Assembling thermoelectric modules into fabric to harvest energy from body heat could one day power multitudinous wearable electronics. However, the invalid 2D architecture of fabric limits the application in thermoelectrics. Here, we make the valid thermoelectric fabric woven out of thermoelectric fibers producing an unobtrusive working thermoelectric module. Alternately doped carbon nanotube fibers wrapped with acrylic fibers are woven into π-type thermoelectric modules. Utilizing elasticity originating from interlocked thermoelectric modules, stretchable 3D thermoelectric generators without substrate can be made to enable sufficient alignment with the heat flow direction. The textile generator shows a peak power density of 70 mWm −2 for a temperature difference of 44 K and excellent stretchability (~80% strain) with no output degradation. The compatibility between body movement and sustained power supply is further displayed. The generators described here are true textiles, proving active thermoelectrics can be woven into various fabric architectures for sensing, energy harvesting, or thermal management.

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Electrocatalytic denitrification is considered as the most promising technology to transform nitrates to nitrogen gas in sewage so far. Although noble metal-based catalysts as a cathode material have reached decent removal capacity of nitrate, the high cost is the main hamper of electrocatalytic reduction. Therefore, the development of alternative catalysis toward highly effective denitrification is imperative yet still remains a significant challenge. Herein, a corchorifolius-like structure, where Fe nanoparticles are sealed in carbon microspheres (CL-Fe@C) with a rough surface, has been elaborately designed by self-assemble strategy. Impressively, the architectured CL-Fe@C microspheres are surrounded with a lot of small iron nanoparticles and contain the high iron content of ∼74%. As a result, an excellent removal capacity of 1816 mg N/g Fe and a high nitrogen selectivity of 98% under a very low nitrate concentration of 100 mg/L are achieved when using the CL-Fe@C microspheres as electrocatalytic denitrification. The present work not only explores high performance electrocatalysis for the denitrification but also promote new inspiration for the preparation of other iron-based functional materials for diverse applications.

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Lead‐free halide double perovskite (HDP) nanocrystals are considered as one of the most promising alternatives to the lead halide perovskite nanocrystals due to their unique characteristics of nontoxicity, robust intrinsic thermodynamic stability, rich and tunable optoelectronic properties. Although lead‐free HDP variants with highly efficient emission are synthesized and characterized, the photoluminescent (PL) properties of colloidal HDP nanocrystals still have enormous challenges for application in light‐emitting diode (LED) devices due to their intrinsic and surface defects, indirect band, and disallowable optical transitions. Herein, recent progress on the synthetic strategies, ligands passivation, and metal doping/alloying for boosting efficiency and stability of HDP nanocrystals is comprehensive summarized. It begins by introducing the crystalline structure, electronic structure, and PL mechanism of lead‐free HDPs. Next, the limiting factors on PL properties and origins of instability are analyzed, followed by highlighting the effects of synthesis strategies, ligands passivation, and metal doping/alloying on the PL properties and stability of the HDPs. Then, their preliminary applications for LED devices are emphasized. Finally, the challenges and prospects concerning the development of highly efficient and stable HDP nanocrystals‐based LED devices in the future are proposed.

A practical and feasible bottom‐up chemistry approach is demonstrated to dramatically enhance thermoelectric properties of the Bi2Te3 matrix by means of exotically introducing silver nanoparticles (AgNPs) for constructing thermoelectric composites with the hierarchical two‐phased heterostructure. By regulating the content of AgNPs and fine‐tuning the architecture of nanostructured thermoelectric materials, more heat‐carrying phonons covering the broad phonon mean free path distribution range can be scattered. The results show that the uniformly dispersed AgNPs not only effectively suppress the growth of Bi2Te3 grains, but also introduce nanoscale precipitates and form new interfaces with the Bi2Te3 matrix, resulting in a hierarchical two‐phased heterostructure, which causes intense scattering of phonons with multiscale mean free paths, and therefore significantly reduce the lattice thermal conductivity. Meanwhile, the improved power factor is maintained due to low‐energy electron filtering and excellent electrical transport property of Ag itself. Consequently, the maximum ZT is amazingly found to be enhanced by 304% arising from the hierarchical heterostructure when the AgNPs content reaches 2.0 vol%. This study offers an easily scalable and low‐cost route to construct a wide range of multiscale hierarchically heterostructured bulk composites with significant enhancement of thermoelectric performance.

Robust and flexible cellulose sponges were prepared by dual-cross-linking cellulose nanofiber (CNF) with γ-glycidoxypropyltrimethoxysilane (GPTMS) and polydopamine (PDA) and used as carriers of metal nanoparticles (NPs), such as palladium (Pd). In situ growth of Pd NPs on the surface of CNF was achieved in the presence of polydopamine (PDA). The modified sponges were characterized with FT-IR, XRD, EDX, SEM, TEM, and TGA. XRD, EDX, and TEM results revealed that the Pd NPs were homogeneously dispersed on the surface of CNF with a narrow size distribution. The catalysts could be successfully applied to heterogeneous Suzuki and Heck cross-coupling reactions. Leaching of Pd was negligible and the catalysts could be conveniently separated from the products and reused.

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