Giant tunnel resistance effect in (SrTiO3)2/(BaTiO3)4/(CaTiO3)2 asymmetric superlattice with enhanced polarization.

In this work, we report the effectively enhanced tunneling electroresistance effect in Au/(SrTiO3)2/(BaTiO3)4/(CaTiO3)2/Nb:SrTiO3 superlattice ferroelectric tunnel junction (FTJ). The stable polarization switching and enhanced ferroelectricity were achieved in the nanoscale thickness high-quality epitaxial superlattice. A high ON/OFF current ratio of more than 105 was obtained at room temperature, which is an order of magnitude larger than the BaTiO3 FTJ with the same structure. Nonvolatile resistance switching controlled by nonvolatile polarization switching was observed in the superlattice FTJ. Driven by increased polarization and intrinsic asymmetric ferroelectricity, a highly asymmetric depolarization field is generated compared with the Au/BaTiO3/Nb:SrTiO3 FTJ, resulting in an enhanced tunneling electroresistance effect. These results provide a potential way to construct FTJ memory devices by constructing asymmetric three-component ferroelectric superlattices.

Enhanced photoluminescence of double perovskite Cs2SnI6 nanocrystals via Na+ doping.

Double perovskites without lead element have attracted great attention in recent years. Further increasing the photoluminescence quantum yield of lead-free double perovskites is necessary for their potential applications. In this work, Na+ doped Cs2SnI6 nanocrystals were synthesized by hot injection method. It was displayed that all the NCs have uniform hexagonal shape with good crystallization. Energy dispersing spectroscopy and X-ray photoelectron spectroscopy proves the Na+ ions were doped in the lattice of perovskite structure. The photoluminescence intensity of doped NCs is increased by 2.7-fold than that of pure NCs. A maximum photoluminescence quantum yield of 72% is obtained. The luminous mechanism was investigated by femtosecond transient absorption spectrum and a self-trap emission was proved by the observation of ground state bleaching and photo-induced absorption signals.

Study on the Up-Conversion Luminescence and Conductivity Behavior of p-Type NiO:Yb,Er Thin Films.

In this work, Li+-doped NiO:Yb,Er thin films are obtained via pulsed laser deposition. It was found that the films exhibit high transparency in the visible region and clearly red up-conversion luminescence under 980 nm excitation. Doping with Li+ can adjust the up-conversion emission intensity of the films. Moreover, all the films have p-type conductivity with a single activation energy of around 360 meV. The sheet resistivity of the films can be improved through changing the doping concentration of Li+ ions. Taken together, 5% is the best doping concentration for the potential application of this kind of film.

Asymmetric liquid crystalline dibenzo[a,h]anthracenes for organic semiconductors with high mobility and thermal stability.

A series of asymmetric organic semiconductors based on N-shaped dibenzo[a,h]anthracene (DBA), Ph-DBA-Cn (n = 8, 10, 12), were developed. All Ph-DBA-Cn compounds had good chemical stability and smectic LC qualities, and thermally stable crystal phase can be maintained under 190 °C due to the suppressed molecular motions by the bent DBA core. High-quality crystalline films can be fabricated using a blade-coating technique. It was revealed that the average mobility of all Ph-DBA-Cn organic thin-film transistors (OTFTs) was estimated to be over 2.8 cm2 V-1 s-1, and a Ph-DBA-C8 device in particular afforded exceptional mobility of up to 11.8 cm2 V-1 s-1. The highly-ordered and uniaxially-oriented crystalline films composed of bilayer units were revealed to be responsible for their excellent electrical device performances. Furthermore, all Ph-DBA-Cn OTFTs can retain operational characteristics up to 160 °C over 1 cm2 V-1 s-1. These findings will be crucial for the development of high-mobility and thermally durable OSCs for practical electronics.

New Approach to Low-Power-Consumption, High-Performance Photodetectors Enabled by Nanowire Source-Gated Transistors.

