| 1. |
- Yang, Chaoran, et al.
(författare)
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Alternate-stacked Li4Ti5O12 nanosheets/d-Ti3C2 flexible film as a current collector-free, high-capacity and robust cathode for rechargeable Mg batteries
- 2020
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Ingår i: Nano select. - : John Wiley & Sons. - 2688-4011. ; 1:1, s. 1-11
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Tidskriftsartikel (refereegranskat)abstract
- Rechargeable magnesium batteries (RMBs) have gained increasing attention owing to its high volumetric capacity, crust abundance, and safety from dendrite-free characteristic. However, the lack of development of high-performance cathode materials with long cycling stability and satisfactory capacity has greatly restricted the development of RMBs. Herein, a self-supported, current collector-free and soft electrode is prepared with delaminated Ti3C2 (d-Ti3C2) and Li4Ti5O12 nanosheets by simple vacuum filtration as flexible cathode in RMBs. Fabricated into a full cell with hybrid AlCl3/MgCl2/Mg(TFSI)2 electrolyte and Mg anode (a thin Mg foil with thickness of 50 μm), the flexible cathode shows high initial specific capacity of 320 mAh g−1 at 20 mA g−1, excellent cycling stability (good retention even after 1000 cycles) and outstanding rate performance. Detailed mechanistic studies reveal that introduction of d-Ti3C2 provide fast transport paths for electrons and Mg2+. The enlarged layer spacing of composited d-Ti3C2 accounts for significant increment in capacity. Benefiting from above-mentioned advantages, the best performance among Ti-based electrode materials is realized and make wearable devices powered by RMBs possible, thus circumventing the safety issues of lithium batteries.
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| 2. |
- Dannemeyer, Melanie, et al.
(författare)
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Fast and robust recombinant protein production utilizing episomal stable pools in WAVE bioreactors
- 2024
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Ingår i: Protein Expression and Purification. - : Elsevier BV. - 1046-5928 .- 1096-0279. ; 221
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Tidskriftsartikel (refereegranskat)abstract
- Protein reagents are essential resources for several stages of drug discovery projects from structural biology and assay development through lead optimization. Depending on the aim of the project different amounts of pure protein are required. Small-scale expressions are initially used to determine the reachable levels of production and quality before scaling up protein reagent supply. Commonly, amounts of several hundreds of milligrams to grams are needed for different experiments, including structural investigations and activity evaluations, which require rather large cultivation volumes. This implies that cultivation of large volumes of either transiently transfected cells or stable pools/stable cell lines is needed. Hence, a production process that is scalable, speeds up the development projects, and increases the robustness of protein reagent quality throughout scales. Here we present a protein production pipeline with high scalability. We show that our protocols for protein production in Chinese hamster ovary cells allow for a seamless and efficient scale-up with robust product quality and high performance. The flexible scale of the production process, as shown here, allows for shorter lead times in drug discovery projects where there is a reagent demand for a specific protein or a set of target proteins.
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| 3. |
- Tegel, Hanna, et al.
(författare)
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High throughput generation of a resource of the human secretome in mammalian cells
- 2020
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Ingår i: New Biotechnology. - : Elsevier BV. - 1871-6784 .- 1876-4347. ; 58, s. 45-54
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Tidskriftsartikel (refereegranskat)abstract
- The proteins secreted by human tissues and blood cells, the secretome, are important both for the basic understanding of human biology and for identification of potential targets for future diagnosis and therapy. Here, a high-throughput mammalian cell factory is presented that was established to create a resource of recombinant full-length proteins covering the majority of those annotated as 'secreted' in humans. The full-length DNA sequences of each of the predicted secreted proteins were generated by gene synthesis, the constructs were transfected into Chinese hamster ovary (CHO) cells and the recombinant proteins were produced, purified and analyzed. Almost 1,300 proteins were successfully generated and proteins predicted to be secreted into the blood were produced with a success rate of 65%, while the success rates for the other categories of secreted proteins were somewhat lower giving an overall one-pass success rate of ca. 58%. The proteins were used to generate targeted proteomics assays and several of the proteins were shown to be active in a phenotypic assay involving pancreatic beta-cell dedifferentiation. Many of the proteins that failed during production in CHO cells could be rescued in human embryonic kidney (HEK 293) cells suggesting that a cell factory of human origin can be an attractive alternative for production in mammalian cells. In conclusion, a high-throughput protein production and purification system has been successfully established to create a unique resource of the human secretome.
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| 4. |
- Wang, Linqin, et al.
(författare)
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A crosslinked polymer as dopant-free hole-transport material for efficient n-i-p type perovskite solar cells
- 2021
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Ingår i: Journal of Energy Chemistry. - : Elsevier BV. - 2095-4956 .- 2096-885X. ; 55, s. 211-218
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Tidskriftsartikel (refereegranskat)abstract
- A new crosslinked polymer, called P65, with appropriate photo-electrochemical, opto-electronic, and thermal properties, has been designed and synthesized as an efficient, dopant-free, hole-transport material (HTM) for n-i-p type planar perovskite solar cells (PSCs). P65 is obtained from a low-cost and easily synthesized spiro[fluorene-9,9′-xanthene]-3′,6′-diol (SFX-OH)-based monomer X65 through a free-radical polymerization reaction. The combination of a three-dimensional (3D) SFX core unit, hole-transport methoxydiphenylamine group, and crosslinked polyvinyl network provides P65 with good solubility and excellent film-forming properties. By employing P65 as a dopant-free hole-transport layer in conventional n-i-p type PSCs, a power conversion efficiency (PCE) of up to 17.7% is achieved. To the best of our knowledge, this is the first time a 3D, crosslinked, polymeric dopant-free HTM has been reported for use in conventional n-i-p type PSCs. This study provides a new strategy for the future development of a 3D crosslinked polymeric dopant-free HTM with a simple synthetic route and low-cost for commercial, large-scale applications in future PSCs.
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