Rechargeable lithium batteries with long calendar life are pivotal in the pursuit of non-fossil and wireless society as energy storage devices. However, corrosion has severely plagued the calendar life of lithium batteries. The corrosion in batteries mainly occurs between electrode materials and electrolytes, which results in constant consumption of active materials and electrolytes and finally premature failure of batteries. Therefore, understanding the mechanism of corrosion and developing strategies to inhibit corrosion are imperative for lithium batteries with long calendar life. In this review, different types of corrosion in batteries are summarized and the corresponding corrosion mechanisms are firstly clarified. Secondly, quantitative studies of the loss of lithium in corrosion are reviewed for an in-depth understanding of the mechanism. Thirdly, the recent progress in inhibiting corrosion is demonstrated. Finally, perspectives to further investigate corrosion mechanism and inhibit corrosion are put forward to promote the development of stable lithium batteries.

Lithium-sulfur (Li-S) battery is considered as a promising energy storage system due to its ultrahigh theoretical energy density of 2,600 Wh·kg⁻¹. Redox mediation strategies have been proposed to promote the sluggish sulfur redox kinetics. Nevertheless, the applicability of redox mediators in practical high-energy-density Li-S batteries has seldomly been manifested. In this work, 5,7,12,14-pentacenetetrone (PT) is proposed as an effective redox mediator to promote the sulfur redox kinetics under practical working conditions. A high initial specific discharge capacity of 993 mAh·g⁻¹ is achieved at 0.1 C with high-sulfur-loading cathodes of 4.0 mg_S·cm⁻² and low electrolyte/sulfur (E/S) ratio of 5 μL·mg_S⁻¹. More importantly, practical Li-S pouch cells with the PT mediator realize an actual initial energy density of 344 Wh·kg⁻¹ and cycle stably for 20 cycles wih a high capacity retention of 88%. This work proposes an effective redox mediator and further verifies the redox mediation strategy for practical high-energy-density Li-S batteries.

Dendrite growth of lithium (Li) metal anode severely hinders its practical application, while the situation becomes more serious at low temperatures due to the sluggish kinetics of Li-ion diffusion. This perspective is intended to clearly understand the energy chemistry of low-temperature Li metal batteries (LMBs). The low-temperature chemistries between LMBs and traditional Li-ion batteries are firstly compared to figure out the features of the low-temperature LMBs. Li deposition behaviors at low temperatures are then discussed concerning the variation in Li-ion diffusion behaviors and solid electrolyte interphase (SEI) features. Subsequently, the strategies to enhance the diffusion kinetics of Li ions and suppress dendrite growth including designing electrolytes and electrode/electrolyte interfaces are analyzed. Finally, conclusions and outlooks are drawn to shed lights on the future design of high-performance low-temperature LMBs.

Oxygen reduction reaction (ORR) constitutes the core process of many energy storage and conversion devices including metal–air batteries and fuel cells. However, the kinetics of ORR is very sluggish and thus high-performance ORR electrocatalysts are highly regarded. Despite recent progress on minimizing the ORR half-wave potential as the current evaluation indicator, in-depth quantitative kinetic analysis on overall ORR electrocatalytic performance remains insufficiently emphasized. In this paper, a quantitative kinetic analysis method is proposed to afford decoupled kinetic information from linear sweep voltammetry profiles on the basis of the Koutecky–Levich equation. Independent parameters regarding exchange current density, electron transfer number, and electrochemical active surface area can be respectively determined following the proposed method. This quantitative kinetic analysis method is expected to promote understanding of the electrocatalytic effect and point out further optimization direction for ORR electrocatalysis.