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1.
ACS Appl Mater Interfaces ; 12(43): 48854-48860, 2020 Oct 28.
Article in English | MEDLINE | ID: mdl-32981323

ABSTRACT

Miniaturized organic single-crystal arrays that are addressed by reading-out circuits are crucial for high performance and high-level integration organic electronics. Here, we report a lithography compatible strategy to fabricate organic single-crystal arrays via area-selective growth and solvent vapor annealing (SVA). The organic semiconducting molecules can first selectively grow on photographically patterned drain-source electrodes, forming ordered amorphous aggregates that can further be converted to discrete single-crystal arrays by SVA. This strategy can be applied to self-align the microsized organic single crystals on predesigned locations. With this method, suppression of cross-talk among devices, organic field-effect transistors, and basic logic gate arrays with reading-out electrodes are further demonstrated.

2.
ACS Appl Mater Interfaces ; 11(39): 36205-36212, 2019 Oct 02.
Article in English | MEDLINE | ID: mdl-31469274

ABSTRACT

Highly ordered organic semiconductor single-crystal (OSSC) arrays are ideal building blocks for functional organic devices. However, most of the current methods are only applicable to fabricate OSSC arrays of a single component, which significantly hinders the application of OSSC arrays in integrated organic circuits. Here, we present a universal approach, termed three-dimensional (3D) wettability-induced sequential assembly that can programmatically and progressively manipulate the crystallization locations of different organic semiconductors at the same spatial position using a 3D microchannel template, for the fabrication of the two-component OSSC arrays. As an example, we successfully prepared two-component, bilayer structured OSSC arrays consisting of n-type N,N'-bis(2-phenylethyl)-perylene-3,4:9,10-tetracarboxylic diimide and p-type 6,13-bis(triisopropylsilylethynyl)pentacene microbelts. The bicomponent OSSCs show ambipolar carrier transport properties with hole and electron mobilities of 0.342 and 0.526 cm2 V-1 s-1, respectively. Construction of complementary inverters is further demonstrated based on the two-component OSSCs. The capability of integration of multicomponent OSSC arrays opens up unique opportunities for future high-performance organic complementary circuits.

3.
ACS Nano ; 13(5): 5910-5919, 2019 May 28.
Article in English | MEDLINE | ID: mdl-31067403

ABSTRACT

High-performance phototransistors made from organic semiconductor single crystals (OSSCs) have attracted much attention due to the high responsivity and solution-processing capability of OSSCs. However, OSSC-based phototransistors capable of dual-band spectral response remain a difficult challenge to achieve because organic semiconductors usually possess only narrow single-band absorption. Here, we report the fabrication of high-performance, dual-band phototransistors from a hybrid structure of a 2,7-dioctyl[1]benzothieno[3,2- b][1]benzothiophene (C8-BTBT) single-crystal array coated with CH3NH3PbI3 nanoparticles (NPs) synthesized by a simple, one-step solution method. In contrast to C8-BTBT and CH3NH3PbI3 NPs with respective absorption in the ultraviolet (UV) and visible (vis) region, their hybrid structure shows broad absorption covering the entire UV-vis range. The hybrid-based phototransistors exhibit an ultrahigh responsivity of >1.72 × 104 A/W in the 252-780 nm region, which represents the best performance for solution-processing, broadband photodetectors. Moreover, integrated phototransistor circuitries from the hybrid CH3NH3PbI3 NPs/C8-BTBT single-crystal array show applications for high-security communication.

4.
Mikrochim Acta ; 185(12): 557, 2018 11 21.
Article in English | MEDLINE | ID: mdl-30465282

ABSTRACT

A molecularly imprinted photonic hydrogel (MIPH) is described for the optical determination of L-histidine (L-His). The inverse opal structure of MIPH was obtained by placing silica particles (230 nm) in molecularly imprinted polymer on a glass slide. After being fully etched by hydrofluoric acid, this inverse opal structure brings about a high specific surface and plentiful binding sites for L-His. If L-His is absorbed by the modified MIPH, its average effective refraction coefficient is increased. This causes the Bragg diffraction peak to be red-shifted by about 34 nm as the concentration of L-His increases from 0 to 100 nM. Much smaller diffraction peak shifts are obtained for other amino acids. The detection limit of this method is 10 pM. The response time towards L-His is as short as 60 s. In addition, the sensor can be recovered by treatment with 0.1 M acetic acid/methanol. It was applied to the determination of L-His in drinks sample. Graphical abstract After absorbing L-histidine, the average effective refractive index of this molecularly imprinted photonic hydrogel (MIPH) is increased, and the Bragg diffraction peak is shifted. The shift of the diffraction peak can be used for the detection of L-His.

