4.7 Article

Tailoring the d-band center of N-doped carbon nanotube arrays with Co4N nanoparticles and single-atom Co for a superior hydrogen evolution reaction

Journal

NPG ASIA MATERIALS
Volume 13, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41427-020-00264-x

Keywords

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Funding

  1. National Natural Science Foundation of China [21522106, 21971117, 21661023, 21601096, 21802076, 21962013, 21971129]
  2. Natural Science Foundation of Inner Mongolia Autonomous Region of China [2018BS05007]
  3. Program of Higher-level Talents of IMU [21300-5155105, 21300-5185111, 21300-5195109]
  4. Cooperation Project of the State Key Laboratory of Baiyun Obo Rare Earth Resource Research and Comprehensive Utilization [2017Z1950]
  5. 111 Project from China [B18030]
  6. National Key R&D Program of China [2017YFA0208000]
  7. Open Funds of the State Key Laboratory of Rare Earth Resource Utilization [RERU2019001]
  8. Functional Research Funds for the Central Universities, Nankai University [ZB19500202]

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A 3D self-supported integrated electrode with Co4N nanoparticles and single-atom Co exhibits robust performance for the hydrogen evolution reaction due to its abundance of active sites and synergistic effects among components, optimizing the d-band center for efficient electrocatalysis.
A 3D self-supported integrated electrode, consisting of heteroatomic nitrogen-doped carbon nanotube arrays on carbon cloth with confined ultrafine Co4N nanoparticles and a distribution of anchored single-atom Co, is fabricated via a cobalt-catalyzed growth strategy using dicyandiamide as the nitrogen and carbon source and a layered cobalt hydroxide-nitrate salt as the precursor. The abundance of exposed active sites, namely, the Co4N nanoparticles, single-atom Co, and heteroatomic N-doped carbon nanotubes, and multiple synergistic effects among these components provide suitable tailoring of the d-band center for facilitating vectorial electron transfer and efficient electrocatalysis. Benefiting from the merits of its structural features and electronic configuration, the prepared electrode exhibits robust performance toward the hydrogen evolution reaction with overpotentials of only 78 and 86 mV at 10 mA cm(-2) in acidic and basic electrolytes, respectively. Density functional theory calculations and X-ray photoelectron spectroscopy valence band measurements reveal that the effective tailoring of the d-band center by Co4N nanoparticles plays a crucial role in optimizing the hydrogen adsorption free energy to a more thermoneutral value for efficient electrocatalysis.

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