviolet (UV) to near infrared (NIR). It shows a high responsivity of 75 mA W-1 and a remarkable short response time of 0.18 ms/0.19 ms. Bi2O3/CuBi2O4 prepared by magnetron sputtering demonstrates great potential for rapid PEC photodetection in a wide optical domain.

Simultaneous co-Photocatalytic CO2 Reduction and Ethanol Oxidation towards Synergistic Acetaldehyde Synthesis.

Photocatalytic conversion of CO2 is of great interest but it often suffers sluggish oxidation half reaction and undesired by-products. Here, we report for the first the simultaneous co-photocatalytic CO2 reduction and ethanol oxidation towards one identical value-added CH3 CHO product on a rubidium and potassium co-modified carbon nitride (CN-KRb). The CN-KRb offers a record photocatalytic activity of 1212.3 µmol h-1 g-1 with a high selectivity of 93.3 % for CH3 CHO production, outperforming all the state-of-art CO2 photocatalysts. It is disclosed that the introduced Rb boosts the *OHCCHO fromation and facilitates the CH3 CHO desorption, while K promotes ethanol adsorption and activation. Moreover, the H+ stemming from ethanol oxidation is confirmed to participate in the CO2 reduction process, endowing near ideal overall atomic economy. This work provides a new strategy for effective use of the photoexcited electron and hole for high selective and sustainable conversion of CO2 paired with oxidation reaction into identical product.

Size-Independent Reconfigurable Logic Gate with Bismuth Oxide Based Photoelectrochemical Device.

XOR gate, an important building block in computational circuits, is often constructed by combining other basic logic gates, and the hybridity inevitably leads to its complexity. A photoelectrochemical device could realize XOR function based on the current change of the photoelectrode; however, such signal is highly sensitive to photoelectrode size and therefore requires precise manufacturing at a high cost. Herein we developed a novel XOR gate based on the light-induced open-circuit potential (OCP) of the Bi2O3 photoelectrode. Surprisingly, the OCP of Bi2O3 does not increase with light intensity according to the traditional logarithmic relationship. Instead, an unusual decrease in OCP is observed at high light intensity, which is attributed to the dramatic light-induced increase in surface states that can be easily regulated by varying the oxygen partial pressure during reactive magnetron sputtering. Based on such a nonmonotonic variation of OCP, a facile Bi2O3-based gate is designed to realize the XOR function. Unlike the commonly used current signal, OCP is size independent, and therefore, the Bi2O3-based gate does not require high manufacturing accuracy. Moreover, in addition to XOR, the Bi2O3-based PEC gate also demonstrates great versatility in realizing other logic functions including AND, OR, NOT, NIH, NAND, and NOR. The strategy of modulating and applying nonmonotonic OCP signal opens a new avenue for designing size-independent reconfigurable logic gates at low manufacturing cost.

Self-passivated CuV2O6 as a universal photoelectrode material for reliable and accurate photoelectrochemical sensing.

Photoelectrochemical (PEC) detection has attracted intensive attention during the past decade. Currently, most research focuses on improving the sensitivity and selectivity of the PEC sensor, but the issue of the stability of the photoelectrode material under the testing environment is often ignored or lacks in-depth investigation. Herein, we develop a novel CuV2O6 photoelectrode exhibiting superior stability under the testing environment through self-passivation. CuV2O6-based PEC sensors are fabricated for the first time for highly selective carcinoembryonic antigen (CEA) and human serum alpha fetoprotein (AFP) detection. The CuV2O6 shows great potential as a universal photoelectrode material for reliable and accurate PEC detection of macromolecules.

Diverse phylogeny and morphology of magnetite biomineralized by magnetotactic cocci.

Magnetotactic bacteria (MTB) are diverse prokaryotes that produce magnetic nanocrystals within intracellular membranes (magnetosomes). Here, we present a large-scale analysis of diversity and magnetosome biomineralization in modern magnetotactic cocci, which are the most abundant MTB morphotypes in nature. Nineteen novel magnetotactic cocci species are identified phylogenetically and structurally at the single-cell level. Phylogenetic analysis demonstrates that the cocci cluster into an independent branch from other Alphaproteobacteria MTB, that is, within the Etaproteobacteria class in the Proteobacteria phylum. Statistical analysis reveals species-specific biomineralization of magnetosomal magnetite morphologies. This further confirms that magnetosome biomineralization is controlled strictly by the MTB cell and differs among species or strains. The post-mortem remains of MTB are often preserved as magnetofossils within sediments or sedimentary rocks, yet paleobiological and geological interpretation of their fossil record remains challenging. Our results indicate that magnetofossil morphology could be a promising proxy for retrieving paleobiological information about ancient MTB.

