02047nas a2200253 4500008004100000022001400041245006800055210006700123260010600190300001600296490000700312520114600319653002901465653002001494653002401514653001201538653002301550100002601573700002201599700002301621700002601644700002401670856009901694 2010 eng d a0360-319900aHydrogen evolution by a low cost photocatalyst: bauxite residue0 aHydrogen evolution by a low cost photocatalyst bauxite residue aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcOCT a10859-108660 v353 a

Bauxite residue or red mud which is an aluminium industry waste has been used as a novel low cost photocatalyst active in visible light for the generation of hydrogen from water. The driving force behind the use of bauxite residue as a photocatalyst is not only the fact that it is widely available but also bauxite residue is a fine grained mixture of oxides and hydroxides (Fe(2)O(3), TiO(2), SiO(2), and Al(2)O(3), Al(OH)3). The photocatalyst was characterized with respect to BET-SA, UV-DRS, XRD, SEM and EDX. Hydrogen yield of 4600 mu mol/h/g of TiO(2) was achieved as compared to hydrogen evolution rate of 164 mu mol/h/g of TiO(2) for commercially available titania Degussa P-25. However, the hydrogen evolution was 20.85 mu mol/h/g of photocatalyst. The results suggest that bauxite residue appears to be a novel low cost photocatalyst. The various operating conditions of photocatalytic hydrogen generation were studied which include amount of catalyst, illumination intensity, illumination time, effect of various sacrificial donors etc. (C) 2009 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.

10aAluminium industry waste10aBauxite residue10aHydrogen generation10aRed mud10aSacrificial donors1 aMangrulkar, Priti, A.1 aJoshi, Meenal, V.1 aKamble, Sanjay, P.1 aLabhsetwar, Nitin, K.1 aRayalu, Sadhana, S. uhttps://library.ncl.res.in/content/hydrogen-evolution-low-cost-photocatalyst-bauxite-residue-002494nas a2200277 4500008004100000022001400041245011500055210006900170260010600239300001600345490000700361520148700368653001501855653001201870653002401882653001701906653001901923100002401942700002201966700001801988700002302006700002102029700001802050700001702068856013102085 2011 eng d a0360-319900aSurfactant tunable hierarchical nanostructures of CdIn2S4 and their photohydrogen production under solar light0 aSurfactant tunable hierarchical nanostructures of CdIn2S4 and th aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcSEP a11628-116390 v363 a

The hierarchical nanostructures of CdIn2S4 were selectively prepared through hydrothermal process in the presence of different surfactants. Structural study demonstrated existence of cubic spinel structure and micro structural study shown a pretty marigold flower like morphology without any surfactant. The effect of surfactants on the morphology and microstructure of CdIn2S4 has been studied by using Polyvinyl pyrrolidone (PVP) and Cetyltrimethyl ammonium bromide (CTAB) as a surfactants. The CdIn2S4 bipyramids with length of 0.7-1 mu m have been obtained using PVP. Interestingly, the nanopetals (thin and transparent) of CdIn2S4 are self assembled into hollow spheres in the presence of CTAB. Considering the importance of these unique nanostructures, the growth mechanism has also been proposed. The optical properties demonstrated the band gap in the range of 2.12-2.29 eV which is well within the visible region. In this contest, photocatalytic activity for hydrogen production using the above nanostructures under visible light was also demonstrated. The prima-fascia observations shows that the bipyramidal CdIn2S4 exhibit excellent photocatalytic activity for hydrogen production (3238 mu molh(-1)) than other nanostructures. Being a nanostructured semiconductor chalcogenide with a good stability will also have potential applications in solar cells and LED. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

