In the field of energy storage technology, the organic electrodes, separators, and electrolytes have unique advantages over inorganic materials, such as low cost, environmental friendliness, and a wide range of applications. Due to the advantages of organics such as light elements, abundant reserves, and recyclability, they have become favorable candidate materials for solving the energy storage problems caused by the fossil energy crisis. In recent years, as a high-performance branch of covalent organic frameworks, covalent triazine structures (CTFs) have attracted great interest due to their applications in electrochemical energy storage. CTFs have gradually become excellent organic materials for metal-ion batteries applications due to their large specific surface area, nitrogen richness, customizable structural features, and electron donor-acceptor/conductive parts. However, the relatively poor conductivity of the triazine ring in the main structure and the harsh polycondensation conditions limit its commercial application. To overcome these challenges, many effective strategies have emerged in terms of structural optimization, functional construction, and triazine-based composites. This review summarizes in detail the synthesis methods and applications of CTFs cathodes, electrolytes, and separators in the past decade. It is found that for CTFs, large-scale synthesis methods and performance regulation strategies have reached a bottleneck. It is hoped that the systematic summary of this review will provide strategic screening and prospects for the further expansion of CTFs research in next-generation batteries.

A dual-molecule reciprocal doping strategy combined with cooperative molecular assembly forms a charge transport network, enabling a champion efficiency of 20.72% in ternary organic solar cells.

Recently, how to enhance the energy density of rechargeable batteries dramatically is becoming a driving force in the field of energy storage research. Among the current energy storage technologies, the lithium-sulfur (Li-S) batteries are one of the most promising candidates for achieving high-capacity and commercial batteries. The theoretical energy density of Li-S batteries reaches to 2,600 Wh kg⁻¹ with the theoretical capacity of 1,675 mA h g⁻¹. Therefore, Li-S batteries are considered as the great potential for developing future energy storage technology. However, some of problems such as Li dendrites growth, the shuttle effect of sulfides and the electronic insulation feature of sulfur, have brought obstacles to the development of Li-S batteries. The covalent organic frameworks (COFs) are a series of porous materials with different topological structures, which show the versatile characteristics of high specific surface area, permanent pores, ordered porous channels and tunable internal structure. Potentially, their ordered channels and extended conjugated frameworks could facilitate rapid Li-ion diffusion and electron transport for the remarkable rate capability. On the basis of these merits, the COFs become the potential electrode materials to solve the above serious problems of Li-S batteries. In this mini review, we summarize the research progress of COFs utilized as electrode materials in the Li-S batteries, including the cathode, separator and anode materials. Accordingly, the outlook of COFs as electrodes for future development in Li-S batteries is also given.

A chiral tether-guided synthesis strategy was introduced for the selective preparation of D _n symmetric chiral conjugated nanorings. These nanorings exhibited exceptional circularly polarized luminescence properties.

Recently, the development of cathode materials is becoming an important issue for lithium-ion batteries (LIBs). Compared with inorganic cathodes, the organic cathodes are developing rapidly, ascribing to their distinct merits in light weight, low cost, massive organic resources and high capacity. In this paper, a cost-efficiency naphthaldiimide (NDI) based derivative, 2,7-bis(2-((2-hydroxyethyl) amino) ethyl) benzo[lmn] [3,8] phenanthroline-1,3,6,8(2H, 7H)-tetraone (NDI-NHOH), was used as organic cathode in LIBs. The NDI-NHOH was synthesized easily via one-step process, and it showed very high thermal stability. Through mixing NDI-NHOH with acetylene black and polyvinylidene fluoride (weight ratio of 6:3:1) as composite cathode in lithium-metal based LIBs, the NDI-NHOH presented versatile electrochemical properties. From cyclic voltammetry (CV) test, it exhibited two reversible peaks for oxidation and reduction in the first cycle, respectively. Notably, the oxidation and reduction peaks were located at 2.54, 3.22 and 2.14, 2.32 V vs. Li⁺/Li, respectively. By employing NDI-NHOH as cathode, it demonstrated a specific capacity of about 80 mAh g⁻¹ in the range of 1.5–3.5 V, where the batteries retained a capacity retention of 50% over 20 cycles. According to the LIBs study, it suggests that the NDI-NHOH-based derivative shows a potentially promising candidate as efficient organic cathode materials for high-performance metal-ions batteries.