Publisher Correction: Architectured ZnO-Cu particles for facile manufacturing of integrated Li-ion electrodes.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Architectured ZnO-Cu particles for facile manufacturing of integrated Li-ion electrodes.

Designing electrodes with tailored architecture is an efficient mean to enhance the performance of metal-ion batteries by minimizing electronic and ionic transport limitations and increasing the fraction of active material in the electrode. However, the fabrication of architectured electrodes often involves multiple laborious steps that are not directly scalable to current manufacturing platforms. Here, we propose a processing route in which Cu-coated ZnO powders are directly shaped into architectured electrodes using a simple uniaxial pressing step. Uniaxial pressing leads to a percolating Cu phase with enhanced electrical conductivity between the active ZnO particles and improved mechanical stability, thus dispensing the use of carbon-based additives and polymeric binders in the electrode composition. The additive-free percolating copper network obtained upon pressing leads to highly loaded integrated anodes displaying volumetric charge capacity 6-10 fold higher than Cu-free ZnO films and that matches the electrochemical performance reported for advanced cathode structures. Achieving this high charge capacity using a readily available pressing tool makes this approach a promising route for the facile manufacturing of high-performance electrodes at large industrial scales.

Correlated X-Ray 3D Ptychography and Diffraction Microscopy Visualize Links between Morphology and Crystal Structure of Lithium-Rich Cathode Materials.

The search for higher performance, improved safety, and lifetime of lithium-ion batteries relies on the understanding of degradation mechanisms. Complementary to methods and studies on primary particles or crystalline structure on bulk materials, here we use spatially correlated ptychographic X-ray computed nanotomography with a 35 nm resolution and scanning X-ray diffraction microscopy with 1 µm resolution to visualize in 3D the hidden morphological and structural degradation processes in individual secondary particles of lithium-rich nickel, cobalt, and manganese oxides. From comparative examination of pristine and cycled particles, we suggest that morphological degradation could have radial dependency and secondary particle size dependency. The same particles were examined to correlate the degradation to crystallinity, which shows surprising core-shell structures. This study reveals the inner 3D structure of the secondary particles while opening up questions on the unexpected crystalline structural distributions, which could offer clues for future studies on this promising cathode material for lithium-ion batteries.

ß-NaMnO2: a high-performance cathode for sodium-ion batteries.

There is much interest in Na-ion batteries for grid storage because of the lower projected cost compared with Li-ion. Identifying Earth-abundant, low-cost, and safe materials that can function as intercalation cathodes in Na-ion batteries is an important challenge facing the field. Here we investigate such a material, ß-NaMnO2, with a different structure from that of NaMnO2 polymorphs and other compounds studied extensively in the past. It exhibits a high capacity (of ca. 190 mA h g(-1) at a rate of C/20), along with a good rate capability (142 mA h g(-1) at a rate of 2C) and a good capacity retention (100 mA h g(-1)after 100 Na extraction/insertion cycles at a rate of 2C). Powder XRD, HRTEM, and (23)Na NMR studies revealed that this compound exhibits a complex structure consisting of intergrown regions of α-NaMnO2 and ß-NaMnO2 domains. The collapse of the long-range structure at low Na content is expected to compromise the reversibility of the Na extraction and insertion processes occurring upon charge and discharge of the cathode material, respectively. Yet stable, reproducible, and reversible Na intercalation is observed.