4,218 publications from this institution
As one of their major goals, researchers attempting to harvest mechanical energy efficiently have continuously sought ways to integrate mature technologies with cutting-edge designs to enhance the performances of triboelectric nanogenerators (TENGs). In this research, we introduced monolayer molybdenum-disulfide (MoS2) into the friction layer of a TENG as the triboelectric electron-acceptor layer in an attempt to dramatically enhance its output performance. As a proof of the concept, we fabricated a vertical contact-separation mode TENG containing monolayer MoS2 as an electron-acceptor layer and found that the TENG exhibited a peak power density as large as 25.7 W/m2, which is 120 times larger than that of the device without monolayer MoS2. The mechanisms behind the performance enhancement, which are related to the highly efficient capture of triboelectric electrons in monolayer MoS2, are discussed in detail. This study indicates that monolayer MoS2 can be used as a functional material for efficient energy harvesting.
Static metal-semiconductor contacts are classified into Ohmic contacts and Schottky contacts. As for dynamic metal-semiconductor contacts, the in-depth mechanism remains to be studied. We here define a "triboelectric junction" model for analyzing dynamic metal-semiconductor contacts, where a space charge region induced by the triboelectric effect dominates the electron-hole separation process. Through theoretical analysis and experiments, we conclude that the triboelectric junction affects the electric output in two aspects: 1) the junction direction determines the output polarity; 2) the junction strength determines the output amplitude. The junction direction and junction strength are both related to the electron-affinity difference between the contact metal and semiconductor. We find that the standard electrode potential in electrochemistry best describes the electron affinity of a dynamic metal-semiconductor contact.
We report on in situ observations of nucleation, growth, and aggregation of hybrid organic–inorganic perovskites by liquid-cell transmission electron microscopy. Direct crystallization of hybrid CH3NH3PbI3 nanoparticles is achieved through an electron beam-assisted solvent evaporation approach. Time-lapse liquid-cell TEM imaging of the nanoparticles reveals a growth trend which is not entirely consistent with the classical Lifshitz–Slyozov–Wagner growth model. Significantly complex dynamical behaviors are observed during the coalescence process of CH3NH3PbI3 nanoparticles. We propose that the chemical instability inherent in the hybrid perovskite iodides should be considered to understand this phenomenon in addition to the oriented attachment mechanism. This study provides a useful reference for understanding the intriguing chemical and physical properties of hybrid organic–inorganic perovskites.
Recently, we have been able to synthesize platinum colloidal nanoparticles of different shapes (Science, 1996, 272, 1924). In this report, we present transmission electron microscopic (TEM) results on the time-dependent shape distribution of platinum nanoparticles during the growth period and its dependence on the concentration of the capping polymer as well as the pH of the solution. The results suggest a shape-controlled growth mechanism in which the difference between the rate of the catalytic reduction process of Pt2+ on the {111} and {100} faces, the competition between the Pt2+ reduction and the capping process on the different nanoparticle surfaces, and the concentration-dependent buffer action of the polymer itself all control the final distribution of the different shapes observed.