Single copper sites dispersed on defective TiO2-x as a synergistic oxygen reduction reaction catalyst

Catalysts containing isolated single atoms have attracted much interest due to their good catalytic behavior, bridging the gap between homogeneous and heterogeneous catalysts. Here, we report an efficient oxygen reduction reaction (ORR) catalyst that consists of atomically dispersed single copper sites confined by defective mixed-phased TiO2-x. This synergistic catalyst was produced by introducing Cu2+ to a metal organic framework (MOF) using the Mannich reaction, occurring between the carbonyl group in Cu(acac)(2) and the amino group on the skeleton of the MOF. The embedding of single copper atoms was confirmed by atomic-resolution high-angle annular dark-field scanning transmission electron microscopy and x-ray absorption fine structure spectroscopy. Electronic structure modulation of the single copper sites coupling with oxygen vacancies was further established by electron paramagnetic resonance spectroscopy and first-principles calculations. Significantly enhanced ORR activity and stability were achieved on this special Cu single site. The promising application of this novel electrocatalyst was demonstrated in a prototype Zn-air battery. This strategy of the stabilization of single-atom active sites by optimization of the atomic and electronic structure on a mixed matrix support sheds light on the development of highly efficient electrocatalysts.

Automated summary

An efficient oxygen reduction reaction (ORR) catalyst consisting of atomically dispersed single copper sites confined by TiO2-x was developed through a synergistic strategy. The stability and activity of single copper atoms coupling with oxygen vacancies were significantly enhanced, showing promising application in Zn-air batteries. This novel electrocatalyst demonstrates the potential of stabilization of single-atom active sites for highly efficient electrocatalysts development.