Sarac, BaranIvanov, Yurii P.Karazehir, TolgaMühlbacher, MarleneSarac, A. SezaiGreer, A. LindsayEckert, Jürgen2025-01-062025-01-0620220360-319910.1016/j.ijhydene.2021.12.0402-s2.0-85121789812https://doi.org/10.1016/j.ijhydene.2021.12.040https://hdl.handle.net/20.500.14669/1483This contribution shows an unusually high hydrogen storage of multilayer amorphous (A)-crystalline (C) Pd–Si based nanosheets when stacked in the right order. Samples with A/C/A/C/A stacking sequence exhibit 40 and 12 times larger hydrogen sorption than monolithic crystalline and amorphous samples, respectively. The maximum capacitance calculated from the fitting of electrochemical impedance measurements of the same sample is twice larger than that of the conventional polycrystalline Pd films of similar thickness. Five times higher diffusion coefficient calculated from modified Cottrell equation is obtained compared to specimens with C/A/C/A/C stacking. For the A/C/A/C/A multilayers, nanobubbles with diameters of 1–2 nm are homogeneously distributed at Si/SiO2 interface, and PdHx crystal formation in these regions confirms hydrogen-metal interactions. Furthermore, corrosion-resistant amorphous top layer permits larger amounts of hydrogen ion transfer to inner layers. Thus, hydrogen storage and production can be enhanced by smart design of multilayers targeted for proton exchange membrane electrolysis or fuel cells. © 2021 Hydrogen Energy Publications LLCeninfo:eu-repo/semantics/closedAccessElectrochemistryHRSTEMHydrogen storageMetallic glassMultilayerPalladium-siliconArticle678810Q1677747