Construction of V2O5@MXene Cathodes toward a High Specific Capacity Aqueous Aluminum-Ion Battery.

Aqueous aluminum-ion batteries (AAIBs) are considered a strong candidate for the new generation of energy storage devices. The lack of suitable cathode materials has been a bottleneck factor hindering the future development of AAIBs. In this work, we design and construct a highly effective cathode with dual morphologies. Two-dimensional (2D) layered MXene materials possessed good conductivity and hydrophilicity, which are used as the substrates to deposit rod-shaped vanadium oxides (V2O5) to form a three-dimensional (3D) cathode. The cathode design provides a strong boost for the rapid electrochemical activities of rod-shaped V2O5 by embedding/extracting both protons (H+) and aluminum-ion (Al3+). As a result, the V2O5@MXene cathode based AAIB delivers an ultrahigh initial specific capacity of 626 mAh/g at 0.1 A/g with a stable cycle performance up to 100 cycles. This work is a breakthrough for the development of cathode materials for AAIBs.

α-MnO2 Cathode with Oxygen Vacancies Accelerated Affinity Electrolyte for Dual-Ion Co-Encapsulated Aqueous Aluminum Ion Batteries.

Aluminum batteries (ABs) are identified as one of the most promising candidates for the next generation of large-scale energy storage elements because of their efficient three-electron reaction. Compared to ionic electrolytes, aqueous aluminum-ion batteries (AAIBs) are considered safer, less costly, and more environmentally friendly. However, considerable cycling performance is a key issue limiting the development of AAIBs. Stable, efficient, and electrolyte-friendly cathodes are most desirable for AAIBs. Herein, a rod-shaped defect-rich α-MnO2 is designed as a cathode, which is capable to deliver high performance with stable cycling for 180 cycles at 500 mA g-1 and maintains a discharge specific capacity of ≈100 mAh g-1. In addition, the infiltrability simulation is effectively utilized to corroborate the rapid electrochemical reaction brought about by the defective mechanism. With the formation of oxygen vacancies, the dual embedding of protons and metal ions is activated. This work provides a brand-new design for the development and characterization of cathodes for AAIBs.

Dual-Salt Mixed Electrolyte for High Performance Aqueous Aluminum Batteries.

A dual-salt electrolyte with 5 M Al(OTF)3 and 0.5 M LiOTF is proposed for aqueous aluminum batteries, which can effectively prevent the corrosion caused by the hydrogen evolution reaction. With the addition of LiOTF in the electrolyte, the solvation phenomenon has changed with the coordination mode of Al3+ conversion from an all octahedral structure to a mixed octahedral and tetrahedral structure. This change can reduce the hydrogen bond between water molecules, which will minimize the occurrence of hydrogen evolution reactions. Moreover, the new electrolyte improves the cycle life of the battery. With MnO as the cathode, 2.1 V high charging platform and 1.5 V high discharge platform can be obtained. The electrochemical stability window (ESW) has been improved to 3.8 V. The first cycle capacity is up to 437 mAh g-1, which can be maintained at 103 mAh g-1 after 100 cycles. This work provides solutions for the future development of electrolyte for aqueous aluminum batteries.

Dual Protection Strategy by Constructing MXene-Coated Cu2Se-Cu1.8Se Heterojunction and CMK-3 Modification for High-Performance Aluminum-Ion Batteries.

The fabrication of cathode materials with ideal kinetic behavior is important to improve the electrochemical performance of aluminum-ion batteries (AIBs). Transition metal selenides have the advantages of abundant reserves and high discharge specific capacity and discharge voltage plateau, which makes them a promising material for rechargeable AIBs. It is well-known that the low structural stability and relatively poor reaction kinetics pose a considerable challenge to the development of AIBs. The cubic structure of Cu2Se-Cu1.8Se can adapt to the volume change of the active material during cycling and facilitate the intercalation and deintercalation of chloroaluminate anions in the cathode material. We created a two-fold protection mechanism for AIBs with a CMK-3 modified separator and a Cu2Se-Cu1.8Se heterojunction coated with MXene in order to better mitigate the detrimental impacts. In addition to offering numerous electronic transmission routes, MXene and CMK-3 help prevent the solubilization of active species. This novel design enables the Cu2Se-Cu1.8Se@MXene composite to have a high initial discharge capacity of 705.5 mAh g-1 at 1.0 A g-1. Even after 1500 cycles at 2.0 A g-1, the capacity is still maintained at 225.1 mAh g-1. Furthermore, the reaction mechanism of AlCl4- intercalated/deintercalated into Cu2Se-Cu1.8Se heterojunction is revealed during charge/discharge. This work to construct novel cathode materials has greatly improved the electrochemical performance of AIBs.

Bimetallic Rechargeable Al/Zn Hybrid Aqueous Batteries Based on Al-Zn Alloys with Composite Electrolytes.

Aluminum is abundant and exhibits a high theoretical capacity and volumetric energy density. Additionally, the high safety of aqueous aluminum-ion batteries makes them strong candidates for large-scale energystorage systems. However, the frequent collapse of the cathode material and passive oxide film results in the difficult development of aqueous aluminum-ion batteries. This work provides a novel battery system, namely, Al-Zn/Al(OTF)3 +HOTF+Zn(OTF)2 /Alx Zny MnO2 ·nH2 O, with a mixed electrolyte. The cathode applies MnO topology transformation to ensure that the cathode forms Alx MnO2 ·nH2 O. Topology transformation alters the structure of the cathode material so that Zn2+ can be intercalated into the Alx MnO2 ·nH2 O spinel structure to provide support for the material structure. Regarding the anode, Zn2+ in the electrolyte is deposited onto Al of the anode to produce a regional Al-Zn alloy. Zn2+ is reduced to Zn metal during discharging, which adds a platform for secondary discharge beneficial for battery capacity enhancement. This system can provide a 1.6 V discharge platform, while the first cycle discharge can reach 554 mAh g-1 , thereby maintaining a high capacity of 313 mAh g-1 after 100 cycles. This study provides a new idea for the further development of aqueous aluminum-ion batteries (AAIBs).

Novel One-Dimensional Nanofiber MnSe/CMK-3 High-Performance Cathode Material for Aluminum Batteries.

Transition metal selenides have shown outstanding performance as cathode materials for aluminum-ion batteries and have thus become a popular choice for cathode materials. Herein, Mn-based carbon fibers (Mn/CNFs) were first synthesized by electrospinning as a precursor, and then MnSe composites were prepared by a melt-diffusion method. However, due to polyselenides and selenides being generated during electrochemical reactions, the cycling stability of MnSe cathode materials is poor. After 200 cycles, the discharge specific capacity is only 176 mA h/g. To suppress the shuttle effect of selenides and polyselenides, a CMK-3-modified separator was used instead of a glass fiber separator. Compared with MnSe-800, the replaced MnSe-800/CMK-3 has a great capacity improvement; the initial discharge specific capacity is 1029.85 mA h/g, which after 3000 cycles, still remains at 297.84 mA h/g. The soft pack battery can still light up the LED normally under different degrees of folding, which proves the application of this material in wearable devices. This work provides a new way to improve the performance of transition metal selenides.