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  • The Electrochemical Society  (64)
  • Unknown  (64)
  • 2020-2024  (64)
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  • The Electrochemical Society  (64)
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  • Unknown  (64)
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  • 2020-2024  (64)
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  • 1
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 167, No. 9 ( 2020-01-07), p. 090527-
    Abstract: Two-dimensional (2D) materials are a promising candidate for the anode material of lithium-ion battery (LIB) and sodium-ion battery (NIB) for their unique physical and chemical properties. Recently, a honeycomb borophene ( h -borophene) has been fabricated by molecular beam epitaxy (MBE) growth in ultra high vacuum. Here, we adopt the first-principles density functional theory calculations to study the performance of monolayer (ML) h -borophene as an anode material for the LIB and NIB. The binding energies of the ML h -borophene-Li/Na systems are all negative, indicating a steady adsorption process. The diffusion barriers of the Li and Na ions in h -borophene are 0.53 and 0.17 eV, respectively, and the anode overall open-circuit voltages for the LIB and NIB are 0.747 and 0.355 V, respectively. The maximum theoretical storage capacity of h -borophene is 1860 mAh·g −1 for NIB and up to 5268 mAh·g −1 for LIB. The latter is more than 14 times higher than that of commercially used graphite (372 mAh·g −1 ) and is also the highest theoretical capacity among all the 2D materials for the LIB discovered to date. Our study suggests that h -borophene is a promising anode material for high capacity LIBs and NIBs.
    Type of Medium: Online Resource
    ISSN: 0013-4651 , 1945-7111
    RVK:
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 2
    Online Resource
    Online Resource
    The Electrochemical Society ; 2022
    In:  Journal of The Electrochemical Society Vol. 169, No. 4 ( 2022-04-01), p. 046507-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 169, No. 4 ( 2022-04-01), p. 046507-
    Abstract: To address issues of global energy sustainability, it is of great practical significance to develop low cost and high efficiency electrocatalysts for the oxygen evolution reaction (OER). In this work, we synthesize amorphous Co 1-x V x S y nanosheets using Co 1-x V x -MOF/NF as a precursor to explore the structural evolution of metal-organic framework (MOF) derivatives during the OER. When tested for OER performance in 1.0 M KOH solution, Co 0.9 V 0.1 S 0.002 /NF exhibits the best catalytic activity, with an overpotential of only 194 mV at a current density of 20 mA cm −2 and a Tafel slope of 28.4 mV dec −1 . We also measured the long-term electrochemical durability of Co 0.9 V 0.1 S 0.002 /NF and found that Co 0.9 V 0.1 S 0.002 /NF maintains its stability for at least 100 h at a current density of 20 mA cm −2 .
    Type of Medium: Online Resource
    ISSN: 0013-4651 , 1945-7111
    RVK:
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2022
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  • 3
    Online Resource
    Online Resource
    The Electrochemical Society ; 2020
    In:  ECS Journal of Solid State Science and Technology Vol. 9, No. 3 ( 2020-02-28), p. 035004-
    In: ECS Journal of Solid State Science and Technology, The Electrochemical Society, Vol. 9, No. 3 ( 2020-02-28), p. 035004-
    Type of Medium: Online Resource
    ISSN: 2162-8777
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 4
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2022-01, No. 7 ( 2022-07-07), p. 645-645
    Abstract: The organic passivated CNT/Si solar cell is a new type of low-cost, high-efficiency solar cell, with challenges concerning the stability of the organic layer used for passivation. In this work, the stability of the organic layer is studied with respect to the internal and external (humidity) water content and additionally long-term stability for low moisture environments. It is found that the organic passivated CNT/Si complex interface is not stable, despite both the organic passivation layer and CNTs being stable on their own and is due to the CNTs providing an additional path for water molecules to the interface. With the use of a simple encapsulation, a record power conversion efficiency (PCE) of 22% is achieved and a stable photovoltaic performance is demonstrated. This work provides a new direction for the development of high-performance/lost-cost photovoltaics in the future and will stimulate the use of nanotubes materials for solar cells applications.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2022
    detail.hit.zdb_id: 2438749-6
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  • 5
    Online Resource
    Online Resource
    The Electrochemical Society ; 2021
    In:  ECS Journal of Solid State Science and Technology Vol. 10, No. 11 ( 2021-11-01), p. 113005-
    In: ECS Journal of Solid State Science and Technology, The Electrochemical Society, Vol. 10, No. 11 ( 2021-11-01), p. 113005-
    Abstract: The heat transfer performance of Flat micro heat pipe (FMHP) is mainly determined by liquid absorption capacity of the wick. A chemical-free laser selective micro-texture technology is proposed for the fabrication of FMHP. Series of samples with different widths of the superhydrophobic-superhydrophilic spacing stripes were prepared by laser micro texturing, and their transport capacity was tested. Scanning electron microscope, three-dimensional optical profiling, and X-ray photoelectron spectroscope techniques were used to characterize the surfaces, and the mechanism of accelerating liquid reflux was investigated. Two samples with the same spacing width were used to make FMHPs. The heat transfer performance of each group of FMHPs was tested, including the start-up time, steady state temperature, and axial maximum temperature difference, and the corresponding thermal resistances were calculated. The results show that the width of superhydrophobic-superhydrophilic spacing stripes can affect the capillary force and hysteresis force during droplet transport, thereby affecting the droplet transport velocity, and in turn, influencing the heat transfer performance of the FMHP. Compared with most current flat micro heat pipes, the laser selective textured heat pipe with superhydrophobic-superhydrophilic stripes can significantly improve the heat transfer performance, and is promising for heat transfer applications in microelectronic equipment.
