Molybdenum disulfide (MoS2 ) quantum dots (QDs) (size <10 nm) possess attractive new properties due to the quantum confinement and edge effects as graphene QDs. However, the synthesis and application of MoS2 QDs has not been investigated in great detail. Here, a facile and efficient approach for synthesis of controllable-size MoS2 QDs with excellent photoluminescence (PL) by using a sulfuric acid-assisted ultrasonic route is developed for this investigation. Various MoS2 structures including monolayer MoS2 flake, nanoporous MoS2 , and MoS2 QDs can be yielded by simply controlling the ultrasonic durations. Comprehensive microscopic and spectroscopic tools demonstrate that the MoS2 QDs have uniform lateral size and possess excellent excitation-independent blue PL. The as-generated MoS2 QDs show high quantum yield of 9.65%, long fluorescence lifetime of 4.66 ns, and good fluorescent stability over broad pH values from 4 to 10. Given the good intrinsic optical properties and large surface area combined with excellent physiological stability and biocompatibility, a MoS2 QDs-based intracellular microRNA imaging analysis system is successfully constructed. Importantly, the MoS2 QDs show good performance as multiphoton bioimaging labeling. The proposed synthesis strategy paves a new way for facile and efficient preparing MoS2 QDs with tunable-size for biomedical imaging and optoelectronic devices application.

Two-dimensional (2D) materials are known to be useful in catalysis. Engineering 3D bulk materials into the 2D form can enhance the exposure of the active edge sites, which are believed to be the origin of the high catalytic activity. Reported herein is the production of 2D "few-layer" antimony (Sb) nanosheets by cathodic exfoliation. Application of this 2D engineering method turns Sb, an inactive material for CO reduction in its bulk form, into an active 2D electrocatalyst for reduction of CO to formate with high efficiency. The high activity is attributed to the exposure of a large number of catalytically active edge sites. Moreover, this cathodic exfoliation process can be coupled with the anodic exfoliation of graphite in a single-compartment cell for in situ production of a few-layer Sb nanosheets and graphene composite. The observed increased activity of this composite is attributed to the strong electronic interaction between graphene and Sb.

Micro-supercapacitors are a promising candidate whose reliability and performances are struggling to meet the energy demands dictated by the incoming generation of miniaturized electronic devices. In this paper, we describe a facile and low-cost method for fabricating flexible and all-solid-state micro supercapacitors by microfluidic etching. The micro-supercapacitor configuration is composed of sub-10-nm-scale MnO(2) nanoparticle interdigital microelectrode fingers prepared by microfluidic etching with H(3)PO(4)-PVA thin films as both the solid-state electrolyte and the flexible substrate. The entire device shows outstanding electrochemical performances with high specific capacitance and stable cycle life, and the performance can be mostly preserved even conditions of under repeated bending. The technique we describe here is a universal method for fabricating a micro-supercapacitor, since the microfluidic etching can be extended to most active materials which can be used for energy- and power-devices, and there are many other choices for the solid electrolyte. Thus, these micro-supercapacitors provide a promising power source in microelectromechanical systems (MEMS), wearable electronics and other general requirements.

Compared with the organic, ionic liquid, and solid-state electrolytes, aqueous electrolytes have the advantages of good security, environmental friendliness, high ionic conductivity, low cost, and high operability in ordinary environments. [1][2][3][4][5] Therefore, aqueous secondary ion batteries/capacitors are more attractive in large-scale energy storage, and have greater application prospects. [6][7][8][9] However, even so, there still exists several disadvantages as follows: 1) The thermodynamic electrochemical stability window (ESW) of water is as narrow as 1.23 V. Even considering the existence of overpotential, the ESWs of conventional aqueous electrolytes are not higher than 2 V. 2) Usually, the electrode materials cannot form stable interface in water, so it is difficult to ensure the cycling stability. 3) Dissolution and even decomposition of electrode materials and discharge/charge products limit the choice of electrode materials. [10] These factors have limited the improvement of key electrochemical performance indicators such as energy density, output voltage, and cycle life of aqueous energy-storage devices Aqueous energy-storage systems have attracted wide attention due to their advantages such as high security, low cost, and environmental friendliness. However, the specific chemical properties of water induce the problems of narrow electrochemical stability window, low stability of water-electrode interface reactions, and dissolution of electrode materials and intermediate products. Therefore, new low-cost aqueous electrolytes with different water chemistry are required. The nature of water depends largely on its hydroxylbased hydrogen bonding structure. Therefore, the super-concentrated hydroxyl-rich sugar solutions are designed to change the original hydrogen bonding structure of water. The super-concentrated sugars can reduce the free water molecules and destroy the tetrahedral structure, thus lowering the binding degree of water molecules by breaking the hydrogen bonds. The ionic electrolytes based on super-concentrated sugars have the expanded electrochemical stability window (up to 2.812 V), wide temperature adaptability (-50 to 80 °C), and fair ionic conductivity (8.536 mS cm −1 ). Aqueous lithium-, sodium-, potassium-ion batteries and supercapacitors using super-concentrated sugar-based electrolytes demonstrate an excellent electrochemical performance. The advantages of ultralow cost and high universality enable a great practical application potential of the superconcentrated sugar-based aqueous electrolytes, which can also provide great experimental and theoretical assistance for further research in water chemistry.

In this study, we develop a new technique to fabricate a reduced graphene oxide (rGO)-based microelectrode array (MEA) with low-cost soft lithography. To prepare patterned rGO, a polydimethylsiloxane (PDMS) mold with an array of microwells on its surface is fabricated using soft lithography, and GO is assembled on an indium tin oxide (ITO) electrode with a layer-by-layer method. The rGO pattern is formed by closely contacting the assembled GO film onto the ITO electrode with the PDMS mold filled with hydrazine solution in the microwells to selectively reduce the localized GO into the rGO. The MEA with patterned rGO as the microelectrode is characterized with Kelvin probe force microscopy (KFM), atomic force microscopy (AFM), and cyclic voltammetry (CV) with ferricyanide in aqueous solution as the redox probe. The KFM and AFM results demonstrate that each rGO pattern prepared under the present conditions is 3 μm in diameter, which is close to that of the PDMS mold we use. The CV results show that the rGO patterned onto the ITO exhibits a sigmoid-shaped voltammogram up to 200 mVs(-1) with a microampere level current response, suggesting that the rGO-based electrode fabricated with soft lithography behalves like a MEA. To demonstrate the potential electroanalytical application of the rGO-based MEA, prussian blue (PB) is electrodeposited onto the rGO-based MEA to form the PB/rGO-based MEA. Electrochemical studies on the formed PB/rGO-based MEA reveal that MEA shows a lower detection limit and a larger current density for the detection of H(2)O(2), as compared with the macroscopic rGO electrode. The method demonstrated here provides a simple and low-cost strategy for the fabrication of graphene-based MEA that are useful for electroanalytical applications.