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Fang, Chengcheng

Publications and source records attributed to Fang, Chengcheng.

24 records · Page 2
All sourcesNASA NTRSDOE OSTI
DOE OSTI2018

Predicting Calendar Aging in Lithium Metal Secondary Batteries: The Impacts of Solid Electrolyte Interphase Composition and Stability

Calendar aging of lithium metal batteries, in which cells’ components degrade internally due to chemical reactions while no current is being applied, is a relatively unstudied field. In this work, a model to predict calendar aging of lithium metal cells is developed using two sets of readily obtainable data: solid electrolyte interphase (SEI) layer composition (measured via X-ray photoelectron spectroscopy) and SEI stability (measured as a degradation rate using a simple constant current–constant voltage charging protocol). Electrolyte properties such as volume and salt concentration are varied in order to determine their effect on SEI stability and composition, with subsequent impacts to calendar aging. Lower salt concentrations produce a solvent-based, more soluble SEI, while the highest concentration produces a salt-based, less soluble SEI. Higher electrolyte volumes promote dissolution of the SEI and thus decrease its stability. The model predicts that lithium metal would be the limiting factor in calendar aging, depleting long before the electrolyte does. Furthermore, the relative composition of the electrolyte during aging is modeled and found to eventually converge to the same value independent of initial salt concentration.

25 ENERGY STORAGE↗
DOE OSTI2018

Modified Coprecipitation Synthesis of Mesostructure-Controlled Li-Rich Layered Oxides for Minimizing Voltage Degradation

In this work, modified carbonate coprecipitation synthesis without addition of chelating agent is introduced to obtain mesostructure-controlled Li-rich layered oxides. The designed mesostructure for target material Li 1.2 Ni 0.2 Mn 0.6 O 2 has uniformly dispersed spherical secondary particles with size around 3 μm. These micrometer-sized particles consist of self-assembled crystallites with size of ~150 nm. This unique design not only decreases the surface area compared with the sample with dispersive particles, but also increases overall structural mechanical stability compared with the sample with larger dense secondary particles as observed by transmission X-ray microscope. As a result, the voltage decay and capacity loss during long-term cycling have been minimized to a large extent. Our findings clearly demonstrate that mesostructure design of Li-rich layered oxides play a key role in optimizing this class of cathode materials. Surprisingly, the voltage fading issue can be partially mitigated by such an approach.

25 ENERGY STORAGE↗
DOE OSTI2017

Narrowing the Gap between Theoretical and Practical Capacities in Li-Ion Layered Oxide Cathode Materials

Although layered lithium oxides have become the cathode of choice for state–of–the–art Li–ion batteries, substantial gaps remain between the practical and theoretical energy densities. With the aim of supporting efforts to close this gap, this work reviews the fundamental operating mechanisms and challenges of Li intercalation in layered oxides, contrasts how these challenges play out differently for different materials (with emphasis on Ni–Co–Al (NCA) and Ni–Mn–Co (NMC) alloys), and summarizes the extensive corpus of modifications and extensions to the layered lithium oxides. Particular emphasis is given to the fundamental mechanisms behind the operation and degradation of layered intercalation electrode materials as well as novel modifications and extensions, including Na–ion and cation–disordered materials.

25 ENERGY STORAGE↗
DOE OSTI2017

Morphological and Surface Structural Changes during Electrochemical Cycling in Li-rich Layered Oxides for Next Generation Li-ion Batteries

Li-rich layered oxides, either as a solid solution or as a nano-composite of layered Li 2 MnO 3 and Li(TM)O 2 (TM=Ni, Co, Mn), draw significant attention as the next-generation cathode materials for high-energy-density Li-ion batteries in electric vehicles. However, there are many issues still unclear, and numerous scientific challenges of these materials that must be overcome to realize their utilization in commercial Li-ion batteries. The first drawback is the irreversible voltage degradation process that limits cycle life. Modified co-precipitation synthesis is introduced to obtain morphology controlled Li-rich material without ammonia addition. This unique design increases meso-structure morphological stability compared with the sample with large secondary particles as proved by Transmission X-ray Microscope. As a result, the voltage decay and capacity loss during long term cycling have been minimized to a large extent. On the other hand, lattice oxygen plays an intriguing role in the electrochemical process of Li-rich material through a reversible redox process as well as an irreversible oxidation with O 2 gas release. To prevent oxygen gas generation, oxygen vacancies have been proposed to form on the surface of the morphology controlled Li-rich layered oxides through the design of a gas-solid interface reaction (GSIR). Dynamic structural changes during the initial two electrochemical cycles of GSIR Li-rich layered oxides are investigated with In operando synchrotron X-ray diffraction (SXRD). Different electrochemical reaction regions dominated by either cations or anions redox are identified in the shifts of the lattice parameters during the first cycle. Changes in lattice parameters, oxygen positions, and microstrain help to explain the lithium de-intercalation mechanism in this class of materials.

Zhang, Minghao↗
DOE OSTI2016

Minimize the Voltage Degradation in Li-rich Layered Oxide Cathode Materials by Morphology Control

Li-rich layered oxides, either as a solid solution or as a nano-composite of layered Li 2 MnO 3 and Li(TM)O 2 (TM=Ni, Co, Mn), draw significant attention as the next-generation cathode materials for high-energy-density lithium ion batteries in electric vehicles. Over the past twenty years, the discharge capacity at room temperature of these cathode materials has been improved from 200 mAh g -1 to over 320 mAh g -1 today, even higher at elevated temperatures. While the research has continued to push the limit of the available capacity of the materials throughout the years, there are many issues still unclear. And numerous scientific challenges, especially voltage degradation during cycling of these materials, that must be overcome to realize their utilization in commercial lithium ion batteries. Here, we report a design of modified co-precipitation method without ammonia addition to synthesize morphology controlled Li-rich material Li 1.2 Ni 0.2 Mn 0.6 O 2 as high energy density cathode for lithium ion batteries. The obtained material has spherical secondary particles with uniform dispersion. The secondary particles are dense, and have an average diameter of approximately 3 μm. These secondary spherical particles consist of primary particles with particle size approximately 150 nm. The morphology controlled sample can minimize voltage decay as well as improve capacity retention during cycling. And furthermore, the influence of morphology control on the cycling performance has been investigated through Transmission X-ray Microscope.

Zhang, Minghao↗