5.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-700033

ABSTRACT

Objective To propose a method for high-energy photon 3D decoding of PET detector to decode reactive crystal position and calculate γ ray depth in the scintillating crystal. Methods Light transmitting windows were set between the crystal arrays, visible photon groups were guided to distribute in the photoelectric sensor array during a single event, and sensor signal intensity was regulated to realize position and depth decoding of the high-energy photon.Monte Carlo method was used to compare the designs of different light transmitting windows to determine the effects of the crystal surface treatment mode on the results. Experiments were executed for further verification. Results The experimental results had consistency with simulation ones;the signal received through the reaction crystal was always stronger than that through the adjacent, which could decode the reaction crystals; the relations between the depth of interaction (DOI) and energy differences of the photo sensors were monotonic with the changes of DOI,and thus could be used to calculate the DOI;when using single window,the DOI vs.Diff.Energy curves had two segments which were not desired for DOI measurement;crystals with rough surfaces were more desired since the qualities of their DOI vs.Diff.Energy curves were better;the dual window method had the best DOI vs.Diff.Energy curves in term of linearity.Conclusion The method can realize 3D decoding of the discrete crystal array,which improves the energy resolution of the PET system. [Chinese Medical Equipment Journal, 2018,39(5):22-28,63]

6.
Methods Enzymol ; 590: 143-167, 2017.
Article in English | MEDLINE | ID: mdl-28411636

ABSTRACT

Jack bean urease is an important enzyme not only because of its numerous uses in medical and other fields but also because of its historical significance-the first enzyme to be crystallized and also the first nickel metalloenzyme. This enzyme hydrolyzes urea into ammonia and carbon dioxide; however, the stability of this enzyme at ambient temperature is a bottleneck for its applicability. To improve urease stability, it was immobilized on different substrates, particularly on polymeric hydrogels. In this study, the enzyme was coupled covalently with poly(acrylamide) hydrogel with an yield of 18µmol/cm3. The hydrogel served as the nanoarmor and protected the enzyme against denaturation. The enzyme immobilized on the polymer hydrogel showed no loss in activity for more than 30 days at ambient temperature, whereas free enzyme lost its activity within a couple of hours. The Michaelis-Menten constant (Km) for free and immobilized urease were 0.0256 and 0.2589mM, respectively, on the first day of the study. The Km of the immobilized enzyme was approximately 10 times higher than that of the free enzyme. The hydrogel technique was also used to prepare light diffracting polymerized colloidal crystal array in which urease enzyme was covalently immobilized. This system was applied for the detection of mercury (Hg2+) with the lower limit as 1ppb, which is below the maximum contaminant limit (2ppb) for mercury ions in water. The experimental details of these studies are presented in this chapter.


Subject(s)
Acrylic Resins/chemistry , Enzymes, Immobilized/chemistry , Urease/chemistry , Disulfides/chemistry , Enzyme Stability , Hydrogels/chemistry , Hydrogen-Ion Concentration , Hydrolysis , Kinetics , Mercury/analysis , Plant Proteins/chemistry , Protein Binding , Urea/chemistry , Water Pollutants, Chemical/analysis , Water Quality
7.
ACS Appl Mater Interfaces ; 8(37): 24753-60, 2016 Sep 21.
Article in English | MEDLINE | ID: mdl-27564727

ABSTRACT

The preparation of uniform large-area highly crystalline organic semiconductor single crystals remains a challenge in the field of organic field-effect transistors (OFETs). Crystal densities in the channel regions of OFETs have not yet reached sufficiently high values to provide efficient charge transport, and improving channel crystal densities remains an important research area. Herein we fabricated densely well-aligned single crystal arrays of the 6,13-bis(triisopropylsilylethynyl)pentacene (TIPS_PEN) semiconductor using a straightforward scooping-up (SU) methodology to quickly produce a large-area self-assembled semiconductor crystal layer. The resulting crystalline TIPS_PEN strip arrays obtained using the SU method revealed a packing density that was 2.76 times the value obtained from the dip-coated channel, and the mean interspatial distance between the crystal strips decreased from 21.5 to 7.8 µm. The higher crystal packing density provided efficient charge transport in the FET devices and directly yielded field-effect mobilities as high as 2.16 cm(2)/(V s). These field-effect mobilities were more than three times the values obtained from the OFETs prepared using dip-coated channels. Furthermore, the contact resistance between the source/drain electrodes and the TIPS_PEN crystals decreased by a factor of 2. These contributions represent a significant step forward in improving semiconductor crystal alignment for the fabrication of large-area high-performance organic electronics.

8.
Article in Korean | WPRIM (Western Pacific) | ID: wpr-93128

ABSTRACT

The purpose of this study is to optimize a parallel-hole collimator for small gamma camera having the pixellated crystal array and evaluate the effect of crystal-collimator misalignment on the image quality using a simulation tool GATE (Geant4 Application for Tomographic Emission). The spatial resolution and sensitivity were measured for the various size of hexagonal-hole and matched square-hole collimators with a Tc-99m point source and the uniformity of flood image was estimated as a function of the angle between crystal array and collimator by misalignment. The results showed that the spatial resolution and sensitivity were greatly improved by using the matched collimator and the uniformity was reduced by crystal-collimator misalignment.


Subject(s)
Gamma Cameras
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