01886nas a2200229 4500008004100000022001400041245012300055210006900178260000800247300001100255490000600266520108400272653002201356653003901378653002701417100001901444700002401463700001801487700001301505700001801518856012001536 2014 eng d a2053-159100aFacile gamma radiolytic synthesis of synergistic Co3O4-rGO nanocomposite: direct use in photocatalytic water splitting0 aFacile gamma radiolytic synthesis of synergistic Co3O4rGO nanoco cDEC a0455070 v13 a

Nanostructured Co3O4 was synthesized through a gamma (gamma)-radiolysis technique using alcoholic (iso-propanol) salt solutions of cobalt ions with and without suspended graphene oxide (GO) nanoparticles, respectively. Formation of Co3O4 accompanied with GO reduction takes place simultaneously (in situ) upon.-ray exposure carried out at a rate of 5.1 KGy h(-1). Reduction of GO and formation of Co3O4 were confirmed by XRD, Raman and UV-vis spectroscopy. XRD and HRTEM results supports the embedding of nano-crystalline Co3O4 in an amorphous matrix. Relatively larger crystallites of cobalt oxide obtained in the presence of rGO proved to be a decisive supporting material for the directional growth of Co3O4. Electrochemical characterization established the fact that rGO is indeed considered as a proficient medium for electrochemical electron transfer process. Photo-assisted H-2 generation studies using Co3O4 and Co3O4-rGO nano-composite yielded 3 and 30 mu mol h(-1) g(-1) of hydrogen (H-2) generation, respectively, supports the action of rGO as an electron trap.

10anano cobalt oxide10aphotocatalytic hydrogen production10aReduced graphene oxide1 aGupta, Bhavana1 aMelvin, Ambrose, A.1 aMatthews, Tom1 aDash, S.1 aTyagi, A., K. uhttps://library.ncl.res.in/content/facile-gamma-radiolytic-synthesis-synergistic-co3o4-rgo-nanocomposite-direct-use02482nas a2200265 4500008004100000022001400041245010400055210006900159260010600228300001400334490000700348520153200355653002101887653001901908653001901927653002701946653000901973100001901982700002402001700001802025700001402043700001802057700001802075856012302093 2015 eng d a0360-319900aFacile gamma radiolytic methodology for TiO2-rGO synthesis: effect on photo-catalytic H-2 evolution0 aFacile gamma radiolytic methodology for TiO2rGO synthesis effect aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcMAY a5815-58230 v403 a

TiO2 (P25) decorated reduced graphene oxide (rGO) is synthesized by gamma-radiolytic technique using water-ethanol solvent medium. Visible light absorpdon was confirmed by UV-Visible spectroscopy. Photoluminescence (PL) study revealed a decline in electron-hole recombination rate signalled by a sharp fall in luminescence of TiO2. Under such scenario, electron transfer from TiO2 conduction band to the conjugated sheet becomes a preferred pathway in the presence of rGO, which is further confirmed by photocurrent measurement. TiO2 -rGO composite with 1 wt. % rGO was found to be the best composition in terms of visible light absorption, while retaining TiO2 crystallinity. Transmission electron microscopy and Raman spectroscopic studies confirmed the coating of rGO sheet with TiO2 nanoparticles. TiO2 -rGO was found to show about 150 times higher photocatalytic H-2 generation under 250 W UV-Visible light irradiation than pristine TiO2. In addition to this, TiO2 -rGO composite shows hydrogen production yield of 35 mu mol/h.g under visible light (lambda = 400 nm) irradiation. Thus gamma-radiolysis can be considered to be a viable technique, which helps in synthesizing photocatalytically active nanocomposite with high H-2 evolution rate. In the light of these interesting aspects, a detail investigation is carried out to study the effect of rGO concentration and illumination time on photocatalytic yield. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

10agamma-radiolysis10aH-2 production10aPhotocatalysis10aReduced graphene oxide10aTiO21 aGupta, Bhavana1 aMelvin, Ambrose, A.1 aMatthews, Tom1 aDhara, S.1 aDash, Sitaram1 aTyagi, A., K. uhttps://library.ncl.res.in/content/facile-gamma-radiolytic-methodology-tio2-rgo-synthesis-effect-photo-catalytic-h-2-002414nas 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-production02322nas a2200229 4500008004100000022001400041245009800055210006900153260000800222300001200230520153600242653001001778653001901788653002101807653001301828653002701841100002501868700002501893700002301918700002401941856012701965 2019 eng d a1862-630000aRealization of efficient field emitter based on reduced graphene oxide-Bi2S3 heterostructures0 aRealization of efficient field emitter based on reduced graphene cJUL a19001213 a

