• Energy Research

AbstractMonolithic all-perovskite tandem photovoltaics promise to combine low-cost and high-efficiency solar energy harvesting with the advantages of all-thin-film technologies. To date, laboratory-scale all-perovskite tandem solar cells have only been fabricated using non-scalable fabrication techniques. In response, this work reports on laser-scribed all-perovskite tandem modules processed exclusively with scalable fabrication methods (blade coating and vacuum deposition), demonstrating power conversion efficiencies up to 19.1% (aperture area, 12.25 cm2; geometric fill factor, 94.7%) and stable power output. Compared to the performance of our spin-coated reference tandem solar cells (efficiency, 23.5%; area, 0.1 cm2), our prototypes demonstrate substantial advances in the technological readiness of all-perovskite tandem photovoltaics. By means of electroluminescence imaging and laser-beam-induced current mapping, we demonstrate the homogeneous current collection in both subcells over the entire module area, which explains low losses (<5%rel) in open-circuit voltage and fill factor for our scalable modules.

Spinel LiNi0.5Mn1.5O4 as one of the high-energy positive electrode materials for next generation Li-ion batteries has attracted significant interest due to its economic and environmental advantages. However, the sensitivity of this type of material upon short to long term ambient storage conditions and the impact on the electrochemical performances remains poorly explored. Nevertheless, this remains an important aspect for practical large-scale synthesis, storage and utilization. Herein, we study and compare the evolution of surface chemistry, bulk crystal structure and elemental content evolution and distribution of LiNi0.5Mn1.5O4 using a variety of characterization techniques including XPS and STEM-EDS-EELS, as well as electrochemical analysis. We show that Mn species dominate the outer surface (0–5 nm), while Ni and Li are preferentially located further away and in the bulk. The studied LiNi0.5Mn1.5O4 material is found to be stable, with minor changes in surface or bulk characteristics detected, even after 12 months of storage under ambient air conditions. The low surface reactivity to air also accounts for the minor changes to the electrochemical performance of the air-exposed LiNi0.5Mn1.5O4, compared to the pristine material. This study provides guidance for the appropriate storage, handling and processing of this high-performance cathode material.

For the first time, a multi-anionic and multi-cationic high entropy oxyhalide is presented as high capacity cathode for Li-ion batteries.

High entropy oxides (HEOs) constitute a promising class of materials with possibly new and largely unexplored properties. The virtually infinite variety of compositions (multi-element approach) for a single-phase structure allows the tailoring of their physical properties and enables unprecedented materials design. Nevertheless, this level of versatility renders their characterization as well as the study of specific processes or reaction mechanisms challenging. In the present work, we report the structural and electrochemical behavior of different multi-cationic HEOs. Phase transformation from spinel to rock-salt was observed upon incorporation of monovalent Li+ ions, accompanied by partial oxidation of certain elements in the lattice. This transition was studied by X-ray diffraction, inductively coupled plasma-optical emission spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, and attenuated total reflection infrared spectroscopy. In addition, the redox behavior was probed using cyclic voltammetry. Especially, the lithiated rock-salt structure HEOs were found to exhibit potential for usage as negative and positive electrode materials in rechargeable lithium-ion batteries.