Polymer−metal composite films with nanostructured metal and/or polymer interfaces show a significant perspective for optoelectronic applications, for example, as sensors or in organic photovoltaics (OPVs). The polymer components used in these devices are mostly nanostructured conductive polymers with conjugated π-electron systems. Enhanced OPV's power conversion efficiencies or sensor sensitivity can be achieved by selective metal deposition on or into polymer templates. In this study, we exploit time-resolved grazing-incidence X-ray scattering to observe the metal−polymer interface formation and the cluster crystallite size in situ during silver (Ag) sputter deposition on a poly(3-hexylthiophene-2,5-diyl)-b-poly(methyl methacrylate) (PMMA-b-P3HT) template. We compare the arising nanoscale morphologies with electronic properties, determine Ag growth regimes, and quantify the selective Ag growth for the diblock copolymer (DBC) template using the corresponding homopolymer thin films (P3HT and PMMA) as a reference. Hence, we are able to describe the influence of the respective polymer blocks and substrate effects on the Ag cluster percolation: the percolation threshold is correlated with the insulator-to-metal transition measured in situ with resistance measurements during the sputter deposition. The Ag cluster percolation on PMMA-b-P3HT starts already on the network of the hexagonal P3HT domain before a complete metal film covers the polymer surface, which is complemented by microscopic measurements. In general, this study demonstrates a possible method for the selective Ag growth as a scaffold for electrode preparation in nanoelectronics and for energy harvesting applications.

Ultra-thin metal layers on polymer thin films attract tremendous research interest for advanced flexible optoelectronic applications, including organic photovoltaics, light emitting diodes and sensors. To realize the large-scale production of...

The most daunting challenge in solid-state polymer electrolyte membranes (PEMs) is to achieve high ionic conductivity close to that of the liquid electrolytes, while maintaining enhanced thermal and mechanical performances. The ionic conductivity in relation to the morphology of PEMs composed of diblock copolymer (polystyrene-block-poly­(ethylene oxide); PS-b-PEO), lithium salt (lithium trifluoromethanesulfonate; LiTf), and ionic liquid (1-ethyl-3-methylimidazolium trifluoromethanesulfonate; EMIMTf) is investigated. The optimized functional nanostructured PEMs are achieved with room-temperature ionic conductivities higher than a 1 mS cm–1 benchmark. The morphology of these microphase-separated electrolytes is composed of a major soft high ionic-conductive PEO/LiTf/IL matrix with minor glassy high-modulus PS nanodomains. The ionic-liquid upload in hybrid electrolytes inhibits the PEO crystallization, reduces the PEO glass transition temperature, promotes an extended PEO chain conformation, and enhances the solubilization of the non-dissociated lithium salt at the PS–PEO domain interfaces. These intrinsic properties caused by the ionic-liquid loading serve to achieve stable and robust nanostructured electrolyte membranes and can explain the achieved benchmark conductivity.

The formation of c-Li3.75Si is known to be detrimental to silicon anodes in lithium-ion batteries. To suppress the formation of this crystalline phase and improve the electrochemical performance of Si-based anodes, three approaches were amalgamated: addition of a nickel adhesion sublayer, alloying of the silicon with titanium, and addition of either carbon or TiO2 as a capping layer. The silicon-based films were analyzed by a suite of methods, including scanning electron microscopy (SEM) and a variety of electrochemical techniques, as well as X-ray photoelectron spectroscopy (XPS) to provide insights into the composition of the resulting solid-electrolyte interphase (SEI). A nickel adhesion layer decreased the extent of delamination of the silicon from the underlying copper substrate, compared to Si deposited directly on Cu, which resulted in less capacity loss. Alloying of silicon with titanium (85% silicon, 15% titanium) further increased the stability. Finally, capping these multilayer electrodes with either a thin 10 nm layer of carbon or TiO2 resulted in the best electrode behavior and lowest cumulative relative irreversible capacity. TiO2 is slightly more effective in enhancing the capacity retention, most likely due to differences in the resulting solid-electrolyte interphase (SEI). The combination of an adhesion layer, alloying, and surface coatings shows a cumulative suppression of the formation of c-Li3.75Si and SEI, resulting in the greatest improvement of capacity retention when all three are incorporated together. However, these strategies appear to only delay the onset of the c-Li3.75Si phase; eventually, the c-Li3.75Si phase will form, and at that point, the capacity degradation rate of all the electrodes becomes similar.

The future of mobility depends on the development of next‐generation battery technologies, such as all‐solid‐state batteries. As the ionic conductivity of solid Li+‐conductors can, in some cases, approach that of liquid electrolytes, a significant remaining barrier faced by solid‐state electrolytes (SSEs) is the interface formed at the anode and cathode materials, with chemical instability and physical resistances arising. The physical properties of space charge layers (SCLs), a widely discussed phenomenon in SSEs, are still unclear. In this work, spectroscopic ellipsometry is used to characterize the accumulation and depletion layers. An optical model is developed to quantify their thicknesses and corresponding concentration changes. It is shown that the Li+‐depleted layer (≈190 nm at 1 V) is thinner than the accumulation layer (≈320 nm at 1 V) in a glassy lithium‐ion‐conducting glass ceramic electrolyte (a trademark of Ohara Corporation). The in situ approach combining electrochemistry and optics resolves the ambiguities around SCL formation. It opens up a wide field of optical measurements on SSEs, allowing various experimental studies in the future.