10aBipyramids10aCdIn2S410aHydrogen generation10ahydrothermal10aSelf-assembled1 aBhirud, Ashwini, P.1 aChaudhari, Nilima1 aNikam, Latesh1 aSonawane, Ravindra1 aPatil, Kashinath1 aBaeg, Jin-Ook1 aKale, Bharat uhttps://library.ncl.res.in/content/surfactant-tunable-hierarchical-nanostructures-cdin2s4-and-their-photohydrogen-production-001869nas a2200289 4500008004100000022001400041245009900055210006900154260007100223300001600294490000600310520085500316653001901171653002401190653002401214653001201238653002201250653003401272653001801306100002001324700002301344700001601367700002101383700002201404700002501426856012801451 2015 eng d a1944-824400aNiS1.97: a new efficient water oxidation catalyst for photoelectrochemical hydrogen generation0 aNiS197 a new efficient water oxidation catalyst for photoelectro a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbAMER CHEMICAL SOCcSEP a20053-200600 v73 a

NiS1.97, a sulfur-deficient dichalcogenide, in nanoscale form, is shown to be a unique and efficient photoelectrochemical (PEC) catalyst for H-2 generation by water splitting. Phase pure NiS1.97 nanomaterial is obtained by converting nickel oxide into sulfide by controlled sulfurization method, which is otherwise difficult to establish. The defect states (sulfur vacancies) in this material increase the carrier density and in turn lead to favorable band line-up with respect to redox potential of water, rendering it to be an effective photoelectrochemical catalyst. The material exhibits a remarkable PEC performance of 1.25 mA/cm(2) vs NHE at 0.68 V in neutral pH, which is almost 1000 times superior as compared with that of the stoichiometric phase of NiS2. The latter is well-known to be a cocatalyst but not as a primary PEC catalyst.

10adichlacogenide10aFaradaic efficiency10aHydrogen generation10aNiS1.9710anonstoichiometric10aphotoelectrochemical catalyst10asulfurization1 aBhosale, Reshma1 aKelkar, Sarika, A.1 aParte, Golu1 aFernandes, Rohan1 aKothari, Dushyant1 aOgale, Satishchandra uhttps://library.ncl.res.in/content/nis197-new-efficient-water-oxidation-catalyst-photoelectrochemical-hydrogen-generation-002119nas a2200253 4500008004100000022001400041245008000055210006900135260010600204300001400310490000700324520123900331653002201570653002401592653001801616653001901634653000901653100001901662700002401681700001801705700001801723700001801741856010601759 2016 eng d a1364-032100aTiO2 modification by gold (Au) for photocatalytic hydrogen (H-2) production0 aTiO2 modification by gold Au for photocatalytic hydrogen H2 prod aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcMAY a1366-13750 v583 a

TiO2 is indeed one of the widely used semiconductors employed for photocatalytic hydrogen production. Most of its photocatalytic activity-is achieved in its crystalline form. However, its photocatalytic activity is limited to ultraviolet region. For making TiO2 visible light active; Au deposition is strongly recommended due to its surface plasmon feature. Au deposition enhances the photocatalytic activity of both crystalline and nanocrystalline TiO2. Efficiency of photocatalytic activity is controlled by shape and size of Au nanoparticle subsequently the synthetic methodology plays an important role. Herein, we furnish a brief description of TiO2-Au nanocomposite synthesis by different methods viz. sol-gel, photodeposition, deposition-precipitation simple reducing method and dispersion method. A discussion on physical properties of the resultant material is also provided. Three different types of mechanism has been described depending on the type of irradiation and form of TiO2 (crystalline and nanocrytalline). A comparative hydrogen production yield is also tabulated to get an idea about the best synthesis methodology and form of TiO2 for efficient photocatalysis. (C) 2016 Elsevier Ltd. All rights reserved.

