Covalent organic frameworks (COFs) with reversible redox behaviors are potential electrode materials for lithium‐ion batteries (LIBs). However, the sluggish lithium diffusion kinetics, poor electronic conductivity, low reversible capacities, and poor rate performance for most reported COF materials limit their further application. Herein, a new 2D COF (TFPB‐COF) with six unsaturated benzene rings per repeating unit and ordered mesoporous pores (≈2.1 nm) is designed. A chemical stripping strategy is developed to obtain exfoliated few‐layered COF nanosheets (E‐TFPB‐COF), whose restacking is prevented by the in situ formed MnO2 nanoparticles. Compared with the bulk TFPB‐COF, the exfoliated TFPB‐COF exhibits new active Li‐storage sites associated with conjugated aromatic π electrons by facilitating faster ion/electron kinetics. The E‐TFPB‐COF/MnO2 and E‐TFPB‐COF electrodes exhibit large reversible capacities of 1359 and 968 mAh g−1 after 300 cycles with good high‐rate capability.

Organic electrodes for low-cost potassium ion batteries (PIBs) are attracting more interest by virtue of their molecular diversity, environmental friendliness, and operation safety. But the sluggish potassium diffusion kinetics, dissolution in organic electrolyte, poor electronic conductivity, and low reversible capacities are several drawbacks compared with inorganic counterparts. Herein, the boronic ester based covalent organic framework (COF) material is successfully prepared on the exterior surface of carbon nanotubes (CNTs) via rational design of the organic condensation reaction and used as an anode material for PIBs. The few-layered structure of COF-10@CNT can provide more exposed active sites and fast K + kinetics. It exhibits ultrahigh potassium storage performances (large reversible capacities of 288 mAh g −1 after 500 cycles at 0.1 A g −1 and 161 mAh g −1 after 4000 cycles at 1 A g −1 ), which is superior to previous organic electrodes and most inorganic electrodes. Moreover, the K-storage mechanism is proposed to be π-cation interaction between K + and conjugated πelectrons of benzene rings.

In order to fulfill the increasing demand for renewable energy, besides the lithium-ion batteries, other alkali (Na, K)-ion batteries are extensively investigated. However, the difficulty to find universal and environmentally benign electrodes for these alkali (Na, K)-ion batteries still severely restricts their development. Promising characteristics, including molecular diversity, low cost, and operation safety, endow the organic electrodes more advantages for applications in alkali-ion batteries. However, organic electrodes usually deliver a reversible capacity smaller than that of their inorganic counterparts due to sluggish ion/electron diffusion and possible dissolution in organic electrolytes. This work introduces fluorine atoms into the covalent triazine frameworks (CTF) to obtain two-dimensional layered fluorinated CTF (FCTF) and its exfoliated few-layered product (E-FCTF) and uses them as anodes of Li, Na, and K organic batteries. Exfoliated E-FCTF electrode delivers high reversible capacities, as well as excellent cycle life for alkali organic batteries (1035 mAh g −1 at 100 mA g −1 after 300 cycles and 581 mAh g −1 at 2 A g −1 after 1000 cycles for lithium organic batteries). In view of the experimental probing and the theoretical calculation, the Li storage mechanism for the E-FCTF can be determined to be an intriguing multielectronic redox reaction originated from lithium storage on the benzene ring and triazine ring units.

The development of the next‐generation lithium ion battery requires environmental‐friendly electrode materials with long cycle life and high energy density. Organic compounds are a promising potential source of electrode materials for lithium ion batteries due to their advantages of chemical richness at the molecular level, cost benefit, and environmental friendliness, but they suffer from low capacity and dissatisfactory cycle life mainly due to hydrophobic dissolution in organic electrolytes and poor electronic conductivity. In this work, two types of triazine‐based covalent organic nanosheets (CONs) are exfoliated and composited with carbon nanotubes. The thin‐layered 2D structure for the exfoliated CONs can activate more functional groups for lithium storage and boost the utilization efficiency of redox sites compared to its bulk counterpart. Large reversible capacities of above 1000 mAh g−1 can be achieved after 250 cycles, which is comparable to high‐capacity inorganic electrodes. Moreover, the lithium‐storage mechanism is determined to be an intriguing 11 and 16 electron redox reaction, associated with the organic groups (unusual triazine ring, piperazine ring, and benzene ring, and common CN, NH groups).

Sensing analysis is significantly important for human health and environmental safety. In this review, POPs used as platforms for various sensing applications have been summarized and discussed.

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Boron/oxygen co‐doped carbons (BOC) have great potentials as sulfur host materials for lithium–sulfur batteries, because they can increase electronic conductivity and anchor polysulfides. However, the doping interface as a key chemically active site still lacks in‐depth understanding owing to the difficulty in design at the molecular scale. Herein, the BOC network derived from covalent organic framework (COF) is prepared on the surface of CNTs via rational design of the organic condensation reaction. This strategy enables boron and oxygen heteroatoms to be uniformly doped throughout porous carbon because of the uniformly‐distributed two elements in the COF precursor. Thereby, the BOC matrix is demonstrated to play a pivotal role in promoting the chemical absorption of polysulfides and enhancing cycling stability. The BOC@CNT with 68.5% sulfur shows superior lithium polysulfides absorptivity and displays superior electrochemical performances as a cathode for Li–S batteries, including a large reversible capacity (1077 mA h g−1 after 200 cycles at 0.2 C), and outstanding cycling stability (794 mA h g−1 after 500 cycles at 1 C). The demonstrated strategy for fabricating BOC network by COF precursor for Li–S batteries provides a new approach to rationally design uniform heteroatom interfaces for good electrochemical performances.

Ultrasmall MoC nanoparticles anchored in 3D networks of N-doped porous carbon are produced and deliver outstanding lithium storage performance.