Fundamental understanding of electrocatalysis over layered double hydroxides from the aspects of crystal and electronic structures

Layered double hydroxides (LDHs) composed of octahedral ligand units centered with various transition metal atoms display unique electronic structures and thus attract significant attention in the field of electrocatalytic oxygen evolution reactions (OER). Intensive experimental explorations have therefore been carried out to investigate the LDHs synthesis, amorphous control, intrinsic material modifications, interfacing with other phases, strain, etc. There is still the need for a fundamental understanding of the structure-property relations, which could hinder the design of the next generation of the LDHs catalysts. In this review, we firstly provide the crystal structure information accompanied by the corresponding electronic structures. Then, we discuss the conflicts of the active sites on the NiFe LDHs and propose the synergistic cooperation among the ligand units during OER to deliver a different angle for understanding the current structure-property relations beyond the single-site-based catalysis process. In the next section of the OER process, the linear relationship-induced theoretical limit of the overpotential is further discussed based on the fundamental aspects. To break up the linear relations, we have summarized the current strategies for optimizing the OER performance. Lastly, based on the understanding gained above, the perspective of the research challenges and opportunities are proposed.

Automated summary

Layered double hydroxides (LDHs) composed of octahedral ligand units centered with various transition metal atoms have unique electronic structures and have attracted significant attention in the field of electrocatalytic oxygen evolution reactions (OER). Further fundamental understanding of the structure-property relations is needed to hinder the design of the next generation of the LDHs catalysts. This review discusses the crystal structure and electronic structures of LDHs, as well as the potential synergistic cooperation and linear relationship limitations in the OER process.