Power consumption makes next-generation large-scale photodetection challenging. In this work, the source-gated transistor (SGT) is adopted first as a photodetector, demonstrating the expected low power consumption and high photodetection performance. The SGT is constructed by the functional sulfur-rich shelled GeS nanowire (NW) and low-function metal, displaying a low saturated voltage of 0.61 V ± 0.29 V and an extremely low power consumption of 7.06 pW. When the as-constructed NW SGT is used as a photodetector, the maximum value of the power consumption is as low as 11.96 nW, which is far below that of the reported phototransistors working in the saturated region. Furthermore, benefiting from the adopted SGT device, the photodetector shows a high photovoltage of 6.6 × 10-1 V, a responsivity of 7.86 × 1012 V W-1, and a detectivity of 5.87 × 1013 Jones. Obviously, the low power consumption and excellent responsivity and detectivity enabled by NW SGT promise a new approach to next-generation, high-performance photodetection technology.

Modifying Jahn-Teller distortion by epitaxial stress in LaMnO3films for tunning electron localization.

The effect of epitaxial stress on Jahn-Teller (JT) distortion in epitaxial LaMnO3(LMO) films has been investigated. Both2θ-ωscans and reciprocal space maps (RSMs) indicate that LMO samples are subjected to compressive stress. Obvious Laue oscillations can be detected in2θ-ωscans, indicating the high quality of samples. RSMs of symmetry peak (001) and asymmetry peak (-103) imply different epitaxial stress for LMO films deposited on different substrates. Raman spectra measurements reveal that the degree of JT distortion can be well tuned via the epitaxial stress which may further influence on the electron localization in the films. This study might benefit to understanding the correlation between crystalline structure and electrical transport properties of LMO films and related LMO-based superlattices.

Enhanced photoluminescence of CsPbBr3-xIx nanocrystals via plasmonic Au nanoarrays.

Large scale ordered Au nanoarrays are fabricated by nanosphere lithography technique. The photoluminescence improvement of CsPbBr3-xIx nanocrystals by more than three times is realized in the CsPbBr3-xIx nanocrystal/Au nanoarray/Si structure. Time-resolved photoluminescence decay curves indicate that the lifetime is decreased by introducing the Au nanoarrays, which results in a increasing radiation recombination rate. The reflection spectra with two major valleys (the dip in the curve) located at ∼325 nm and 545 nm of Au nanoarray/Si structure, which illustrates two plasmonic resonance absorption peaks of the Au nanoarrays. The enhancement of photoluminescence is ascribed to a well match between the excitation/emission of CsPbBr3-xIx nanocrystals and localized surface plasmon/gap plasmon resonance absorption of the ordered Au nanoarrays, as also revealed from the finite-difference time-domain simulation analysis. Our work offers an effective strategy to improve the fluorescence of perovskite nanocrystals and provide the potential for further applications.

Enhanced upconversion red light emission of TiO2:Yb,Er thin film via Mn doping.

TiO2:Yb,Er films with different concentrations of Mn2+ are grown on SiO2 glass substrates by pulsed laser deposition. It is found that the introduction of Mn2+ enhanced the intensity of upconversion emission. In particular, TiO2:Yb,Er thin film with 5% Mn2+ ions exhibits the brightest upconversion emission. The upconversion red emission intensity is increased by 2.5-fold than that of a TiO2:Yb,Er thin film without Mn2+ ions, which is ascribed to the multi-photon absorption and efficient exchange-energy transfer process between Er3+ and Mn2+. The high transmittance and good conductivity of the films made them possible to act as electron transport layer in solar cells.

Enhancing the bulk photovoltaic effect by tuning domain walls in epitaxial BiFeO3films.

