Abstract
The reversibility of phase transformation influences the functionality of electrode materials in batteries. In many battery materials, nanosized grains favor phase reversibility but at the cost of cyclability due to aggravated side reactions with the electrolyte. In this study, we present a novel approach to enhance the phase transformation reversibility of layered oxide cathodes, exemplified by Na2/3Fe1/2Mn1/2O2 through proton irradiation. In addition to forming defects, proton irradiation at sufficiently high doses can subdivide single grains into multiple nanodomains without physically rupturing them. Hence, the single grains of the material assume a pseudo-secondary particle nature without reducing the overall grain size. Preserving the grain size is advantageous, as it reduces side reactions, which is not possible with conventional grain size reduction methods. While chemical transformations and defect formation induced through proton irradiation can influence the stability of battery materials, it is expected that structural reorganization due to cycling-induced phase transformation will be contained within these nanodomains. Such confinement of phase transformation is potentially responsible for enhancing the reversibility of layered oxide materials in our study. Thus, our study suggests that grain subdivision could become an effective microstructure tuning strategy for managing electrochemical cycling-induced phase changes in battery electrodes.
| Original language | English |
|---|---|
| Pages (from-to) | 5106-5114 |
| Number of pages | 9 |
| Journal | Journal of Materials Chemistry A |
| Volume | 14 |
| Issue number | 9 |
| DOIs | |
| State | Published - Feb 5 2026 |
Funding
This work was supported by The Thomas F. and Kate Miller Jeffress Memorial Trust, Bank of America, Trustee, and the Jeffress Trust Awards Program in Interdisciplinary Research. The Na cathode was developed based on a project funded by the National Science Foundation (No. CBET-1912885). This research uses beamline 7-BM at the National Synchrotron Light Source II, a US DOE Office of Science user facility operated for the DOE Office of Science by Brookhaven National Laboratory under contract number DE-SC0012704. This work used resources of the Center for Functional Nanomaterials (CFN), a U.S. Department of Energy Office of Science User Facility at Brookhaven National Laboratory under Contract No. DE-SC0012704. This work also used beamlines 10-1 and 11-3 at the Stanford Synchrotron Radiation Lightsource, a Directorate of SLAC National Accelerator Laboratory and an Office of Science User Facility. Use of the Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, is supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences under Contract No. DE-AC02-76SF00515. This research used beamline 34-ID-C at the Advanced Photon Source; an Office of Science User Facility operated for the U.S. Department of Energy (DOE) Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. The irradiation work was performed at the Center for Integrated Nanotechnologies (CINT) through User Proposal #2019AU0116, an Office of Science User Facility operated for the U.S. Department of Energy (DOE) Office of Science. Los Alamos National Laboratory, an affirmative action equal opportunity employer, is managed by Triad National Security, LLC for the U.S. Department of Energy's NNSA, under contract 89233218CNA000001.
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