GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    In: Acta Physica Sinica, Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences, Vol. 62, No. 18 ( 2013), p. 188501-
    Abstract: In a magnetic flux modulated DC superconducting quantum interference device (SQUID) readout, the matching transformer could realize the function of signal amplification and impedance matching, which is the key element of a low noise SQUID readout. We use a simulated DC SQUID readout to test the characteristics of matching transformer, study the transmission characteristics of transformer with different turns, and confirm its best turn ratio. In the coupling network that the transformer picks up voltage signals of SQUID, We also study the transmission characteristics of transformers with different matching capacitances, realize the matching of the parameters and the optimization in the transformer coupling network. At room temperature, for the matching transformer with a turn ratio of 1:20, when matching capacitance is 1 μF, the gain of output voltage source could reach 21.2 and its bandwidth could reach 210 kHz. Finally, in magnetic flux modulation DC SQUID readout, we evaluate the performance of the matching transformer.
    Type of Medium: Online Resource
    ISSN: 1000-3290 , 1000-3290
    Language: Unknown
    Publisher: Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences
    Publication Date: 2013
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Online Resource
    Online Resource
    Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences ; 2009
    In:  Acta Physica Sinica Vol. 58, No. 4 ( 2009), p. 2364-
    In: Acta Physica Sinica, Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences, Vol. 58, No. 4 ( 2009), p. 2364-
    Abstract: We have studied experimentally the dipole orientation and reorientation dynamics of single dye molecules at room temperature. The dipole rotation of individual dye molecules which are physisorbed to glass and embedded in spin-cast polymer films is measured with the confocal scanning optical microscopy and the method of fluorescence polarization analysis, the probability of reorientation of single molecules found to be about 5%—9% when embedded in polymer, and about 26% when absorbed to glass by using the statistic analysis. It is found the quantum jumps for molecule dipole reorientation are distributed in several different polarization states by measuring the polarization degree of fluorescent photons.
    Type of Medium: Online Resource
    ISSN: 1000-3290 , 1000-3290
    Language: Unknown
    Publisher: Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences
    Publication Date: 2009
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    In: Acta Physica Sinica, Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences, Vol. 62, No. 9 ( 2013), p. 098501-
    Abstract: Noise suppression is a key technique in retrieving weak magnetic signal from human heart. In order to improve the signal-to-noise ratio (SNR) of magnetocardiography (MCG) signals, signal average method is widely used. However, due to the existence of local environmental interference, averaging the whole section data would unavoidable bring distortion to the average signal. In this paper, the authors proposed a kind of selective average method by using the template matching. The results showed that this method can effectively eliminate the data section with interference such as low frequency fluctuation, pulse burr etc. Thus averaging MCG signal with high SNR and fidelity will be obtained.
    Type of Medium: Online Resource
    ISSN: 1000-3290 , 1000-3290
    Language: Unknown
    Publisher: Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences
    Publication Date: 2013
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    In: Acta Physica Sinica, Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences, Vol. 66, No. 24 ( 2017), p. 248201-
    Abstract: Study of the relationship between conformation and photophysics of individual -conjugated polymer chain is one of the most important problems in polymer nanoscience and nanotechnology, which will facilitate the application of conjugated polymer in a range of electronic devices such as organic field-effect transistors, light-emitting diodes, and solar cells. Single-molecule spectroscopy has emerged as a powerful tool to unravel structure and dynamic heterogeneities that are hidden in ensemble average. Identification of the emitting segments through fluorescence of single conjugated polymer molecules and their dependence on the conformation can help reveal the mechanism and the extent of energy transfer process in a single polymer chain. In this paper, the photophysical properties of individual poly[2, 7-(9, 9-dioctylfluorene)-alt-4, 7-bis(thiophen-2-yl) benzo-2, 1, 3-thiadiazole] (PFO-DBT) conjugated polymer molecules are measured based on the defocused wide-field microscopy of single molecules. The single PFO-DBT molecules are prepared on cleaned glass coverslips by spin-coating solution of poly[methyl methacrylate] (PMMA) containing 110-9 mol/L PFO-DBT molecules in chloroform and toluene, respectively. Defocused imaging of single conjugated polymer molecule is performed based on a wide-field fluorescence microscope system. The change of defocused patterns of individual polymer chain maps the angular distribution of emitted chromophore and thus the emitting dipole orientation. Fluorescence trajectory and corresponding emission dipole moments of single conjugated polymer molecules are analyzed to identify the emitting conjugated segments. It is found that single PFO-DBT conjugated polymer molecules prepared by chloroform solvent show extended conformation. The intrachain energy transfer is dominant in the single conjugated polymer molecules that take extended conformation, which leads to photophysical properties of multiple chromophores. In contrast, single PFO-DBT conjugated polymer molecules prepared by toluene solvent hold folded conformation, which exhibit emission from single chromophore due to efficient interchain energy transfer. The emitting chromophore is not constant in a single PFO-DBT conjugated polymer molecule with folded conformation. About 35% of the single conjugated molecules prepared with toluene show only one constant emitting chromophore before photobleaching. However, about 65% of single conjugated polymer molecules prepared with toluene show two or more sequencely emitting chromophores. It can be concluded that the energy transfer properties of single PFO-DBT conjugated polymer molecule is greatly dependent on the conformation, which can be reflected in its photophysical properties. The study on the influence of single conjugated polymer conformation on energy transfer efficiency can provide the reference for the preparation and performance of optoelectronic devices and molecular devices based on conjugated polymer.
