Robust Co-catalytic Performance of Nanodiamonds Loaded on WO3 for the Decomposition of Volatile Organic Compounds under Visible Light

Proper co-catalysts (usually noble metals), combined with semiconductor materials, are commonly needed to maximize the efficiency of photocatalysis. Search for cost-effective and practical alternatives for noble-metal co-catalysts is under intense investigation. In this work, nanodiamond (ND), which is a carbon nanomaterial with a unique sp(3)(core)/sp(2)(shell) structure, was combined with WO3 (as an alternative co-catalyst for Pt) and applied for the degradation of volatile organic compounds under visible light. NDs-loaded WO3 showed a highly enhanced photocatalytic activity for the degradation of acetaldehyde (similar to 17 times higher than bare WO3), which is more efficient than other well-known co-catalysts (Ag, Pd, Au, and CuO) loaded onto WO3 and comparable to Pt-loaded WO3. Various surface modifications of ND and photoelectochemical measurements revealed that the graphitic carbon shell (sp(2)) on the diamond core (spa) plays a crucial role in charge separation and the subsequent interfacial charge transfer. As a result, ND/WO3 showed much higher production of OH radicals than bare WO3 under visible light. Since ND has a highly transparent characteristic, the light shielding that is often problematic with other carbon-based co-catalysts was considerably lower with NDs-loaded WO3. As a result, the photocatalytic activity of NDs/WO3 was higher than that of WO3 loaded with other carbon-based co-catalysts (graphene oxide or reduced graphene oxide). A range of spectroscopic and photo(electro)chemical techniques were systematically employed to investigate the properties of NDs-loaded WO3. ND is proposed as a cost-effective and practical nanomaterial to replace expensive noble-metal co-catalysts.1124Ysciescopu

Boosting Up the Low Catalytic Activity of Silver for H2 Production on Ag/TiO2 Photocatalyst: Thiocyanate as a Selective Modifier

Noble metal cocatalysts like Pt have been widely employed as an essential ingredient in many kinds of photocatalytic materials for solar hydrogen production. The high material cost of Pt is the biggest limitation. Silver is far less expensive but much less active than Pt and Au as a hydrogen evolving catalyst. Here we demonstrate a new strategy to boost up the activity of silver in Ag/TiO2 for photocatalytic H-2 production via forming a simple surface complexation of thiocyanate (SCN-) on silver. The addition of thiocyanate in the suspension of Ag/TiO2 markedly enhanced the photocatalytic production of H-2 by about 4 times. Thiocyanate was not consumed at all during the photoreaction, which ruled out the role of thiocyanate as an electron donor. Such a positive role of thiocyanate was not observed with bare TiO2, Pt/TiO2, and Au/TiO2. The selective chemisorption of thiocyanate on silver was confirmed by the analyses of Raman spectroscopy and spot-profile energy-dispersive spectroscopy. In the presence of thiocyanate, the overpotential for water reduction on Ag/TiO2 electrode was slightly reduced, and the interfacial charge transfer resistance on Ag/TiO2 (measured by electrochemical impedance spectroscopy) was significantly decreased, whereas other electrode systems (bare TiO2, Au/TiO2, and Pt/TiO2) showed the opposite effect of thiocyanate. These results indicate that the adsorption of thiocyanate on Ag facilitates the transfer of photogenerated electrons on the Ag/TiO2 electrode. It is proposed that the formation of Ag-SCN surface complex enhances the interfacial electron transfer rate and facilitates the reduction of protons on Ag/TiO2.115640Ysciescopu

Selective Dual-purpose Photocatalysis for Simultaneous H2 Evolution and Mineralization of Organic Compound Enabled by Cr2O3 Barrier Layer Coated on Rh/SrTiO3

Dual-functional photocatalysis for H-2 evolution with the simultaneous mineralization of 4-chlorophenol was achieved under de-aerated conditions using a Cr2O3/Rh/SrTiO3 photocatalyst which has Rh nanoparticles covered with a thin Cr2O3 barrier layer to selectively control and maximize the dual-functional photocatalytic activity.111511Ysciescopu

Parameter-robust linear quadratic Gaussian technique for multi-agent slung load transportation

This paper copes with parameter-robust controller design for transportation system by multiple unmanned aerial vehicles. The transportation is designed in the form of string connection. Minimal state-space realization of slung-load dynamics is obtained by Newtonian approach with spherical coordinates. Linear quadratic Gaussian / loop transfer recovery (LQG/LTR) is implemented to control the position and attitude of all the vehicles and payloads. The controller's robustness against variation of payload mass is improved using parameter-robust linear quadratic Gaussian (PRLQG) method. Numerical simulations are conducted with several transportation cases. The result verifies that LQG/LTR shows fast performance while PRLQG has its strong point in robustness against system variation

Photochemical deposition of metal nanoparticles on reduced graphene oxide sheets using polyoxometalate

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Bezier-curve Navigation Guidance for Impact Time and Angle Control

This paper addresses a novel impact time and angle control guidance law using a Bézier curve. The 2nd order Bézier curve consists of one control point and two boundary points; initial point P0, middle point P1 and end point P2. The curve is tangent to the line P0-P1 and the line P1-P2, respectively, and always exists in the convex hull of the control points. Proposed Bézier curve navigation guidance, makes the missile follow the Bézier curve with the feedback form of guidance command so that the missile hits the target on the desired time in the desired direction. We conducted numerical simulations on several terminal conditions to demonstrate the performance of proposed method

Photocatalytic production of H2O2 through selective two-electron reduction of O2

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CHAPTER 5. Photoexcitation in Pure and Modified Semiconductor Photocatalysts

Semiconductor photocatalysis has great promise for applications in solar energy conversion and environmental remediation because it is inexpensive, versatile, and environmentally benign. However, some critical factors such as limited light absorption and fast electron-hole pair recombination restrict the practical applications. Because no pure-phase semiconductors efficiently utilize solar irradiation, semiconductor materials have been modified in various ways to enhance their light-absorption properties. In this chapter, photoexcitation in modified semiconductor systems that include the impurity-doped, coupled, dye-sensitized, ligand-to-metal charge transfer (LMCT)-sensitized, and local surface plasmon resonance (LSPR)-sensitized semiconductors are discussed. In particular, the photoexcitation mechanism, charge transfer pathway, applications, and limitations of each method are described. © 2016 The Royal Society of Chemistry.FALS