    Type of Medium: Online Resource
    ISSN: 2162-8769 , 2162-8777
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2021
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  • 6
    Online Resource
    Online Resource
    The Electrochemical Society ; 2020
    In:  ECS Journal of Solid State Science and Technology Vol. 9, No. 12 ( 2020-12-01), p. 126003-
    In: ECS Journal of Solid State Science and Technology, The Electrochemical Society, Vol. 9, No. 12 ( 2020-12-01), p. 126003-
    Abstract: CsPbBr 3 :xBi 3+ quantum dot glass was prepared by using traditional melting-quenching and heat treatment processes. The effects of Bi doing on the sinter of the precursor of glass and the crystalline of the perovskite quantum dot were discussed detailly. By doping Bi 2 O 3 into the borosilicate glass matrix, the melting temperature was reduced to 900 °C. The tunable emission of CsPbBr 3 quantum dots from 523 to 493 nm was achieved with suitable Bi 2 O 3 doping. Due to the protection of the inorganic glass matrix, the prepared CsPbBr 3 quantum dots still exhibit excellent thermal stability after multiple thermal cycles and thermal shocks. This provides a good solution to the problem of poor thermal stability of perovskite quantum dots.
    Type of Medium: Online Resource
    ISSN: 2162-8769 , 2162-8777
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 7
    Online Resource
    Online Resource
    The Electrochemical Society ; 2020
    In:  ECS Meeting Abstracts Vol. MA2020-02, No. 2 ( 2020-11-23), p. 369-369
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2020-02, No. 2 ( 2020-11-23), p. 369-369
    Abstract: Silicon monoxide (SiO) is a very promising anode material for the next generation high energy lithium ion batteries due to its high theoretical specific capacity of 1710 mAh/g and volumetric capacity of 1547 Ah/L.[1] Compared to commercially used graphite, SiO can offer 18% cell stack level improvement in volumetric energy density and 11% in gravimetric energy density (calculated based on the same cell stack model), enabling utilization of smaller and lighter batteries. It also offers more stable cycle performance compared to Si due to less volume change (134% initial volume expansion and 117% reversible volume expansion), making it a more practical choice for lithium ion batteries in the near future. SiO is composed of Si nanodomains in a SiO 2 matrix. An interphase region of transitional stoichiometry (SiO x , 0 〈 x 〈 2) is also present between Si and SiO 2 and takes up 20-25 at.% of the entire composition.[2] During the lithiation and delithiation, the Si nanodomains react reversibly with lithium, similar to amorphous silicon, to give the reversible capacity. The SiO 2 matrix reacts irreversibly with lithium to form lithium silicates and lithium oxide. Therefore, the Si domain size and interphase suboxide between Si and SiO 2 have effect on the electrochemical performance of SiO. In this study, we gradually changed the microstructure of SiO via annealing treatment and thoroughly studied the change of the SiO microstructure and its impact on the electrochemical performance of the SiO. Together with electrode formulation optimization, up to 99% capacity retention during 50 cycles was obtained in full cells when using pure SiO as anode and LiNi 0.5 Mn 0.3 Co 0.2 O 2 as cathode. Acknowledgement We gratefully acknowledge the support from Peter Faguy at the U.S. Department of Energy’s (DOE) office of Energy Efficiency & Renewable Energy (EERE) - Vehicle Technologies Office. This work is conducted under the Cell Analysis, Modeling, and Prototyping (CAMP) Facility at Argonne National Laboratory. Argonne National Laboratory is a U.S. Department of Energy Office of Science Laboratory operated under Contract No. DE-AC02-06CH11357. Reference: Obrovac, M. N.; Chevrier, V. L., Alloy Negative Electrodes for Li-Ion Batteries. Chemical Reviews 2014, 114 (23), 11444-11502. Hirata, A.; Kohara, S.; Asada, T.; Arao, M.; Yogi, C.; Imai, H.; Tan, Y.; Fujita, T.; Chen, M., Atomic-scale disproportionation in amorphous silicon monoxide. Nature Communications 2016, 7, 11591.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
