Compressible and Elastic Reduced Graphene Oxide Sponge for Stable and Dendrite-Free Lithium Metal Anodes.

Dendritic Li deposition, an unstable solid-electrolyte interphase (SEI), and a nearly infinite relative volume change during cycling are three major obstacles to the practical application of Li metal batteries. Herein, we introduce a compressible and elastic reduced graphene oxide sponge (rGO-S) to simultaneously eliminate Li dendrite growth, stabilize the SEI, and accommodate the volume change. The volume change is contained by compressing and expanding the rGO-S anode, which effectively releases the Li plating-induced stress during cycling. The smooth and dense Li metal is deposited on rGO-S without dendrites, which preserves the SEI, reduces consumption of the electrolyte, and prevents the formation of Li debris. The half-cells employing rGO-S show a steady and high Coulombic efficiency. The Li@rGO-S symmetric cells demonstrate excellent cycling stability over 1200 cycles with a low overpotential. When paired with LiFePO4 (LFP), the Li@rGO-S||LFP full cells exhibit a high specific capacity (150.3 mAh g-1 at 1C), superior rate performance, and good capacity retention.

Portable Triboelectric Electrostatic Tweezer for External Manipulation of Droplets within a Closed Femtosecond Laser-Treated Superhydrophobic System.

Controllable droplet manipulation has diverse applications; however, limited methods exist for externally manipulating droplets in confined spaces. Herein, we propose a portable triboelectric electrostatic tweezer (TET) by integrating electrostatic forces with a superhydrophobic surface that can even manipulate droplets in an enclosed space. Electrostatic induction causes the droplet to be subjected to an electrostatic force in an electrostatic field so that the droplet can be moved freely with the TET on a superhydrophobic platform. Characterized by its high precision, flexibility, and robust binding strength, TET can manipulate droplets under various conditions and achieve a wide range of representative fluid applications such as droplet microreactors, precise self-cleaning, cargo transportation, the targeted delivery of chemicals, liquid sorting, soft droplet robotics, and cell labeling. Specifically, TET demonstrated the ability to manipulate internal droplets from the outside of a closed system, such as performing cell labeling experiments within a sealed Petri dish without opening the culture system.

A Hierarchical Anodic Aluminum Oxide Template.

Anodic aluminum oxide (AAO) templates are widely used for the development of various functional nanomaterials due to their highly ordered and tunable porous structures. Here, we report a new hierarchical AAO (hAAO) template with the hexagonally ordered unit cells and the radially distributed nanochannels. It is formed by integrating the self-assembled polystyrene microsphere template into the AAO fabrication process and rationalized in terms of mechanical stress and electric-field-induced oxide dissolution. The back side of the hAAO template resembles a moth-eye-like nanoarray, which shows good hydrophobicity. A variety of radial nanopillar arrays and moth-eye-like nanoarrays are fabricated by a series of materials and synthesis techniques employing the hAAO template. These unique nanoarrays demonstrate many physicochemical properties that are distinct from those obtained from the conventional AAO template.

A New Organic Interlayer Spacer for Stable and Efficient 2D Ruddlesden-Popper Perovskite Solar Cells.

Two-dimensional (2D) perovskite materials have exhibited great possibilities toward the fabrication of highly efficient and stable solar cell devices. The large degree of structural versatility due to the viable choices of organic interlayer spacers promises new and valuable 2D perovskite species. Herein, phenyltrimethylammonium (PTA+) is successfully employed as the organic interlayer spacer to prepare the 2D Ruddlesden-Popper perovskite films that exhibit exceptional optoelectronic properties. By adding Cl- ions during film growth, the (PTA)2(MA)3Pb4I13 (MA = methylammonium) perovskite films are effectively prepared with a tunable crystal orientation and film morphology. The optimized devices fabricated with the assistance of Cl- ions deliver the power conversion efficiency up to 11.53%, which is ascribed to the simultaneous reductions of charge transfer resistance and defect-induced charge recombination. Moreover, the PTA-based 2D perovskite solar cells demonstrate remarkable environmental and thermal stabilities.

Multifunctional Electrostatic Droplet Manipulation on the Femtosecond Laser-Prepared Slippery Surfaces.

