TY - JOUR A1 - Sun, Fu A1 - Osenberg, Markus A1 - Dong, Kang A1 - Zhou, Dong A1 - Hilger, Andre A1 - Jafta, Charl J. A1 - Risse, Sebastian A1 - Lu, Yan A1 - Markoetter, Henning A1 - Manke, Ingo T1 - Correlating Morphological Evolution of Li Electrodes with Degrading Electrochemical Performance of Li/LiCoO2 and Li/S Battery Systems BT - Investigated by Synchrotron X-ray Phase Contrast Tomography JF - ACS energy letters / American Chemical Society N2 - Efficient Li utilization is generally considered to be a prerequisite for developing next-generation energy storage systems (ESSs). However, uncontrolled growth of Li microstructures (LmSs) during electrochemical cycling has prevented its practical commercialization. Herein, we attempt to understand the correlation of morphological evolution of Li electrodes with degrading electrochemical performances of Li/LiCoO2 and Li/S systems by synchrotron X-ray phase contrast tomography technique. It was found that the continuous transformation of the initial dense Li bulk to a porous lithium interface (PL1) structure intimately correlates with the gradually degrading overall cell performance of these two systems. Additionally, the formation mechanism of the PLI and its correlation with previously reported inwardly growing LmS and the lithium-reacted region have been intensively discussed. The information that we gain herein is complementary to previous investigations and may provide general insights into understanding of degradation mechanisms of Li metal anodes and also provide highly needed guidelines for effective design of reliable next-generation Li metal-based ESSs. Y1 - 2018 U6 - https://doi.org/10.1021/acsenergylett.7b01254 SN - 2380-8195 VL - 3 IS - 2 SP - 356 EP - 365 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Rudolph, Nicole A1 - Esser, Hanna G. A1 - Carminati, Andrea A1 - Moradi, Ahmad B. A1 - Hilger, Andre A1 - Kardjilov, Nikolay A1 - Nagl, Stefan A1 - Oswald, Sascha T1 - Dynamic oxygen mapping in the root zone by fluorescence dye imaging combined with neutron radiography JF - Journal of soils and sediments : protection, risk assessment and remediation N2 - The rooted zone of a soil, more precisely the rhizosphere, is a very dynamic system. Some of the key processes are water uptake and root respiration. We have developed a novel method for measuring the real-time distribution of water and oxygen concentration in the rhizosphere as a biogeochemical interface in soil. This enables understanding where and when roots are active in respect to root respiration and water uptake and how the soil responds to it. We used glass containers (15 x 15 x 1 cm), which were filled with a quartz sand mixture. Sensor foils for fluorescence dye imaging of O-2 were installed on the inner side of the containers. A lupine plant was grown in each container for 2 weeks under controlled conditions. Then we took time series of fluorescence images for time-lapsed visualization of oxygen depletion caused by root respiration. Changing water content was mapped in parallel by non-invasive neutron radiography, which yields water content distributions in high spatial resolution. Also it can detect the root system of the lupine plants. By this combined imaging of the samples, a range of water contents and different oxygen concentration levels, both induced by root activities, could be assessed. We monitored the dynamics of these vital parameters induced by roots during a period of several hours. We observed that for high water saturation, the oxygen concentration decreased in parts of the container. The accompanying neutron radiographies gave us the information that these locations are spatially correlated to roots. Therefore, it can be concluded that the observed oxygen deficits close to the roots result from root respiration and show up while re-aeration from atmosphere by gas phase transport is restricted by the high water saturation. Our coupled imaging setup was able to monitor the spatial distribution and temporal dynamics of oxygen and water content in a night and day cycle. This reflects complex plant activities such as photosynthesis, transpiration, and metabolic activities impacting the root-soil interface. Our experimental setup provides the possibility to non-invasively visualize these parameters with high resolution. The particular oxygen imaging method as well as the combination with simultaneously mapping the water content by neutron radiography is a novelty. KW - Fluorescence imaging KW - Neutron radiography KW - Oxygen mapping KW - Rhizosphere KW - Root respiration KW - Water distribution Y1 - 2012 U6 - https://doi.org/10.1007/s11368-011-0407-7 SN - 1439-0108 VL - 12 IS - 1 SP - 63 EP - 74 PB - Springer CY - Heidelberg ER - TY - JOUR A1 - Sun, Fu A1 - Dong, Kang A1 - Osenberg, Markus A1 - Hilger, Andre A1 - Risse, Sebastian A1 - Lu, Yan A1 - Kamm, Paul H. A1 - Klaus, Manuela A1 - Markoetter, Henning A1 - Garcia-Moreno, Francisco A1 - Arlt, Tobias A1 - Manke, Ingo T1 - Visualizing the morphological and compositional evolution of the interface of InLi-anode|thio-LISION electrolyte in an all-solid-state Li-S cell by in operando synchrotron X-ray tomography and energy dispersive diffraction JF - Journal of materials chemistry : A, Materials for energy and sustainability N2 - Dynamic and direct visualization of interfacial evolution is helpful in gaining fundamental knowledge of all-solid-state-lithium battery working/degradation mechanisms and clarifying future research directions for constructing next-generation batteries. Herein, in situ and in operando synchrotron X-ray tomography and energy dispersive diffraction were simultaneously employed to record the morphological and compositional evolution of the interface of InLi-anode|sulfide-solid-electrolyte during battery cycling. Compelling morphological evidence of interfacial degradation during all-solid-state-lithium battery operation has been directly visualized by tomographic measurement. The accompanying energy dispersive diffraction results agree well with the observed morphological deterioration and the recorded electrochemical performance. It is concluded from the current investigation that a fundamental understanding of the phenomena occurring at the solid-solid electrode|electrolyte interface during all-solid-state-lithium battery cycling is critical for future progress in cell performance improvement and may determine its final commercial viability. Y1 - 2018 U6 - https://doi.org/10.1039/c8ta08821g SN - 2050-7488 SN - 2050-7496 VL - 6 IS - 45 SP - 22489 EP - 22496 PB - Royal Society of Chemistry CY - Cambridge ER -