    Type of Medium: Online Resource
    ISSN: 1000-3290 , 1000-3290
    Language: Unknown
    Publisher: Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences
    Publication Date: 2017
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Online Resource
    Online Resource
    Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences ; 2014
    In:  Acta Physica Sinica Vol. 63, No. 16 ( 2014), p. 167302-
    In: Acta Physica Sinica, Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences, Vol. 63, No. 16 ( 2014), p. 167302-
    Abstract: The fluorescence blinking characteristics of the single CdSe/ZnS core/shell quantum dots (QDs) absorbed on the cover glass surface, indium-tin oxide (ITO) nanoparticles, and polymethyl methacrylate (PMMA) film surface are measured by a laser scanning confocal fluorescence microscopy. It is found that all the distributions of bright state duration time of QDs on the three different interfaces can be described by a truncated power law P(t)∝ t-αexp(-t/μ). The statistical on-time durations of single QDs absorbed on the ITO nanoparticles is shorter than on the glass. In addition, the on-time duration with single QDs absorbed on the PMMA is longer than on the others. These differences can be attributed to the diverse interfacial electron transfers between QD and different materials.
    Type of Medium: Online Resource
    ISSN: 1000-3290 , 1000-3290
    Language: Unknown
    Publisher: Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences
    Publication Date: 2014
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    In: Acta Physica Sinica, Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences, Vol. 67, No. 6 ( 2018), p. 066802-
    Abstract: The strong, broad and tunable fluorescence emission of graphene oxide (GO) has shown the exciting optical applications in many areas, such as fluorescence imaging in living cell, high sensitive detection of heavy metal ions, and the fabrication of optoelectronic devices. However, the intrinsic heterogeneous fluorescence intensity resulting from the variability in the power density of excitation laser and the non-uniform thickness of GO film, hinders its further applications in the micropatterning, information storage and display technology, which requires homogeneous fluorescence emission. In contrast to the fluorescence intensity, the fluorescence lifetime of GO is determined by the intrinsic nature of chromophores, rather than the film thickness or excitation power density. Here we report that the fluorescence lifetime is homogeneous for GO film, which eliminates the anisotropic optical properties of GO film. By reducing the GO film through the irradiation from a 405 nm continuous-wave laser at a certain power density on a home-built scanning confocal microscope, we find that the lifetime can be precisely modulated by controlling the duration of laser irradiation. It is determined that the lifetime gradually decreases with the increase of duration. As reported in the previous researches, the GO fluorescence originates from the graphene-like confined sp2 clusters and sp3 domains consisting of oxygen-containing functional groups, where the lifetime of sp3 domain is about 1.4 ns, and that of sp2 domain is 0.14 ns. During the photoreduction, the long-lived sp3 domains will decrease or convert into short-lived sp2 domains, resulting in the decrease of lifetime. Hence, by controlling the reduction degree or the ratio of the two domains, the lifetime of GO film can be determined. More importantly, the lifetime distributions of the reduction areas are very narrow, leading to a relatively homogenous background. The precise manipulation of lifetime can be used to fabricate micropatterns with high contrast. Combining with laser direct writing with features of maskless, facile processing ability and high spatial resolution, many versatile micropatterns, such as quick response code, barcode, graphic, alphabet, and numbers can be readily created based on the modulation of fluorescence lifetime. By using three optimized durations of laser irradiation, three distributions with narrow widths are obtained. Based on this processing, the micropatterns with three colors are determined, which indicates that the multimode optical recording can be created on the GO film based on the modulation of fluorescence lifetime. Furthermore, the multilayer micropatterns are also created. The robust and versatile micropatterns with film-thickness and excitation-power-independent features show their promising applications in electronics, photonics, display technology and information storage.
