Jia‐Qi Huang

Abstract Portable electronic devices (PEDs) are promising information‐exchange platforms for real‐time responses. Their performance is becoming more and more sensitive to energy consumption. Rechargeable batteries are the primary energy source of PEDs and hold the key to guarantee their desired performance stability. With the remarkable progress in battery technologies, multifunctional PEDs have constantly been emerging to meet the requests of our daily life conveniently. The ongoing surge in de

Lithium-sulfur batteries hold great promise for serving as next generation high energy density batteries. However, the shuttle of polysulfide induces rapid capacity degradation and poor cycling stability of lithium-sulfur cells. Herein, we proposed a unique lithium-sulfur battery configuration with an ultrathin graphene oxide (GO) membrane for high stability. The oxygen electronegative atoms modified GO into a polar plane, and the carboxyl groups acted as ion-hopping sites of positively charged

The stability of a battery is strongly dependent on the feature of solid electrolyte interphase (SEI). The electrical double layer forms prior to the formation of SEI at the interface between the Li metal anode and the electrolyte. The fundamental understanding on the regulation of the SEI structure and stability on Li surface through the structure of the electrical double layer is highly necessary for safe batteries. Herein, the interfacial chemistry of the SEI is correlated with the initial Li

Lithium–sulfur batteries attract great attention due to their high energy density, while their real applications are still hindered by the rapid capacity degradation. Despite great efforts devoted to solving the polysulfide shuttle between the cathode and anode electrodes, it remains a serious challenge to build highly-stable lithium–sulfur batteries. Herein we demonstrate a strategy of introducing an ion selective membrane to improve the stability and coulombic efficiency of lithium–sulfur batt

Abstract Lithium (Li) metal has been pursued as “Holy Grail” among various anode materials due to its high specific capacity and the lowest reduction potential. However, uncontrolled growth of Li dendrites and extremely unstable interfaces during repeated Li plating/stripping ineluctably plague the practical applications of Li metal batteries. Herein, an artificial protective layer with synergistic soft–rigid feature is constructed on the Li metal anode to offer superior interfacial stability du

The development of energy-storage devices has received increasing attention as a transformative technology to realize a low-carbon economy and sustainable energy supply. Lithium-sulfur (Li-S) batteries are considered to be one of the most promising next-generation energy-storage devices due to their ultrahigh energy density. Despite the extraordinary progress in the last few years, the actual energy density of Li-S batteries is still far from satisfactory to meet the demand for practical applica

Abstract Rechargeable lithium–sulfur batteries have attracted tremendous scientific attention owing to their superior energy density. However, the sulfur electrochemistry involves multielectron redox reactions and complicated phase transformations, while the final morphology of solid‐phase Li 2 S precipitates largely dominate the battery's performance. Herein, a triple‐phase interface among electrolyte/CoSe 2 /G is proposed to afford strong chemisorption, high electrical conductivity, and superb

The lithium metal anode is regarded as a promising candidate in next-generation energy storage devices. Lithium nitrate (LiNO₃ ) is widely applied as an effective additive in ether electrolyte to increase the interfacial stability in batteries containing lithium metal anodes. However, because of its poor solubility LiNO₃ is rarely utilized in the high-voltage window provided by carbonate electrolyte. Dissolution of LiNO₃ in carbonate electrolyte is realized throu

A cooperative interface constructed by "lithiophilic" nitrogen-doped graphene frameworks and "sulfiphilic" nickel-iron layered double hydroxides (LDH@NG) is proposed to synergistically afford bifunctional Li and S binding to polysulfides, suppression of polysulfide shuttles, and electrocatalytic activity toward formation of lithium sulfides for high-performance lithium-sulfur batteries. LDH@NG enables high rate capability, long lifespan, and efficient stabilization of both sulfur and lithium ele

The rational combination of conductive nanocarbon with sulfur leads to the formation of composite cathodes that can take full advantage of each building block; this is an effective way to construct cathode materials for lithium–sulfur (Li–S) batteries with high energy density. Generally, the areal sulfur‐loading amount is less than 2.0 mg cm −2 , resulting in a low areal capacity far below the acceptable value for practical applications. In this contribution, a hierarchical free‐standing carbon

Solid-state electrolytes (SSEs) are widely considered as an “enabler” to inhibit dendrite growth of lithium-metal anodes for high-energy and highly safe next-generation batteries. However, recent studies demonstrated that lithium dendrites form in working SSEs. Theoretically, dendrite inhibition can be achieved in perfect SSEs without any defects, while dendrite growth is extensively observed in practical SSEs with poor interface stability, large grain boundaries, voids, and partial electronic c

Lithium metal batteries (such as lithium-sulfur, lithium-air, solid state batteries with lithium metal anode) are highly considered as promising candidates for next-generation energy storage systems. However, the unstable interfaces between lithium anode and electrolyte definitely induce the undesired and uncontrollable growth of lithium dendrites, which results in the short-circuit and thermal runaway of the rechargeable batteries. Herein, a dual-layered film is built on a Li metal anode by the