Batteries & Supercaps www.batteries-supercaps.org Review doi.org/10.1002/batt.202200160Multivalent secondary batteries (MSBs) have attracted great attention in view of their rich resources, low cost, and high safety. However, its development and application are still plagued by electrode materials. With their renewable and highly adjustable structures, organic electrode materials (OEMs) have several advantages over traditional inorganic electrode materials (IEMs), which has become the current research hotspot of electrode materials for MSBs. In this review, we present the recent developments in OEMs used for secondary batteries, including carbonyl compounds, imine compounds, conductive polymers, covalent organic frameworks, organic cyanides, organosulfur polymers and so on. An overview of the structural characteristics, energy storage mechanism, and electrochemical performance of OEMs in MSBs is given. Furthermore, to reveal the reasons for the high performance of the preponderant organic electrode materials, the relationships between material structures, electrolyte system, and battery properties are discussed in detail. Finally, we hope that this review could provide a fundamental guide to developing and designing high-performance MSBs in the future.

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As a class of flexible and designable materials, organic electrode materials would greatly facilitate the progress of potassium-ion batteries (PIBs), especially when the dissolution issue is ameliorated. Ionic liquid electrolytes (ILEs) do not merely alleviate the dissolution of organic materials but provide reliable security. Herein, Pillar[5]­quinone (P5Q) as the cathode of PIBs is demonstrated for the first time, and the electrochemical performance of two common ILEs is investigated. In the 0.3 M KFSI-PY13FSI electrolyte with better conductivity, the P5Q cathode maintains a large reversible capacity of 232 mAh g–1 (450 Wh kg–1) after 100 cycles at 0.2C at 1.2–4.0 V. When a current density of 2.0C is applied, the cell retains a capacity of 101 mAh g–1 (211 Wh kg–1) after 1000 cycles and 61 mAh g–1 (125 Wh kg–1) even over 5000 cycles. This research would inspire research on organic electrodes and advance the application of PIBs.

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Alkali vapor cells are the core components of atomic sensing instruments such as atomic gyroscopes, atomic magnetometers, atomic clocks, etc. Emerging integrated atomic sensing devices require high-performance miniaturized alkali vapor cells, especially micro-fabricated vapor cells. In this review, bonding methods for vapor cells of this kind are summarized in detail, including anodic bonding, sacrificial micro-channel bonding, and metal thermocompression bonding. Compared with traditional through-lighting schemes, researchers have developed novel methods for micro-fabricated vapor cells under both single- and double-beam schemes. In addition, emerging packaging methods for alkali metals in micro-fabricated vapor cells can be categorized as physical or chemical approaches. Physical methods include liquid transfer and wax pack filling. Chemical methods include the reaction of barium azide with rubidium chloride, ultraviolet light decomposition (of rubidium azide), and the high-temperature electrolysis of rubidium-rich glass. Finally, the application trend of micro-fabricated alkali vapor cells in the field of micro-scale gyroscopes, micro-scale atomic clocks, and especially micro-scale biomagnetometers is reviewed. Currently, the sensing industry has become a major driving force for the miniaturization of atomic sensing devices, and in the near future, the micro-fabricated alkali vapor cell technology of atomic sensing devices may experience extensive developments.