| 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. |
- Li, Fusheng, 1985-, et al.
(författare)
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Electroless Plating of NiFeP Alloy on the Surface of Silicon Photoanode for Efficient Photoelectrochemical Water Oxidation
- 2020
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Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 12:10, s. 11479-11488
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Tidskriftsartikel (refereegranskat)abstract
- N- type silicon is a kind of semiconductor with a narrow band gap that has been reported as an outstanding light-harvesting material for photoelectrochemical (PEC) reactions. Decorating a thin catalyst layer on the n-type silicon surface can provide a direct and effective route toward PEC water oxidation. However, most of catalyst immobilization methods for reported n-type silicon photoanodes have been based on energetically demanding, time-consuming, and high-cost processes. Herein, a high-performance NiFeP alloy (NiFeP)-decorated n-type micro-pyramid silicon array (n-Si) photoanode (NiFeP/n-Si) was prepared by a fast and low-cost electroless deposition method for light-driven water oxidation reaction. The saturated photocurrent density of NiFeP/n-Si can reach up to similar to 40 mA cm(-2) and a photocurrent density of 15.5 mA cm(-2) can be achieved at 1.23 V-RHE under light illumination (100 mW cm(-2), AM1.5 filter), which is one of the most promising silicon-based photoanodes to date. The kinetic studies showed that the NiFeP on the silicon photoanodes could significantly decrease the interfacial charge recombination between the n-type silicon surface and electrolyte.
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| 3. |
- Li, Gang, et al.
(författare)
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Selective Electrochemical Alkaline Seawater Oxidation Catalyzed by Cobalt Carbonate Hydroxide Nanorod Arrays with Sequential Proton-Electron Transfer Properties
- 2021
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Ingår i: ACS Sustainable Chemistry and Engineering. - : American Chemical Society (ACS). - 2168-0485. ; 9:2, s. 905-913
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Tidskriftsartikel (refereegranskat)abstract
- Seawater oxygen evolution is one of the promising energy conversion technologies for large-scale renewable energy storage. It requires efficient catalysts to accelerate the oxygen evolution reaction (OER) for sustained water oxidation, avoiding chlorine evolution under acidic conditions or hypochlorite formation in alkaline solutions. Conventional metal oxide-based OER catalysts follow the adsorbate evolution mechanism that involves concerted proton-electron transfer steps at the active sites. Thus, on the scale of reversible hydrogen electrode, their catalytic activity is independent of the pH of electrolytes. In the present study, nanostructured cobalt carbonate hydroxide (CoCH) with sequential proton-electron transfer properties was tested as a catalyst for seawater oxygen evolution. CoCH exhibited pH-dependent water oxidation activities, thereby providing larger potential and current operating windows for selective water oxidation compared to the catalysts with pH-independent OER activities. The operating window can be further expanded by increasing the pH of the electrolyte.
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| 4. |
- Li, Yingzheng, et al.
(författare)
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Influence of O-O formation pathways and charge transfer mediator on lipid bilayer membrane-like photoanodes for water oxidation
- 2024
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Ingår i: Journal of Energy Chemistry. - : Elsevier. - 2095-4956 .- 2096-885X. ; 93, s. 526-537
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Tidskriftsartikel (refereegranskat)abstract
- Inspired by the function of crucial components in photosystem II (PSII), electrochemical and dyesensitized photoelectrochemical (DSPEC) water oxidation devices were constructed by the selfassembly of well-designed amphipathic Ru(bda)-based catalysts (bda = 2,2'-bipyrdine-6,6'-dicarbonoxyl acid) and aliphatic chain decorated electrode surfaces, forming lipid bilayer membrane (LBM)-like structures. The Ru(bda) catalysts on electrode-supported LBM films demonstrated remarkable water oxidation performance with different O-O formation mechanisms. However, compared to the slow charge transfer process, the O-O formation pathways did not determine the PEC water oxidation efficiency of the dyesensitized photoanodes, and the different reaction rates for similar catalysts with different catalytic paths did not determine the PEC performance of the DSPECs. Instead, charge transfer plays a decisive role in the PEC water oxidation rate. When an indolo[3,2-b] carbazole derivative was introduced between the Ru (bda) catalysts and aliphatic chain-modified photosensitizer in LBM films, serving as a charge transfer mediator for the tyrosine-histidine pair in PSII, the PEC water oxidation performance of the corresponding photoanodes was dramatically enhanced.
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| 5. |
- Li, Yingzheng, et al.
