| 1. |
- Duan, Shanghong, 1992, et al.
(författare)
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BUILDING AND CHARACTERIZATION OF SYMMETRIC STRUCTURAL BATTERY
- 2022
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Ingår i: ECCM 2022 - Proceedings of the 20th European Conference on Composite Materials: Composites Meet Sustainability. ; 3, s. 1169-1174
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Konferensbidrag (refereegranskat)abstract
- Recently, a structural battery with multifunctional carbon fibre anode has been reported. The energy density of active material is not fully extracted due to the low ionic conductivity inside the battery. To identify the main region that attributes to the low ion transportation, we assemble a symmetric structural battery with one anode layer in the centre sandwiched between two cathode layers. Such a design can also be treated as a combination of two asymmetric batteries with one full thickness cathode layer plus one half thickness anode layer. Thus, the travelled distance of lithium ions is shortened only in the anode part. It is found that the area energy density of the symmetric structural battery is doubled compared to a reference asymmetric battery. Thus, the additional cathode layer activates the double amount of carbon fibres in the anode. A plausible reason is that only the carbon fibres next to the separator is activated in the battery.
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| 2. |
- Li, Ziyao, et al.
(författare)
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Atomic-level orbital coupling in a tri-metal alloy site enables highly efficient reversible oxygen electrocatalysis
- 2023
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 11:5, s. 2155-2167
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Tidskriftsartikel (refereegranskat)abstract
- Complex multi-metallic alloys with ultra-small sizes have received extensive attention in the fields of Zn-air battery and water splitting, because of their unique advantages including adjustable composition, tailorable active sites, and optimizable electronic structure. In this effort, an atomic-level orbital coupling strategy is presented to effectively regulate the electronic structures of ultra-small tri-metal Fe-Co-Ni nanoalloy particles confined in an N-doped carbon hollow nanobox. As expected, the optimal nanoalloy hybrid material exhibited notable bi-functional catalytic performances toward the oxygen reduction reaction (half-wave potential of 0.902 V) and oxygen evolution reaction (1.589 V at 10 mA cm−2) with a small ΔE of 0.687 V, exceeding the precious-metal-based and many previously reported catalysts. Furthermore, the as-assembled Zn-air device also displayed a superior specific capacity of 894 mA h g−1, a maximal power density of 247 mW cm−2, and impressive durability (over 100 hours). Ultraviolet photoelectron spectroscopy and density functional theory calculations revealed that the electronic structures could be finely tuned and optimized through ternary metal alloying, resulting in a suitable d-band center and advantageous interfacial charge-transfer, which in turn could effectively reduce the involved energy barriers in the electrocatalytic process and significantly boost its intrinsic activity of reversible oxygen catalysis. Thus, this work affords an effective method for the rational creation of bi-functional non-noble-metal-based electrocatalysts for sustainable energy technology.
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| 3. |
- Wu, Junru, et al.
(författare)
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Unique tridentate coordination tailored solvation sheath towards highly stable lithium metal batteries
- 2023
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Ingår i: Advanced Materials. - : Wiley-VCH Verlagsgesellschaft. - 0935-9648 .- 1521-4095. ; 35:38
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Tidskriftsartikel (refereegranskat)abstract
- Electrolyte optimization by solvent molecule design has been recognized as an effective approach for stabilizing lithium (Li) metal batteries. However, the coordination pattern of Li+ with solvent molecules has been sparsely considered. Here, we report an electrolyte design strategy based on bi/tridentate chelation of Li+ and solvent to tune the solvation structure. As a proof of concept, a novel solvent with multi oxygen coordination sites is demonstrated to facilitate the formation of an anion-aggregated solvation shell, enhancing the interfacial stability and de-solvation kinetics. As a result, the as-developed electrolyte exhibits ultra-stable cycling over 1400 h in symmetric cells with 50 ?m-thin Li foils. When paired with high-loading LiFePO4, full cells maintain 92% capacity over 500 cycles and deliver improved electrochemical performances over a wide temperature range from -10 °C to 60 °C. Furthermore, the concept is validated in a pouch cell (570 mAh), achieving a capacity retention of 99.5% after 100 cycles. This brand-new insight on electrolyte engineering provides guidelines for practical high-performance Li metal batteries. This article is protected by copyright. All rights reserved
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| 4. |
- Zhang, Xin, et al.
(författare)
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Increasing Electrocatalytic Oxygen Evolution Efficiency through Cobalt-Induced Intrastructural Enhancement and Electronic Structure Modulation
- 2021
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Ingår i: ChemSusChem. - : Wiley-VCH Verlagsgesellschaft. - 1864-5631 .- 1864-564X. ; 14:1, s. 467-478
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Tidskriftsartikel (refereegranskat)abstract
- Electrolytic water splitting using surplus electricity represents one of the most cost-effective and promising strategies for hydrogen production. The high overpotential of the oxygen-evolution reaction (OER) caused by the multi-electron transfer process with a high chemical energy barrier, however, limits its competitiveness. Here, a highly active and stable OER electrocatalyst was designed through a cobalt-induced intrastructural enhancement strategy combined with suitable electronic structure modulation. A carved carbon nanobox was embedded with tri-metal phosphide from a uniform Ni-Co-Fe Prussian blue analogue (PBA) nanocube by sequential NH3 center dot H2O etching and thermal phosphorization. The sample exhibited an OER activity in an alkaline medium, reaching a current density of 10 mA cm(-2) at an overpotential of 182 mV and displayed a small Tafel slope of 47 mV dec(-1), superior to the most recently reported OER electrocatalysts. Moreover, it showed impressive electrocatalytic durability, increasing by approximately 2.7 % of operating voltage after 24 h of continuous testing. The excellent OER activity and stability are ascribed to a favorable transfer of mass and charge provided by the porous carbon shell, synergistic catalysis between the three-component metal phosphides originating from appropriate electronic structure modulation, more exposed catalytic sites on the hollow structure, and chainmail catalysis resulting from the carbon protective layer. It is foreseen that this successfully demonstrated design concept can be easily extended to other heterogeneous catalyst designs.
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