Hydroxide ion-conducting viologen-bakelite organic frameworks for flexible solid-state zinc-air battery applications

Adaptable polymer-based solid-state electrolytes can be a game-changer toward safe, lightweight flexible batteries. We present a robust Bakelite-type organic polymer covalently decked with viologen, triazine, and phenolic moieties. Its flexible structure with cationic viologen centers incorporates c...

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Veröffentlicht in:Nanoscale horizons 2023-01, Vol.8 (2), p.224-234
Hauptverfasser: Rase, Deepak, Illathvalappil, Rajith, Singh, Himan Dev, Shekhar, Pragalbh, Leo, Liya S, Chakraborty, Debanjan, Haldar, Sattwick, Shelke, Ankita, Ajithkumar, Thalasseril G, Vaidhyanathan, Ramanathan
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container_issue 2
container_start_page 224
container_title Nanoscale horizons
container_volume 8
creator Rase, Deepak
Illathvalappil, Rajith
Singh, Himan Dev
Shekhar, Pragalbh
Leo, Liya S
Chakraborty, Debanjan
Haldar, Sattwick
Shelke, Ankita
Ajithkumar, Thalasseril G
Vaidhyanathan, Ramanathan
description Adaptable polymer-based solid-state electrolytes can be a game-changer toward safe, lightweight flexible batteries. We present a robust Bakelite-type organic polymer covalently decked with viologen, triazine, and phenolic moieties. Its flexible structure with cationic viologen centers incorporates counter-balancing free hydroxide ions into the polymeric framework. By design, the aromatic groups and heteroatoms in the framework can be activated under an applied potential to prompt a push-pull drive, setting off the towing of hydroxide ions via weak electrostatic, van der Waals, and hydrogen-bond interactions. The frontier orbitals from a DFT-modeled structure certify this. The hydroxyl-polymer requires minimal KOH wetting to maintain a humid environment for Grotthuss-type transport. The hydroxide ion conductivity reaches a value of 1.4 × 10 −2 S cm −1 at 80 °C and 95% RH, which is retained for over 15 h. We enhanced its practical utility by coating it as a thin solid-state separator-cum-electrolyte on readily available filter paper. The composite exhibits a conductivity of 4.5 × 10 −3 S cm −1 at 80 °C and 95% RH. A zinc-air battery (ZAB) constructed using this polymer-coated paper as electrolyte yields a maximum power density of 115 mW cm −2 and high specific capacitance of 435 mA h g −1 . The power density recorded for our ZAB is among the best reported for polymer electrolyte-based batteries. Subsequently, the flexible battery fabricated with IISERP-POF11_OH@FilterPaper exhibits an OCV of 1.44 V, and three batteries in series power a demo traffic signal. To underscore the efficiency of hydroxide ion transport through the complex multifunctional backbone of the polymer, we calculated the diffusion coefficient for OH − (Exp: 2.9 × 10 −5 cm 2 s −1 ; Comp. 5.2 × 10 −6 cm 2 s −1 ) using electrochemical methods and MD simulations. Climbing-edge NEB calculations reveal a large energy barrier of 2.11 eV for Zn 2+ to penetrate the polymer and identify hydroxide ions within the polymer, suggesting no undesirable Zn 2+ crossover. Our findings assert the readily accessible C-C-linked cationic polymer's capacity as a solid-state electrolyte for ZABs and any anion-conducting membrane. A cationic bakelite-viologen polymer with counter-balancing hydroxide ions serves as a solid-state electrolyte for zinc-air battery.
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We present a robust Bakelite-type organic polymer covalently decked with viologen, triazine, and phenolic moieties. Its flexible structure with cationic viologen centers incorporates counter-balancing free hydroxide ions into the polymeric framework. By design, the aromatic groups and heteroatoms in the framework can be activated under an applied potential to prompt a push-pull drive, setting off the towing of hydroxide ions via weak electrostatic, van der Waals, and hydrogen-bond interactions. The frontier orbitals from a DFT-modeled structure certify this. The hydroxyl-polymer requires minimal KOH wetting to maintain a humid environment for Grotthuss-type transport. The hydroxide ion conductivity reaches a value of 1.4 × 10 −2 S cm −1 at 80 °C and 95% RH, which is retained for over 15 h. We enhanced its practical utility by coating it as a thin solid-state separator-cum-electrolyte on readily available filter paper. The composite exhibits a conductivity of 4.5 × 10 −3 S cm −1 at 80 °C and 95% RH. A zinc-air battery (ZAB) constructed using this polymer-coated paper as electrolyte yields a maximum power density of 115 mW cm −2 and high specific capacitance of 435 mA h g −1 . The power density recorded for our ZAB is among the best reported for polymer electrolyte-based batteries. Subsequently, the flexible battery fabricated with IISERP-POF11_OH@FilterPaper exhibits an OCV of 1.44 V, and three batteries in series power a demo traffic signal. To underscore the efficiency of hydroxide ion transport through the complex multifunctional backbone of the polymer, we calculated the diffusion coefficient for OH − (Exp: 2.9 × 10 −5 cm 2 s −1 ; Comp. 5.2 × 10 −6 cm 2 s −1 ) using electrochemical methods and MD simulations. Climbing-edge NEB calculations reveal a large energy barrier of 2.11 eV for Zn 2+ to penetrate the polymer and identify hydroxide ions within the polymer, suggesting no undesirable Zn 2+ crossover. Our findings assert the readily accessible C-C-linked cationic polymer's capacity as a solid-state electrolyte for ZABs and any anion-conducting membrane. 