A Bio‐Inspired Multifunctional Hydrogel Network with Toughly Interfacial Chemistry for Highly Reversible Flexible Zinc Batteries DOI
Song Yang,

Qing Wu,

Yue Li

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(44)

Published: Aug. 8, 2024

Abstract Flexible and high‐performance aqueous zinc‐ion batteries (ZIBs), coupled with low cost safe, are considered as one of the most promising energy storage candidates for wearable electronics. Hydrogel electrolytes present a compelling alternative to liquid due their remarkable flexibility clear advantages in mitigating parasitic side reactions. However, hydrogel suffer from poor mechanical properties interfacial chemistry, which limits them suppressed performance levels flexible ZIBs, especially under harsh strains. Herein, bio‐inspired multifunctional electrolyte network (polyacrylamide (PAM)/trehalose) improved adhesive was developed via simple trehalose network‐repairing strategy stabilize chemistry dendrite‐free long‐life ZIBs. As result, trehalose‐modified PAM exhibits superior strength stretchability up 100 kPa 5338 %, respectively, well strong various substrates. Also, PAM/trehalose provides anti‐corrosion capability Zn anode regulates nucleation/growth, resulting achieving high Coulombic efficiency 98.8 long‐term stability over 2400 h. Importantly, Zn//MnO 2 pouch cell excellent cycling different bending conditions, offers great potential energy‐related applications beyond.

Language: Английский

Cation‐Conduction Dominated Hydrogels for Durable Zinc–Iodine Batteries DOI
Jin‐Lin Yang, Tuo Xiao, Tao Xiao

et al.

Advanced Materials, Journal Year: 2024, Volume and Issue: 36(21)

Published: Feb. 13, 2024

Abstract Zinc–iodine batteries have the potential to offer high energy‐density aqueous energy storage, but their lifetime is limited by rampant dendrite growth and concurrent parasite side reactions on Zn anode, as well shuttling of polyiodides. Herein, a cation‐conduction dominated hydrogel electrolyte designed holistically enhance stability both zinc anode iodine cathode. In this electrolyte, anions are covalently anchored chains, major mobile ions in restricted be 2+ . Specifically, such cation‐conductive results ion transference number (0.81) within guides epitaxial nucleation. Furthermore, optimized solvation structure reconstructed hydrogen bond networks chains contribute reduced desolvation barrier suppressed corrosion reactions. On cathode side, electrostatic repulsion between negative sulfonate groups polyiodides hinders loss active material. This all‐round design renders zinc–iodine with reversibility, low self‐discharge, long lifespan.

Language: Английский

Citations

57

Recent Progress in Using Covalent Organic Frameworks to Stabilize Metal Anodes for Highly‐Efficient Rechargeable Batteries DOI Creative Commons
Jianlu Sun, Fangyuan Kang,

Dongbo Yan

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(28)

Published: May 7, 2024

Alkali metals (e.g. Li, Na, and K) multivalent Zn, Mg, Ca, Al) have become star anodes for developing high-energy-density rechargeable batteries due to their high theoretical capacity excellent conductivity. However, the inevitable dendrites unstable interfaces of metal pose challenges safety stability batteries. To address these issues, covalent organic frameworks (COFs), as emerging materials, been widely investigated regular porous structure, flexible molecular design, specific surface area. In this minireview, we summarize research progress COFs in stabilizing anodes. First, present origins delve into advantages based on physical/chemical properties alkali metals. Then, special attention has paid application host design anodes, artificial solid electrolyte interfaces, additives, solid-state electrolytes, separator modifications. Finally, a new perspective is provided from pore modulation, synthesis COFs.

Language: Английский

Citations

38

Recent advances in zinc-ion dehydration strategies for optimized Zn–metal batteries DOI
Haoyu Li, Sijie Li,

Ruilin Hou

et al.

