Modulation engineering of in-situ cathodic activation of FePx based on W-incorporation for hydrogen evolution
In-situ electrochemical activation as a new pretreating method to adjust electrocatalytic performance attracts extensive attention. However, the activation mechanisms of electrocatalysts are still ambiguous. Herein, we propose a facile modulation strategy of in-situ cathodic activation of FePx based on W-incorporation (W-FePx/IF) for hydrogen evolution reaction (HER). The activated W-FeOx with obvious surface reconstruction demonstrates the role of W-incorporation for driving the cathodic activation of FePx, which suggests the larger surface area and more active sites. In fact, W incorporation can not only accelerate cathodic activation process but also act as the adsorption sites for Had to form synergistic effect with FeOx for water dissociation. The obtained W-FeOx/IF exhibits greatly enhanced HER activity featuring decreased overpotential from 237.7 to 154.0 mV at 100 mA cm-2, which may be ascribed to W-FeOx with double catalytic active sites after cathodic activation. Additionally, the modulation effects of cathodic activation can be exactly achieved by changing electrochemical parameters such as CV cycles. W-FeOx/IF also shows excellent long-term stability for at least 100 h at 100 mA cm-2. This modulation engineering based on metal doping is expected to provide inspiration for the understanding of cathodic activation process for efficient electrocatalysts.