4.5 Article

In Situ Growth of Cobalt Nanoparticles Encapsulated Nitrogen-Doped Carbon Nanotubes among Ti3C2Tx (MXene) Matrix for Oxygen Reduction and Evolution

Journal

ADVANCED MATERIALS INTERFACES
Volume 5, Issue 16, Pages -

Publisher

WILEY
DOI: 10.1002/admi.201800392

Keywords

carbon nanotubes; MXene; oxygen reduction and evolution; X-ray absorption spectra

Funding

  1. MOST [2017YFA0303500, 2014CB848900]
  2. NSFC [U1532112, 11574280, 11605201, 21706248]
  3. Innovative Research Groups of NSFC [11621063]
  4. CAS Key Research Program of Frontier Sciences [QYZDB-SSW-SLH018]
  5. CAS Interdisciplinary Innovation Team, China Postdoctoral Science Foundation [BH2310000033]
  6. Innovative Program of Development Foundation of Hefei Center for Physical Science and Technology [2016FXCX003]
  7. 111 project [B12015]
  8. Shanghai synchrotron Radiation Facility [14W1]
  9. Beijing Synchrotron Radiation Facility [1W1B]

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MXene with unique layered structure and rich chemical compositions has been extensively investigated for lithium-ion batteries, electrochemical capacitors, and hydrogen storage medium, but less attention has been paid to its electrocatalytic potential might due to nonideal activity. Here, an in situ growth strategy is developed to synthesize a new type of composite with carbon nanotubes (CNTs) supported on the surface of Ti3C2Tx MXene (Co/N-CNTs@Ti3C2Tx) as bifunctional electrocatalyst toward oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). By combining the X-ray photoelectron detection with synchrotron-based soft X-ray spectroscopic characterizations, the strong interfacial coupling and electron transfer are efficiently identified, which can effectively facilitate the bifunctional electrocatalytic performance of Co/N-CNTs@Ti3C2Tx toward ORR and OER in alkaline solution. The present strategy provides a facile route for the design of the hybrids of CNTs and MXene for bifunctional electrocatalysis.

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