(författare)
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Switching the O-O Bond Formation Pathways of Ru-pda Water Oxidation Catalyst by Third Coordination Sphere Engineering
- 2021
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Ingår i: RESEARCH. - : American Association for the Advancement of Science (AAAS). - 2639-5274. ; 2021
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Tidskriftsartikel (refereegranskat)abstract
- Water oxidation is a vital anodic reaction for renewable fuel generation via electrochemical- and photoelectrochemical-driven water splitting or CO2 reduction. Ruthenium complexes, such as Ru-bda family, have been shown as highly efficient water-oxidation catalysts (WOCs), particularly when they undergo a bimolecular O-O bond formation pathway. In this study, a novel Ru(pda)-type (pda(2-) = 1,10-phenanthroline-2,9-dicarboxylate) molecular WOC with 4-vinylpyridine axial ligands was immobilized on the glassy carbon electrode surface by electrochemical polymerization. Electrochemical kinetic studies revealed that this homocoupling polymer catalyzes water oxidation through a bimolecular radical coupling pathway, where interaction between two Ru(pda)-oxyl moieties (I2M) forms the O-O bond. The calculated barrier of the I2M pathway by density-functional theory (DFT) is significantly lower than the barrier of a water nucleophilic attack (WNA) pathway. By using this polymerization strategy, the Ru centers are brought closer in the distance, and the O-O bond formation pathway by the Ru (pda) catalyst is switched from WNA in a homogeneous molecular catalytic system to I2M in the polymerized film, providing some deep insights into the importance of third coordination sphere engineering of the water oxidation catalyst.
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| 6. |
- Liu, Chang, et al.
(författare)
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A dendritic Sb2Se3/In2S3 heterojunction nanorod array photocathode decorated with a MoSx catalyst for efficient solar hydrogen evolution
- 2020
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 8:44, s. 23385-23394
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Tidskriftsartikel (refereegranskat)abstract
- Developing cost-effective photocathodes that show desirable performance for use in commercial photoelectrochemical water splitting devices remains a fundamental and practical challenge. Sb2Se3 semiconductors satisfy most of the demands expected for an ideal highly efficient photocathode, including favorable cost and optoelectronic properties. Herein, we have demonstrated outstanding photoelectrodes using a noble-metal-free catalyst, namely, a MoSx-decorated low-cost Sb2Se3/In2S3 heterojunction, as the photocathode. This enabled a maximum photocurrent density of up to -27 mA cm(-2) (0 V vs. RHE, 100 mW cm(-2), AM 1.5G filter) with a remarkable half solar-to-hydrogen conversion efficiency (STH) of 2.6%, obtained via decreasing charge recombination and accelerating charge transfer through morphological optimization of the In2S3 layer.
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| 7. |
- Zhao, Yilong, et al.
(författare)
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Efficient urea electrosynthesis from carbon dioxide and nitrate via alternating Cu–W bimetallic C–N coupling sites
- 2023
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Ingår i: Nature Communications. - : Springer Nature. - 2041-1723. ; 14:1
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Tidskriftsartikel (refereegranskat)abstract
- Electrocatalytic urea synthesis is an emerging alternative technology to the traditional energy-intensive industrial urea synthesis protocol. Novel strategies are urgently needed to promote the electrocatalytic C–N coupling process and inhibit the side reactions. Here, we report a CuWO4 catalyst with native bimetallic sites that achieves a high urea production rate (98.5 ± 3.2 μg h−1 mg−1cat) for the co-reduction of CO2 and NO3− with a high Faradaic efficiency (70.1 ± 2.4%) at −0.2 V versus the reversible hydrogen electrode. Mechanistic studies demonstrated that the combination of stable intermediates of *NO2 and *CO increases the probability of C–N coupling and reduces the potential barrier, resulting in high Faradaic efficiency and low overpotential. This study provides a new perspective on achieving efficient urea electrosynthesis by stabilizing the key reaction intermediates, which may guide the design of other electrochemical systems for high-value C–N bond-containing chemicals.
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| 8. |
- Han, Ziqi, et al.
(författare)
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Regulating the miscibility of donors/acceptors to manipulate the morphology and reduce non-radiative recombination energy loss enables efficient organic solar cells
- 2024
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Ingår i: Journal of Materials Chemistry C. - : ROYAL SOC CHEMISTRY. - 2050-7526 .- 2050-7534.
