4.7 Article

Rational design and in-situ formation of nickel-cobalt nitride multi-core/hollow N-doped carbon shell anode for Li-ion batteries

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 420, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.129630

Keywords

Transition metal nitride; Prussian blue analogue; Polydopamine; N-doped carbon shell; Li-ion battery

Funding

  1. National Research Foundation of Korea (NRF) - Korean government (MSIT) [2019R1C1C1007886, 2019M3D1A2104105, 2018R1A5A1025224, 2021R1A2C2007804]
  2. ''World Class 300 Project (R&D)'' of the MOTIE, MSS (Korea) [S2561932]
  3. Korea Technology & Information Promotion Agency for SMEs (TIPA) [S2561932] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. National Research Foundation of Korea [2019M3D1A2104105, 2021R1A2C2007804, 2019R1C1C1007886] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

Ask authors/readers for more resources

The construction of a carbon-encapsulated multi-core nanostructure based on transition metal nitride is an effective approach to enhance Li-ion storage capacity and cycle stability. The rational synthetic strategy of the unique hybrid nanoarchitecture through in-situ formation of polymer-coated metal-organic frameworks plays a key role in improving the electrochemical performance of Li-ion battery anodes.
The construction of a carbon-encapsulated multi-core nanostructure based on transition metal nitride is a preferred approach to efficiently mitigate volume expansion with improved sustainability and to enhance conductivity with more active sites for Li-ion cell reaction. Herein, we report the in-situ formation of carbon-coated nickel-cobalt nitride multi-core nanoparticles encapsulated by hollow N-doped carbon shell via monodispersed Ni-3[Co(CN)(6)](2) Prussian blue analogue/polydopamine precursors using by simultaneous nitridation and calcination process. The (Ni/Co)(3)N multi-core nanoparticles (Ni:Co = 3:2) were highly dispersed in conductive and hollow N-doped carbon shell, thereby (i) mitigating mechanical stress by volume change during the conversion reaction of nitrides, (ii) stabilizing the electrochemical reaction surface with a thin solid electrolyte interphase, and (iii) maintaining the original structure and hierarchical morphologies even after long cycles. The (Ni/Co)(3)N multi-core@hollow N-doped carbon shell demonstrated better electrochemical performance than the (Ni/Co)(3) N@carbon shell without the outer hollow N-doped carbon shell for the Li-ion battery anode, which has an excellent reversible capacity of similar to 440 mAh g(-1)- and a stable cycle life of 130 cycles at 200 mA g(-1). The rational synthetic strategy of the unique hybrid nanoarchitecture via in-situ formation of polymer-coated metal-organic frameworks is key in improving the Li-ion storage capacity and cycle stability.

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