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We present a robust Bakelite-type organic polymer covalently decked with viologen, triazine, and phenolic moieties. Its flexible structure with cationic viologen centers incorporates counter-balancing free hydroxide ions into the polymeric framework. By design, the aromatic groups and heteroatoms in the framework can be activated under an applied potential to prompt a push-pull drive, setting off the towing of hydroxide ions via weak electrostatic, van der Waals, and hydrogen-bond interactions. The frontier orbitals from a DFT-modeled structure certify this. The hydroxyl-polymer requires minimal KOH wetting to maintain a humid environment for Grotthuss-type transport. The hydroxide ion conductivity reaches a value of 1.4 × 10 −2 S cm −1 at 80 °C and 95% RH, which is retained for over 15 h. We enhanced its practical utility by coating it as a thin solid-state separator-cum-electrolyte on readily available filter paper. The composite exhibits a conductivity of 4.5 × 10 −3 S cm −1 at 80 °C and 95% RH. A zinc-air battery (ZAB) constructed using this polymer-coated paper as electrolyte yields a maximum power density of 115 mW cm −2 and high specific capacitance of 435 mA h g −1 . The power density recorded for our ZAB is among the best reported for polymer electrolyte-based batteries. Subsequently, the flexible battery fabricated with IISERP-POF11_OH@FilterPaper exhibits an OCV of 1.44 V, and three batteries in series power a demo traffic signal. To underscore the efficiency of hydroxide ion transport through the complex multifunctional backbone of the polymer, we calculated the diffusion coefficient for OH − (Exp: 2.9 × 10 −5 cm 2 s −1 ; Comp. 5.2 × 10 −6 cm 2 s −1 ) using electrochemical methods and MD simulations. Climbing-edge NEB calculations reveal a large energy barrier of 2.11 eV for Zn 2+ to penetrate the polymer and identify hydroxide ions within the polymer, suggesting no undesirable Zn 2+ crossover. Our findings assert the readily accessible C-C-linked cationic polymer's capacity as a solid-state electrolyte for ZABs and any anion-conducting membrane. 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We present a robust Bakelite-type organic polymer covalently decked with viologen, triazine, and phenolic moieties. Its flexible structure with cationic viologen centers incorporates counter-balancing free hydroxide ions into the polymeric framework. By design, the aromatic groups and heteroatoms in the framework can be activated under an applied potential to prompt a push-pull drive, setting off the towing of hydroxide ions via weak electrostatic, van der Waals, and hydrogen-bond interactions. The frontier orbitals from a DFT-modeled structure certify this. The hydroxyl-polymer requires minimal KOH wetting to maintain a humid environment for Grotthuss-type transport. The hydroxide ion conductivity reaches a value of 1.4 × 10 −2 S cm −1 at 80 °C and 95% RH, which is retained for over 15 h. We enhanced its practical utility by coating it as a thin solid-state separator-cum-electrolyte on readily available filter paper. The composite exhibits a conductivity of 4.5 × 10 −3 S cm −1 at 80 °C and 95% RH. A zinc-air battery (ZAB) constructed using this polymer-coated paper as electrolyte yields a maximum power density of 115 mW cm −2 and high specific capacitance of 435 mA h g −1 . The power density recorded for our ZAB is among the best reported for polymer electrolyte-based batteries. Subsequently, the flexible battery fabricated with IISERP-POF11_OH@FilterPaper exhibits an OCV of 1.44 V, and three batteries in series power a demo traffic signal. To underscore the efficiency of hydroxide ion transport through the complex multifunctional backbone of the polymer, we calculated the diffusion coefficient for OH − (Exp: 2.9 × 10 −5 cm 2 s −1 ; Comp. 5.2 × 10 −6 cm 2 s −1 ) using electrochemical methods and MD simulations. Climbing-edge NEB calculations reveal a large energy barrier of 2.11 eV for Zn 2+ to penetrate the polymer and identify hydroxide ions within the polymer, suggesting no undesirable Zn 2+ crossover. Our findings assert the readily accessible C-C-linked cationic polymer's capacity as a solid-state electrolyte for ZABs and any anion-conducting membrane. 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source Royal Society Of Chemistry Journals
subjects Bakelite
Cationic polymerization
Diffusion coefficient
Electrolytes
Filter paper
Flexible structures
Hydrogen bonds
Ion transport
Ions
Maximum power density
Metal air batteries
Molten salt electrolytes
Polymer coatings
Polymers
Solid electrolytes
Solid state
Traffic signals
Vinyl resins
Wetting
Zinc-oxygen batteries
title Hydroxide ion-conducting viologen-bakelite organic frameworks for flexible solid-state zinc-air battery applications
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