Chemical Society Reviews, Journal Year: 2024, Volume and Issue: 53(15), P. 7742 - 7783

Published: Jan. 1, 2024

Aqueous Zn-metal batteries have attracted increasing interest for large-scale energy storage owing to their outstanding merits in terms of safety, cost and production. However, they constantly suffer from inadequate density poor cycling stability due the presence zinc ions fully hydrated solvation state. Thus, designing dehydrated structure can effectively address current drawbacks aqueous batteries. In this case, considering lack studies focused on strategies dehydration ions, herein, we present a systematic comprehensive review deepen understanding zinc-ion regulation. Two fundamental design principles component regulation pre-desolvation are summarized environment formation interfacial desolvation behavior. Subsequently, specific strategy based distinct carefully discussed, including preparation methods, working mechanisms, analysis approaches performance improvements. Finally, general summary issues addressed using strategies, four critical aspects promote presented as an outlook, involving updating (de)solvation theories, revealing evolution, enhancing techniques developing functional materials. We believe that will not only stimulate more creativity optimizing electrolytes but also provide valuable insights into other battery systems.

Language: Английский

Citations

38

Advanced electrolytes for high-performance aqueous zinc-ion batteries DOI

Jie Wei,

Pengbo Zhang,

Jingjie Sun

et al.

Chemical Society Reviews, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

This review presents an comprehensive overview of various advanced aqueous electrolytes for zinc-ion batteries, including “water-in-salt” electrolytes, eutectic molecular crowding and hydrogel electrolytes.

Language: Английский

Citations

38

Designing single-ion conductive electrolytes for aqueous zinc batteries DOI
Jin‐Lin Yang, Peihua Yang, Tao Xiao

et al.

Matter, Journal Year: 2024, Volume and Issue: 7(6), P. 1928 - 1949

Published: April 18, 2024

Language: Английский

Citations

28

A Hydrogel Electrolyte with High Adaptability over a Wide Temperature Range and Mechanical Stress for Long‐Life Flexible Zinc‐Ion Batteries DOI
Jingran Zhang,

Chuyuan Lin,

Lingxing Zeng

et al.

Small, Journal Year: 2024, Volume and Issue: 20(30)

Published: March 6, 2024

Abstract Flexible zinc‐ion batteries have garnered significant attention in the realm of wearable technology. However, instability hydrogel electrolytes a wide‐temperature range and uncontrollable side reactions Zn electrode become main problems for practical applications. Herein, N,N‐dimethylformamide (DMF) to design binary solvent (H 2 O‐DMF) is introduced combined it with polyacrylamide (PAM) ZnSO 4 synthesize electrolyte (denoted as PZD). The synergistic effect DMF PAM not only guides 2+ deposition on Zn(002) crystal plane isolates H O from anode, but also breaks hydrogen bonding network between water improve stability electrolytes. Consequently, symmetric cell utilizing PZD can stably cycle over 5600 h at 0.5 mA cm − @0.5 mAh −2 . Furthermore, Zn//PZD//MnO full exhibits favorable adaptability (for 16000 cycles 3 A g −1 under 25 °C, 750 98 0.1 ‐20 °C) outstanding mechanical properties lighting up LEDs conditions pressure, bending, cutting, puncture). This work proposes useful modification designing high‐performance electrolyte, which provides reference investigating flexible aqueous batteries.

Language: Английский

Citations

25

Constructing Lysozyme Protective Layer via Conformational Transition for Aqueous Zn Batteries DOI
Yifan Pan, Zhicheng Zuo, Yucong Jiao

et al.

