TY - JOUR
T1 - Single- or Poly-Crystalline Ni-Rich Layered Cathode, Sulfide or Halide Solid Electrolyte
T2 - Which Will be the Winners for All-Solid-State Batteries?
AU - Han, Yoonjae
AU - Jung, Sung Hoo
AU - Kwak, Hiram
AU - Jun, Seunggoo
AU - Kwak, Hunho H.
AU - Lee, Jong Hoon
AU - Hong, Seung Tae
AU - Jung, Yoon Seok
N1 - Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2021/6/2
Y1 - 2021/6/2
N2 - 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 °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.
AB - 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 °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.
KW - (electro)chemo-mechanical effects
KW - Ni-rich layered oxide cathodes
KW - halides
KW - solid-state batteries
KW - sulfides
UR - http://www.scopus.com/inward/record.url?scp=85104374761&partnerID=8YFLogxK
U2 - 10.1002/aenm.202100126
DO - 10.1002/aenm.202100126
M3 - Article
AN - SCOPUS:85104374761
SN - 1614-6832
VL - 11
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 21
M1 - 2100126
ER -