| 1. |
- Beal, Jacob, et al.
(författare)
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Robust estimation of bacterial cell count from optical density
- 2020
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Ingår i: Communications Biology. - : Springer Science and Business Media LLC. - 2399-3642. ; 3:1
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Tidskriftsartikel (refereegranskat)abstract
- Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data.
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| 2. |
- Xi, Ning, et al.
(författare)
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Polyhedral Coordination Determined Co-O Activity for Electrochemical Oxidation of Biomass Alcohols
- 2023
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Ingår i: Advanced Energy Materials. - 1614-6832 .- 1614-6840. ; 13:37
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Tidskriftsartikel (refereegranskat)abstract
- Earth-abundant transition metal oxides are promising electrocatalysts for oxidation of biomass alcohols. Here, CoO and Co3O4 are selected as representative cobalt oxide catalysts and grown on carbon fiber paper (CFP) electrodes to reveal the interplay between electronic structure and catalytic activity of catalysts for oxidation of glycerol, diols, and monohydric alcohols. In situ electrochemical tests elucidate that the CoO/CFP electrode has lower interfacial impedance, higher charge transfer, faster oxidation rate, and thereby the higher catalytic activity for alcohol oxidation than the Co3O4/CFP electrode. Especially for glycerol oxidation, the CoO/CFP electrode only requires 1.32 V to reach 10 mA cm−2, the potential is 120 mV lower than that for the Co3O4/CFP electrode. The CoO/CFP electrode can also produce value-added products such as formate, acetate, and glycolate with high selectivity and efficiency at low energy consumptions from oxidation of biomass alcohols. Theoretical calculations further confirm the dominant role of octahedrally coordinated Co-O sites in adsorption, activation, and oxidation of C3-C1 alcohols. This work sheds light on the design of highly efficient transition metal oxide catalysts for oxidation of alcohols by populating octahedral sites in the crystal structure.
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| 3. |
- Wang, Longwei, et al.
(författare)
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Regulation of functional groups enable the metal-free PDINH/GO advisable antibacterial photocatalytic therapy
- 2023
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Ingår i: Chemical Engineering Journal. - : Elsevier BV. - 1385-8947. ; 451
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Tidskriftsartikel (refereegranskat)abstract
- N-type organic semiconductor perylene-3,4,9,10-tetracarboxylic acid diimide (PDINH) are well-investigated photocatalyst. However, the photocatalytic potential for antibacterial therapy has been underexplored owing to the insufficient light absorption and rapid recombination of light-induced carriers. Herein, functional group-regulated is introduced by recrystallizing PDINH on the surface of GO in situ, endowing the PDINH/GO with enhanced photocatalytic properties, which harvest light energy across the full spectrum form ultraviolet to near-infrared. Simultaneously, the enhanced photogenerated carriers can activate Lewis base of GO to form an amide bond on the interface between bacteria and material, exhibiting high-efficient and steady bacteria trap. Compared with PDINH, both in vitro and in vivo all demonstrated PDINH/GO possess excellent antibacterial effect. In addition, as a non-metallic semiconductor, PDINH/GO shows capacity of enhancing epidermal cells proliferation and migration, resulting in successful infectious wound regeneration in mice and the side effects in vivo are negligible. Such the integration of wide-spectrum response, high efficiency of carrier separation, intentional bacterial capture and accelerated would healing of PDINH/GO not only enables an effective antibacterial therapy but also contributes to a successful example to activate nanomaterials by regulation of functional groups.
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| 4. |
- Chang, Jian, 1990-, et al.
(författare)
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Tailor-Made White Photothermal Fabrics : A Bridge between Pragmatism and Aesthetic
- 2023
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Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 35:41
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Tidskriftsartikel (refereegranskat)abstract
- Maintaining human thermal comfort in the cold outdoors is crucial for diverse outdoor activities, e.g., sports and recreation, healthcare, and special occupations. To date, advanced clothes are employed to collect solar energy as a heat source to stand cold climates, while their dull dark photothermal coating may hinder pragmatism in outdoor environments and visual sense considering fashion. Herein, tailor-made white webs with strong photothermal effect are proposed. With the embedding of cesium–tungsten bronze (CsxWO3) nanoparticles (NPs) as additive inside nylon nanofibers, these webs are capable of drawing both near-infrared (NIR) and ultraviolet (UV) light in sunlight for heating. Their exceptional photothermal conversion capability enables 2.5–10.5 °C greater warmth than that of a commercial sweatshirt of six times greater thickness under different climates. Remarkably, this smart fabric can increase its photothermal conversion efficiency in a wet state. It is optimal for fast sweat or water evaporation at human comfort temperature (38.5 °C) under sunlight, and its role in thermoregulation is equally important to avoid excess heat loss in wilderness survival. Obviously, this smart web with considerable merits of shape retention, softness, safety, breathability, washability, and on-demand coloration provides a revolutionary solution to realize energy-saving outdoor thermoregulation and simultaneously satisfy the needs of fashion and aesthetics.
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| 5. |
- Farmand, Maryam, et al.
(författare)
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Near-edge X-ray refraction fine structure microscopy
- 2017
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Ingår i: Applied Physics Letters. - : AMER INST PHYSICS. - 0003-6951 .- 1077-3118. ; 110:6
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Tidskriftsartikel (refereegranskat)abstract
- We demonstrate a method for obtaining increased spatial resolution and specificity in nanoscale chemical composition maps through the use of full refractive reference spectra in soft x-ray spectro- microscopy. Using soft x-ray ptychography, we measure both the absorption and refraction of x-rays through pristine reference materials as a function of photon energy and use these reference spectra as the basis for decomposing spatially resolved spectra from a heterogeneous sample, thereby quantifying the composition at high resolution. While conventional instruments are limited to absorption contrast, our novel refraction based method takes advantage of the strongly energy dependent scattering cross-section and can see nearly five-fold improved spatial resolution on resonance.
