Substitution of Fe in hydroxyapatite as an efficient single-atom catalyst for oxygen reduction reaction in biofuel cells: A first-principles study

Single-atom biological catalysts have attracted enormous attentions for low cost, high stability and catalytic activity in therapeutics and biomedical devices. The properties of Fe atom substituted CaII in HAP surface (Fe@HAP) and Fe adsorbed over HAP surface (Fe/HAP), and the detailed kinetic and thermodynamic behaviors of the oxygen reduction reaction (ORR) processes have been investigated by using the first-principles study. It is found that Fe dopant by substituted CaII ion into HAP surface could be more stably anchored at HAP surface than Fe adsorbate, and the introduced Fe dopant can enormously increase the endogenous ORR catalytic activity of magnetic HAP catalysts. Furthermore, the ORR process on Fe@HAP prefers to the 4epathway with the small reaction barrier (0.73 eV) for the rate-limiting step, and the two OH species formed from the hydrogenation of the adsorbed O-2 prefer to further hydrogenate into two H2O molecules and their self-dehydrogenation is not preferable according to the transition states simulation, which is also confirmed by the Gibbs free energy calculation. Consequently, our results revealed that the Fe@HAP could be an efficient catalyst as cathode material in the applications of the implantable biofuel cells and shed light on the design of biomaterials for various applications.

Automated summary

The properties and behaviors of Fe@HAP and Fe/HAP were investigated using first-principles study, revealing that Fe@HAP can be stably anchored and enhance the ORR catalytic activity. The ORR process on Fe@HAP prefers the 4e pathway and the hydrogenated OH species tend to further hydrogenate.