First-principles design of hetero CoM (M = 3d, 4d, 5d block metals) double-atom catalysts for oxygen evolution reaction under alkaline conditions.

As an extension of single-atom catalysts, the development of double-atom catalysts with high electrocatalytic activity for the oxygen evolution reaction (OER) is vital to facilitate hydrogen production and industrial applications. The CoM (M = 3d, 4d, 5d block metals) homo and double-atom catalysts supported on nitrogen-doped graphene (CoM/NG) were prepared for electrochemical water oxidation under alkaline conditions, and the electrocatalytic activity was studied through density functional theory (DFT) calculations. The hetero CoCu/NG double-atom catalyst indicated the highest OER activity with an onset potential of 0.

Conformation-modulated three-dimensional electrocatalysts for high-performance fuel cell electrodes.

Unsupported Pt electrocatalysts demonstrate excellent electrochemical stability when used in polymer electrolyte membrane fuel cells; however, their extreme thinness and low porosity result in insufficient surface area and high mass transfer resistance. Here, we introduce three-dimensionally (3D) customized, multiscale Pt nanoarchitectures (PtNAs) composed of dense and narrow (for sufficient active sites) and sparse (for improved mass transfer) nanoscale building blocks. The 3D-multiscale PtNA fabricated by ultrahigh-resolution nanotransfer printing exhibited excellent performance (45% enhanced maximum power density) and high durability (only 5% loss of surface area for 5000 cycles) compared to commercial Pt/C.