J. Mater. Sci. Technol. ›› 2025, Vol. 231: 256-269.DOI: 10.1016/j.jmst.2025.01.020

• Research article • Previous Articles     Next Articles

Enhancing corrosion resistance of Mg-Alloys by regulating precipitates at grain boundaries using rare earth oxides

Wei Chena,*, Chenyang Gonga, Peipei Jiangb, Lang Gana, Yanjie Renc, Cong Lia, Jian Chena, Wei Qiua,*   

  1. aSchool of Energy and Power Engineering, Changsha University of Science & Technology, Changsha 410114, China;
    bSchool of Resources Environment and Safety Engineering, University of South China, Hengyang 421001, China;
    cSchool of Mechanical & Energy Engineering, Zhejiang University of Science & Technology, Hangzhou 310023, China
  • Received:2024-11-19 Revised:2025-01-10 Accepted:2025-01-10 Published:2025-10-01 Online:2025-02-26
  • Contact: *E-mail addresses: weichen@csust.edu.cn (W. Chen), yekyek2009@126.com(W. Qiu).

Abstract: This study delved into the corrosion behavior of ZK60 Mg alloy in saturated NaCl solution, particularly focusing on the effects of the addition of rare earth oxide, namely CeO2 (forming ZKC alloy) and La2O3 (forming ZKL alloy). The results indicate that the introduction of CeO2 and La2O3 promotes the precipitation of T-(Mg1-x, Znx)11RE phases (Mg-Zn-RE phases, where RE represents Ce or La) at grain boundaries. The presence and distribution pattern of the T-phase have a profound impact on the corrosion resistance of the Mg alloy. Specifically, the ZKC alloy exhibits the most outstanding corrosion resistance. This superior performance is attributed to the uniform distribution of (Mg1-x, Znx)11Ce phase at grain boundaries in ZK60-0.5 wt% CeO2, effectively hindering the penetration of corrosive media into the matrix. Additionally, scanning kelvin probe force microscopy (SKPFM) analysis reveals that the (Mg1-x, Znx)11Ce phase exhibits the smallest potential difference with the matrix, significantly mitigating the tendency for galvanic corrosion. In contrast, the ZKL alloy displays less precipitation and uneven distribution of the (Mg1-x, Znx)11La phase, resulting in inferior corrosion resistance compared to the ZKC alloy. The disparities in the precipitation of the two phases, as derived from first-principles calculations, stem from the spontaneous reduction of CeO2 under Mg conditions, whereas the reduction reaction between La2O3 and Mg cannot proceed spontaneously. Furthermore, SKPFM analysis and CALPHAD method found that as the addition of CeO2/La2O3 increases, the atomic ratio of Zn in the Mg-Zn-RE ternary phase rises, accompanied by an increase in the potential difference between the Mg-Zn-RE phase and the Mg matrix. This suggests that fine-tuning the addition of rare earth oxides can modify the atomic ratio of the Mg-Zn-RE ternary phase, thereby enhancing the corrosion resistance of the Mg alloy. In summary, this study not only unravels the specific mechanisms of how CeO2 and La2O3 affect the corrosion behavior of ZK60 Mg alloy but also provides new strategies and insights for the development of low-cost, high-performance corrosion-resistant Mg alloy materials.

Key words: Mg alloy, Rare earth oxide, Corrosion behavior, T-Phase, SKPFM