4.7 Article

Cobalt-embedded in ultrahigh boron and nitrogen codoped hierarchically porous carbon nanowires as excellent catalysts toward water splitting

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 446, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.137111

Keywords

Hierarchically porous carbon nanowires; Boron and nitrogen codoping; Cobalt@BNC; Hydrogen evolution reaction; Oxygen evolution reaction; Full water splitting

Funding

  1. National Science Foundation of China (NSFC) [51902146]
  2. Applied Basic Research Plan of Yunnan Province [2019FD039]
  3. Kunming University of Science and Technology of introducing talents [130214119417]

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Novel three-dimensional cobalt nanoparticles-embedded ultrahigh boron and nitrogen doped hierarchically porous carbon nanowires (Co@BNPCFs) were successfully synthesized and exhibited excellent water splitting performances and electrolysis stability.
The low heteroatoms doping amount and uncontrollable formation of electrochemically inactive boron (B)-nitrogen (N) bonds have hindered the electrocatalytic activities of B and N codoped carbonaceous catalysts. Herein, the novel three-dimensional (3D) cobalt (Co) nanoparticles (NPs)-embedded and ultrahigh B and N doped hierarchically porous carbon nanowires (denoted as Co@BNPCFs) have been successfully synthesized via pyrolyzing the 3D cobalt acetate/hydroxybenzeneboronic acid/polyvinylpyrrolidone precursor networks woven by electrospinning. After optimizing the pyrolysis temperatures, the optimal Co@BNPCFs-800 owns a large surface area and abundant carbon edges/defects. Especially, 6.86 atom % of B and 6.59 atom % of N atoms are doped into carbon frameworks with affording 13.45 atom % of B/N active centers (i.e. BC3, pyridinic-N, Co-Nx-C, pyrrolic-N, and graphitic-N). In alkaline solution, the hydrogen evolution reaction overpotential at 10 mA cm-2 of the optimal Co@BNPCFs-800 (151.3 mV) is just 82.4 mV larger than 20 wt% Pt/C (68.9 mV). Especially, the oxygen evolution reaction potential at 10 mA cm-2 of the optimal Co@BNPCFs-800 (1.554 V vs. RHE) is even 2 mV more negative than RuO2 (1.556 V vs. RHE). For full water splitting, Co@BNPCFs-800 based electrolysis cell just requires a small voltage of 1.596 V to achieve 10 mA cm-2, which is 19 mV smaller than that of the state-ofthe-art 20 wt% Pt/C||RuO2 benchmark (1.615 V). The perfect 3D hierarchically porous structures and fairly abundant electrocatalytic active sites dispersed along Co@BNPCFs-800 ' s surface are responsible for the outstanding water splitting performances. In addition, as the good structural and chemical stabilities, Co@BNPCFs-800 nanowires based water electrolysis cell also displays excellent water electrolysis stability.

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