4.8 Article

Single- or Poly-Crystalline Ni-Rich Layered Cathode, Sulfide or Halide Solid Electrolyte: Which Will be the Winners for All-Solid-State Batteries?

期刊

ADVANCED ENERGY MATERIALS
卷 11, 期 21, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202100126

关键词

(electro)chemo‐ mechanical effects; halides; Ni‐ rich layered oxide cathodes; solid‐ state batteries; sulfides

资金

  1. Technology Development Program to Solve Climate Changes through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT AMP
  2. Future Planning [NRF-2017M1A2A2044501]
  3. Samsung Science and Technology Foundation [SRFC-MA2002-04]

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The use of single-crystalline NCA and oxidation-tolerable Li3YCl6 in all-solid-state batteries shows promising results in terms of discharge capacity, initial Coulombic efficiency, cycling performance, and rate capability. The overlooked contribution of side reactions to the degradation of polycrystalline NCA is revealed for the first time in this study through rigorous characterization and analysis.
Two newly emerging materials for application in all-solid-state batteries, namely, single-crystalline Ni-rich layered oxide cathode and halide solid electrolyte (SE), are of utmost interest because of their superior properties (good microstructural integrity and excellent electrochemical oxidation stability, respectively) to conventional polycrystalline layered oxides and sulfide SEs. In this work, four electrodes employing single- or polycrystalline LiNi0.88Co0.11Al0.01O2 (NCA) and Li3YCl6 or Li6PS5Cl0.5Br0.5 are rigorously characterized by complementary analyses. It is shown that the synergy of employing cracking-free single-crystalline NCA and oxidation-tolerable Li3YCl6 can be achieved by considering intercoupled engineering factors that are prone to overlook, such as size, lightness, and mixing of particles. Accordingly, the highest level of performances in terms of discharge capacity (199 mA h g(-1) at 0.1C), initial Coulombic efficiency (89.6%), cycling performance (96.8% of capacity retention at the 200th cycle), and rate capability (130 mA h g(-1) at 4C) are demonstrated at 30 degrees C. Severe side reactions occurring at the Li6PS5Cl0.5Br0.5/NCA interfaces are also quantified and probed. Importantly, an overlooked but significant contribution of the side reaction of Li6PS5Cl0.5Br0.5 to the detrimental electrochemo-mechanical degradation of polycrystalline NCA is revealed for the first time by postmortem scanning electron microscopy and operando electrochemical pressiometry measurements.

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