The design and synthesis of hollow and porous nanostructured
electrode
materials is an effective strategy to improve the electrochemical
performance of lithium-ion batteries and the hydrogen evolution reaction
(HER). Herein, we synthesize hollow and porous Co@Co3O4 nanoparticles embedded in N-doped CNTs (N-CNTs) with rich
surface defects through a two-step calcination strategy. The formation
mechanism is explored. The influence of oxygen vacancies regulated
by the nanoscale Kirkendall effect on the electrochemical performance
of the electrode is elucidated. The Co@Co3O4@N-CNTs exhibit remarkable activity for catalyzing the HER with a
low onset overpotential of 296 mV (a low Tafel slope of 116.2 mV dec–1), much better than Co3O4@N-CNTs
(315 mV for overpotential and 124.2 mV dec–1 for
Tafel slope). Significantly, the Co@Co3O4@N-CNTs
deliver a high discharge capacity of 990 mA h g–1 after 600 cycles at 0.1 A g–1. Our nanostructure
strategy can provide new insights into the strategy for high-rate
and highly stable energy storage systems.
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