We use micro-bubble based thermo-optical tweezers to simultaneously synthesize, dope, and pattern conducting polymers to obtain unprecedented conductivity values.
We have designed a supramolecularly bound multi-component catalytic material based on a soft oxometalate (SOM) and a porous organic framework (POF) material, which shows high catalytic conversion efficiency.
A microbubble nucleated due to the absorption of a tightly focused laser at the interface of a liquid−solid substrate enables directed and irreversible self-assembly of mesoscopic particles dispersed in the liquid at the bubble base. This phenomenon has facilitated a new microlithography technique which has grown rapidly over the past decade and can now reliably pattern a vast range of soft materials and colloids, ranging from polymers to metals to proteins. In this review, we discuss the science behind this technology and the present state-of-the-art. Thus, we describe the physics of the self-assembly driven by the bubble, the techniques for generating complex mesoarchitectures, both discrete and continuous, and their properties, and the various applications demonstrated in plastic electronics, site-specific catalysis, and biosensing. Finally, we describe a roadmap for the technique to achieve its potential of successfully patterning "everything" mesoscopic and the challenges that lie therein.
The propagation of flexural gravity waves, routinely used to model wave interaction with sea ice, is studied, including the effect of compression and current. A number of significant and surprising properties are shown to exist. The occurrence of blocking above a critical value of compression is illustrated. This is analogous to propagation of surface gravity waves in the presence of opposing current and light wave propagation in the curved space-time near a black hole, therefore providing a novel system for studying analogue gravity. Between the blocking and buckling limit of the compressive force, the dispersion relation possesses three positive real roots, contrary to an earlier observation of having a single positive real root. Negative energy waves, in which the phase and group velocity point in opposite directions, are also shown to exist. In the presence of an opposing current and certain critical ranges of compressive force, the second blocking point shifts from the positive to the negative branch of the dispersion relation. Such a shift is known as the Hawking effect from the analogous behaviour in the theory of relativity which leads to Hawking radiation. The theory we develop is illustrated with simulations of linear waves in the time domain.
We report soft-oxometalate catalytic systems based on various metal oxide catalysts to oxidize H2O and utilize the generated H+s and e−s for reduction of CO2 with a TON of 1366 (effectively 1.4 x 106).
Photocatalytic CO2 reduction in water is one of the most attractive research pursuits of our time. In this article we report a giant polyoxometalate {Mo368} based homogeneous catalytic system, which efficiently reduces CO2 to formic acid with a maximum turnover number (TON) of 27,666, turnover frequency (TOF) of 4,611 h−1 and external quantum efficiency of the reaction is 0.6%. The catalytic system oxidizes water and releases electrons, and these electrons are further utilized for the reduction of CO2 to formic acid. A maximum of 8.3 mmol of formic acid was observed with the loading of 0.3 μmol of the catalyst. Our catalyst material is also stable throughout the reaction. The starting materials for this experiment are CO2 and H2O and the end products are HCOOH and O2. The formic acid formed in this reaction is an important H2 gas carrier and thus significant in renewable energy research.
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