<p>Designing novel conducting polymers as energy storage materials is a viable route to construct energy storage devices with high performance. Here, 1,10-phenanthroline and its derivatives (5-amino-1,10-phenanthroline and 1,10-phenanthroline-5,6-dione) are electropolymerized in aqueous electrolytes under anodic potentials. All polymers exhibit layered morphology, but with different contents of O and N in the structure. Three aqueous electrolytes, 1&#xa0;M H<sub>2</sub>SO<sub>4</sub>, 1&#xa0;M ZnSO<sub>4</sub>, and 1&#xa0;M Na<sub>2</sub>SO<sub>4</sub>, are chosen to investigate the charge storage performance of these polymers. The poly(1,10-phenanthroline-5,6-dione) (PPD/CP) exhibits the best performance in all three electrolytes, with 146.3 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup> in 1&#xa0;M H<sub>2</sub>SO<sub>4</sub>. The high specific capacity arises from the plentiful redox-active sites available. The cycling stability of these polymers is systematically evaluated. All polymers exhibit battery-type behavior in aqueous electrolytes. The charge storage mechanism of PPD/CP is investigated, revealing that the process involves redox reactions of amino/imino and hydroxyl/carbonyl functional groups, accompanied by the reversible insertion and extraction of cations. A two-electrode device using PPD/CP, a zinc foil, and 1&#xa0;M ZnSO<sub>4</sub> is assembled and exhibits a specific capacity of 154.2 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup>. The device achieves an energy density of 71.25 Wh kg<sup>−1</sup> at a power density of 450 W kg<sup>−1</sup>. A capacity retention of 81.9% is maintained after 2000 cycles at a current density of 5 A g<sup>−1</sup>.</p>

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Electropolymerization of 1,10-phenanthroline derivatives and their electrochemical energy storage properties in aqueous electrolytes

  • Shuling Liu,
  • Gege Feng,
  • Yihao Li,
  • Jiatuo Li,
  • Yuhang Cao,
  • Chao Wang

摘要

Designing novel conducting polymers as energy storage materials is a viable route to construct energy storage devices with high performance. Here, 1,10-phenanthroline and its derivatives (5-amino-1,10-phenanthroline and 1,10-phenanthroline-5,6-dione) are electropolymerized in aqueous electrolytes under anodic potentials. All polymers exhibit layered morphology, but with different contents of O and N in the structure. Three aqueous electrolytes, 1 M H2SO4, 1 M ZnSO4, and 1 M Na2SO4, are chosen to investigate the charge storage performance of these polymers. The poly(1,10-phenanthroline-5,6-dione) (PPD/CP) exhibits the best performance in all three electrolytes, with 146.3 mAh g−1 at 1 A g−1 in 1 M H2SO4. The high specific capacity arises from the plentiful redox-active sites available. The cycling stability of these polymers is systematically evaluated. All polymers exhibit battery-type behavior in aqueous electrolytes. The charge storage mechanism of PPD/CP is investigated, revealing that the process involves redox reactions of amino/imino and hydroxyl/carbonyl functional groups, accompanied by the reversible insertion and extraction of cations. A two-electrode device using PPD/CP, a zinc foil, and 1 M ZnSO4 is assembled and exhibits a specific capacity of 154.2 mAh g−1 at 1 A g−1. The device achieves an energy density of 71.25 Wh kg−1 at a power density of 450 W kg−1. A capacity retention of 81.9% is maintained after 2000 cycles at a current density of 5 A g−1.