    Type of Medium: Online Resource
    ISSN: 1000-3290 , 1000-3290
    Language: Unknown
    Publisher: Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences
    Publication Date: 2018
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    In: Acta Physica Sinica, Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences, Vol. 65, No. 21 ( 2016), p. 218201-
    Abstract: The optical signals of single molecules provide information about structures and dynamic behaviors of their nanoscale environments, and eliminations of space and time averaging effect. These are particularly useful whenever complex structures or dynamic behaviors are present, especially in polymers. The single molecules absorbed onto polymer chains rotate with rotational relaxation of polymer chains. Thus, we can measure the dynamic properties of polymer thin films by measuring the rotational properties of single molecules. Here, we use single Nile Red(NR) dye molecules as nano-probes to measure polymer dynamic behaviors of poly(methyl acrylate)(PMA) polymer film. The polymer films are prepared on cleaned glass coverslips by spin-coating 1.0 wt.%solution of PMA containing ~10-9 mol/L NR molecules in toluene. Defocused wide-field fluorescence microscopy is used to measure the three-dimensional molecular rotational diffusion of single NR molecules in PMA polymer thin film. The local environmental change driven by heterogeneous dynamics of the polymer can be probed by parallel imaging of several molecules. It is found that at Tg+19 K, rotations of NR single molecules in different nano-areas are in two different ways, i.e., rotational way(rotational molecules account for ~83%) and non-rotaional way(non-rotational molecules occupy~17%). The rotational molecules include the single molecules of intermittent rotation with a short time and a long time. The different rotational patterns indicate that there is still a spatial and temporal heterogeneity of dynamics in PMA polymer film at a temperature of Tg+19 K. The autocorrelation function C(t) of angular change of dipole orientation of NR single molecules is calculated to reveal the property of polymer dynamics. The decay of C(t) can be fitted by Kohlrausch-Williams-Watt stretched exponential function. The averaged timescale of rotational diffusion c for 183 rotational NR single molecules indicates that the timescale of polymer dynamics at 300 K is~3 s. In order to investigate the temporal heterogeneity of PMA polymer dynamics, we define a threshold to separate the single molecular rotation into two parts:rotational state and non-rotational state. According to the statistics of duration time of rotational state and non-rotational state, we can obtain the probability densities of duration time of rotational states and non-rotational states of the single molecules. The probability densities obey a truncated power law, which indicates that there are still the behaviors of trapping and self-trapping in PMA polymer chains at Tg+19 K. The researches of spatial and temporal heterogeneity of dynamics of PMA polymers in nano-environment have great significance for preparing the high performance materials.
    Type of Medium: Online Resource
    ISSN: 1000-3290 , 1000-3290
    Language: Unknown
    Publisher: Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences
    Publication Date: 2016
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    Online Resource
    Online Resource
    Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences ; 2013
    In:  Acta Physica Sinica Vol. 62, No. 23 ( 2013), p. 233601-
    In: Acta Physica Sinica, Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences, Vol. 62, No. 23 ( 2013), p. 233601-
    Abstract: We have changed the resonance energy of the graphene oxide molecular clusters by using the external electric field. From the graphene oxide resonance fluorescence we could study the polarization dynamics of graphene oxide under the electric field. It is found that the electric field makes the FWHM of fluorescence resonance peak tend to be saturated, and the temporal change of fluorescence resonance of the graphene oxide molecular clusters reflects the directional polarization and the deformation polarization generated in the graphene oxide due to the electric field.
    Type of Medium: Online Resource
    ISSN: 1000-3290 , 1000-3290
    Language: Unknown
    Publisher: Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences
    Publication Date: 2013
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    Online Resource
    Online Resource
    Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences ; 2015
    In:  Acta Physica Sinica Vol. 64, No. 24 ( 2015), p. 247803-
    In: Acta Physica Sinica, Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences, Vol. 64, No. 24 ( 2015), p. 247803-
    Abstract: Single quantum dots (QDs) always exhibit strong blinking in fluorescence intensity when they are on some inert substrates. The blinking activity is attributed to the photoinduced charging of QDs by electron transfer (ET) to trap states in QDs and the surrounding matrix, which has been considered as an undesirable property in many applications. Here, we use N-doped indium tin oxide (ITO) semiconductor nanoparticles to suppress fluorescence blinking activity of single CdSe/ZnS core/shell QDs. The fluorescence characteristics of single QDs in ITO and on SiO2 cover glass are measured by a laser scanning confocal fluorescence microscopy, respectively. It is found that the on-and off-state probability densities of QDs on different substrates both can be fit by a truncated power law. Blinking rates for single QDs on glass and in ITO are also calculated. By contrast, single QDs doped in ITO show that their blinking rate and fluorescence lifetime both decrease. The on-state probability density of single QDs in ITO is approximately two orders of magnitude higher than that of QDs on SiO2 cover glass. It means that single QDs doped in ITO have a longer time to be on-state. Because the Fermi level in QDs is lower than in ITO, when they are in contact, electrons in ITO will transfer to QDs. As a result, the equilibration of their Fermi levels leads to the formation of negatively charged QDs. These electrons fill in the holes of QDs shell and enhance the on-state probability of QDs. Fluorescence decays of single QDs on glass and in ITO are measured by TAC/MCA, and they can be fit by biexponential function. The two lifetime values correspond to the single exciton lifetime and biexciton lifetime of QDs, respectively. It is worth noting that the distribution of the amplitude weighted average lifetime for single QDs in ITO is approximately 41% of that for single QDs on SiO2 cover glass and its full width at half maximum (FWHM) is changed to 50%. For the conduction band potential of QDs is higher than that of ITO, which contributes to photoinduced interfacial electron transfer from QDs to ITO and leads to the increase of nonradiative transition. These indicate that ITO can reduce single exciton and biexciton lifetime of QDs. The study demonstrates that ITO can effectively suppress the blinking activity of QDs.
    Type of Medium: Online Resource
    ISSN: 1000-3290 , 1000-3290
    Language: Unknown
    Publisher: Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences
    Publication Date: 2015
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...