Abstract
The hydrogen peroxide oxidation reaction (HPOR) plays a vital role in the emerging H2-H2O2 cycle energy storage system, in which the rational design of HPOR electrocatalyst is essential for achieving high system efficiency. Herein, we establish the HPOR activity trends using structurally well-defined metal phthalocyanines (MPc) as model catalysts via a combined experimental and computational approach. The measured activity sequence follows the order of CoPc > FePc > MnPc > ZnPc > H2Pc > NiPc > CuPc based on their site-normalized exchange current (i
0-s). Theoretical calculations indicate that the binding free energy of hydroperoxyl intermediate, HOO*, on MPc (ΔG
HOO*) is the activity descriptor for HPOR. A volcano-type activity trend is observed by correlating the logarithm of i
0-s (logi
0-s) with the ΔG
HOO* values and agrees with the theoretical predictions. This HPOR activity trend provides insights into the design of highly active electrocatalysts for HPOR and related energy applications.
Funder
Institute of Coal Chemistry, Chinese Academy of Sciences
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences
Natural Science Foundation of Shanxi Province
Publisher
The Electrochemical Society