In this letter, the role of domain wall (DW) on bulk photovoltaic effect (BPV) effect in BiFeO3(BFO) films was studied by x-ray reciprocal space mapping and conductive atomic force microscope. It was found that the domain structure and DW can be tuned by controlling the epitaxial orientation of BFO film. Remarkably, under 1 sun AM 1.5 G illumination, the 109° DW enhances the transport of photogenerated carriers and simultaneously improves the conductivity and power conversion efficiency (PCE). The short-circuit current density and PCE can reach 171.15µA cm-2and 0.1127%, respectively. Therefore, our study reveals the correlation between the DW and the BPV effect in BFO film and provides a new pathway to improve the PCE of BFO-based photovoltaic device.

Highly Conductive P-Type MAPbI3 Films and Crystals via Sodium Doping.

To regulate the optical and electrical properties of the crystals and films of the intrinsic methylammonium lead iodide (CH3NH3PbI3), we dope them with sodium (Na) by selecting sodium iodide (NaI) as a dopant source. The highly conductive p-type sodium-doped CH3NH3PbI3 (MAPbI3: Na) perovskite single crystals and thin films are successfully grown using the inverse temperature crystallization (ITC) method and antisolvent spin-coating (ASC) method, respectively. With the increase of Na+ doping concentration, the grain size of the film increases, the surface becomes smoother, and the crystallinity improves. Hall effect results demonstrate that both the MAPbI3: Na thin films and single crystals change their quasi-insulating intrinsic conductivity to a highly conductive p-type conductivity. The room-temperature photoluminescence (PL) peaks of doped MAPbI3 films slightly blue shift, while the photocarriers' lifetime becomes longer. The optical fingerprints of the doped levels in MAPbI3: Na perovskites can be identified by temperature-dependent PL. Obvious fingerprints of Na-related acceptor (A0X) levels in the doped MAPbI3: Na were observed at 10 K. These results suggest that sodium doping is an effective way to grow highly conductive p-type MAPbI3 perovskites.

Continuous, Ultra-lightweight, and Multipurpose Super-aligned Carbon Nanotube Tapes Viable over a Wide Range of Temperatures.

In extreme environments, such as at ultrahigh or ultralow temperatures, the amount of tape used should be minimal so as to reduce system contamination and unwanted residues. However, tapes made from conventional materials typically lose their adhesiveness or leave residues difficult to remove under such conditions. Thus, the development of more versatile, lightweight, and easily removable tapes for applications in such extreme environments has received considerable attention. Here, we report that horizontally superaligned carbon nanotube (SACNT) tapes can be used to provide perfect van der Waals (vdW) interface contacts over a wide range of temperatures (from -196 to 1000 °C), yielding outstanding adhesiveness with specific adhesion strengths up to ∼1.1 N/µg. With a surface density of only 0.5-5 µg/cm2, hundreds of times lighter than the vertically aligned CNT adhesives, the SACNT tapes can be cost-effectively provided in hundreds of meters. They have multipurpose adhesive abilities for versatile materials and are also easily separated from samples even after exposure to extreme temperature regimes. First-principles calculations confirm the mechanism of vdW adhesion and reveal that ultraflat and nanometer-thick SACNT tapes may yield far greater adhesive abilities. These SACNT tapes show great potential for use in mechanical bonding, electrical bonding, and thermal dissipation in electronic devices.

Laser-Induced Flash-Evaporation Printing CH3NH3PbI3 Thin Films for High-Performance Planar Solar Cells.

Organic-inorganic hybrid perovskites have been emerging as promising light-harvesting materials for high-efficiency solar cells recently. Compared to solution-based methods, vapor-based deposition technologies are more suitable in preparing compact, uniform, and large-scale perovskite thin films. Here, we utilized flash-evaporation printing (FEP), a laser-induced ultrafast single source evaporation method employing a carbon nanotube evaporator, to fabricate high-quality methylammonium lead iodide perovskite thin films. Stoichiometric films with pure tetragonal perovskite phase can be achieved using a controlled methylammonium iodide to lead iodide ratio in evaporation precursors. The film crystallinity and crystal grain growth could further be promoted after postannealing. Planar solar cells (0.06 cm2) employing these perovskite films exhibit a champion power conversion efficiency (PCE) of 16.8% with insignificant hysteresis, which is among the highest reported PCEs using vapor-based deposition methods. Large-area (1 cm2) devices based on such perovskite films also achieved a stabilized PCE of 11.2%, indicating the feasibility and scalability of our FEP method in fabricating large-area perovskite films for other optoelectronic applications.

