High Na‐ion conductivity and mechanical integrity of anion‐exchanged polymeric hydrogel electrolytes for flexible sodium ion hybrid energy storage

Author:

Hong Jung Woo1,Rana Harpalsinh H.1,Park Jeong Hee1,Kim Jun Su1,Lee Sang Joon1,Jang Gun1,Kang Tae Hoon1,Shin Kang Ho1,Baek Sang Ha1,Yang Wooseok1234,Kim Kwang Ho123,Lee Ju‐Hyuk5,Park Ho Seok12346

Affiliation:

1. School of Chemical Engineering Sungkyunkwan University Suwon Republic of Korea

2. Clean Energy Research Center Korea Institute of Science and Technology (KIST) Seoul Republic of Korea

3. KIST‐SKKU Carbon‐Neutral Research Center Sungkyunkwan University (SKKU) Suwon Republic of Korea

4. SKKU Institute of Energy Science and Technology (SIEST) Sungkyunkwan University Suwon Republic of Korea

5. COSMOS LAB / 92 Jomaru‐ro 385beon‐gil Bucheon‐si Republic of Korea

6. SKKU Advanced Institute of Nano Technology (SAINT) Sungkyunkwan University Suwon Republic of Korea

Abstract

AbstractThe polymeric gel electrolytes are attractive owing to their higher ionic conductivities than those of dry polymer electrolytes and lowered water activity for enlarged potential window. However, the ionic conductivity and mechanical strength of the Na‐ion conducting polymeric gel electrolytes are limited by below 20 mS cm−1 and 2.2 MPa. Herein, we demonstrate Na‐ion conducting and flexible polymeric hydrogel electrolytes of the chemically coupled poly(diallyldimethylammonium chloride)‐dextrin‐N,N′‐methylene‐bis‐acrylamide film immersed in NaClO4 solution (ex‐DDA‐Dex + NaClO4) for flexible sodium‐ion hybrid capacitors (f‐NIHC). In particular, the anion exchange reaction and synergistic interaction of ex‐DDA‐Dex with the optimum ClO4 enable to greatly improve the ionic conductivity up to 27.63 mS cm−1 at 25°C and electrochemical stability window up to 2.6 V, whereas the double networking structure leads to achieve both the mechanical strength (7.48 MPa) and softness of hydrogel electrolytes. Therefore, the f‐NIHCs with the ex‐DDA‐Dex + NaClO4 achieved high specific and high‐rate capacities of 192.04 F g−1 at 500 mA g−1 and 116.06 F g−1 at 10 000 mA g−1, respectively, delivering a large energy density of 120.03 W h kg−1 at 906 W kg−1 and long cyclability of 70% over 500 cycles as well as demonstrating functional operation under mechanical stresses.

Funder

National Research Foundation

Korea Institute for Advancement of Technology

Publisher

Wiley

Subject

General Medicine

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