Tuning the electronic-state of metal cobalt/cobalt iron alloy hetero-interface embedded in nitrogen-doped carbon nanotube arrays for boosting electrocatalytic overall water splitting

The formed a Co/Co7Fe3 hetero-interface induce changes in hetero-interface electrons and the well-dispersed carbon nanotube arrays with superhydrophilic and superaerophobic characteristic promotes electrolyte permeation and bubbles escape, which collectively enhance the catalytic kinetics, activity, and stability of Co/Co7Fe3-10@NCNT/NF. [Display omitted] Maximizing the utilization of active sites and tuning the electronic-state are crucial yet extremely challenging in enhancing the ability of alloy-based catalysts to catalyze hydrogen and oxygen evolution reactions (HER and OER). Here, the 3D self-supported N-doped carbon nanotube arrays (NCNTAs) was synthesized on Ni foam by the drop-casting and calcination method, where the metal Co and Co7Fe3 alloy were enclosed at the NCNT tip (denoted as Co/Co7Fe3@NCNT/NF). The Co/Co7Fe3 hetero-interface formation led to changes in the electronic state, which can optimize the adsorption free energy of reaction intermediates and thereby boost the intrinsic catalytic performance. The well-dispersed carbon nanotube arrays with superhydrophilic and superaerophobic characteristic promotes electrolyte permeation and bubbles escape. Therefore, the optimized Co/Co7Fe3-10@NCNT/NF exhibits superior bifunctional activities with overpotential of 93 and 174 mV at 10 mA cm−2 for HER and OER, respectively. For overall water splitting (OWS), the assembled dual electrode device with Co/Co7Fe3-10@NCNT/NF only requires a low voltage of 1.56 V to achieve 10 mA cm−2 and stabilizes for 24 h at 100 mA cm−2. The result underscores the importance of hetero-interface electronic effect and carbon nanotube arrays in catalytic water splitting, providing valuable insights for the design of more advanced bifunctional electrocatalysts for OWS.