4.8 Article

Natural Polysaccharide Strengthened Hydrogel Electrolyte and Biopolymer Derived Carbon for Durable Aqueous Zinc Ion Storage

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 20, 页码 23452-23464

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c03323

关键词

hydrogel electrolyte; polysaccharide; N-doped carbon microsphere; zinc-ion hybrid supercapacitor; dendrite suppression

资金

  1. National Natural Science Foundation of China [21805237, 21965033, U2003216, U2003132, U2003123]
  2. Natural Science Foundation of Xinjiang Uygur Autonomous Region [2022D01C25, 2019D01C075, 2020D01C021]
  3. Opening Foundation of the State Key Laboratory of Fine Chemicals [KF2003]
  4. Tianchi Doctor Program of Education Department of Xinjiang Uygur Autonomous Region, Talents Project Key Training Object Project of Urumqi
  5. Doctor Starting Fund of Xinjiang University

向作者/读者索取更多资源

In this study, a natural polysaccharide strengthened hydrogel electrolyte and a biopolymer-derived N-doped carbon microsphere cathode material were developed for aqueous zinc-ion hybrid supercapacitors (ZHSCs), demonstrating excellent performance.
Aqueous zinc-ion hybrid supercapacitors (ZHSCs) represent one of the current research subjects because of their flame retardancy, ease of manufacturing, and exceptional roundtrip efficiency. With the evolution into real useful energy storage cells, the bottleneck factors of the corrosion and dendrite growth problems must be properly resolved for largely boosting their cycling life and energy efficiency. Herein, a natural polysaccharide strengthened hydrogel electrolyte (denoted as PAAm/agar/Zn(CF3SO3)(2)) was engineered by designing an asymmetric dual network of covalently cross-linked polyacrylamide (denoted as PAAm) and physically cross-linked loose polysaccharide (e.g., agar) followed by intense uptake of Zn(CF3SO3)(2) aqueous electrolyte. In this polymeric matrix, the PAAm chains are responsible for constructing the soft domains to immobilize the water molecules, and the agar component boosts the mechanical performance (by using its inherent reversible sacrificial bonds) and favors the electrolyte ion transport. Due to these reasons, the as-designed hydrogel electrolyte effectively inhibits the zinc dendrite growth, realizes the uniform Zn deposition, and affords a satisfactory ionic conductivity of 1.55 S m(-1), excellent tensile strength (78.9 kPa at 507.7% stretchable), and high compression strength (118.0 kPa at 60.0% strain). Additionally, a biopolymer-derived N-doped carbon microsphere cathode material with a highly interconnected porous carbonaceous network (denoted as NC) was also synthesized, which delivers a high capacity of 92.8 mAh g(-1), along with superb rate capability and long duration cycling lifespan (95.4% retention for 10000 cycles) in the aqueous Zn//NC ZHSC. More notably, with integrated merits of the PAAm/agar/Zn(CF3SO3)(2) hydrogel electrolyte and NC, the as-built quasi-solid-state ZHSC achieves a high specific capacity of 73.4 mAh g(-1) and superior energy density of 61.3 Wh kg(-1) together with excellent cycling stability for 10000 cycles. This work demonstrated favorable practicability in the structural design of the hydrogel electrolytes and electrode materials for advanced ZHSC applications.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据