Abstract
Water splitting is considered a promising approach for renewable and sustainable energy conversion. The development of water splitting electrocatalysts that have low-cost, long-lifetime, and high-performance is an important area of research for the sustainable generation of hydrogen and oxygen gas. Here, we report a metal-free porphyrin-based two-dimensional crystalline covalent organic polymer obtained from the condensation of terephthaloyl chloride and 5,10,15,20-tetrakis(4-aminophenyl) porphyrin which is stabilized by an extensive hydrogen bonding network. This material exhibits bifunctional electrocatalytic performance towards water splitting with onset overpotentials, η, of 36 mV and 110 mV for HER (in 0.5 M H(2)SO(4)) and OER (in 1.0 M KOH), respectively. The as-synthesized material is also able to perform water splitting in neutral phosphate buffer saline solution, with 294 mV for HER and 520 mV for OER, respectively. Characterized by electrochemical impedance spectroscopy (EIS) and chronoamperometry, the as-synthesized material also shows enhanced conductivity and stability compared to its molecular counterpart. Inserting a non-redox active zinc metal center in the porphyrin unit leads to a decrease in electrochemical activity towards both HER and OER, suggesting the four-nitrogen porphyrin core is the active site. The high performance of this metal-free material towards water splitting provides a sustainable alternative to the use of scarce and expensive metal electrocatalysts in energy conversion for industrial applications.