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Structural DNA nanotechnology can produce a wide range of 3D nanostructures with programmable structure and size at <5 nm resolution. However, it is challenging to dry these structures without capillary force-induced damage. As a result, the applications of 3D DNA nanostructures have long been limited in aqueous environments. Ready access to free-standing 3D DNA nanostructures in the dry state could revolutionize many research areas, especially in the development of low-density, high-strength materials. Here we report a method to obtain free-standing wireframe 3D DNA tetrahedra in air on a solid substrate, such as SiO 2 and mica, by absorbing uranyl acetate and lyophilization. The dried DNA tetrahedron structure, 93 ± 2 nm in height, withstands 42 ± 22 nN of loading force. The effective hardness (9.1 ± 5.1 MPa) and Young's modulus (77 ± 48 MPa) of this low-density (70.7 kg/m 3 ) DNA-inorganic hybrid nanostructure are comparable to other reported low-density high-strength materials.

A number of inherent and thorny obstacles still stand in the way of the practical application of Li-O 2 batteries, which require development of an advanced lithium anode and O 2 cathode. Herein, the strategy of a symmetrical Li-O 2 battery is presented. Specifically, Cu nanoneedle arrays with a nanoengineered Au coating are grown directly on a Cu foam substrate (Au/Cu@FCu), which can act as both the anode backbone and the cathode in a Li-O 2 battery. The excellent conductivity, high porosity, large specific surface, and superior lithiophilicity as well as high catalytic activity of the Au/Cu@FCu electrodes can simultaneously regulate the deposition behavior of the lithium metal in the anode and catalyze the formation/decomposition of Li 2 O 2 in the cathode. As a result, the Li uniformly deposited on the Au/Cu@FCu anode without Li dendrites, showing a high Coulombic efficiency over 96% and a long and stable cycle lifetime over 970 h. At the same time, the Au/Cu@FCu cathode demonstrates extremely low overpotentials (0.64 V) and a much higher specific capacity of 27 270 mAh g -1 compared to the Li-O 2 batteries with a carbon-free cathode reported to date. Moreover, the "ebb and flow" phenomenon of the anode and cathode morphology is also observed in the Li-O 2 battery.

Dendrite growth of metal anodes is one of the key hindrances for both secondary aqueous metal batteries and nonaqueous metal batteries. In this work, a freestanding Ti 3 C 2 T x MXene@Zn paper is designed as both zinc metal anode and lithium metal anode host to address the issue. The binder-free Ti 3 C 2 T x MXene@Zn paper exhibits merits of good mechanical flexibility, high electronic conductivity, hydrophilicity, and lithiophilicity. The crystal growth mechanism of Zn metal on common Zn foil and Ti 3 C 2 T x MXene@Zn composite is also studied. It is found that the Ti 3 C 2 T x MXene@Zn paper can effectively suppress the dendrite growth of Zn, enabling reversible and fast Zn plating/stripping kinetics in an aqueous electrolyte. Moreover, the Ti 3 C 2 T x MXene@Zn paper can be used as a 3D host for a lithium metal anode. In this host, Zn is utilized as a nucleation agent to suppress the Li dendrite growth. The freestanding Ti 3 C 2 T x MXene@Zn@Li anode exhibits superior reversibility with high Coulombic efficiency (97.69% over 600 cycles at 1.0 mA cm -2 ) and low polarization compared with the Cu@Li anode. These findings may be useful for the design of dendrite-free metal-based energy storage systems.

Droplets suspended by acoustic levitation provide genuine substrate-free environments for understanding unconventional fluid dynamics, evaporation kinetics, and chemical reactions by circumventing solid surface and boundary effects. Using a fully levitated air-water interface by acoustic levitation in conjunction with drying-mediated nanoparticle self-assembly, here, we demonstrate a general approach to fabricating free-standing nanoassemblies, which can totally avoid solid surface effects during the entire process. This strategy has no limitation for the sizes or shapes of constituent metallic nanoparticle building blocks and can also be applied to fabricate free-standing bilayered and trilayered nanoassemblies or even three-dimensional hollow nanoassemblies. We believe that our strategy may be further extended to quantum dots, magnetic particles, colloids, etc. Hence, it may lead to a myriad of homogeneous or heterogeneous free-standing nanoassemblies with programmable functionalities.