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| 6. |
- Gao, Wenqiang, et al.
(författare)
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Construction of diluted magnetic semiconductor to endow nonmagnetic semiconductor with spin-regulated photocatalytic performance
- 2023
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Ingår i: Nano Energy. - : Elsevier BV. - 2211-2855 .- 2211-3282. ; 110
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Tidskriftsartikel (refereegranskat)abstract
- Electron spinning polarization has now attracted extensive attention due to its significant effect on improving catalysis. However, only a few photocatalysts possess the electron spinning modification property. How to endow nonmagnetic semiconductors with spintronic properties to realize spinning-regulated photocatalysis enhancement is a great challenge. Herein, based on the diluted magnetic semiconductor concept, we proposed a novel strategy to endow photocatalysts a spinning tunable property. In this work, a diluted magnetic semiconductor photocatalyst with spin polarization was constructed by only doping magnetic ions into CdS/MoS2. The spin polarization with a higher ferromagnetic property was detected in CdS and MoS2 of the Ni-doped CdS/MoS2 diluted magnetic semiconductor photocatalyst. The magnetic field-derived spin polarization reduced the charge recombination in CdS, and improved the interface transfer efficiency between CdS and MoS2, which resulted in a 3.89-fold improvement of the photocatalytic hydrogen production under an external magnetic field. This work provides a new strategy to endow nonmagnetic semiconductors with spin-regulated photocatalytic performance by constructing diluted magnetic semiconductor photocatalysts.
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| 7. |
- Martín-Yerga, Daniel, et al.
(författare)
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In situ catalyst reactivation for enhancing alcohol electro-oxidation and coupled hydrogen generation
- 2020
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Ingår i: Chemical Communications. - : Royal Society of Chemistry (RSC). - 1359-7345 .- 1364-548X. ; 56:28, s. 4011-4014
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Tidskriftsartikel (refereegranskat)abstract
- A novel method exploiting the in situ reactivation of a PdNi catalyst to enhance the electro-oxidation of alcohols is reported. The periodic regeneration of the catalyst surface leads to significant gains in terms of conversion rate, energy requirements and stability compared to the conventional potentiostatic method.
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| 8. |
- Subbotina, Elena, et al.
(författare)
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Oxidative cleavage of C-C bonds in lignin
- 2021
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Ingår i: Nature Chemistry. - : Springer Science and Business Media LLC. - 1755-4330 .- 1755-4349. ; 13, s. 1118-1125
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Tidskriftsartikel (refereegranskat)abstract
- Lignin is an aromatic polymer that constitutes up to 30 wt% of woody biomass and is considered the largest source of renewable aromatics. Valorization of the lignin stream is pivotal for making biorefining sustainable. Monomeric units in lignin are bound via C–O and C–C bonds. The majority of existing methods for the production of valuable compounds from lignin are based on the depolymerization of lignin via cleavage of relatively labile C–O bonds within lignin structure, which leads to yields of only 36–40 wt%. The remaining fraction (60 wt%) is a complex mixture of high-molecular-weight lignin, generally left unvalorized. Here we present a method to produce additional valuable monomers from the high-molecular-weight lignin fraction through oxidative C–C bond cleavage. This oxidation reaction proceeds with a high selectivity to give 2,6-dimethoxybenzoquinone (DMBQ) from high-molecular-weight lignin in 18 wt% yield, thus increasing the yield of monomers by 32%. This is an important step to make biorefining competitive with petroleum-based refineries.
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| 9. |
- Subbotina, Elena, et al.
(författare)
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Oxidative Cleavage of C-C Bonds in Lignin
- 2022
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Ingår i: Synlett. - : GEORG THIEME VERLAG KG. - 0936-5214 .- 1437-2096. ; 33:04, s. A44-A46
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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| 10. |
- Yu, Xiaowen, et al.
(författare)
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Electrocatalytic Glycerol Oxidation with Concurrent Hydrogen Evolution Utilizing an Efficient MoOx/Pt Catalyst
- 2021
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Ingår i: Small. - : Wiley. - 1613-6810 .- 1613-6829. ; 17:44
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Tidskriftsartikel (refereegranskat)abstract
- Glycerol electrolysis affords a green and energetically favorable route for the production of value-added chemicals at the anode and H2 production in parallel at the cathode. Here, a facile method for trapping Pt nanoparticles at oxygen vacancies of molybdenum oxide (MoOx) nanosheets, yielding a high-performance MoOx/Pt composite electrocatalyst for both the glycerol oxidation reaction (GOR) and the hydrogen evolution reaction (HER) in alkaline electrolytes, is reported. Combined electrochemical experiments and theoretical calculations reveal the important role of MoOx nanosheets for the adsorption of glycerol molecules in GOR and the dissociation of water molecules in HER, as well as the strong electronic interaction with Pt. The MoOx/Pt composite thus significantly enhances the specific mass activity of Pt and the kinetics for both reactions. With MoOx/Pt electrodes serving as both cathode and anode, two-electrode glycerol electrolysis is achieved at a cell voltage of 0.70 V to reach a current density of 10 mA cm−2, which is 0.90 V less than that required for water electrolysis.
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