01171nas a2200157   4500008004100000245007900041210006900120260000800189300002300197490000700220520061800227100002200845700001900867700001900886856010800905       2006                        eng d00aElectrical bistability in a xanthene class molecule: conduction mechanisms0 aElectrical bistability in a xanthene class molecule conduction m  cOCT  aArticle No: 1421100 v893 a<p>The author study conduction mechanism in two conducting states of a bistable device at range. They find that in the electrical bistable devices, electrical switching is associated with a change in the conduction mechanism. Device current in the low-conducting state follows an injection-limited mechanism. The current in the high-conducting state conforms a bulk-dominated mechanism, namely, space-charge limited conduction with an exponential distribution of traps. The bistability has an associated memory phenomenon. The devices exhibit read-only and random-access memory applications for several hours.</p>1 aRath, Arup, Kumar1 aSahu, Satyajit1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/electrical-bistability-xanthene-class-molecule-conduction-mechanisms01212nas a2200145   4500008004100000245007300041210006900114260000800183300001400191490000700205520072000212100002200932700001900954856009300973       2007                        eng d00aConductance switching in an organic material: from bulk to monolayer0 aConductance switching in an organic material from bulk to monola  cSEP  a9831-98350 v233 a<p>Fluorescein sodium, which does not exhibit electrical bistability in thin films, can be switched to a high conducting state by the introduction of carbon nanotubes as channels for carrier transport. Thin films based on fluorescein sodium/carbon nanotubes display memory switching phenomenon among a low conducting state and several high conducting states. Read-only and random-access memory applications between the states resulted in multilevel memory in these systems. Results in thin films and in a monolayer (deposited via layer-by-layer assembly) show that instead of different molecular conformers, multilevel conducting states arise from the different density of high conducting fluorescein molecules.</p>1 aRath, Arup, Kumar1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/conductance-switching-organic-material-bulk-monolayer01383nas a2200169   4500008004100000245014600041210006900187260000800256300001600264490000700280520071200287100002200999700001901021700002201040700001901062856013201081       2008                        eng d00aNanowires of metal-organic complex by photocrystallization: a system to achieve addressable electrically bistable devices and memory elements0 aNanowires of metalorganic complex by photocrystallization a syst  cMAY  a5937–59410 v243 a<p>A new method has been achieved to form a Cu:benzoquinone derivative (DDQ) charge-transfer complex by the photoexcitation of [Cu(DDQ)2(CH3COO)2] (1) that has been synthesized by the reaction of DDQ and hydrated cupric acetate in acetonitrile. Photoexcitation of coordinated complex 1 leads to the formation of charge-transfer complex Cu2+(DDQ•−)2 (2). The charge transfer complex 2, when spun on solid substrates, forms nanowires. Sandwich structures of 2 exhibit electrical bistability associated with memory phenomenon. Read-only and random-access memory phenomena are evidenced in nanowires of 2 providing a route to attend the issues pertaining to the addressibility of organic memory devices.</p>1 aRath, Arup, Kumar1 aDhara, Koushik1 aBanerjee, Pradyot1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/nanowires-metal-organic-complex-photocrystallization-system-achieve-addressable-electrically01195nas a2200145   4500008004100000245009400041210006900135260000800204300001400212490000600226520065500232100002200887700001900909856012100928       2008                        eng d00aResistive switching in rose bengal and other xanthene molecules is a molecular phenomenon0 aResistive switching in rose bengal and other xanthene molecules   cFEB  a495–5000 v93 a<p>There has been a debate on the mechanism of resistive switching in Rose Bengal and other Xanthene class molecules. While some authors proposed that the switching was due to an oxide layer at the Rose Bengal/Aluminum interface, some inferred the switching as an extrinsic effect like filament formation. We show results from Rose Bengal and other Xanthene class molecules on doped Si. Conductance switching in such monolayers induced by Pt/Ir tip of a scanning tunneling microscope (STM) in a non-contact mode shows that resistive switching in these molecules, initially reported by us in 2003 (in thin films), is indeed a molecular phenomenon.