Oxygen Reduction Activity of B←N-Containing Organic Molecule Affected by Asymmetric Regulation

Organic molecular catalysts have received great attention as they have the merits of well-controlled molecular structures for the development of catalytic chemistry. Herein, the electronic distribution of active sites is regulated by asymmetrically introducing S-heterocycle on one side of the molecular core. As a result, the asymmetric as-PYT and as-BNT show higher oxygen reduction performance than their symmetric counterparts without (s-PY, s-PY2T) or with two S-heterocycle units (s-BN, s-BN2T). Density functional theory calculations reveal that the carbon atoms (site-12) at symmetric s-BN and s-BN2T are the catalytic active sites, while for asymmetric as-BNT, it has changed to amino-N atom (site-14). Due to the non-uniform charge distribution and increased dipole moment of as-BNT caused by asymmetric molecular configuration, the kinetics of catalytic reaction has changed significantly. The catalytically active sites of specific N atoms are further verified experimentally and theoretically by using sterically hindered phenyl groups. This work provides a simple but efficient method to design metal-free oxygen reduction electrocatalysts.

Automated summary

Organic molecular catalysts with well-controlled molecular structures have attracted attention for catalytic chemistry. By asymmetrically introducing S-heterocycles, the electronic distribution of active sites is regulated, leading to improved oxygen reduction performance. Asymmetric structure of as-BNT alters the catalytic active sites and changes the kinetics of catalytic reaction due to non-uniform charge distribution and increased dipole moment.