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Spontaneous redox reactions occur abundantly in nature. The chemical reaction occurring in a disposable AA battery powering our remote controls is one such example of a spontaneous redox reaction. Another example is the immersion of coiled copper wire into an aqueous silver nitrate solution. The reaction shows a gradual, visually impressive color change from colorless to bright blue and the formation of a grey precipitate on the copper wire. In this experiment,...
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Interphase Self-Optimization Enables Stable Magnesium Anode in Hydrogel Electrolyte.

Xinyuan Zhang1,2,3, Hengyue Xu4, Heng Jiang3

  • 1School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore, Singapore.

Advanced Materials (Deerfield Beach, Fla.)
|March 24, 2026
PubMed
Summary
This summary is machine-generated.

Researchers developed a novel hydrogel electrolyte to stabilize magnesium anodes in aqueous batteries. This innovation prevents corrosion and passivation, enabling stable magnesium plating and stripping for long-term battery performance.

Keywords:
aqueous electrolytesdynamic interfacehydrogel electrolytesion‐conductive interphasemagnesium batteriesmetal anode protection

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Energy Storage

Background:

  • Magnesium (Mg) metal is a cost-effective anode for high-energy aqueous batteries.
  • Mg anodes suffer from severe corrosion and passivation, limiting their practical application.
  • Existing strategies to mitigate these issues have limited effectiveness or sacrifice active metal.

Purpose of the Study:

  • To develop a stable and efficient Mg anode for aqueous batteries.
  • To address the challenges of corrosion and surface passivation in Mg anodes.
  • To enable long-term cycling stability in Mg-based energy storage systems.

Main Methods:

  • Formulation of a hydrogel electrolyte containing a tridentate chelant and MgCl2.
  • Investigation of the anode-electrolyte interface dynamics.
  • Testing of Mg anode performance in symmetric cells and hybrid cells with different cathodes.

Main Results:

  • A self-optimized, dynamic, Mg2+-conductive interphase (magnesium oxychloride) was formed on the Mg anode surface.
  • The hydrogel electrolyte mitigated parasitic reactions and enabled complete conversion of MgO byproduct.
  • Reversible Mg plating/stripping was achieved for over 600 hours in symmetric cells.
  • Hybrid cells demonstrated stable cycling for up to 500 cycles with 69% capacity retention.

Conclusions:

  • The developed hydrogel electrolyte effectively stabilizes the Mg anode by forming a dynamic interphase.
  • This approach overcomes the limitations of previous strategies for Mg anode protection.
  • The findings pave the way for high-energy, cost-effective, and stable aqueous magnesium batteries.