Herein, Bi2S3 nanorods and reduced graphene oxide (rGO)-Bi2S3 heterostructures are synthesized using a simple hydrothermal method. The structural, morphological, chemical, and elemental analysis of as-synthesized materials is performed using X-ray diffraction (XRD), Raman spectroscopy, field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). Field emission (FE) studies are carried out on both pristine Bi2S3 nanorods and rGO-Bi2S3 heterostructure samples at a base pressure of approximate to 1 x 10(-8) mbar. The results show that the rGO-Bi2S3 heterostructure emitter has superior FE performance compared to pristine Bi2S3 emitters in terms of the turn-on field (2.6 V mu m(-1) at 10 mu A cm(-2)) and threshold field (4.0 V mu m(-1) at 100 mu A cm(-2)) along with a high emission current density of approximate to 1464 mu A cm(-2) at an applied electric field of 7.0 V mu m(-1). The rGO-Bi2S3 heterostructure emitter exhibits very good emission current stability, tested for more than 3 h duration, characterized by standard deviation values approximate to 2.84 and 4.06, corresponding to preset values 12 and 100 mu A. This study implies that one-step hydrothermal route can be efficiently used to synthesize organic-inorganic heterostructures that possess unique morphology. Furthermore, the synthesized rGO-Bi2S3 heterostructure emitter shows potential as an electron source for practical application in vacuum microelectronic devices.

10aBi2S310afield emission10aHeterostructures10aNanorods10aReduced graphene oxide1 aGote, Gorkshnath, H.1 aBhopale, Somnath, R.1 aMore, Mahendra, A.1 aLate, Dattatray, J. uhttps://library.ncl.res.in/content/realization-efficient-field-emitter-based-reduced-graphene-oxide-bi2s3-heterostructures02005nas a2200229 4500008004100000022001400041245012300055210006900178260000800247300001200255490000600267520117600273653002201449653003101471653003001502653001401532653002701546100002401573700002301597700002601620856012901646 2020 eng d a2637-611300aNanoporous reduced graphene oxide and polymer composites as efficient counter electrodes in dye-sensitized solar cells0 aNanoporous reduced graphene oxide and polymer composites as effi cMAR a626-6340 v23 a

The introduction of an efficient and precious platinum (Pt) free counter electrode (CE) for dye-sensitized solar cells (DSSCs) is an important aspect to address. In this report, we have employed nanoporous reduced graphene oxide (PG) containing PEDOT:PSS-PG composite on FTO substrate as CEs, which have shown excellent diffusion of I-3(-), remarkable photocatalytic activity, and better device performance along with desired stability. The investigated cathode material has been prepared by mixing PGs and highly conducting PEDOT:PSS. Experimental measurements and analyses such as electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and so on indicate that PEDOT:PSS-PG is a promising cathode material for a Pt-free CE in DSSCs. EIS indicates that the PEDOT:PSS-PGs have lower interfacial charge-transfer resistance because of their high electrical conductivity and superior electrocatalytic activity. The achieved photoconversion efficiency (eta) of a DSSC employing the Pt-free PEDOT:PSS-PG/FTO CE is 9.57%, which is found to be comparable to that of Pt/FTO CE based DSSC (9.64%) under a simulated solar light illumination of 100 mW/cm(2).

10acounter electrode10aDye-sensitized solar cells10aelectrocatalytic activity10aPEDOT:PSS10aReduced graphene oxide1 aSudhakar, Vediappan1 aSingh, Anup, Kumar1 aChini, Mrinmoy, Kumar uhttps://library.ncl.res.in/content/nanoporous-reduced-graphene-oxide-and-polymer-composites-efficient-counter-electrodes-dye02272nas a2200289 4500008004100000022001400041245009400055210006900149260000900218490000700227520134800234653003101582653002001613653002701633653001601660653002101676100001901697700001501716700001901731700001501750700001601765700002101781700002101802700002101823700002101844856011701865 2024 eng d a0947-653900aRobust spin liquidity in 2D metal-organic framework Cu3 (HHTP)2 with S=1/2 kagome lattice0 aRobust spin liquidity in 2D metalorganic framework Cu3 HHTP2 wit cJAN 0 v303 a