10aGold nanoparticle10aHydrogen generation10aNanocomposite10aPhotocatalysis10aTiO21 aGupta, Bhavana1 aMelvin, Ambrose, A.1 aMatthews, Tom1 aDash, Sitaram1 aTyagi, A., K. uhttps://library.ncl.res.in/content/tio2-modification-gold-au-photocatalytic-hydrogen-h-2-production-002432nas a2200265 4500008004100000245014900041210006900190260000800259300000900267490000800276520151200284653002801796653002401824653001401848653001901862653002201881653002201903100002001925700001701945700001701962700001601979700003001995700001802025856012302043 2017 eng d00aBand alignment and charge transfer pathway in three phase anatase-rutile-brookite TiO2 nanotubes: an efficient photocatalyst for water splitting0 aBand alignment and charge transfer pathway in three phase anatas cDEC a9-190 v1283 aThe study reports electrochemical synthesis, phase evolution and hydrogen generation efficiency of anatase, anatase-rutile and anatase-rutile-brookite (ARB) TiO2 nanotubes for the first time. The SEM and TEM micrographs confirm the tubular morphology of the samples. The presence of anatase, rutile and brookite phases in a single nanotube is confirmed from high resolution TEM analysis. The water splitting efficiency of the three systems are studied under one sun illumination. It is observed that the anatase-rutile-brookite TiO2 nanotubes are highly efficient compared to anatase-rutile or anatase TiO2 nanotubes. The hydrogen generated by ARB composites, after four hours of one sun illumination, is found to be nearly twice that of anatase TiO2 nanotubes and 1.6 times that of anatase-rutile TiO2 nanotubes. The results suggest that the ARB in single nanotube having two junction interfaces, highly facilitate interparticle charge transfer compared to single junction anatase-rutile or bare anatase TiO2 nanotubes. From the deconvolution of PL spectra and the synchrotron radiation assisted valence band edge analysis, the band diagram for the anatase-rutile-brookite phase is constructed. The charge separation and its transfer pathway for efficient photo-assisted water splitting are delineated. This opens a new route for the simple synthesis and study of tri-phase TiO2 for efficient photocatalytic water splitting compared to the widely studied two phase TiO2. (C) 2017 Published by Elsevier B.V.10aAnatase-Rutile-Brookite10aHydrogen generation10ananotubes10aPhotocatalysis10aphotoluminescence10aValence band edge1 aPreethi, L., K.1 aMathews, Tom1 aNand, Mangla1 aJha, S., N.1 aChinnakonda, Gopinath, S.1 aDash, Sitaram uhttps://library.ncl.res.in/content/band-alignment-and-charge-transfer-pathway-three-phase-anatase-rutile-brookite-tio202414nas a2200337 4500008004100000022001400041245008500055210006900140260000800209300001400217490000700231520136300238653002701601653001401628653001501642653001301657653002401670653001801694653002401712653001901736653003401755653002001789653002701809653000901836653003301845653003001878653001001908100001901918700002401937856011501961 2017 eng d a1364-032100aTiO2/RGO composites: Its achievement and factors involved in hydrogen production0 aTiO2RGO composites Its achievement and factors involved in hydro cSEP a1384-13920 v763 a

The immense potential shown by TiO2 to participate as a designer material resulting into a new class of high performing photocatalyst has acclaimed it to become an important player in the designing and synthesis of various solar harvesting materials. This role has further been explored by the introduction of graphene into TiO2 matrix. TiO2/reduced graphene oxide (TiO2/RGO) or TiO2/graphene (TiO2/GR) has shown its prospects or relevance to be considered as the next generation photocatalyst for hydrogen production by its reported values in terms of producing hydrogen gas. Hence, there is a requirement of having a detailed up to date write up on the work done in this area in terms of its synthetic procedures, properties and its effect on hydrogen production. Herein, we discuss the different methods involved in the synthesis of such highly efficient materials followed by a brief explanation on its structural and morphological properties. Furthermore, a comparative study on the recent developments in terms of hydrogen evolution efficiency along with a mechanistic approach is also described. Finally, the current challenge and possibility of the future development in this direction is emphasized.

10aAu-tio2 Photocatalysts10aEvolution10aGeneration10agraphene10aHydrogen generation10aNanocomposite10aNitrogen-doped Tio210aPhotocatalysis10aPhotocatalytic H-2 Production10aRecent Progress10aReduced graphene oxide10aTiO210aTio2-graphene Nanocomposites10aVisible-light Irradiation10aWater1 aGupta, Bhavana1 aMelvin, Ambrose, A. uhttps://library.ncl.res.in/content/tio2rgo-composites-its-achievement-and-factors-involved-hydrogen-production01655nas a2200277 4500008004100000022001400041245015600055210006900211260000900280300001400289490000600303520071700309653001901026653000901045653001101054653002401065653001801089653001901107653002001126100002301146700002001169700002301189700001501212700002401227856012601251 2020 eng d a2574-096200aPhotocatalytic hydrogen generation and CO2 conversion using g-C3N4 decorated dendritic fibrous nanosilica: role of interfaces between silica and g-C3N40 aPhotocatalytic hydrogen generation and CO2 conversion using gC3N cSEP  a8150-81580 v33 a

