High Corrosion Resistance of NiFe‐Layered Double Hydroxide Catalyst for Stable Seawater Electrolysis Promoted by Phosphate Intercalation
Baoshan Zhang, Shuo Liu, Shaojie Zhang, Yu Cao, Huili Wang, Chengyu Han, Jie Sun
Abstract
Abstract Sustainable production of hydrogen from seawater electrolysis has attracted much attention in recent years. Considering that Cl ‐ might corrode metal substrate by crossing through the covered catalyst, the conventional Ni(II)Fe(III)‐layered double hydroxide (NiFe‐LDH) loaded on metal substrate, as a favorable oxygen evolution catalyst, cannot be directly used for seawater electrolysis. Herein, an anti‐corrosion strategy of PO 4 3‐ intercalation in NiFe‐LDH is proposed, in which the highly negatively charged PO 4 3‐ in the interlayers can prevent the Ni substrate from Cl ‐ corrosion by electrostatic repulsion. In order to verify the anti‐corrosion effect, the two electrodes of the pristine NiFe‐LDH and the PO 4 3‐ intercalated NiFe‐LDH are evaluated in a solution with high Cl ‐ concentration. PO 4 3‐ can effectively hinder the migration of Cl ‐ between the interlayers of NiFe‐LDH, thus the corrosion life of the PO 4 3‐ intercalated NiFe‐LDH is more than 100 times longer than that of the pristine NiFe‐LDH. The improvement of stability is attributed to the inhibition effect of Cl ‐ passing through the interlayers of NiFe‐LDH, leading to the protection of Ni substrate. This work provides a design strategy for the catalysts loaded on the metal substrate, which has excellent Cl ‐ ‐corrosion resistance and can be widely used in hydrogen generation from seawater electrolysis.