Emerging aqueous manganese-based batteries: Fundamental understanding, challenges, and opportunities DOI Open Access

Jiafeng Lei,

Liwei Jiang, Yi‐Chun Lu

et al.

Chemical Physics Reviews, Journal Year: 2023, Volume and Issue: 4(2)

Published: May 22, 2023

Aqueous manganese (Mn)-based batteries are promising candidates for grid-scale energy storage due to their low-cost, high reversibility, and intrinsic safety. However, further development is impeded by controversial reaction mechanisms low density with unsatisfactory cycling stability. Here, we summarized various types of emerging aqueous Mn-based based on the active redox couples, including liquid–solid deposition/dissolution reactions Mn0/Mn2+ Mn2+/MnO2, liquid–liquid conversion Mn2+/Mn3+ MnO42−/MnO4−, solid–solid intercalation XMnOy/MnOy (X: cations) oxide as host materials. A critical review fundamental understanding physicochemical properties in each reaction, scientific challenges, improvement strategies presented. Finally, perspectives design future commercialization highlighted.

Language: Английский

Nanomicellar Electrolyte To Control Release Ions and Reconstruct Hydrogen Bonding Network for Ultrastable High-Energy-Density Zn–Mn Battery DOI
Yongqi Deng, Hongfei Wang,

Ming‐Hui Fan

et al.

Journal of the American Chemical Society, Journal Year: 2023, Volume and Issue: 145(36), P. 20109 - 20120

Published: Sept. 1, 2023

Zn–Mn batteries with two-electron conversion reactions simultaneously on the cathode and anode harvest a high voltage plateau energy density. However, zinc faces dendrite growth parasitic side while Mn2+/MnO2 reaction involves oxygen evolution possesses poor reversibility. Herein, novel nanomicellar electrolyte using methylurea (Mu) has been developed that can encapsulate ions in nanodomain structure to guide homogeneous deposition of Zn2+/Mn2+ form controlled release under an external electric field. Consecutive hydrogen bonding network is broken favorable local system established, thus inhibiting water-splitting-derived reactions. Concomitantly, solid–electrolyte interface protective layer situ generated Zn anode, further circumventing corrosion issue resulting from penetration water molecules. The reversibility also significantly enhanced by regulating interfacial wettability improving nucleation kinetics. Accordingly, modified endows symmetric Zn∥Zn cell extended cyclic stability 800 h suppressed dendrites at areal capacity 1 mAh cm–2. assembled electrolytic battery demonstrates exceptional retention nearly 100% after cycles superior density Wh kg–1 0.5

Language: Английский

Citations

83

Dynamic Balance of Partial Charge for Small Organic Compound in Aqueous Zinc‐Organic Battery DOI

Tianjiang Sun,

Zhehan Yi, Weijia Zhang

et al.

Advanced Functional Materials, Journal Year: 2023, Volume and Issue: 33(47)

Published: July 8, 2023

Abstract Organic cathodes for aqueous zinc‐ion batteries (AZIBs) feature intrinsic flexibility and favorable kinetics, but they suffer from high solubility. Herein, a partial charge regulation strategy is deployed by designing small organic molecule with extended π ‐conjugated plane, namely benzo[i]benzo[6′,7′]quinoxalino[2′,3′:9,10]phenanthro[4,5‐abc]phenazine‐5,10,16,21‐tetraone (PTONQ). The equalization of active sites induced the plane PTONQ combined aromaticity renders low solubility, fast transfer, structural stability. fabricated Zn//PTONQ battery cycles more than 500 h at 175 mA g −1 capacity reduction, charged/discharged anti‐freeze performance (below ‐20°C). By series ex situ characterizations, it attested that originates mainly Zn 2+ insertion/removal without H + incorporation, which also accounts formation x (CF 3 SO ) y (OH) 2x‐y ·nH 2 O by‐products. This result benefits understanding by‐product mechanism cathode paves new way to advance Zn‐organic batteries.

Language: Английский

Citations

60

Synergetic impact of oxygen and vanadium defects endows NH4V4O10 cathode with superior performances for aqueous zinc-ion battery DOI
Shijia Li, Xieyu Xu, Weixin Chen

et al.

Energy storage materials, Journal Year: 2023, Volume and Issue: 65, P. 103108 - 103108

Published: Dec. 11, 2023

Language: Английский

Citations

50

Unlocking the critical role of Mg doping in α-MnO2 cathode for aqueous zinc ion batteries DOI

Qiongguang Li,

Cun Wang,

Yue Zhu

et al.

Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 485, P. 150077 - 150077

Published: Feb. 29, 2024

Language: Английский

Citations

34

Critical challenges and solutions: quasi-solid-state electrolytes for zinc-based batteries DOI
Haoyang Ge, Xian Xie, Xuesong Xie

et al.

Energy & Environmental Science, Journal Year: 2024, Volume and Issue: 17(10), P. 3270 - 3306

Published: Jan. 1, 2024

QSSEs are emerging in aqueous ZBs and modern applications. By summarizing the fundamentals of materials properties, battery performance applications QSSEs, this review provides insight into future development optimization wider application fields.

Language: Английский

Citations

29

Activating the redox chemistry of MnO2/Mn2+ in aqueous Zn batteries based on multi-ions doping regulation DOI
Yajun Zhao, Xiaoyu Xia,

Qi Li

et al.

Energy storage materials, Journal Year: 2024, Volume and Issue: 67, P. 103268 - 103268

Published: Feb. 15, 2024

Language: Английский

Citations

23

Hydroxylated Manganese Oxide Cathode for Stable Aqueous Zinc‐Ion Batteries DOI
Mengxue Li, Chang Liu,

Jianming Meng

et al.

Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown

Published: May 1, 2024

Abstract Manganese (Mn) oxides are promising cathode materials for rechargeable aqueous Zn‐ion batteries. However, the Mn dissolution in weakly acidic electrolytes always hinders development of better Zn–Mn Herein, a hydroxylated manganese oxide material (H‐MnO 2 ) is fabricated using an electrochemical method stable batteries without relying on 2+ electrolyte additives. The partial hydroxylation leads to charge redistribution material, changing reaction thermodynamics and kinetics. Theoretical simulation suggests that promotes both Zn adsorption diffusion kinetics surface H‐MnO but weakens interaction between H + electrode. Therefore, ions can be more reactive with than ions. Experimental results show insertion mechanism dominates storage process 2, ‐induced effectively alleviated. Importantly, exhibits good cycling stability 95% capacity retention over 5000 cycles at current density 3.8 A g −1 ZnSO 4 electrolyte, outperforming state‐of‐the‐art batteries, even those findings provide new insights designing cathodes

Language: Английский

Citations

23

In situ formation of liquid crystal interphase in electrolytes with soft templating effects for aqueous dual-electrode-free batteries DOI
Yuqi Li,

Xueli Zheng,

Evan Z. Carlson

et al.

Nature Energy, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 20, 2024

Language: Английский

Citations

22

A cyano cobalt “electron transfer bridge” boosting the two-electron reaction of a MnO2 cathode with long lifespan in aqueous zinc batteries DOI
Yaozhi Liu, Lin Lu, Tengsheng Zhang

et al.

Energy & Environmental Science, Journal Year: 2024, Volume and Issue: 17(7), P. 2521 - 2529

Published: Jan. 1, 2024

An electron transfer bridge based on Mn–NC–Co interactions is applied for a MnO 2 cathode to boost its reversible two-electron reaction in conventional zinc cells.

Language: Английский

Citations

16

Electrochromic windows with fast response and wide dynamic range for visible-light modulation without traditional electrodes DOI Creative Commons

Zhuofei Jia,

Yiming Sui,

Long Qian

et al.

Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)

Published: July 20, 2024

Abstract Electrochromic (EC) devices represent an emerging energy-saving technology, exhibiting the capability to dynamically modulate light and heat transmittance. Despite their promising potential, commercialization of EC faces substantial impediments such as high cost, intricate fabrication process, low optical contrast inherent in conventional materials relying on ion insertion/extraction mechanism. In this study, we introduce innovative “electrode-free” electrochromic device, termed EECD, which lacks EC-layer electrodes during device assembling bleached state. This features a simplified process delivers superior modulation. It achieves ranging from 68-85% across visible spectrum boasts rapid response time, reaching 90% coloring just 17 seconds. addition, EECD exhibits stable cycling for over 10,000 cycles without noticeable degradation maintains functionality broad temperature range (0 °C 50 °C). Furthermore, fabricated large-area (40 cm × 40 cm) demonstrate excellent tinting uniformity, suggesting scalability approach. Our study establishes paradigmatic breakthrough smart windows.

Language: Английский

Citations

16