Abstract
The electrocatalytic 2e(-) oxygen reduction reaction (2e(-) ORR) provides an appealing pathway to produce hydrogen peroxide (H(2)O(2)) in a decentralized and clean manner, which drives the demand for developing high selectivity electrocatalysts. However, current understanding on selectivity descriptors of 2e(-) ORR electrocatalysts is still insufficient, limiting the optimization of catalyst design. Here we study the catalytic performances of a series of metal phthalocyanines (MPcs, M = Co, Ni, Zn, Cu, Mn) for 2e(-) ORR by combining density functional theory calculations with electrochemical measurements. Two descriptors (ΔG (*O) - ΔG (*OOH) and ΔG (*H(2)O(2)) ) are uncovered for manipulating the selectivity of H(2)O(2) production. ΔG (*O) - ΔG (*OOH) reflects the preference of O-O bond breaking of *OOH, affecting the intrinsic selectivities. Due to the high value of ΔG (*O) - ΔG (*OOH), the molecularly dispersed electrocatalyst (MDE) of ZnPc on carbon nanotubes exhibits high selectivity, even superior to the previously reported NiPc MDE. ΔG (*H(2)O(2)) determines the possibility of further H(2)O(2) reduction to affect the measured selectivities. Enhancing the hydrophobicity of the catalytic layer can increase ΔG (*H(2)O(2)) , leading to selectivity improvement, especially under high H(2)O(2) production rates. In the gas diffusion electrode measurements, both ZnPc and CoPc MDEs with polytetrafluoroethylene (PTFE) exhibit low overpotentials, high selectivities, and good stability. This study provides guidelines for rational design of 2e(-) ORR electrocatalysts.