Second-Shell N Dopants Regulate Acidic O<sub>2</sub> Reduction Pathways on Isolated Pt Sites
Baoxin Ni, Peng Shen, Guiru Zhang, Jiajun Zhao, Honghe Ding, Yifan Ye, Zhouying Yue, Hui Yang, Hao Wei, Kun Jiang
Abstract
Pt is a well-known benchmark catalyst in the acidic oxygen reduction reaction (ORR) that drives electrochemical O 2 -to-H 2 O conversion with maximum chemical energy-to-electricity efficiency. Once dispersing bulk Pt into isolated single atoms, however, the preferential ORR pathway remains a long-standing controversy due to their complex local coordination environment and diverse site density over substrates. Herein, using a set of carbon nanotube supported Pt–N–C single-atom catalysts, we demonstrate how the neighboring N dopants regulate the electronic structure of the Pt central atom and thus steer the ORR selectivity; that is, the O 2 -to-H 2 O 2 conversion selectivity can be tailored from 10% to 85% at 0.3 V versus reversible hydrogen electrode. Moreover, via a comprehensive X-ray-radiated spectroscopy and shell-isolated nanoparticle-enhanced Raman spectroscopy analysis coupled with theoretical modeling, we reveal that a dominant pyridinic- and pyrrolic-N coordination within the first shell of Pt–N–C motifs favors the 4e – ORR, whereas the introduction of a second-shell graphitic-N dopant weakens *OOH binding on neighboring Pt sites and gives rise to a dominant 2e – ORR. These findings underscore the importance of the chemical environment effect for steering the electrochemical performance of single-atom catalysts.