A strategy to manipulate droplets on the lubricated slippery surfaces using tribostatic electricity is proposed. By employing femtosecond laser-induced porous microstructures, we prepared a slippery surface with ultralow adhesion to various liquids. Electrostatic induction causes the charges within the droplet to be redistributed; thus, the droplet on the as-prepared slippery surfaces can be guided by electrostatic force under the electrostatic field, with controllable sliding direction and unlimited transport distance. The combination of electrostatic interaction and slippery surfaces allows us to manipulate droplets with a wide volume range (from 100 nL to 0.5 mL), charged droplets (including electrostatic attraction and repulsion), corrosive droplets, and even organic droplets with ultralow surface tension. In addition, droplets on tilted surfaces, curved surfaces, and inverted slippery surfaces can also be manipulated. Especially, the slippery surfaces can even allow the electrostatic interaction to manipulate alcohol with surface tension as low as 22.3 mN/m and liquid droplets suspended on a downward surface, which is not possible with reported superhydrophobic substrates. The features of slippery surfaces make the electrostatic manipulation successfully applied in versatile droplet manipulation, droplet patterning, chemical microreaction, transport of solid cargo, targeted delivery of chemicals, and liquid sorting.

A nanomesh electrode for self-driven perovskite photodetectors with tunable asymmetric Schottky junctions.

Self-driven photodetectors are essential for many applications where it is unpractical to provide or replace power sources. Here, we report a new device architecture for self-driven photodetectors with tunable asymmetric Schottky junctions based on a nanomesh electrode. The vertical-channel nanomesh scaffold is composed of a hexagonally ordered nanoelectrode array fabricated via the nanosphere lithography technique. The top and bottom nanoelectrodes are separated by only 30 nm and the areal ratio of the two nanoelectrodes can be fine-tuned, which effectively modifies the geometric asymmetricity of the Schottky junctions in the photodetector devices. The self-driven photodetectors are fabricated by depositing the (FAPbI3)0.97(MAPbBr3)0.03 (MA = methylammonium, FA = formamidinium) perovskite films onto the nanomesh electrodes. Under the self-driven mode, the optimized device demonstrates a high detectivity of 1.05 × 1011 Jones and a large on/off ratio of 2.1 × 103. This nanomesh electrode is very versatile and can be employed to investigate the optoelectronic properties of various semiconducting materials.

Improving efficiency and stability of colorful perovskite solar cells with two-dimensional photonic crystals.

Colorful solar cells have been much sought after because they can generate electricity and concurrently satisfy ornamentation purposes. Owing to their outstanding power conversion efficiency and flexibility in processing, perovskite solar cells (PSCs) have the great potential to become both efficient and aesthetically appealing. Here, we specially devise and fabricate two novel electron transport layers (ETLs) for PSCs with two-dimensional (2D) photonic crystal structures, namely the 2D inverse opal (IO) structured SnO2 (IOS) and SnO2-TiO2 composite (IOST), using the template-assisted spin-coating method. The synergistic structure and material modifications to the ETLs lead to a number of unique features, including the remarkable electron transfer ability, vivid colors and good protection to the infiltrated perovskite films. Furthermore, the IOS and IOST ETLs are effectively incorporated into the CH3NH3PbI3-based PSC devices that deliver the best efficiency of 16.8% with structural colors.

In Situ Real-Time Study of the Dynamic Formation and Conversion Processes of Metal Halide Perovskite Films.

Metal halide perovskite solar cells (PSCs) have advanced to the forefront of solution-processed photovoltaic techniques and made stunning progress in power conversion efficiency (PCE). Further improvements in device performances rely on perfecting the structure and morphology of perovskite films. However, undesirable defects such as pinholes and grain boundaries are often created in film preparations due to lack of knowledge of the precise reaction mechanism. Here, in situ grazing-incidence X-ray diffraction (GI-XRD) investigations are performed, facilitated by other techniques, on the formation of the widely adopted MAPbI3 (MA = methylammonium) perovskite films from their intermediate adduct (IA) phases. The influences of solvent vapor atmospheres on MAPbI3 films are also systematically investigated, where the dynamic conversion processes between different phases are visualized in real time. Further in situ GI-XRD and infrared spectroscopy measurements reveal that the IA phases contain both N,N-dimethylformamide and dimethyl sulfoxide (DMSO) as coordinating molecules. By tuning the DMSO concentration in perovskite precursors, the ideal perovskite film is formed and the best PCE is achieved for the planar MAPbI3 -based PSCs. These findings highlight the role of IA phases and the effect of solvent atmospheres on the quality of perovskite films, providing direct insights into their growth mechanism.