GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Xia, Xianming  (3)
  • Yu, Yan  (3)
Material
Language
Years
Subjects(RVK)
  • 1
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Nanoscale Horizons Vol. 7, No. 8 ( 2022), p. 899-907
    In: Nanoscale Horizons, Royal Society of Chemistry (RSC), Vol. 7, No. 8 ( 2022), p. 899-907
    Abstract: Sodium (Na) metal is a very encouraging anode material for next-generation rechargeable batteries owing to its high specific capacity, earth-abundance and low-cost. However, the application of Na metal anodes (SMAs) is hampered by dendrite growth and “dead” Na formation caused by the uncontrollable Na deposition, leading to poor cycle life and even safety concerns. Herein, a high-performance Na anode is designed by introducing an artificial VN interlayer on the Na metal surface (Na/VN) by a simple mechanical rolling process to regulate Na nucleation/deposition behaviors. The density functional theory (DFT) and experiment results uncover that the VN possesses high “sodiophilicity”, which can facilitate the initially homogeneous Na nucleation and cause Na to distribute evenly on the VN interlayer. Therefore, uniform Na deposition with dendrite-free morphology and prolonged cycling lifespan (over 1060 h at 0.5 mA cm −2 /1 mA h cm −2 ) can be realized. Moreover, the full cell assembled by coupling a Na 3 V 2 (PO 4 ) 3 (NVP) cathode and Na/VN anode presents superior cycling performance ( e.g. , 96% capacity retention even after 800 cycles at 5C). This work provides a promising direction for regulating Na nucleation and deposition to achieve dendrite-free metal anodes.
    Type of Medium: Online Resource
    ISSN: 2055-6756 , 2055-6764
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    In: Advanced Materials, Wiley, Vol. 35, No. 11 ( 2023-03)
    Abstract: The sodium (Na)‐metal anode with high theoretical capacity and low cost is promising for construction of high‐energy‐density metal batteries. However, the unsatisfactory interface between Na and the liquid electrolyte induces tardy ion transfer kinetics and dendritic Na growth, especially at ultralow temperature (−40 °C). Herein, an artificial heterogeneous interphase consisting of disodium selenide (Na 2 Se) and metal vanadium (V) is produced on the surface of Na (Na@Na 2 Se/V) via an in situ spontaneous chemical reaction. Such interphase layer possesses high sodiophilicity, excellent ionic conductivity, and high Young's modulus, which can promote Na‐ion adsorption and transport, realizing homogenous Na deposition without dendrites. The symmetric Na@Na 2 Se/V cell exhibits outstanding cycling life span of over 1790 h (0.5 mA cm −2 /1 mAh cm −2 ) in carbonate‐based electrolyte. More remarkably, ab initio molecular dynamics simulations reveal that the artificial Na 2 Se/V hybrid interphase can accelerate the desolvation of solvated Na + at −40 °C. The Na@Na 2 Se/V electrode thus exhibits exceptional electrochemical performance in symmetric cell (over 1500 h at 0.5 mA cm −2 /0.5 mAh cm −2 ) and full cell (over 700 cycles at 0.5 C) at −40 °C. This work provides an avenue to design artificial heterogeneous interphase layers for superior high‐energy‐density metal batteries at ambient and ultralow temperatures.
    Type of Medium: Online Resource
    ISSN: 0935-9648 , 1521-4095
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 1474949-X
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Online Resource
    Online Resource
    Wiley ; 2022
    In:  Advanced Functional Materials Vol. 32, No. 10 ( 2022-03)
    In: Advanced Functional Materials, Wiley, Vol. 32, No. 10 ( 2022-03)
    Abstract: Sodium (Na) metal as an anode is one of the ultimate choices for the high‐energy rechargeable batteries in virtue of its intrinsic high theoretical capacity (1166 mAh g −1 ) and low redox potential (−2.71V vs standard hydrogen electrode (SHE)), as well as its low cost and broad sources. Nevertheless, the dendrite‐related hazards seriously block its practical application. Na dendrite formation mainly emanates from the uncontrolled Na deposition behavior. Therefore, it seems particularly important to employ appropriate strategies towards the homogeneous deposition of Na for the dendrite‐free metal anode. In this review, the challenge of regulating Na homogeneous deposition for dendrite‐free Na anodes is first discussed. Then, recent advances in the strategies of regulating the Na uniform deposition are summarized, including adjusting Na + flux near the solid‐liquid interface and improving sodiophilicity on the biphase interface. Lastly, perspectives on further research and important factors toward the practical application of high‐energy‐density Na metal batteries are emphasized in detail.
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2029061-5
    detail.hit.zdb_id: 2039420-2
    SSG: 11
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...