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Active crystal facets can generate special properties for various applications. Herein, we report a (001) faceted nanosheet-constructed hierarchically porous TiO2/rGO hybrid architecture with unprecedented and highly stable lithium storage performance. Density functional theory calculations show that the (001) faceted TiO2 nanosheets enable enhanced reaction kinetics by reinforcing their contact with the electrolyte and shortening the path length of Li+ diffusion and insertion-extraction. The reduced graphene oxide (rGO) nanosheets in this TiO2/rGO hybrid largely improve charge transport, while the porous hierarchy at different length scales favors continuous electrolyte permeation and accommodates volume change. This hierarchically porous TiO2/rGO hybrid anode material demonstrates an excellent reversible capacity of 250 mAh g-1 at 1 C (1 C = 335 mA g-1) at a voltage window of 1.0-3.0 V. Even after 1000 cycles at 5 C and 500 cycles at 10 C, the anode retains exceptional and stable capacities of 176 and 160 mAh g-1, respectively. Moreover, the formed Li2Ti2O4 nanodots facilitate reversed Li+ insertion-extraction during the cycling process. The above results indicate the best performance of TiO2-based materials as anodes for lithium-ion batteries reported in the literature.

The rapid development of the Internet of Things (IoT)-enabled applications and connected automation are increasingly making sensing technologies the heart of future intelligent systems. The potential applications have wide-ranging implications, from industrial manufacturing and chemical process control to agriculture and nature conservation, and even to personal health monitoring, smart cities, and national defence. Devices that can detect trace amounts of analyte gases represent the most ubiquitous of these sensor platforms. In particular, the advent of nanostructured organic and inorganic materials has significantly transformed this field. Highly sensitive, selective, and portable sensing devices are now possible due to the large surface to volume ratios, favorable transport properties and tunable surface chemistry of the sensing materials. Here, we present a review on the recent development of printed gas sensors. We first introduce the state-of-the-art printing techniques, and then describe a variety of gas sensing materials including metal oxides, conducting polymers, carbon nanotubes and two-dimensional (2D) materials. Particular emphases are given to the working principles of the printing techniques and sensing mechanisms of the different material systems. Strategies that can improve sensor performance via materials design and device fabrication are discussed. Finally, we summarize the current challenges and present our perspectives in opportunities in the future development of printed gas sensors.

As an extraordinarily lightweight and porous functional nanomaterial family, aerogels have attracted considerable interest in academia and industry in recent decades. Despite the application scopes, the modest mechanical durability of aerogels makes their processing and operation challenging, in particular, for situations demanding intricate physical structures. "Bottom-up" additive manufacturing technology has the potential to address this drawback. Indeed, since the first report of 3D printed aerogels in 2015, a new interdisciplinary research area combining aerogel and printing technology has emerged to push the boundaries of structure and performance, further broadening their application scope. This review summarizes the state-of-the-art of printed aerogels and presents a comprehensive view of their developments in the past 5 years, and highlights the key near- and mid-term challenges.

Metal-organic frameworks (MOFs) have received great attention in recent years as potential adsorbents for CO2 capture due to their unique properties. However, the high cost and their tedious synthesis procedures impede their industrial application. A series of new CO2-philic oxalamide-functionalized MOFs have been solvothermally synthesized: {[Zn-3(mu(8)-OATA)(1.5)(H2O)(2)(DMF)]center dot 5/2H(2)O center dot 5DMF}(n) (Zn-OATA), {[NH2(CH3)(2)][Cd(mu(4)-HOATA)]center dot H2O center dot DMF}(n) (Cd-OATA), and {[Co-2(mu(7)-OATA)(H2O)(DMF)(2)]center dot 2H(2)O center dot 3DMF}(n) (Co-OATA) (H(4)OATA = N,N'-bis(3,5-dicarboxyphenyl)oxalamide). In Zn-OATA, the [Zn-2(CO2)(4)] SBUs are connected by OATA(4-) ligands into a 3D framework with 4-connected NbO topology. In Cd-OATA, two anionic frameworks with a dia topology interpenetrated each other to form a porous structure. In Co-OATA, [Co-2(CO2)(4)] units are linked by four OATA(4-) to form a 3D framework with binodal 4,4-connected 4(2)center dot 8(4) PtS-type topology. Very interestingly, Cu-OATA can be prepared from Zn-OATA by a facile metal ions exchange procedure without damaging the structure while the CO2 adsorption ability can be largely enhanced when Zn(II) metal ions are exchanged to Cu(II). These new MOFs possess channels decorated by the CO2-philic oxalamide groups and accessible open metal sites, suitable for highly selective CO2 adsorption. Cu-OATA exhibits a significant CO2 adsorption capacity of 25.35 wt % (138.85 cm(3)/g) at 273 K and 9.84 wt % (50.08 cm(3)/g) at 298 K under 1 bar with isosteric heat of adsorption (Qst) of about 25 kJ/mol. Cu-OATA presents a very high selectivity of 5.5 for CO2/CH4 and 43.8 for CO2/N-2 separation at 0.1 bar, 298 K. Cd-OATA exhibits a CO2 sorption isotherm with hysteresis that can be originated from structural rearrangements. Cd-OATA adsorbs CO2 up to 11.90 wt % (60.58 cm(3)/g) at 273 K and 2.26 wt % (11.40 cm(3)/g) at 298 K under 1 bar. Moreover, these new MOFs exhibit high stability in various organic solvents, water, and acidic or basic media. The present work opens a new opportunity in the development of improved and cost-effective MOF adsorbents for highly efficient CO2 capture.Y