We present a superconducting bolometer fabricated by a rolled-up technology that allows one to combine the two-dimensionality (2D) of the superconducting layer with a helical spiral curvature. The bolometer is formed as a free-standing Nb nanohelix acting as an ultrathin transition-edge sensor (TES) and having a negligible thermal contact to the substrate. We demonstrate the functionality of the thin-film TES by examining its microwave-detection performance in comparison with a commercial cryogenic bolometer from QMC Instruments. The nanohelix has been revealed to feature a noise equivalent power (NEP) of about 2 × 10 -10 W Hz -1/2 at a microwave radiation power of 9 W m -2 , which is 4 orders of magnitude smaller than the NEP of the QMC sensor at a similar radiation power. Furthermore, the forecast for the nanohelix is a 1 to 2 orders of magnitude shorter response time as compared to sensors based on commonly used 1 μm thick Si 3 N 4 membranes. The reason is the extremely low heat capacity of the 50 nm thick supporting material and the few contact points between the TES and the substrate. Our findings indicate that microwave radiation detection can be substantially improved by extending 2D superconducting structures into the 3D space.

Hollow nanocone array (HNCA) films (cm × cm), composed of two Ag and Au nanoshells, are fabricated via a low-cost and efficient colloidal lithography technique. The relative position of the Ag and Au nanoshells can be controlled to generate various chiral asymmetries. A pronounced chiroptical response is observed in the ultraviolet-visible region with the anisotropy factor up to 10 -1 , which is rooted in the asymmetric current oscillations and electric field distributions. Beyond previous reports on plasmonic chiral metamaterials, the HNCA can be free-standing and further transferred to other functional and flexible substrates, such as polydimethylsiloxane (PDMS), highly curved surfaces, prepatterned films, and hydrogels, while keeping the original features. The good transferability would make HNCA more flexible in specific applications. Furthermore, the chiral HNCAs offer a series of chiral resonance cavities, which are conducive for the research of chiral sensing, confinement, chiral signal transmission, and amplification. Overall, this work provides a scalable metamaterial to tune the plasmonic chiral response, and HNCA would be a promising candidate of the components in chiral optical devices and sensors.

Lithium-ion batteries have been regarded as one of the most promising energy storage devices, and development of low-cost batteries with high energy density is highly desired so that the cost per watt-hour ($/Wh) can be minimized. In this work, we report using ball-milled low-cost silicon (Si) as the starting material and subsequent carbon coating to produce low-cost hierarchical carbon-coated (HCC) Si. The obtained particles prepared from different Si sources all show excellent cycling performance of over 1000 mAh/g after 1000 cycles. Interestingly, we observed in situ formation of porous Si, and it is well confined in the carbon shell based on postcycling characterization of the hierarchical carbon-coated metallurgical Si (HCC-M-Si) particles. In addition, lightweight and free-standing electrodes consisting of the HCC-M-Si particles and carbon nanofibers were fabricated, which achieved 1015 mAh/g after 100 cycles based on the total mass of the electrodes. Compared with conventional electrodes, the lightweight and free-standing electrodes significantly improve the energy density by 745%. Furthermore, LiCoO 2 and LiNi 0.5 Mn 1.5 O 4 cathodes were used to pair up with the HCC-M-Si anode to fabricate full cells. With LiNi 0.5 Mn 1.5 O 4 as cathode, an energy density up to 547 Wh/kg was achieved by the high-voltage full cell. After 100 cycles, the full cell with a LiNi 0.5 Mn 1.5 O 4 cathode delivers 46% more energy density than that of the full cell with a LiCoO 2 cathode. The systematic investigation on low-cost Si anodes together with their applications in lightweight free-standing electrodes and high-voltage full cells will shed light on the development of high-energy Si-based lithium-ion batteries for real applications.

A rotary disc-structured triboelectric nanogenerator (rd-TENG) on the basis of free-standing electrification has been designed, where the aluminum composite panel has not been tailored to the stator becauseit is commercially available and cost-effective, has good electronic conductivity, and is easily processed. With the rotating speed increasing from 200 to 1000 rpm, the short-circuit current (I sc ) is sharply enhanced from 50 μA to 200 μA, while the measured open-circuit voltage (V oc ) and transferred charge (Q tr ) almost keep constant, 600 V and 0.4 μC, respectively. The matched load for the rd-TENG at a rotating speed of 600 rpm is 2.7 MΩ, generating a maximum power of 19.75 mW, which corresponds to a maximum power density of 2.28 W m -2 . Using the electric power generated by such a rd-TENG, highly toxic and carcinogenic 4-aminoazobenzene can be selectively treated to produce CO 2 or an oligomer via reasonably controlling electrochemical oxidation potentials. The underlying mechanism is tentatively proposed based on the cyclic voltammogram, gas chromatograph-mass spectrometer, electrochemical impedance spectroscopy, and UV-vis spectra. Here the electrochemical degradation in a single-compartment cell is more valid, preferable, and feasible. The output V oc and rectified current of rd-TENG guarantee its extensive application to self-power electrochemical degradation of other azo compounds, i.e., 2-(4-dimethylaminophenylazo) benzoic acid, to CO 2 . This work suggests that rd-TENG, sustainable energy, can be feasibly designed to self-power a practical electrochemical treatment of dyeing wastewater by harvesting vibration energy.