One Step Synthesis of Tetragonal-CuBi2O4/Amorphous-BiFeO3 Heterojunction with Improved Charge Separation and Enhanced Photocatalytic Properties.

Tetragonal CuBi2O4/amorphous BiFeO3 (T-CBO/A-BFO) composites are prepared via a one-step solvothermal method at mild conditions. The T-CBO/A-BFO composites show expanded visible light absorption, suppressed charge recombination, and consequently improved photocatalytic activity than T-CBO or A-BFO alone. The T-CBO/A-BFO with an optimal T-CBO to A-BFO ratio of 1:1 demonstrates the lowest photoluminescence signal and highest photocatalytic activity. It shows a removal rate of 78.3% for the photodegradation of methylene orange under visible light irradiation for 1 h. XPS test after the cycle test revealed the reduction of Bi3+ during the photocatalytic reaction. Moreover, the as prepared T-CBO/A-BFO show fundamentally higher photocatalytic activity than their calcinated counterparts. The one-step synthesis is completed within 30 min and does not require post annealing process, which may be easily applied for the fast and cost-effective preparation of photoactive metal oxide heterojunctions.

Short-Time Hydrothermal Synthesis of CuBi2O4 Nanocolumn Arrays for Efficient Visible-Light Photocatalysis.

In this article, a short-time hydrothermal method is developed to prepare CuBi2O4 nanocolumn arrays. By using Bi(NO3)3·5H2O in acetic acid and Cu(NO3)2·3H2O in ethanol as precursor solutions, tetragonal CuBi2O4 with good visible light absorption can be fabricated within 0.5 h at 120 °C. Tetragonal structured CuBi2O4 can be formed after 15 min hydrothermal treatment, however it possesses poor visible light absorption and low photocatalytic activity. Extending the hydrothermal treatment duration to 0.5 h results in a significant improvement invisible light absorption of the tetragonal CuBi2O4. The CuBi2O4 obtained through 0.5 h hydrothermal synthesis shows a band gap of 1.75 eV and exhibits the highest photocatalytic performance among the CuBi2O4 prepared with various hydrothermal time. The removal rate of methylene blue by the 0.5 h CuBi2O4 reaches 91% under visible light irradiation for 0.5 h. This study proposes a novel strategy to prepare photoactive CuBi2O4 nanocolumn arrays within 0.5 h at a moderate temperature of 120 °C. The hydrothermal method provides a facile strategy for the fast synthesis of metal-oxide-based photocatalysts at mild reaction conditions.

Short-Chain Modified SiO2 with High Absorption of Organic PCM for Thermal Protection.

Organic phase change materials (PCMs) have great potential in thermal protection applications but they suffer from high volumetric change and easy leakage, which require "leak-proof" packaging materials with low thermal conductivity. Herein, we successfully modify SiO2 through a simple 2-step method consisting of n-hexane activation followed by short-chain alkane silanization. The modified SiO2 (M-SiO2) exhibits superior hydrophobic property while maintaining the intrinsic high porosity of SiO2. The surface modification significantly improves the absorption rate of RT60 in SiO2 by 38%. The M-SiO2/RT60 composite shows high latent heat of 180 J·g-1, low thermal conductivity of 0.178 W·m-1·K-1, and great heat capacity behavior in a high-power thermal circuit with low penetrated heating flow. Our results provide a simple approach for preparing hydrophobic SiO2 with high absorption of organic PCM for thermal protection applications.

Gradient Self-Doped CuBi2O4 with Highly Improved Charge Separation Efficiency.