Crystalline multiwall carbon nanotubes and their application as a field emission electron source.

Using super-aligned carbon nanotube (CNT) film, we have fabricated van der Waals crystalline multiwall CNTs (MWCNT) by adopting high pressure and high temperature processing. The CNTs keep parallel to each other and are distributed uniformly. X-ray diffraction characterization shows peaks at the small angle range, which can be assigned to the spacing of the MWCNT crystals. The mechanical, electrical and thermal properties are all greatly improved compared with the original CNT film. The field emission properties of van der Waals crystalline MWCNTs are tested and they show a better surface morphology stability for the large emission current. We have further fabricated a field emission x-ray tube and demonstrated a precise resolution imaging ability.

Design, synthesis and in vitro biological evaluation of novel [1,2,3]triazolo[4,5-d]pyrimidine derivatives containing a thiosemicarbazide moiety.

A series of hybrid molecules containing [1,2,3]triazolo[4,5-d]pyrimidine and thiosemicarbazide moieties were designed, synthesized and evaluated for their antiproliferative activities against MGC-803, NCI-H1650 and PC-3 human cancer cells. Some of the synthesized compounds showed moderate to good activity against three selected cancer cell lines. Among these compounds, compound 29 displayed the most potent antiproliferative activity as well as good selectivity between cancer cells and normal cells. Further mechanism studies revealed that compound 29 could obviously inhibit the colony formation and migration of MGC-803 as well as induced apoptosis.

Identification of thiazolo[5,4-d]pyrimidine derivatives as potent antiproliferative agents through the drug repurposing strategy.

A series of thiazolo[5,4-d]pyrimidine derivatives were synthesized and evaluated for their antiproliferative activities on three cancer cell lines. The structure-activity relationship studies were conducted through the variation in the three regions of the thiazolo-pyrimidine core. Substitution with morpholine led to compound 24, which exerted the most potent antiproliferative activity as well as good selectivity between cancer and normal cells (IC50 values of 1.03 µM against MGC803 and 38.95 µM against GES-1). In addition, compound 24 inhibited the colony formation and migration of MGC803 as well as induced apoptosis. Western blot experiments indicated the expression changes of apoptosis-related proteins, including up-regulation of Bax and caspase-3/9, as well as down-regulation of Bcl-2.

Epitaxial Growth of Aligned and Continuous Carbon Nanofibers from Carbon Nanotubes.

Exploiting the superior properties of nanomaterials at macroscopic scale is a key issue of nanoscience. Different from the integration strategy, "additive synthesis" of macroscopic structures from nanomaterial templates may be a promising choice. In this paper, we report the epitaxial growth of aligned, continuous, and catalyst-free carbon nanofiber thin films from carbon nanotube films. The fabrication process includes thickening of continuous carbon nanotube films by gas-phase pyrolytic carbon deposition and further graphitization of the carbon layer by high-temperature treatment. As-fabricated nanofibers in the film have an "annual ring" cross-section, with a carbon nanotube core and a graphitic periphery, indicating the templated growth mechanism. The absence of a distinct interface between the carbon nanotube template and the graphitic periphery further implies the epitaxial growth mechanism of the fiber. The mechanically robust thin film with tunable fiber diameters from tens of nanometers to several micrometers possesses low density, high electrical conductivity, and high thermal conductivity. Further extension of this fabrication method to enhance carbon nanotube yarns is also demonstrated, resulting in yarns with ∼4-fold increased tensile strength and ∼10-fold increased Young's modulus. The aligned and continuous features of the films together with their outstanding physical and chemical properties would certainly promote the large-scale applications of carbon nanofibers.