</p>1 aRath, Arup, Kumar1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/resistive-switching-rose-bengal-and-other-xanthene-molecules-molecular-phenomenon02049nas a2200157   4500008004100000245011700041210006900158260000800227300001600235490000700251520144300258100001901701700002201720700001901742856013001761       2009                        eng d00aHybrid core-shell nanoparticles: photoinduced electron-transfer for charge separation and solar cell application0 aHybrid coreshell nanoparticles photoinduced electrontransfer for  cOCT  a5292–52990 v213 a<p>We report growth and formation of hybrid core−shell nanoparticle systems, where photoinduced electron-transfer takes place from the II−VI semiconducting core to an organic shell. With the hybrid core−shell nanoparticles, we fabricate devices so that the photoinduced electron-transfer can finally yield photocurrent and result photovoltaic solar cells. Formation of an organic shell-layer on CdSe nanoparticles is supported by electronic absorption spectroscopy. Electron-transfer from the nanoparticle in the core to a number of organic molecules in the shell is established from quenching of photoluminescence intensity of CdSe nanoparticles as well as from a change in the lifetime of photoluminescence emission. Devices based on the hybrid core−shell nanoparticles in a suitable hole-transporting layer with two dissimilar metal electrodes show efficient photovoltaic performance. Here, following the electron-transfer, electrons flow through the organic molecules and holes, left in the nanoparticles, move through the hole-transporting polymer to the opposite electrodes to yield photovoltaic short-circuit current. The role of CdSe nanoparticles in light-harvesting and charge-generation has been substantiated by control experiments with ZnS nanoparticles in the core. In ZnS-based hybrid core−shell systems, photovoltaic performance is low since photoinduced electron-transfer does not occur from ZnS to the dye.</p>1 aGuchhait, Asim1 aRath, Arup, Kumar1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/hybrid-core-shell-nanoparticles-photoinduced-electron-transfer-charge-separation-and-solar01262nas a2200145   4500008004100000245009500041210006900136260000800205300001600213490000700229520071400236100002200950700001900972856012500991       2009                        eng d00aInduce negative differential resistance in organic devices through a ferroelectric polymer0 aInduce negative differential resistance in organic devices throu  cJUN  a1116–11190 v103 a<p>We report how ferroelectric materials induce negative differential resistance (NDR) in organic devices. Fluorescein, which exhibits semiconducting current–voltage characteristics, shows NDR effect in a ferroelectric matrix. Here, we vary the concentration of fluorescein in the ferroelectric matrix to study its effect on NDR. We also show how the degree of polarization controls NDR. We infer that under a suitable bias, the ferroelectric polymer becomes polarized to facilitate electron-injection in the device followed by a double-reduction of fluorescein molecules. From the capacitance–voltage measurements, we substantiate the role of polarization in inducing NDR effect in organic molecules.</p>1 aRath, Arup, Kumar1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/induce-negative-differential-resistance-organic-devices-through-ferroelectric-polymer01353nas a2200133   4500008004100000245009200041210006900133260000800202490000700210520083300217100002201050700001901072856012801091       2009                        eng d00aOrganic memory and electrical bistability in a quinone –based charge transfer complex0 aOrganic memory and electrical bistability in a quinone based cha  cAUG0 v973 a<p>We present an overview of the issues of organic memory devices and discuss the mechanisms involved in conductance switching. To make the memory elements addressable, we introduce nanostructures of a quinone-based charge-transfer complex. The devices based on charge-transfer complexes exhibit electrical bistability. Apart from characterizing complex formation, we study characteristics of memory devices based on the complexes. The mechanism of bistability has been discussed in terms of electroreduction of the quinone derivative with the formation of a percolating network of conducting molecules or channels across the device. Depending on the device architecture, a device may exhibit memoryswitching or threshold-switching phenomenon. The former system has displayed read-only and random-access memory applications.