01813nas a2200169   4500008004100000022001400041245015400055210006900209260000900278300001600287490000800303520112500311100002701436700003001463700003101493856011901524       2020                        eng d  a1932-744700aPhase- and morphology-controlled synthesis of tunable plasmonic MoO3-x nanomaterials for ultrasensitive surface-enhanced raman spectroscopy detection0 aPhase and morphologycontrolled synthesis of tunable plasmonic Mo  cSEP   a21082-210930 v1243 a<p>The enhancement of the surface-enhanced Raman scattering (SERS) property of the plasmonic metal oxide semiconductor nanostructures by controlling their phase, shape, size, and oxygen vacancy to detect trace amounts of organics is of significant interest. In this study, a simple surfactant-free hydrothermal strategy was proposed to fabricate crystalline h-MoO3-x and alpha-MoO3-x nanomaterials with tunable plasmonic properties. Herein, the crystal phase, morphology, and oxygen vacancy of MoO3-x nanostructures were precisely controlled under suitable synthetic conditions. The plasmonic properties of the as-synthesized h-MoO3-x and alpha-MoO3-x micro-/nanostructures were controlled by adjusting the residual volume in the autoclaving chamber. In addition, the plasmonic MoO3-x exhibited SERS activity with a detection limit as low as 1.0 x 10(-9) M and the maximum enhancement factor (EF) up to 6.99 x 10(5) for h-MoO3-x, while for alpha-MoO3-x, the detection limit was 1.0 x 10(-7) M with the corresponding EF up to 8.51 x 10(3), comparable with plasmonic noble metal nanomaterials without a ``hot spot''.</p>
1 aPatil, Manoj, Krishnat1 aGaikwad, Supriya, Hanmant1 aMukherjee, Shatabdi, Porel  uhttp://library.ncl.res.in/content/phase-and-morphology-controlled-synthesis-tunable-plasmonic-moo3-x-nanomaterials02350nas a2200229   4500008004100000022001400041245011400055210006900169260000800238490000700246520155000253653001601803653000801819653002001827653002301847100001801870700002701888700003101915700003001946700001901976856012501995       2022                        eng d  a1861-472800aScalable mechanochemical synthesis of beta-ketoenamine-linked covalent organic frameworks for methane storage0 aScalable mechanochemical synthesis of betaketoenaminelinked cova  cDEC0 v173 a<p>
	In the current scenario of increased pollution and releasing toxic gases by burning petroleum products, switching to natural gas is more promising for reducing CO2 emissions and air pollutants. Hence, research on Liquefied Natural Gas and Compressed Natural Gas is gaining more value. However, natural gas primarily consists of CH4, which has less energy density than conventional fuels. Interestingly, since the C-H ratio of CH4 gas is 1 : 4, it is easily combustible, gives less carbon footprint, and reduces unburnt hydrocarbon pollution. Hence, research on storing and transporting CH4 has utmost importance, and porous materials are one of the suitable candidates for storing CH4. Herein we report the scalable synthesis of highly porous and crystalline covalent organic frameworks for storing CH4 at room temperature and pressure. Two COFs, namely, Tp-Azo and Tp-Azo-BD(Me)(2), synthesized in 1 kg at similar to 45 g batch scale using a Planetary mixer, displayed a maximum BET surface area of around 3345 m(2)/g, and 2342 m(2)/g and CH4 storage of 174.10 cc/cc and 151 cc/cc, respectively. A comparison of the CH4 sorption of Tp-Azo and Tp-Azo-BD(Me)(2) COFs synthesized in different batches has a variation of only +/- 5 cc/cc and shows the consistency in bulk scale synthesis of COFs. The cyclic equilibrium CH4 adsorption studies showed the COFs are stable with consistent CH4 adsorption and desorption cycles. The present study is a step towards the scalable mechanochemical synthesis of COFs for gas storage applications.</p>
10aCH4 storage10aCOF10aporous material10ascalable synthesis1 aAsokan, Kiran1 aPatil, Manoj, Krishnat1 aMukherjee, Shatabdi, Porel1 aSukumaran, Santhosh, Babu1 aNandakumar, T.  uhttp://library.ncl.res.in/content/scalable-mechanochemical-synthesis-beta-ketoenamine-linked-covalent-organic-frameworks