Design, synthesis, and biological evaluation of new thiazolo[5,4-d]pyrimidine derivatives as potent antiproliferative agents.

A series of thiazolo[5,4-d]pyrimidine derivatives were synthesized and evaluated for their antiproliferative activities against several human cancer cell lines. Structure-activity relationship studies were carried out, showing that most of the target compounds had good inhibition against the tested cell lines. Among them, compound 7i exhibited potent inhibition against human gastric cancer cells MGC-803 and HGC-27 with IC50 values of 4.64 and 5.07 µM, respectively and around 12-fold selectivity between MGC-803 and GES-1, indicating a relatively low toxicity to normal cells. The potency and low toxicity of compound 7i make the thiazolo[5,4-d]pyrimidine an attractive scaffold for designing new derivatives selectively targeting MGC-803 cells.

Design, synthesis and biological evaluation of [1,2,3]triazolo[4,5-d]pyrimidine derivatives possessing a hydrazone moiety as antiproliferative agents.

A series of [1,2,3]triazolo[4,5-d]pyrimidine derivatives bearing a hydrazone moiety were designed, synthesized and evaluated for their antiproliferative activity against several cancer cell lines of different origins by MTT assay. Most of the synthesized compounds demonstrated moderate to good activity against the cancer cell lines selected. Especially, compound 43 showed the most potent antiproliferative activity as well as good selectivity between cancer and normal cells (IC50 values of 0.85 µM against MGC-803 and 56.17 µM against GES-1). In addition, compound 43 evidently inhibited the colony formation of MGC-803 cells at 0.8 µM. Further mechanism studies revealed that compound 43 could induce apoptosis of MGC-803 cells probably through the mitochondrial pathway accompanied with decrease of the mitochondrial membrane potential (MMP), activations of caspase-9/3, up-regulation of the expression of Bax, Bak and PUMA, as well as down-regulation of that of Bcl-2 and Mcl-1.

Observation of Charge Generation and Transfer during CVD Growth of Carbon Nanotubes.

Carbon nanotube (CNT) is believed to be the most promising material for next generation IC industries with the prerequisite of chirality specific growth. For various approaches to controlling the chiral indices of CNTs, the key is to deepen the understanding of the catalytic growth mechanism in chemical vapor deposition (CVD). Here we show our discovery that the as-grown CNTs are all negatively charged after Fe-catalyzed CVD process. The extra electrons come from the charge generation and transfer during the growth of CNTs, which indicates that an electrochemical process happens in the surface reaction step. We then designed an in situ measurement equipment, verifying that the CVD growth of CNTs can be regarded as a primary battery system. Furthermore, we found that the variation of the Fermi level in Fe catalysts have a significant impact on the chirality of CNTs when different external electric fields are applied. These findings not only provide a new perspective on the growth of CNTs but also open up new possibilities for controlling the growth of CNTs by electrochemical methods.

Ice-assisted transfer of carbon nanotube arrays.

Decoupling the growth and the application of nanomaterials by transfer is an important issue in nanotechnology. Here, we developed an efficient transfer technique for carbon nanotube (CNT) arrays by using ice as a binder to temporarily bond the CNT array and the target substrate. Ice makes it an ultraclean transfer because the evaporation of ice ensures that no contaminants are introduced. The transferred superaligned carbon nanotube (SACNT) arrays not only keep their original appearance and initial alignment but also inherit their spinnability, which is the most desirable feature. The transfer-then-spin strategy can be employed to fabricate patterned CNT arrays, which can act as 3-dimensional electrodes in CNT thermoacoustic chips. Besides, the flip-chipped CNTs are promising field electron emitters. Furthermore, the ice-assisted transfer technique provides a cost-effective solution for mass production of SACNTs, giving CNT technologies a competitive edge, and this method may inspire new ways to transfer other nanomaterials.