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Tidskriftsartikel (refereegranskat)abstract
- Due to the high exciton binding energy and relatively low charge carrier mobilities of organic photovoltaic materials, it is crucial to optimize the active layer morphology of organic solar cells (OSCs) to well juggle exciton dissociation and charge carrier transport, and inhibit charge carrier recombination for high power conversion efficiencies (PCEs). Herein, we efficiently improve the crystallinity and miscibility of fused ring electron acceptors (FREAs) via lengthening the side chains and developing four FREAs, BTP-nC8, BTP-C8, BTP-C12 and BTP-C20. The dual functions of lengthening the side chains of FREAs make PM6:FREA blend films present the tendency of first improving then deteriorating in crystallinity, phase separation, domain purity and thus charge carrier dynamics, which leads the JSC and FF of PM6:FREA-based OSCs to show the same trend along with the side-chain length of FREAs. More importantly, enhancing the miscibility between PM6 and FREA facilitates the spatial registry to reduce the formation and recombination rate of triplet excitons in the PM6:FREA blend films, thus inhibiting the non-radiative recombination for decreased Delta Enr, and then increasing VOC in OSCs. Among them, PM6:BTP-C8 based OSCs well balance the multiple impacts of lengthening the side chains to achieve the highest PCE of 17.77%. This work demonstrates that it is important to finely control the crystallinity and miscibility of organic photovoltaic materials to achieve high PCEs in OSCs. The miscibility and crystallinity of fused ring electron acceptors is regulated to study the effects on the morphology and energy loss of organic solar cells (OSCs). BTP-C8 based OSCs juggle multiple impacts to gain the best efficiency.
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| 9. |
- Yu, Shuang, et al.
(författare)
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Imidazole additives in 2D halide perovskites : impacts of -CN versus -CH3 substituents reveal the mediation of crystal growth by phase buffering
- 2022
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Ingår i: Energy and Environmental Science. - : Royal Society of Chemistry (RSC). - 1754-5692 .- 1754-5706. ; 15:8, s. 3321-3330
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Tidskriftsartikel (refereegranskat)abstract
- The unique sandwich structure and favorable crystallization kinetics have endowed two-dimensional (2D) halide perovskites with excellent ambient stability and facile film formation compared to those of their three-dimensional counterparts. However, the heterogeneous crystallization of multiple n-value phases during solution-casting of 2D perovskite thin films results in random and disordered crystalline alignment in conjunction with numerous lattice defects, all of which ultimately impair the device performance. Herein we demonstrate that highly ordered lattice arrangements in 2D lead halide perovskites, exemplified as a paradigm phenylethylamine (PEA) spacer, can be achieved using the 4,5-dicyanoimidazole (DCI) additive without any post-treatment. Electrostatic potential distribution mapping and X-ray photoelectron spectroscopy collectively confirm the Lewis acid-base interaction between -CN− units in DCI and Pb2+, which is conducive to homogeneous nucleation during perovskite crystallization. A sequence of in situ grazing-incident wide-angle X-ray scattering and high-resolution transmission electron microscopy characterization unravel the epitaxial growth of multi-phases that gradually buffer the internal lattice strain and consequently regulate the lattice orientation, which markedly leads to a reduction of trap density and a prolongation of carrier lifetime. The resulting planar solar cells based on 2D PEA2MA3Pb4I13 (n = 4) deliver an outstanding efficiency of ∼17.0% along with excellent operational stability.
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| 10. |
- Zhao, Jinli, et al.
(författare)
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Cloud-Edge Collaboration-Based Local Voltage Control for DGs With Privacy Preservation
- 2023
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Ingår i: IEEE Transactions on Industrial Informatics. - : IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC. - 1551-3203 .- 1941-0050. ; 19:1, s. 98-108
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Tidskriftsartikel (refereegranskat)abstract
- The increased distributed generators (DGs) have exacerbated voltage violations in active distribution networks (ADNs). Local reactive power control of DG inverters can realize a fast response to frequent voltage fluctuations. However, commonly used model-based voltage control depends upon accurate network parameters and entire ADN data, which may cause the sensitive information leakage of ADN and DG behaviors in practical operation. In this article, a cloud-edge collaboration-based local voltage control strategy for DGs is proposed with privacy preservation. First, a local voltage control framework is established based on cloud-edge collaboration, in which a surrogate model is built based on the graph convolutional neural networks to estimate the ADN voltages. By transferring the surrogate model, the edge side can obtain the exact voltage estimation in the local curve tuning process without the authority of the whole ADN data, preserving the network parameters of ADN. Then, the interarea coordination based on federated learning is proposed to realize the parameter updating of DG control curves, which can achieve better voltage control performance. By updating surrogate submodels based on private data distributed across multiple edge devices, federated learning can effectively preserve DG behaviors. Finally, the effectiveness and adaptability of the proposed control strategy are validated using the modified IEEE 33-node system. The proposed local DG control strategy can effectively cope with voltage problems and enhance the adaptability to variations in practical operation states while considering privacy preservation.
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