A new strategy of using forward gradient self-doping to improve the charge separation efficiency in metal oxide photoelectrodes is proposed. Gradient self-doped CuBi2O4 photocathodes are prepared with forward and reverse gradients in copper vacancies using a two-step, diffusion-assisted spray pyrolysis process. Decreasing the Cu/Bi ratio of the CuBi2O4 photocathodes introduces Cu vacancies that increase the carrier (hole) concentration and lowers the Fermi level, as evidenced by a shift in the flat band toward more positive potentials. Thus, a gradient in Cu vacancies leads to an internal electric field within CuBi2O4, which can facilitate charge separation. Compared to homogeneous CuBi2O4 photocathodes, CuBi2O4 photocathodes with a forward gradient show highly improved charge separation efficiency and enhanced photoelectrochemical performance for reduction reactions, while CuBi2O4 photocathodes with a reverse gradient show significantly reduced charge separation efficiency and photoelectrochemical performance. The CuBi2O4 photocathodes with a forward gradient produce record AM 1.5 photocurrent densities for CuBi2O4 up to -2.5 mA/cm2 at 0.6 V vs RHE with H2O2 as an electron scavenger, and they show a charge separation efficiency of 34% for 550 nm light. The gradient self-doping accomplishes this without the introduction of external dopants, and therefore the tetragonal crystal structure and carrier mobility of CuBi2O4 are maintained. Lastly, forward gradient self-doped CuBi2O4 photocathodes are protected with a CdS/TiO2 heterojunction and coated with Pt as an electrocatalyst. These photocathodes demonstrate photocurrent densities on the order of -1.0 mA/cm2 at 0.0 V vs RHE and evolve hydrogen with a faradaic efficiency of ∼91%.

Magnetotactic Coccus Strain SHHC-1 Affiliated to Alphaproteobacteria Forms Octahedral Magnetite Magnetosomes.

Magnetotactic bacteria (MTB) are morphologically and phylogenetically diverse prokaryotes. They can form intracellular chain-assembled magnetite (Fe3O4) or greigite (Fe3S4) nanocrystals each enveloped by a lipid bilayer membrane called a magnetosome. Magnetotactic cocci have been found to be the most abundant morphotypes of MTB in various aquatic environments. However, knowledge on magnetosome biomineralization within magnetotactic cocci remains elusive due to small number of strains that have been cultured. By using a coordinated fluorescence and scanning electron microscopy method, we discovered a unique magnetotactic coccus strain (tentatively named SHHC-1) in brackish sediments collected from the estuary of Shihe River in Qinhuangdao city, eastern China. It phylogenetically belongs to the Alphaproteobacteria class. Transmission electron microscopy analyses reveal that SHHC-1 cells formed many magnetite-type magnetosomes organized as two bundles in each cell. Each bundle contains two parallel chains with smaller magnetosomes generally located at the ends of each chain. Unlike most magnetotactic alphaproteobacteria that generally form magnetosomes with uniform crystal morphologies, SHHC-1 magnetosomes display a more diverse variety of crystal morphology even within a single cell. Most particles have rectangular and rhomboidal projections, whilst others are triangular, or irregular. High resolution transmission electron microscopy observations coupled with morphological modeling indicate an idealized model-elongated octahedral crystals, a form composed of eight {111} faces. Furthermore, twins, multiple twins and stack dislocations are frequently observed in the SHHC-1 magnetosomes. This suggests that biomineralization of strain SHHC-1 magnetosome might be less biologically controlled than other magnetotactic alphaproteobacteria. Alternatively, SHHC-1 is more sensitive to the unfavorable environments under which it lives, or a combination of both factors may have controlled the magnetosome biomineralization process within this unique MTB.

Single-Cell Resolution of Uncultured Magnetotactic Bacteria via Fluorescence-Coupled Electron Microscopy.