We have synthesized g-C3N4 decorated over dendritic fibrous nanosilica (DFNS). The generation of C-N-Si interfaces by coating each fiber of DFNS with g-C3N4 not only provided high surface area but also affected the optical and electronic properties of the composite. The catalyst synthesis reproducibility issue of g-C3N4 was resolved using a vacuum-sealed quartz tube. The extended light absorption in the visible region, enhanced lifetime of photogenerated charge carriers due to the formation of interfaces between silica and g-C3N4 (confirmed by solid-state NMR), and increased surface area result in the improved photocatalytic activity of DFNS/g-C(3)N(4)for hydrogen generation and CO2 conversion.

10aCO2 conversion10aDFNS10ag-C3N410aHydrogen generation10ananocatalysts10aphotocatalysts10aSolid-state NMR1 aRawool, Sushma, A.1 aSamanta, Anupam1 aAjithkumar, T., G.1 aKar, Yusuf1 aPolshettiwar, Vivek uhttps://library.ncl.res.in/content/photocatalytic-hydrogen-generation-and-co2-conversion-using-g-c3n4-decorated-dendritic02718nas a2200241 4500008004100000022001400041245011600055210006900171260000800240300001100248490000800259520187500267653002602142653001802168653001802186653002402204653002502228100002202253700002402275700003002299700001702329856013002346 2025 eng d a1387-700300aEfficient hydrogen liberation from autocatalytic wastewater treatment by green synthesized Ag2SeO3 nanocatalyst0 aEfficient hydrogen liberation from autocatalytic wastewater trea cMAY a1141060 v1753 a

Concerns about wastewater management, secure hydrogen storage, and interest in an affordable, effective, and user-friendly technique for releasing hydrogen have grown globally. Developing sustainable synthetic processes that result in industrially significant nanocatalyst to synergistically accelerate the evolution of hydrogen from wastewater treatment is extremely desirable. This work, for the first time, demonstrates the design and green fabrication of bactericidal silver selenite nanoparticles (Ag2SeO3 NPs) using the fungus Aspergillus niger for autocatalytic hydrogen production and methylene blue dye reduction by hydrolytic dehydrogenation of NaBH4. The morphology of Ag2SeO3 nanocatalysts with an average particle size of 60 nm was assessed by FETEM, while their surface chemistry, crystal structure, and optical properties were examined using XPS, XRD, and FTIR/ UV-Visible spectrophotometers, respectively. The sigmoidal trajectory of NaBH4 dehydrogenation with turnover frequencies (TOF) of 4750 mL g- 1 min- 1 suggested good autocatalytic activity of Ag2SeO3 NPs. The mechanistic study unveiled that autocatalysis was made possible by the creation of novel, active Ag co-catalyst which works synergistically with Ag2SeO3 NPs. For in-situ, real time assessment of Ag concentration during catalysis, hydrolysis of NaBH4 was carried out in the presence of methylene blue dye. The results showed that the active cocatalyst centers have a significant influence on autocatalytic hydrogen production at room temperature, reducing 98.8 % methylene blue (MB) dye in 6 min with a lesser hydrogen generation rate of 4174 mL g- 1 min- 1. The catalyst exhibited excellent stability and durability after fourth consecutive cycle, demonstrating its promise for long-term and recurring application in hydrogen liberation from autocatalytic MB dye reduction.

10aAg2SeO3 nanoparticles10aAntibacterial10aautocatalysis10aHydrogen generation10aWastewater treatment1 aIslam, Sk, Najrul1 aAnsari, Ifra, Ilyas1 aGopinath, Chinnakonda, S.1 aAhmad, Absar uhttps://library.ncl.res.in/content/efficient-hydrogen-liberation-autocatalytic-wastewater-treatment-green-synthesized-ag2seo3