Stabilizing Cathode–Electrolyte Interphase of Nickel-Rich Single-Crystal Cathodes for Lithium-Ion BatteriesSource: Journal of Electrochemical Energy Conversion and Storage:;2026:;volume( 023 ):;issue:002Author:Farrell, Collin
,
Dixit, Marm
,
Preefer, Molleigh
,
Sahore, Ritu
,
Islam, Saiful M.
,
Roy, Subrata Chandra
,
Li, Mengya
DOI: 10.1115/1.4070915Publisher: The American Society of Mechanical Engineers (ASME)
Abstract: Abstract. Nickel-rich single-crystal (SC) layered oxides are promising cathode candidates for next-generation lithium-ion batteries (LIBs) owing to their high energy density and structural robustness against intergranular cracking. However, their intrinsic surface reactivity with liquid electrolytes accelerates parasitic reactions at the cathode–electrolyte interphase (CEI), leading to transition-metal dissolution, gas generation, and impedance buildup. In this work, we synthesized SC-LixNi0.9Mn0.05Co0.05O2 (NMC9055, 1 ≤ x ≤ 1.2) using a eutectic-assisted method and investigated interface stabilization strategies. A nickel-deficient LixNi0.6Mn0.2Co0.2O2 (NMC622, 1 ≤ x ≤ 1.2) coating was applied via evaporation-based deposition to suppress CEI degradation pathways. Structural and compositional analyses confirmed uniform shell formation and preserved particle integrity. Half-cell electrochemical testing against lithium metal revealed ∼10% higher capacity retention and improved reversibility compared with pristine SC NMC9055, particularly under high-voltage operation. These results highlight the critical role of controlled surface chemistry in mitigating CEI instability in nickel-rich SC cathodes, offering a pathway toward enabling durable high-energy LIBs.
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| contributor author | Farrell, Collin | |
| contributor author | Dixit, Marm | |
| contributor author | Preefer, Molleigh | |
| contributor author | Sahore, Ritu | |
| contributor author | Islam, Saiful M. | |
| contributor author | Roy, Subrata Chandra | |
| contributor author | Li, Mengya | |
| date accessioned | 2026-08-23T07:51:54Z | |
| date available | 2026-08-23T07:51:54Z | |
| date copyright | 2026/05/01 | |
| date issued | 2026 | |
| identifier issn | 2381-6872 | |
| identifier other | jeecs-25-1193.pdf | |
| identifier uri | http://yetl.yabesh.ir/yetl1/handle/yetl/4315724 | |
| description abstract | Abstract. Nickel-rich single-crystal (SC) layered oxides are promising cathode candidates for next-generation lithium-ion batteries (LIBs) owing to their high energy density and structural robustness against intergranular cracking. However, their intrinsic surface reactivity with liquid electrolytes accelerates parasitic reactions at the cathode–electrolyte interphase (CEI), leading to transition-metal dissolution, gas generation, and impedance buildup. In this work, we synthesized SC-LixNi0.9Mn0.05Co0.05O2 (NMC9055, 1 ≤ x ≤ 1.2) using a eutectic-assisted method and investigated interface stabilization strategies. A nickel-deficient LixNi0.6Mn0.2Co0.2O2 (NMC622, 1 ≤ x ≤ 1.2) coating was applied via evaporation-based deposition to suppress CEI degradation pathways. Structural and compositional analyses confirmed uniform shell formation and preserved particle integrity. Half-cell electrochemical testing against lithium metal revealed ∼10% higher capacity retention and improved reversibility compared with pristine SC NMC9055, particularly under high-voltage operation. These results highlight the critical role of controlled surface chemistry in mitigating CEI instability in nickel-rich SC cathodes, offering a pathway toward enabling durable high-energy LIBs. | |
| publisher | The American Society of Mechanical Engineers (ASME) | |
| title | Stabilizing Cathode–Electrolyte Interphase of Nickel-Rich Single-Crystal Cathodes for Lithium-Ion Batteries | |
| type | Journal Paper | |
| journal volume | 23 | |
| journal issue | 2 | |
| journal title | Journal of Electrochemical Energy Conversion and Storage | |
| identifier doi | 10.1115/1.4070915 | |
| tree | Journal of Electrochemical Energy Conversion and Storage:;2026:;volume( 023 ):;issue:002 | |
| contenttype | Fulltext |