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Updated: Jan 9, 2026

In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries
Published on: November 10, 2014
Addressing first cycle irreversible capacity in lithium-rich layered oxides by blending with delithiated active
Dimitrios Chatzogiannakis1,2,3, Violetta Arszelewska4, Pierre-Etienne Cabelguen4
1Institut de Ciència de Materials de Barcelona, ICMAB-CSIC Campus UAB, 08193 Bellaterra Catalonia Spain rosa.palacin@icmab.es.
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Lithium-rich oxides (LRO), derived from NMC-type materials, are among the most promising next-generation positive electrode candidates for lithium-ion batteries. Despite their potential, their practical application is hinderend by inherently low first-cycle coulombic efficency, caused by the irreversible loss of lithium. In this work, we address this drawback by chemically delithiating secondary active materials - LiMn2O4 (LMO) or LiFePO4- and subsequentyly blending them with the cobalt-free lithium rich oxide Li1.15Ni0.3Mn0.55O2. The incorporation of these delithiated components improves not only first-cycle efficiency but also capacity retention, with the degree of enhancement proportional to the fraction of added material. Differential scanning calorimetry (DSC) further reveals improved thermal stability for LRO:FePO4 blends evidenced by a higher decomposition temperature and lower overall heat released. In contrast, blending LRO with λ-MnO2 blends results in a detrimental effect related to increased moisture sensitivity. Operando synchrotron X-ray diffraction on blended electrodes confirms that the secondary active material actively participates in the electrochemical processes. Our findings demonstrate a simple and industry-compatible strategy to mitigate one of the major drawbacks of LROs, paving the way for more sustainable and high performance lithium-ion batteries.
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