    detail.hit.zdb_id: 2438749-6
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  • 8
    Online Resource
    Online Resource
    The Electrochemical Society ; 2020
    In:  Journal of The Electrochemical Society Vol. 167, No. 2 ( 2020-01-29), p. 020538-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 167, No. 2 ( 2020-01-29), p. 020538-
    Type of Medium: Online Resource
    ISSN: 1945-7111
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 9
    In: ECS Journal of Solid State Science and Technology, The Electrochemical Society, Vol. 10, No. 3 ( 2021-03-01), p. 036004-
    Abstract: Series of Ba 1.98 Mg 1− x Al 2 x Si 2− x O 7 :0.02Eu 2+ phosphors were synthesized by the solid-state reaction method. Ba 1.98 Mg 1− x Al 2 x Si 2− x O 7 :0.02Eu 2+ shows efficient green emission under the near ultra violet light excitation. As Al-Al replacing Mg-Si, the changes of the structure and the morphology, the variations of the photoluminescence spectra and lifetime, and the evolutions of the thermal stability were investigated and discussed. With Mg-Si replacement by Al-Al, the crystal field splitting strength of the 5d electron of Eu 2+ increases, which causes the red shift of the emission band. The photoluminescence intensity and lifetime of Eu 2+ is decreased. The physical mechanisms for the variations of the photoluminescence intensity and lifetime were discussed. The thermal stability can be evidently improved with Al-Al replacing Mg-Si in the host structure. The forbidden band width has been calculated with the measurements of the reflection spectra, which is extended firstly and then narrowed. The extended forbidden band width limits the Eu 2+ 5d electron self-ionization from the splitting levels to the conduction band, which is resulted in the improvement of the thermal stabilities. These results show Al-Al replacing Si-Mg can be a suitable route for the photoluminescence tune for Ba 2 MgSi 2 O 7 :Eu 2+ phosphors.
    Type of Medium: Online Resource
    ISSN: 2162-8769 , 2162-8777
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2021
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  • 10
    Online Resource
    Online Resource
    The Electrochemical Society ; 2022
    In:  Journal of The Electrochemical Society Vol. 169, No. 3 ( 2022-03-01), p. 034501-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 169, No. 3 ( 2022-03-01), p. 034501-
    Abstract: Non-precious metal catalysts for oxygen reduction reaction (ORR) are urgently needed in clean energy conversion systems, such as fuel cells and metal-air batteries. Cobalt nanoparticles supported on nitrogen, sulfur and fluorine tri-doped carbon (Co/NSF-C) is a new class of non-precious metal materials, which exhibit ORR catalysis in alkaline media. These catalysts are prepared by pyrolyzing cobalt chloride and melamine sulfuric acid hydrogen fluoride with carbon black in a nitrogen atmosphere at temperatures from 600 °C to 900 °C with Co content from 0 to15wt%. The electrochemical performance of the catalysts shows hat the best temperatures and the best cobalt contents in descending order are 700 °C 〉 600 °C 〉 800 °C 〉 900 °C and 10 wt% ≈ 5 wt% 〉 15 wt% 〉 0 wt%, respectively. The catalyst with cobalt content of 10 wt% and prepared at 700 °C (Co/NSF-C700) has a mesopore surface with high heteroatom defect density and a specific surface area of 875 m 2 g −1 . Co/NSF-C700 exhibits the best ORR catalytic performance with a mainly 4-electron reaction pathway, an ORR peak potential of 0.856 V and the half-wave potential of 0.855 V, as well as a good stability in 0.1 M KOH.
    Type of Medium: Online Resource
    ISSN: 0013-4651 , 1945-7111
    RVK:
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2022
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