On one hand electron or hole doping of quantum spin liquid (QSL) may unlock high-temperature superconductivity and on the other hand it can disrupt the spin liquidity, giving rise to a magnetically ordered ground state. Recently, a 2D MOF, Cu-3(HHTP)(2) (HHTP - 2,3,6,7,10,11-hexahydroxytriphenylene), containing Cu(II) S = 1/2 frustrated spins in the Kagome lattice is emerging as a promising QSL candidate. Herein, we present an elegant in situ redox-chemistry strategy of anchoring Cu-3(HHTP)(2) crystallites onto diamagnetic reduced graphene oxide (rGO) sheets, resulting in the formation of electron-doped Cu-3(HHTP)(2)-rGO composite which exhibited a characteristic semiconducting behavior (5 K to 300 K) with high electrical conductivity of 70 S . m(-1) and a carrier density of similar to 1.1 x 10(18) cm(-3) at 300 K. Remarkably, no magnetic transition in the Cu-3(HHTP)(2)-rGO composite was observed down to 1.5 K endorsing the robust spin liquidity of the 2D MOF Cu-3(HHTP)(2). Specific heat capacity measurements led to the estimation of the residual entropy values of 28 % and 34 % of the theoretically expected value for the pristine Cu-3(HHTP)(2) and Cu-3(HHTP)(2)-rGO composite, establishing the presence of strong quantum fluctuations down to 1.5 K (two times smaller than the value of the exchange interaction J).

10a2D Metal-organic Framework10aElectron doping10aReduced graphene oxide10aSpin Liquid10aSpin-frustration1 aNinawe, Pranay1 aJain, Anil1 aSangole, Mayur1 aAnas, Mohd1 aUgale, Ajay1 aMalik, Vivek, K.1 aYusuf, Seikh, M.1 aSingh, Kirandeep1 aBallav, Nirmalya uhttps://library.ncl.res.in/content/robust-spin-liquidity-2d-metal-organic-framework-cu3-hhtp2-s12-kagome-lattice02180nas a2200265 4500008004100000022001400041245014600055210006900201260000800270490000600278520120700284653002501491653001901516653002701535653003001562653002701592100003101619700002001650700003001670700002401700700001601724700001801740700002701758856012901785 2025 eng d a2366-748600aRational design of reduced graphene oxide/TiO2/gold nanorod nanocomposite for complete degradation of polystyrene microplastics in wastewater0 aRational design of reduced graphene oxideTiO2gold nanorod nanoco cAUG0 v93 a

Our planet is being devoured by plastic consumption every day. Water, soil, and air are deliberately polluted by the ingredients of these nondegradable plastics. Extensive usage of plastic has serious consequences in the environment, wildlife, and human health. A comprehensive approach to eradicate plastics from the planet is therefore imperative. Herein, a ternary nanocomposite subsumed of reduced graphene oxide (rGO), titanium dioxide (TiO2), and gold nanorods (AuNRs) is synthesized and effectively deployed to remove plastics from water as well as degradation of polymer film by both chemically and photocatalytically. The hydrothermally prepared nanocomposite completely removes polystyrene molecules from water, and 1.2 mg of plastic degradation is observed during the photolysis. Conversely, chemical degradation pathway induces the weight loss of 10.7 mg. Both Plasmon-induced interfacial charge transfer transition (PICTT) and Plasmon-induced hot electron transfer (PHET) assist the formation of reactive oxygen species (ROS) that collectively degrades the polymer strands. The spectrochemical and microscopic studies validate the degradation studies with cautious conclusions.

10achemical degradation10aPhotocatalysis10aplasmonic hot electron10apolystyrene microplastics10aReduced graphene oxide1 aUshaVipinachandran, Varsha1 aNaveenkumar, K.1 aHaroon, Kabir, Hussain Ba1 aAshokan, Indhumathi1 aSinha, Arup1 aMaity, Pradip1 aBhunia, Susanta, Kumar uhttps://library.ncl.res.in/content/rational-design-reduced-graphene-oxidetio2gold-nanorod-nanocomposite-complete-degradation