Recent Strategies for the Synthesis of Phase-Pure Ultrathin 1T/1T' Transition Metal Dichalcogenide Nanosheets.

The past few decades have witnessed a notable increase in transition metal dichalcogenide (TMD) related research not only because of the large family of TMD candidates but also because of the various polytypes that arise from the monolayer configuration and layer stacking order. The peculiar physicochemical properties of TMD nanosheets enable an enormous range of applications from fundamental science to industrial technologies based on the preparation of high-quality TMDs. For polymorphic TMDs, the 1T/1T' phase is particularly intriguing because of the enriched density of states, and thus facilitates fruitful chemistry. Herein, we comprehensively discuss the most recent strategies for direct synthesis of phase-pure 1T/1T' TMD nanosheets such as mechanical exfoliation, chemical vapor deposition, wet chemical synthesis, atomic layer deposition, and more. We also review frequently adopted methods for phase engineering in TMD nanosheets ranging from chemical doping and alloying, to charge injection, and irradiation with optical or charged particle beams. Prior to the synthesis methods, we discuss the configuration of TMDs as well as the characterization tools mostly used in experiments. Finally, we discuss the current challenges and opportunities as well as emphasize the promising fields for the future development.

Retarding the Shuttling Ions in the Electrochromic TiO2 with Extensive Crystallographic Imperfections.

To understand the role of structure imperfections on the performance of electrochromic transition metal oxide (ETMO) is challenging for the design of efficient smart windows. Herein, we investigate the performance evolution with tunable crystallographic imperfections for rutile TiO2 nanowire film (TNF). Structure imperfections, originating mainly from the copious oxygen deficiency, are apt to cumulatively retard the shuttling ions, resulting in the response rate for raw TNF being less than the half that of TNF annealed at 500 °C. We describe ion accommodation sites as a convolution of normal site and abnormal site, in which the normal site performs reversible coloration but the abnormal site contributes only to charge storage, which gives a rationale for the non-linear coloration and rate capability loss. These findings give a clear picture of the ion shuttling process, which is insightful for enhancing the electrochromic performance via structure reprogramming.

Electron Transport in Low Dimensional Solids: A Surface Chemistry Perspective.

Electron transport is a fundamental process that controls the intrinsic chemical and physical properties of solid materials. The surface phase becomes dominant when downsized dimensionality into cluster scale in nanomaterials, and surface chemistry plays more and more important role in regulating electron transport. During past decades, varieties of chemical approaches have been developed to modify the surface of low dimensional solids, substantially providing versatile perspectives on engineering electron transport. In this Perspective, we focus on recent researches concerning surface chemical modification strategies, such as surface molecular adsorption, atomic incorporation, defect engineering and spin scattering to engineer electron transport of typical one-/two-dimensional systems. Under the framework of Drude's transport model, we highlight the core role of micro degrees of freedom, i.e., charge, lattice, and spin, in molecular-level understanding and optimizing the regulation effect of surface chemistry. Finally, based on the discussion and current achievements of surface chemistry effect on electron transport of low dimensional solids, some personal perspectives on the future development are also presented.

Orthogonal navigation of multiple visible-light-driven artificial microswimmers.

Nano/microswimmers represent the persistent endeavors of generations of scientists towards the ultimate tiny machinery for device manufacturing, targeted drug delivery, and noninvasive surgery. In many of these envisioned applications, multiple microswimmers need to be controlled independently and work cooperatively to perform a complex task. However, this multiple channel actuation remains a challenge as the controlling signal, usually a magnetic or electric field, is applied globally over all microswimmers, which makes it difficult to decouple the responses of multiple microswimmers. Here, we demonstrate that a photoelectrochemically driven nanotree microswimmer can be easily coded with a distinct spectral response by loading it with dyes. By using different dyes, an individual microswimmer can be controlled and navigated independently of other microswimmers in a group. This development demonstrates the excellent flexibility of the light navigation method and paves the way for the development of more functional nanobots for applications that require high-level controllability.

A Silicon Nanowire as a Spectrally Tunable Light-Driven Nanomotor.

Over the last decades, scientists have endeavored to develop nanoscopic machines and envisioned that these tiny machines could be exploited in biomedical applications and novel material fabrication. Here, a visible-/near-infrared light-driven nanomotor based on a single silicon nanowire is reported. The silicon nanomotor harvests energy from light and propels itself by the self-electrophoresis mechanism. Due to the high efficiency, the silicon nanowire can be readily driven by visible and near-infrared illumination at ultralow light intensity (≈3 mW cm-2 ). The experimental study and numerical simulation also show that the detailed structure around the concentrated reaction center determines the migration behavior of the nanomotor. Importantly, due to the optical resonance inside the silicon nanowire, the spectral response of the nanowire-based nanomotor can be readily modulated by the nanowire's diameter. Compared to other methods, light controlling potentially offers more freedom and flexibility, as light can be modulated not only with its intensity and direction, but also with the frequency and polarities. This nanowire motor demonstrates a step forward to harness the advantages of light, which opens up new opportunities for the realization of many novel functions such as multiple channels communication to nanorobots and controllable self-assembly.

Programmable artificial phototactic microswimmer.

Phototaxis is commonly observed in motile photosynthetic microorganisms. For example, green algae are capable of swimming towards a light source (positive phototaxis) to receive more energy for photosynthesis, or away from a light source (negative phototaxis) to avoid radiation damage or to hide from predators. Recently, with the aim of applying nanoscale machinery to biomedical applications, various inorganic nanomotors based on different propulsion mechanisms have been demonstrated. The only method to control the direction of motion of these self-propelled micro/nanomotors is to incorporate a ferromagnetic material into their structure and use an external magnetic field for steering. Here, we show an artificial microswimmer that can sense and orient to the illumination direction of an external light source. Our microswimmer is a Janus nanotree containing a nanostructured photocathode and photoanode at opposite ends that release cations and anions, respectively, propelling the microswimmer by self-electrophoresis. Using chemical modifications, we can control the zeta potential of the photoanode and program the microswimmer to exhibit either positive or negative phototaxis. Finally, we show that a school of microswimmers mimics the collective phototactic behaviour of green algae in solution.