Abstract

Research on entropy-stabilized oxides (ESO) [1] has primarily focused on exploring new single-phase structures with diverse chemistries, or unique properties, such as high Li-ion conductivity, high dielectric constant, low thermal conductivity, good electrochemical cycling stability, and high storage capacity retention [2]. However, few studies discuss the impact of secondary phase formation on functionality such as electrical conductivity [3] despite the fact that annealing this single-phase ESO causes it to undergo a phase transformation leading to the formation of Cu-rich and Co-rich secondary phases [4]. To address this gap, this work [5] investigates the electrical transport mechanisms in the canonical entropy-stabilized oxide (Co,Cu,Mg,Ni,Zn)O as a function of secondary phase content. Here, the structure and composition of single-phase and multiphase ESOs, and their GBs and HIs are probed using atomic-resolution imaging by scanning transmission electron microscopy (STEM) coupled with nanoscale spectroscopy by electron energy-dispersive spectroscopy (EDS) and electron energy-loss spectroscopy (EELS). Our findings suggest that when single-phase, the oxide is an oxygen ion conductor. After 2 h of heat treatment, Cu-rich tenorite particles form at some grain boundaries, turning the grain interior rocksalt oxide into a mixed ionic-electronic conductor via oxygen ions and small hole polaron Co2+/Co3+ and Cu2+/Cu+ pairs. 24 h of heat treatment leads to the full coverage of Cu-rich tenorite particles at all grain boundaries and the formation of anisotropic Cu-rich tenorite and equiaxed Co-rich spinel particles in the grains. While the grain interiors exhibit similar mixed ionic-electronic conduction, Cu-rich tenorite grain boundary phases create a pathway for Cu2+/Cu3+ small hole polarons. The ability to selectively grow secondary phases nucleated at grain boundaries enables tuning of electrical properties in entropy-stabilized and complex concentrated oxides using microstructure design, nanoscale engineering, and heat treatment, paving the way to develop many novel materials.[1] C. M. Rost, J.-P. Maria, Nat Commun, 2015.[2] A. Salian, S. Mandal, Critical Reviews in Solid State and Materials Sciences, 2022.[3] M. Moździerz, K. Świerczek, Acta Materialia, 2021.[4] A. D. Dupuy, J. M. Schoenung, Journal of the European Ceramic Society, 2021.[5] H. Vahidi...W. J. Bowman (submitted). Acknowledgments This research was primarily supported by the National Science Foundation Materials Research Science and Engineering Center program through the UC Irvine Center for Complex and Active Materials (DMR-2011967). WJB and HV acknowledge partial support from the UCI new faculty startup funding. The authors acknowledge the use of facilities and instrumentation at the UC Irvine Materials Research Institute (IMRI) supported in part by the National Science Foundation Materials Research Science and Engineering Center program through the UC Irvine Center for Complex and Active Materials (DMR-2011967).

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