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Conventional metal-organic framework (MOF) powders have periodic micro/mesoporous crystalline architectures tuned by their three-dimensional coordination of metal nodes and organic linkers. To add practical macroscopic shapeability and extrinsic hierarchical porosity, fibrous MOF aerogels were produced by synthesizing MOF crystals on the template of TEMPO-cellulose nanofibrils. Cellulose nanofibrils not only offered extrinsic porosities and mechanical flexibility for the resultant MOF aerogels, but also shifted the balance of nucleation and growth for synthesizing smaller MOF crystals, and further decreased their aggregation possibilities. Thanks to their excellent shapeability, hierarchical porosity up to 99%, and low density below 0.1 g/cm, these MOF aerogels could make the most of their pores and accessible surface areas for higher adsorption capacity and rapid adsorption kinetics of different molecules, in sharp contrast to conventional MOF powders. Thus, this scalable and low-cost production pathway is able to convert MOF powders into a shapeable and flexible form and thereby extend their applications in more broad fields, for example, adapting a conventional filtration setup.

Nanometerization of liquid metal in organic systems can facilitate deposition of liquid metals onto substrates and then recover its conductivity through sintering. Although having broader potential applications, producing stable aqueous inks of liquid metals keeps challenging because of rapid oxidation of liquid metal when exposing to water and oxygen. Here, a biocompatible aqueous ink is produced by encapsulating alloy nanodroplets of gallium and indium (EGaIn) into microgels of marine polysaccharides. During sonicating bulk EGaIn in aqueous alginate solution, alginate not only facilitates the downsizing process via coordination of their carboxyl groups with Ga ions but also forms microgel shells around EGaIn droplets. Due to the deceasing oxygen-permeability of microgel shells, aqueous ink of EGaIn nanodroplets can maintain colloidal and chemical stability for a period of >7 d. Crosslinked alginate-gel with tunable thickness can retard the generation and release of toxic cations, thereby affording high biocompatibility. The soft alginate shells also enable to recover electric conductivity of EGaIn layers by "mechanical sintering" for applications in microcircuits, electric-thermal actuators, and wearable sensors, offering huge potential for electronic tattoos, artificial limbs, electric skins, etc.