Engineering Layered Double Hydroxides for Photochemical and Electrochemical Hydrogen Evolution: Mechanistic Insights and Structure-Property Relationships

Abstract

Being a multifaceted class of 2D materials, layered double hydroxides possess great potential for the hydrogen evolution reaction. LDHs own lamellar structure, defect-rich framework, and adjustable cation composition that are active in tuning their electronic structures and reaction interfaces for facilitated proton adsorption. This work surveys recent developments in comprehending the structure-activity relationships of LDHs in accordance with photochemical and electrochemical HER processes. The roles of lattice architecture, interlayer anions, and cation interactions in controlling charge migration, active site attainability, and adsorption energetics have been emphasized more in this work. The chemical strategies to alter the catalytic efficacy of LDH-based materials toward HER have been scrutinized, including heterostructure design, strain engineering, elemental doping, and interface adjustments. The catalytic mechanism of LDH-based catalysts in the light of theoretical modelling and operando/in-situ characterizations is discussed in detail. This review will be a torchbearer in bridging the gap between heterogeneous catalysis and LDH catalytic systems and will guide the researchers to engineer high-performing LDH-derived HER catalysts.