Advanced Materials, Journal Year: 2024, Volume and Issue: 36(29)

Published: May 8, 2024

The practical applications for aqueous Zn ion batteries (ZIBs) are promising yet still impeded by the severe side reactions on metal. Here, a lysozyme protective layer (LPL) is prepared metal surface simple and facile self-adsorption strategy. LPL exhibits extremely strong adhesion to provide stable interface during long-term cycling. In addition, strategy triggered hydrophobicity-induced aggregation effect endows with gap-free compacted morphology which can reject free water effective reaction inhibition performance. More importantly, conformation transformed from α-helix β-sheet structure before formation, thus abundant functional groups exposed interact

Language: Английский

Citations

25

Polyelectrolyte Membrane Enables Highly Reversible Zinc Battery Chemistry via Immobilizing Anion and Stabilizing Water DOI
Yubin He, Rui Zhang, Peichao Zou

et al.

Journal of the American Chemical Society, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 17, 2025

The integration of water-based electrolytes into zinc-ion batteries encounters challenges due to the limited voltage window water, interfacial side reactions mobile counterions, and growth zinc metal (Zn0) dendrites during charge. In this study, we introduce a nonfluorinated, cation-conducting polyelectrolyte membrane (PEM) designed alleviate these by suppressing reactivities both water counterions. This PEM forms hydrogen bonds with molecules through its proton-accepting chains, thus shifting lowest unoccupied molecular orbital (LUMO) energy from −0.37 −0.14 eV inducing negative shift in onset potential for evolution 110 mV. Additionally, it immobilizes counteranions onto polymer backbones via covalent bonding, hence making Zn2+ transference number nearly unity (0.96). Meanwhile, high modulus establishes solid-state diffusion barrier homogenize flux, leading 3D in-plane compact Zn0 plating within (002) plane. Atomic resolution scanning transmission electron microscopy (STEM) reveals corrosion-free deposition without electrolyte degradation, while operando transition X-ray (TXM) further illustrates real-time dendrite-free process at 5 mA/cm2. Consequently, unique properties water-binding anion-tethering enable enhanced electrochemical performance employing highly fluorinated expensive anions. demonstrates durability 3800 h Zn0–Zn0 symmetric cells lifetime 6000 cycles Zn0–LiV3O8 full cells.

Language: Английский

Citations

2

Improvements and Challenges of Hydrogel Polymer Electrolytes for Advanced Zinc Anodes in Aqueous Zinc-Ion Batteries DOI
Huili Peng, Dongdong Wang, Fenglong Zhang

et al.

ACS Nano, Journal Year: 2024, Volume and Issue: 18(33), P. 21779 - 21803

Published: Aug. 12, 2024

Aqueous zinc-ion batteries (AZIBs) are widely regarded as desirable energy storage devices due to their inherent safety and low cost. Hydrogel polymer electrolytes (HPEs) cross-linked polymers filled with water zinc salts. They not only used in flexible but also represent an ideal electrolyte candidate for addressing the issues associated Zn anode, including dendrite formation side reactions. In HPEs, abundance of hydrophilic groups can form strong hydrogen bonds molecules, reducing activity inhibiting decomposition. At same time, special

Language: Английский

Citations

13

In‐Situ Spontaneous Electropolymerization Enables Robust Hydrogel Electrolyte Interfaces in Aqueous Batteries DOI
Liangyuan Chen, Tuo Xiao, Jin‐Lin Yang

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(21)

Published: March 23, 2024

Abstract Hydrogels hold great promise as electrolytes for emerging aqueous batteries, which establishing a robust electrode‐hydrogel interface is crucial mitigating side reactions. Conventional hydrogel fabricated by ex situ polymerization through either thermal stimulation or photo exposure cannot ensure complete interfacial contact with electrodes. Herein, we introduce an in electropolymerization approach constructing electrolytes. The spontaneously generated during the initial cycling of battery, eliminating need additional initiators polymerization. involvement electrodes synthesis yields well‐bonded and deep infiltrated electrode‐electrolyte interfaces. As case study, attest that, situ‐formed polyanionic Zn‐MnO 2 battery substantially improves stability kinetics both Zn anode porous MnO cathode owing to This research provides insight function electrolyte interfaces constitutes critical advancement designing highly durable batteries.

Language: Английский

Citations

11