Magnetotactic bacteria (MTB) form intracellular chain-assembled nanocrystals of magnetite or greigite termed magnetosomes. The characterization of magnetosome crystals requires electron microscopy due to their nanoscopic sizes. However, electron microscopy does not provide phylogenetic information for MTB. We have developed a strategy for the simultaneous and rapid phylogenetic and biomineralogical characterization of uncultured MTB at the single-cell level. It consists of four steps: (i) enrichment of MTB cells from an environmental sample, (ii) 16S rRNA gene sequencing of MTB, and (iii) fluorescence in situ hybridization analyses coordinated with (iv) transmission or scanning electron microscopy of the probe-hybridized cells. The application of this strategy identified a magnetotactic Gammaproteobacteria strain, SHHR-1, from brackish sediments collected from the Shihe River estuary in Qinhuangdao City, China. SHHR-1 magnetosomes are elongated prismatic magnetites which can be idealized as hexagonal prisms. Taxonomic groups of uncultured MTB were also identified in freshwater sediments from Lake Miyun in northern Beijing via this novel coordinated fluorescence and scanning electron microscopy method based on four group-specific rRNA-targeted probes. Our analyses revealed that major magnetotactic taxonomic groups can be accurately determined only with coordinated scanning electron microscopy observations on fluorescently labeled single cells due to limited group coverage and specificity for existing group-specific MTB fluorescence in situ hybridization (FISH) probes. Our reported strategy is simple and efficient, offers great promise toward investigating the diversity and biomineralization of MTB, and may also be applied to other functional groups of microorganisms.IMPORTANCE Magnetotactic bacteria (MTB) are phylogenetically diverse and biomineralize morphologically diverse magnetic nanocrystals of magnetite or greigite in intracellular structures termed magnetosomes. However, many uncultured MTB strains have not been phylogenetically identified or structurally investigated at the single-cell level, which limits our comprehensive understanding of the diversity of MTB and their role in biomineralization. We developed a fluorescence-coupled electron microscopy method for the rapid phylogenetic and biomineralogical characterization of uncultured MTB at the single-cell level. Using this novel method, we successfully identified taxonomic groups of several uncultured MTB and one novel magnetotactic Gammaproteobacteria strain, SHHR-1, from natural environments. Our analyses further indicate that strain SHHR-1 forms elongated prismatic magnetites. Our findings provide a promising strategy for the rapid characterization of phylogenetic and biomineralogical properties of uncultured MTB at the single-cell level. Furthermore, due to its simplicity and generalized methodology, this strategy can also be useful in the study of the diversity and biomineralization properties of microbial taxa involved in other mineralization processes.

Surfactant-free ionic liquid-based nanofluids with remarkable thermal conductivity enhancement at very low loading of graphene.

We report for the first time the preparation of highly stable graphene (GE)-based nanofluids with ionic liquid as base fluids (ionic liquid-based nanofluids (Ionanofluids)) without any surfactant and the subsequent investigations on their thermal conductivity, specific heat, and viscosity. The microstructure of the GE and MWCNTs are observed by transmission electron microscope. Thermal conductivity (TC), specific heat, and viscosity of these Ionanofluids were measured for different weight fractions and at varying temperatures, demonstrating that the Ionanofluids exhibit considerably higher TC and lower viscosity than that of their base fluids without significant specific heat decrease. An enhancement in TC by about 15.5% and 18.6% has been achieved at 25 °C and 65 °C respectively for the GE-based nanofluid at mass fraction of as low as 0.06%, which is larger than that of the MWCNT-dispersed nanofluid at the same loading. When the temperature rises, the TC and specific heat of the Ionanofluid increase clearly, while the viscosity decreases sharply. Moreover, the viscosity of the prepared Ionanofluids is lower than that of the base fluid. All these advantages of this new kind of Ionanofluid make it an ideal fluid for heat transfer and thermal storage.

[The clinical features of acute pancreatitis in 10 cities in Shandong Province].

OBJECTIVE: To investigate and obtain a more comprehensive view of the etiology and clinical features of acute pancreatitis (AP) in Shandong Province. METHODS: 1471 cases admitted to hospital for AP were studied and collected from the ten cities of Shandong Province from January 1992 to December 2002 retrospectively. Data of each enrolled patient was recorded in a standardized form. RESULTS: In the 1471 patients, the ratio of male: female was 854:617, and also the mean age of them and the range was 43.3 and from 13 - 82 years old. 1280 had mild AP, and 191 had sever AP. Cholelithiasis (20.2%), alcohol (17.3%) and diet-induced (12.4%) were the most frequent etiologic factors, followed by biliary tract infections (5.6%), hyperlipemia (2.3%), other factors (5.1%). But in about 36.1% cases, the etiology of AP still remains unexplained. In coastal regions, cholelithiasis is the most frequent factor but in interior regions alcohol ranked first. In male, a small predominance of alcohol over cholelithiasis was seen (27.4 vs.14.3%, P < 0.01); and in female, there was a clear predominance of cholelithiasis over alcohol (28.4 vs. 3.2%, P < 0.01). The complications of AP were pancreatic pseudocyst, ascites and peritonitis, pulmonary infections, multiple organ failure, diabetes mellitus-2 and shock, etc. according to their frequencies. CONCLUSIONS: Cholelithiasis, alcohol and diet-induced factor were main etiologic factors in Shandong Province, whereas cholelithiasis alone predominated in the females. In about 36.1% cases, the etiology remains unknown. So that more attention should be paid to study the etiology of AP.