ABSTRACT
A bubble-releasing assisted pulse electrodeposition method was developed to create metallic alloy, NiFe, nanotube arrays in one step. The NiFe alloy nanotube array exhibited excellent bifunctional electrolytic activities, achieving low overpotentials of 100 mV for the hydrogen evolution reaction and 236 mV for the oxygen evolution reaction at 10 mA cm-2, both in 1 M KOH at room temperature. For overall water splitting, the NiFe alloy nanotube array delivered 10 mA cm-2 at an ultralow cell voltage of 1.58 V, among the top tier of the state-of-the-art bifunctional electrocatalysts. The NiFe alloy nanotube array also exhibited ultrastability at high current densities, experiencing only a minor chronoamperometric decay of 6.5% after a 24 h operation at 400 mA cm-2. The success of the present binder-free nanotube array-based electrode can be attributed to the much enlarged reaction surface area, one-dimensionally guided charge transport and mass transfer offered by the nanotube structure, and improved product crystallinity provided by the pulse current electrodeposition. The nanotube array structure proves to be a promising new architecture design for electrocatalysts.
ABSTRACT
Mixed NiO/NiCo2O4 nanocrystals grown in situ from the skeleton of a 3D porous nickel network (3DPNN) were prepared with a simple hydrothermal method followed by a low temperature calcination, exhibiting outstanding electrocatalytic efficiencies toward oxygen evolution reactions (OER). The 3DPNN was prepared with a novel leaven dough method and served as both the nickel source for growth of the mixed NiO/NiCo2O4 nanocrystals and the charge transport highway to accelerate the sluggish kinetics of the OER. The mixed NiO/NiCo2O4 nanocrystals exhibited pronounced synergistic effects to achieve a high mass activity of 200 A g-1 at the catalyst mass loading of 0.5 mg cm-2, largely outperforming the corresponding single component nanocrystal systems, NiO (5.87) and NiCo2O4 (9.35). The NiO/NiCo2O4@3DPNN composite electrocatalyst achieved a low overpotential of 264 mV at the current density of 10 mA cm-2 and 389 mV at the practically high current density of 250 mA cm-2, which compete favorably among the top tier of previously reported OER electrocatalysts. Moreover, it exhibited good stability even at the high current density of 250 mA cm-2, showing only 9.40% increase in working applied potential after a continuous 12 h operation. The present work demonstrates a new design for highly efficient OER catalysts with in situ growth of mixed oxide nanocrystals of pronounced synergistic effects.
ABSTRACT
A superfast, room-temperature, one-step carrier-solvent-assisted interfacial reaction process was developed to prepare Ag/AgFeO2 composite nanocrystals (NCs) of less than 10 nm in size within a 1 min reaction time. These composite NCs were with a direct energy band gap of 2.0 eV and were paramagnetic, making them suitable for optical activation and magnetic manipulation. These composite NCs, applied as a photocatalyst for the treatment of HeLa cells, achieved a significant reduction of 74% in cell viability within 30 min. These Ag/AgFeO2 composite NCs proved to be a promising magnetically guidable photocatalyst for cancer cell treatment.