</p>1 aRath, Arup, Kumar1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/organic-memory-and-electrical-bistability-quinone-%E2%80%93based-charge-transfer-complex01258nas a2200157   4500008004100000245011600041210006900157260000800226300002700234490000700261520064500268100002200913700002000935700001900955856012600974       2010                        eng d00aMn-doped nanocrystals in light-emitting diodes: energy-transfer to obtain electroluminescence from quantum dots0 aMndoped nanocrystals in lightemitting diodes energytransfer to o  cSEP  aArticle number: 1135020 v973 a<p>We fabricatelight-emitting diodes(LEDs) based on Mn-doped ZnSnanocrystals along with hole-transporting bis(3-methylphenyl)--diphenyl-benzidine (TPD). With Mn-doping, ZnSnanostructures exhibit a strong photoluminescence. The LEDs exhibit electroluminescence(EL) from Mn-doped ZnSquantum dots and TPD. In order to open up channels for energy-transfer from TPD to quantum dots and to achieve EL from only the nanoparticles, we grow core-shell nanoparticles with Mn-doped ZnS in the core and CdS as the shell layer. Excitons formed in TPD can now transfer their energy directly to the shell-layer to yield EL from only the nanoparticles.</p>1 aRath, Arup, Kumar1 aBhaumik, Saikat1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/mn-doped-nanocrystals-light-emitting-diodes-energy-transfer-obtain-electroluminescence01259nas a2200157   4500008004100000245012600041210006900167260000800236300002300244490000700267520063700274100001900911700002200930700001900952856013000971       2010                        eng d00aNear-IR activity of hybrid solar cells: enhancement of efficiency by dissociating excitons generated in PbS nanoparticles0 aNearIR activity of hybrid solar cells enhancement of efficiency   cFEB  aArticle no: 0735050 v963 a<p>Photovoltaic devices based on PbSnanoparticles remained inactive in the near-IR region due to a not-so-favorable energy band-diagram that does not allow dissociation of excitons generated in PbS. In this work, with the introduction of nanostructures in the PbS-based hybrid system, we show an enhancement of photovoltaic performance in both visible and near-IR regions. The addition of increases the power conversion efficiency from 0.006% to 0.12%. With the aid of energy band-diagram, we show that excitons generated in PbS even in the near-IR range can now become dissociated to yield photocurrent in the external circuit.</p>1 aGuchhait, Asim1 aRath, Arup, Kumar1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/near-ir-activity-hybrid-solar-cells-enhancement-efficiency-dissociating-excitons-generated01721nas a2200157   4500008004100000245010700041210006900148260000800217300001400225490000700239520112500246100001901371700002201390700001901412856013201431       2011                        eng d00aTo make polymer: quantum dot hybrid solar cells NIR-active by increasing diameter of PbS nanoparticles0 aTo make polymer quantum dot hybrid solar cells NIRactive by incr  cOCT  a651–6560 v953 a<p>We fabricate NIR-active solar cells based on PbS quantum dots and a conventional conjugated polymer. These devices act as solar cells under exclusively NIR wavelengths above 650 nm. Here PbS nanoparticles absorb photons in the NIR range that in turn generate excitons. We show that with an assistance from a strong electron-acceptor (TiO2), these excitons can be dissociated to electrons and holes to yield a photocurrent in the external circuit. We then aim to extend the spectral window of the solar cells to higher wavelength region by increasing the diameter of PbS nanoparticles to make the cells further NIR-active. We observe that the short-circuit current (JSC) shows a peak when the diameter of PbS nanoparticles increases. Here, the spectral window can be extended till conduction band-edge of PbS quantum dots falls below that of TiO2 nanostructures cutting off the electron-transfer pathway. The NIR-active photovoltaic solar cells yield a short-circuit current (JSC) of 1.0 mA/cm2, open-circuit voltage (VOC) of 0.42 V, and power conversion efficiency (η) of 0.16% and remain operative till 1200 nm.</p>1 aGuchhait, Asim1 aRath, Arup, Kumar1 aPal, Amlan, J.  uhttps://library.ncl.res.in/content/make-polymer-quantum-dot-hybrid-solar-cells-nir-active-increasing-diameter-pbs-nanoparticles