4.8 Article

Performance-improved Li-O-2 batteries by tailoring the phases of MoxC porous nanorods as an efficient cathode

Journal

NANOSCALE
Volume 10, Issue 31, Pages 14877-14884

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8nr04319a

Keywords

-

Funding

  1. Natural Science Basic Research Plan in Shaanxi Province of China [2018JQ5004]
  2. China Postdoctoral Science Foundation [2018M631191]
  3. Fundamental Research Funds for the Central Universities of China [G2017KY0311]
  4. Singapore MOE AcRF [RG113/15, 2016-T1-002-065]
  5. Singapore EMA [EIRP 12/NRF2015EWT-EIRP002-008]
  6. National Research Foundation of Singapore (NRF) [NRF2016NRF-NRFI001-22]

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Novel nitrogen-doped porous molybdenum carbide (alpha-MoC1-x and beta-Mo2C) architectures were prepared using Mo-based metal-organic frameworks (MOFs) as the precursor. The synthesized molybdenum carbides consist of numerous nanocrystals organized into micro-sized rods with interpenetrating mesoporous-channels and macroporous-tunnels along the axial direction. When employed as the cathode catalyst for Li-O-2 batteries, this dual pore configuration offers abundant active sites for the electrochemical reaction and many nucleation sites for the discharge product of Li2O2; hence, decent performances were obtained. Among the two synthesized molybdenum carbides, the alpha-MoC1-x electrode stands out as being better due to its lower charge transfer resistance (395.8 Omega compared to 627.9 Omega) and better O-2 adsorption (binding energy of -1.87 eV of alpha-(111)-Mo compared to -0.72 eV of beta-(101)-Mo). It delivered a high full discharge of 20 212 mA h g(-1) with a discharge voltage of 2.62 V at 200 mA g(-1). A good cycling stability was also obtained: i.e. 100 stable cycles with a fixed capacity of 1000 mA h g(-1) (at a current density of 200 mA g(-1)) with a charging voltage of 4.24 V and maintaining a respectable round-trip efficiency of similar to 70%.

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