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Interfacial charge transfer efficiency and electronic states of active sites are two essential issues to restrict catalytic activity of electrocatalysts for oxygen evolution reaction (OER). In this work, we show that although Au is recognized to be inert towards OER, the catalytic activity of Fe 3 O 4 catalyst for OER was highly boosted by coupling Fe 3 O 4 with Au to address these two issues. Here, Au nanoparticles were attached to hierarchical Fe 3 O 4 microsphere through electrochemical deposition, a mild and rapid approach that can be accomplished within 3 min and requires no sophisticated equipment. With the coupling of Au, interfacial charge transfer resistance of Fe 3 O 4 declined remarkably. On the other hand, oxidability of Fe sites and electron accepting capability of Au sites was elevated due to strong interaction between Au and Fe 3 O 4. Owing to these two merits induced by Au, Fe 3 O 4 exhibited enhanced catalytic activity for OER. The potential of Fe 3 O 4 to obtain 10 mA/cm2 decreased by 640 mV, the current density was amplified up to 2.5 fold at the potential of 2 V (vs SCE), and the Tafel slop was reduced by 146 mV/dec. This work shows that the catalytic activity of an earth-abundant electrocatalyst (Fe 3 O 4) for OER reaction was boosted by coupling it with OER-inert Au. It is found that the coupling of Au not only facilitated charge transfer efficiency of the catalyst, but elevated the oxidability of Fe sites and electron accepting capability of Au sites. Thereby, when coupled with Au, Fe 3 O 4 exhibited enhanced current density, reduced overpotential, and smaller Tafel slop. [Display omitted] • Enhance catalytic activity of Fe 3 O 4 for OER reaction via coupling of OER-inert Au. • Effectively promoted interfacial charge transfer with the decoration of Au. • Modify the state of Fe sites and Au sites by strong interaction of Au with Fe 3 O 4. • An easy-to-handle and rapid way to couple Au with hierarchical Fe 3 O 4 microspheres. [ABSTRACT FROM AUTHOR]

Electrochemical water splitting is considered as a promising approach to storing renewable electricity in the form of hydrogen fuel. In this work, we report the design and electrocatalytic properties of chiral CuO@Ni with three dimensional (3D) continuous macroporous framework. With the chiral CuO@Ni as anode, the OER overpotential required to achieve the current density of 10 mA/cm2 was as low as 110 mV in 0.1 M KOH electrolyte, and the hydrogen production rate of water splitting reaction could reach 1070 nL/s. Moreover, the OER overpotential could be regulated easily by controlling the deposition time of chiral CuO layer on Ni. The high catalytic activity of chiral CuO@Ni for water splitting is closely associated with the Chiral-induced spin selectivity ( CISS ) effect, the large reactive area provided by its 3D macroporous structure, and the effective cooperation between chiral CuO and Ni foam that facilitated the transportation of spin aligned electrons from chiral CuO layer to Ni. The results shown in this work indicate a simple and promising strategy to improve the electrocatalytic activity of other chiral earth-abundant catalysts for water splitting. This work shows the design and properties of chiral CuO@Ni with three dimensional continuous macroporous framework. The chiral CuO@Ni exhibited lower OER overpotential and larger current density than many CuO-based catalysts. Its high catalytic activity for water splitting reaction is attributed to the CISS effect of chiral CuO, the large reactive area of its 3D porous structure, and the synergistic interaction between the chiral CuO and the Ni foam. Image 1 • Chiral CuO@Ni with three dimensional continuous macroporous framework. • Low OER overpotential (110 mV) to achieve 10 mA/cm2 current density. • Easy and effective way to enhance the activity of chiral earth-abundant catalyst. [ABSTRACT FROM AUTHOR]