The preparation of materials exhibiting structural colors has been intensively studied in biomimetic science and technology. Utilizing a newly synthesized cholesteric liquid-crystal (CLC) monomer (abbreviated as BP 1 CRM), we have prepared CLC films. Photoinitiated copolymerization of this monomer with a common achiral liquid-crystalline monomer produced free-standing films with homogeneous and nanoscale pitch distributions. Employing the thermal sensitivity of the CLC monomer, chirophotonic crystal reflectors were prepared exhibiting a range of colors. The free-standing and circular-polarizing chirophotonic crystal films maintain excellent thermal, mechanical, and chemical stabilities, and the composition can readily be applied as polarized optical films and smart paints.

Mechanical instability has been shown to play an important role in the formation of wrinkle structures in biofilms, which not only can adopt instability modes as templates to regulate their 3D architectures but also can tune internal stresses to achieve stable patterns. Inspired by nature, we report a mechanical-chemical coupling method to fabricate free-standing conducting films with instability-driven hierarchical micro/nanostructured patterns. When polypyrrole (PPy) film is grown on an elastic substrate via chemical oxidation polymerization, differential growth along with in situ self-reinforcing effect induces stable wrinkle patterns with different scales of wavelengths. The self-reinforcing effect modifies the internal stresses, hence PPy films with intact wrinkles can be removed from substrates and further transferred onto target substrates for functional device fabrication. To understand the buckling mechanics, we construct a model which reveals the formation of hierarchical wrinkle patterns.

A simple and scalable method which combines traditional powder metallurgy and chemical vapor deposition is developed for the synthesis of mesoporous free-standing 3D graphene foams. The powder metallurgy templates for 3D graphene foams (PMT-GFs) consist of particle-like carbon shells which are connected by multilayered graphene that shows high specific surface area (1080 m(2) g(-1)), good crystallization, good electrical conductivity (13.8 S cm(-1)), and a mechanically robust structure. The PMT-GFs did not break under direct flushing with DI water, and they were able to recover after being compressed. These properties indicate promising applications of PMT-GFs for fields requiring 3D carbon frameworks such as in energy-based electrodes and mechanical dampening.

Free-standing electrodes with high gravimetric/volumetric capacitance will open up potential applications in miniaturized consumer electronics. Herein, we report a simple synthesis technology of free-standing orthorhombic Nb2O5 (T-Nb2O5)/graphene composite papers for Li-intercalating pseudocapacitive electrodes. Through a facile polyol-mediated solvothermal reaction, the Nb2O5 nanodots are homogeneously decorated onto the surface of reduced graphite oxide (rGO), which can form a homogeneous Nb2O5/rGO colloidal suspension that can be easily fabricated into flexible composite papers. The heat-treated T-Nb2O5/graphene composite papers exhibit a nanoporous layer-stacked structure with good ionic-electric conductive pathways, high T-Nb2O5 loading of 74.2%, and high bulk density of 1.55 g cm(-3). Such T-Nb2O5/graphene composite papers show a superior pseudocapacitor performance as free-standing electrodes, as evidenced by an ultrahigh gravimetric/volumetric capacitance (620.5 F g(-1) and 961.8 F cm(-3) at 1 mV s(-1)) and excellent rate capability. Furthermore, an organic electrolyte-based asymmetric supercapacitor is assembled based on T-Nb2O5/graphene composite papers, which can deliver a high energy density of 47 W h kg(-1) and power density of 18 kW kg(-1).

The synthesis of rebar graphene on Cu substrates is described using functionalized boron nitride nanotubes (BNNTs) that were annealed or subjected to chemical vapor deposition (CVD) growth of graphene. Characterization shows that the BNNTs partially unzip and form a reinforcing bar (rebar) network within the graphene layer that enhances the mechanical strength through covalent bonds. The rebar graphene is transferrable to other substrates without polymer assistance. The optical transmittance and conductivity of the hybrid rebar graphene film was tested, and a field effect transistor was fabricated to explore its electrical properties. This method of synthesizing 2D hybrid graphene/BN structures should enable the hybridization of various 1D nanotube and 2D layered structures with enhanced mechanical properties.