The Role of Na Doping in Li-Rich Li–Mn–Ni–O Layered Oxides

Lithium- and manganese-rich layered oxides, especially cobalt-free compositions, have gained considerable attention as sustainable and cost-effective cathode materials for lithium-ion batteries. This attention is largely due to the relative abundance and low cost of Mn compared to Ni and Co. However, these materials face critical challenges, including voltage and capacity fade, structural instability, and transition metal (TM) dissolution. Sodium doping has been proposed as a promising strategy to address these issues by expanding the lithium interlayer spacing, reducing cation mixing, and introducing stabilizing defects. Herein, we present the impact of sodium substitution across a broad compositional range (0–20%) in Li1+xNay(Ni0.35Mn0.65)1–x–yO2 by synthesizing and characterizing 128 compositions within the Li–Na–Ni + Mn pseudoternary system. Using high-throughput X-ray diffraction, elemental analysis, and electrochemical testing of all samples, we accurately mapped the layered solid-solution region, despite substantial Li and Na loss during synthesis. The solid-solution region extends to high sodium content (13% of all cations) and spans both stoichiometric Li contents and Li-rich compositions. We uncover strong relationships between composition, structural stability, and electrochemical performance. Our results show that moderate sodium doping (∼2–8%) stabilizes the layered phase at low Li content and enhances electrochemical performance at high Li content. Additionally, several lithium-rich multiphase compositions display extreme capacity growth (e.g., 250% over 7 cycles), which yields the highest discharge capacity after 10 cycles of approximately 225 mA h g–1. Furthermore, we systematically quantified TM dissolution under aggressive cycling and found that high Li content is needed to suppress TM dissolution and that this is resilient to the addition of sodium. Thus, we determine the optimal sodium content that improves battery performance while also showing good stability against TM dissolution due to the high Li content. These results highlight the importance of systematically exploring complex composition spaces, as small compositional changes can dramatically impact performance.

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Journal
ACS Applied Energy Materials
Published
2025-12-01
DOI
https://doi.org/10.1021/acsaem.5c03108
Primary Topic
Advancements in Battery Materials
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article
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article

The Role of Na Doping in Li-Rich Li–Mn–Ni–O Layered Oxides

Jack Wright, Eric McCalla, Nooshin Zeinali Galabi, Maxime Blangero et al.
ACS Applied Energy Materials
Advancements in Battery Materials
article

The Role of Na Doping in Li-Rich Li–Mn–Ni–O Layered Oxides

Jack Wright, Eric McCalla, Nooshin Zeinali Galabi, Maxime Blangero, Dae Hyun Kim, Sibyl Martasek
article en

Abstract

Lithium- and manganese-rich layered oxides, especially cobalt-free compositions, have gained considerable attention as sustainable and cost-effective cathode materials for lithium-ion batteries. This attention is largely due to the relative abundance and low cost of Mn compared to Ni and Co. However, these materials face critical challenges, including voltage and capacity fade, structural instability, and transition metal (TM) dissolution. Sodium doping has been proposed as a promising strategy to address these issues by expanding the lithium interlayer spacing, reducing cation mixing, and introducing stabilizing defects. Herein, we present the impact of sodium substitution across a broad compositional range (0–20%) in Li1+xNay(Ni0.35Mn0.65)1–x–yO2 by synthesizing and characterizing 128 compositions within the Li–Na–Ni + Mn pseudoternary system. Using high-throughput X-ray diffraction, elemental analysis, and electrochemical testing of all samples, we accurately mapped the layered solid-solution region, despite substantial Li and Na loss during synthesis. The solid-solution region extends to high sodium content (13% of all cations) and spans both stoichiometric Li contents and Li-rich compositions. We uncover strong relationships between composition, structural stability, and electrochemical performance. Our results show that moderate sodium doping (∼2–8%) stabilizes the layered phase at low Li content and enhances electrochemical performance at high Li content. Additionally, several lithium-rich multiphase compositions display extreme capacity growth (e.g., 250% over 7 cycles), which yields the highest discharge capacity after 10 cycles of approximately 225 mA h g–1. Furthermore, we systematically quantified TM dissolution under aggressive cycling and found that high Li content is needed to suppress TM dissolution and that this is resilient to the addition of sodium. Thus, we determine the optimal sodium content that improves battery performance while also showing good stability against TM dissolution due to the high Li content. These results highlight the importance of systematically exploring complex composition spaces, as small compositional changes can dramatically impact performance.

ACS Applied Energy MaterialsVol. 8(24)
Umicore (Belgium) (BE), McGill University (CA)
Openalex Percentile: Top 63%
Advancements in Battery Materials
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