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Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
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On comparing the reactivity of silver and lead, it is observed that the two ionic species, Ag+ (aq) and Pb2+ (aq), show a difference in their redox reactivity towards copper: the silver ion undergoes spontaneous reduction, while the lead ion does not. This relative redox activity can be easily quantified in electrochemical cells by a property called cell potential. This property is commonly known as cell voltage in electrochemistry, and it is a measure of the energy which accompanies the charge...
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A battery is a galvanic cell that is used as a source of electrical power for specific applications. Modern batteries exist in a multitude of forms to accommodate various applications, from tiny button batteries such as those that power wristwatches to the very large batteries used to supply backup energy to municipal power grids. Some batteries are designed for single-use applications and cannot be recharged (primary cells), while others are based on conveniently reversible cell reactions that...
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In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
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EDTA titrations may necessitate masking and demasking agents to temporarily protect a particular metal ion in a mixture from the EDTA reaction. These agents facilitate the sequential analysis of the metal ions by forming stable complexes with some—but not all—metal ions during certain steps.
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Electroactive Chelating Groups Enable High-Performance Aqueous Zinc-Organic Batteries.

Jin Zhou1, Hongbin Xu2, Peifang Guo1

  • 1College of Smart Materials and Future Energy, State Key Laboratory of Coatings for Advanced Equipment, Fudan University, Shanghai, 200438, China.

Angewandte Chemie (International Ed. in English)
|November 3, 2025
PubMed
Summary
This summary is machine-generated.

Introducing electroactive chelating groups enhances p-type organic electrode materials for aqueous zinc-ion batteries (ZIBs). This innovation boosts capacity and cycling stability, overcoming key limitations for practical ZIB applications.

Keywords:
Electroactive chelating groupsOrganic electrodeZinc‐ion batteriesZinc‐supramolecular networks

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Energy Storage

Background:

  • P-type organic electrode materials offer fast kinetics and high redox potential for aqueous zinc-ion batteries (ZIBs).
  • Current limitations include low capacity and poor cycling stability, hindering practical ZIB applications.

Purpose of the Study:

  • To improve the capacity and cycling stability of p-type triphenylamine derivative-based electrodes for ZIBs.
  • To investigate the role of electroactive chelating groups in enhancing electrode performance.

Main Methods:

  • Synthesis of poly(1,4-naphthoquinone-1,3,5-tri(4-aminophenyl)benzene) incorporating electroactive chelating groups.
  • Electrochemical performance testing (capacity, rate capability, cycling stability).
  • In/ex situ spectroscopic analysis and theoretical investigations.

Main Results:

  • The modified electrode exhibits a high reversible capacity of 311 mAh g⁻¹ at 50 mA g⁻¹.
  • Superior rate performance was achieved, with 199 mAh g⁻¹ at 10 A g⁻¹.
  • Exceptional cycling stability was demonstrated, retaining 83%-96% capacity over 5000 cycles.

Conclusions:

  • Electroactive chelating groups significantly enhance capacity and stability in p-type organic electrodes for ZIBs.
  • These groups promote stable zinc-supramolecular network formation, mitigating material dissolution and electrolyte decomposition.
  • The developed material sets a new benchmark for organic electrode materials in high-performance ZIBs.