ABSTRACT
Zn-ion energy storage devices will play important roles in the future energy storage field. However, Zn-ion device development suffers significantly from adverse chemical reactions (dendrite formation, corrosion, and deformation) on the Zn anode surface. Zn dendrite formation, hydrogen evolution corrosion, and deformation combine to degrade Zn-ion devices. Zincophile modulation and protection using covalent organic frameworks (COF) inhibited dendritic growth by induced uniform Zn ion deposition, which also prevented chemical corrosion. The Zn@COF anode circulated stably for more than 1800 cycles even at high current density in symmetric cells and maintained a low and stable voltage hysteresis. This work explains the surface state of the Zn anode and provides information for further research.
ABSTRACT
The high Zn ion desolvation energy, sluggish Zn deposition kinetics, and top Zn plating pattern are the key challenges toward practical Zn anodes. Herein, these key issues are addressed by introducing zinc pyrovanadate (ZVO) as a solid zinc-ion conductor interface to induce smooth and fast Zn deposition underneath the layer. Electrochemical studies, computational analysis, and in situ observations reveal the boosted desolvation and deposition kinetics, and uniformity by ZVO interface. In addition, the anti-corrosion ability of Zn anodes is improved, resulting in high Zn stripping/plating reversibility. Consequently, the ZVO layer renders fast rechargeability and durable life in both Zn symmetric cells (1050 h at 10 mA cm-2 , 1 mAh cm-2 ) and Zn/V2 O5 batteries (79.1% capacity retention after 1000 cycles at 2 A g-1 ) with low electrode polarization. This work provides insights into the design of solid zinc-ion conductor interface to enhance the interface stability and kinetics of Zn metal anodes.
ABSTRACT
Aqueous Zn-ion batteries (ZIBs) show great potential in energy storage systems because of their high theoretical capacities, high safety, low cost, and environmental friendliness. The lack of suitable cathode materials for sustaining the Zn2+ intercalation/deintercalation severely restricts their further application. Herein, calcium-intercalated birnessite MnO2 anchored on carbon nanotubes (CNTs) was designed as a cathode for ZIBs. The cathode material can be facilely produced by a simple one-pot reaction process. The external calcium-intercalated MnO2 with large layer spacing affords a fast ionic migration rate and the internal CNTs serving as a structural framework endow the electrode with better electrical conductivity. Benefiting from the larger interlayer spacing and the enhanced electrical conductivity, the CNT-CaMO cathode shows a high specific capacity of 351.8 mA h g-1 at 200 mA g-1 and a long cycle life over 6000 cycles. Besides, the H+ and Zn2+ co-intercalation storage mechanism was confirmed by ex situ XRD, SEM, and XPS analyses. This work opens up a new way to develop aqueous ZIB cathode materials with a high reversible capacity and long cycle life.
ABSTRACT
The rechargeable zinc-iodine (Zn-I2) battery is a promising energy-storage system due to its low cost and good security, but the practical use of the battery is largely constrained by the shuttle effect and high dissolvability of iodides. Here a multifunctional iodine host, constructed with nitrogen-doped porous carbon nanocages (NCCs) by the polymerization carbonization activation method, is exploited to improve the electrochemical performance and lifespan of the Zn-I2 battery, achieving a high specific capacity of 259 mAh g-1, a good rate performance (maintaining 50.6% expanding 50 times), and a high cycle stability (retention of 100% after 1000 cycles). On the basis of the experimental results and theoretical calculations, NCCs via the introduction of N doping and nanosized porous structure can simultaneously provide rich and robust anchoring and catalytic sites to carry out the electrostatic adsorption of iodides and facilitate the reversible conversion between iodine and iodides. This work shows a novel and efficient strategy to develop high-performance and long-life Zn-I2 batteries.
ABSTRACT
Searching for high active, low cost and durable catalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) remains challenge in developing metal-air battery cathodes. Herein, we proposed a novel bifunctional catalyst derived from the pyrolysis of Co/Fe/Zn trimetallic zeolitic imidazolite framework. The obtained Co@CoFe0.01NC catalyst displays desirable activity for both ORR and OER (E1/2 = 0.844 V, Ej=10 = 1.654 V). The Zn-air battery equipped with Co@CoFe0.01NC catalyst on the cathode exhibits a high peak power density of 174.1 mW cm-2, which is much superior than that of commercial 20% Pt/C (87.6 mW cm-2). Significantly, the designed Co@CoFe0.01NC presents an outstanding stability for over 100 h in rechargeable Zn-air battery.
