“…In the PBA crystal system, the N-coordinated high-spin P cations and C-coordinated low-spin R cations are interlinked with C≡N bridges, forming an open face-centered cubic structure that provides distinctive advantages such as high porosity, large specific surface area, and tunable metal active sites, which are beneficial for various applications, such as catalysis, energy storage, and sensors [33][34][35][36][37]. Currently, among the wide selection of PBA family, the metal hexacyanoferrates (HCFs), in which lowspin R cations are replaced with Fe and high-spin cations are replaced with transition metal ions (mostly Co, Ni, Cu, and Zn), are of interest owing to their chemical stability over a wide pH range, tunable physicochemical properties, and catalytic activities, which are comparable to those of metal oxides [31,38]. Despite these technical advantages, metal HCFs still suffer from low current densities and mechanical resistance owing to their conductivity and poor interfacial bonding with the electrode surfaces; subsequently, limiting their application.…”