Quantum Tricritical Point in the Spin-Boson Model with an Ohmic Bath

The dynamics of the spin-boson model with an Ohmic bath at finite temperature is studied by a variational calculation. Numerical solution of the self-consistent equation derived from the variational method shows that the transition from incoherent to coherent phases is discontinuous. It indicates that （T = 0, s = 1） is a tricritical point, i.e. the transition changes from continuous to discontinuous by tuning from T = 0 to T≠ 0. The discontinuous transition at finite temperature is analysed by Landau theory and the relation to the experimental observation on the coherent state is also discussed.     

Photoresponse of the In0.3Ga0.7N metal-insulator-semiconductor photodetectors

In0.3Ga0.7N metal-insulator-semiconductor （MIS） and metal-semiconductor （MS） surface barrier photodetectors have been fabricated. The In0.3Ga0.7N epilayers were grown on sapphire by metalorganic chemical vapour deposition （MOCVD）. The photoresponse and reverse current-voltage characteristics of the In0.3Ga0.7N MIS and MS photodetectors were measured. A best zero bias responsivity of 0.18 A/W at 450 nm is obtained for the In0.3Ga0.7N MIS photodetector with 10 nm Si3N4 insulator layer, which is more than ten times higher than the In0.3Ga0.7N MS photodetector. The reason is attributed to the decrease of the interface states and increase of surface barrier height by the inserted insulator. The influence of the thickness of the Si3N4 insulator layer on the photoresponsivity of the MIS photodetector is also discussed.     

光纤量子密码网络

 数字通信和数字信号处理领域的快速发展直接推动了20世纪后半叶兴起的信息革命。今天的数字信息系统仍然只在经典物理的范畴。每一个比特的信息都能完全的被经典器件描述，比如说一个晶体管或者微处理器的输入电压高低来代表0或者1。然而，信息也能通过量子力学的方式来处理和传输，这就产生了全新的量子信息科学。量子信息科学的一个典型应用就是量子密码术，在过去的十几年中发展十分迅速，美国和欧洲甚至都已经有比较成熟的商业产品。那么，什么是量子密码术，它的基本工作原理是什么，量子密码网络又是解决什么问题的。希望通过本文的叙述，读者能有大致的了解。     

Quantum secure direct communication and deterministic secure quantum communication

In this review article, we review the recent development of quantum secure direct communication (QSDC) and deterministic secure quantum communication (DSQC) which both are used to transmit secret message, including the criteria for QSDC, some interesting QSDC protocols, the DSQC protocols and QSDC network, etc. The difference between these two branches of quantum communication is that DSQC requires the two parties exchange at least one bit of classical information for reading out the message in each qubit, and QSDC does not. They are attractive because they are deterministic, in particular, the QSDC protocol is fully quantum mechanical. With sophisticated quantum technology in the future, the QSDC may become more and more popular. For ensuring the safety of QSDC with single photons and quantum information sharing of single qubit in a noisy channel, a quantum privacy amplification protocol has been proposed. It involves very simple CHC operations and reduces the information leakage to a negligible small level. Moreover, with the one-party quantum error correction, a relation has been established between classical linear codes and quantum one-party codes, hence it is convenient to transfer many good classical error correction codes to the quantum world. The one-party quantum error correction codes are especially designed for quantum dense coding and related QSDC protocols based on dense coding.      

Perylene diimide copolymers with dithienothiophene and dithienopyrrole: Use in n‐channel and ambipolar field‐effect transistors

Solution‐processable polymers consisting of perylene diimide (PDI) acceptor moieties alternating with dithienothiophene (DTT), N‐dodecyl‐dithienopyrrole (DTP), or oligomers of these donor groups have been synthesized. We have, in addition to varying the donor, varied the N,N′ substituents of the PDIs. The thermal, optical, electrochemical, and charge‐transport properties of the polymers have been investigated. The polymers show broad absorption extending from 300 to 1000 nm with optical band gaps as low as 1.2 eV; the band gap decreases with increasing the conjugation length of donor block, or by replacement of DTT by DTP. The electron affinities of the polymers, estimated from electrochemical data, range from ?3.87 to ?4.01 eV and are slightly affected by the specific choice of donor moiety, while the estimated ionization potentials (?5.31 to ?5.92 eV) are more sensitive to the choice of donor. Bottom‐gate top‐contact organic field‐effect transistors based on the polymers generally exhibit n‐channel behavior with electron mobilities as high as 1.7 × 10^–2 cm²/V/s and on/off ratios as high as 10⁶; one PDI‐DTP polymer is an ambipolar transport material with electron mobility of 4 × 10^–4 cm²/V/s and hole mobility of 4 × 10^–5 cm²/V/s in air. There is considerable variation in the charge transport properties of the polymers with the chemical structures. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013     

Enzyme-Inspired Chiral Secondary-Phosphine-Oxide Ligand with Dual Noncovalent Interactions for Asymmetric Hydrogenation

Inspired by the unique character of enzymes, we developed novel chiral SPO (secondary-phosphine-oxide) ligand (SPO-Wudaphos) which can enter into both ion pair and H-bond noncovalent interactions. The novel chiral SPO-Wudaphos exhibited excellent results in the asymmetric hydrogenation of α-methylene-γ-keto carboxylic acids, affording the chiral γ-keto acids with up to over 99 % ee. A series of control experiments and DFT calculations were conducted to illustrate the critical roles of both the ion pair and H-bond noncovalent interactions.     

Triazine Dendrimers for Drug Delivery: Evaluation of Solubilization Properties,Activity in Cell Culture,and In Vivo Toxicity of a Candidate Vehicle

Three criteria are evaluated to assess the potential of a dendrimer based on triazines, 1, for use as a vehicle for drug delivery. These criteria are: (1) its ability to solubilize small hydrophobic guests as measured spectrophotometrically; (2) its ability to deliver a drug in vitro as evaluated using a gene reporter assay; and (3) its in vivo toxicity in mice as determined by autopsy and screens of liver and kidney function. Vehicle 1 solubilizes pyrene to a similar extent to dendrimers based on poly(arylether)s, 4, encapsulating approximately 0.2 molecules of pyrene per dendrimer. This activity is approximately 10-fold greater than that of the more polar poly(propyleneimine) and poly(amidoamine) dendrimers, 2 and 3. Gas-phase computational models reveal that both 1 and 4 have cores that are accessible to solvent, suggesting that these dendrimers can occupy much greater volumes than 2 and 3 whose cores are confined toward the interior of the structure. Electrostatic potential maps can be used to rationalize differences in solubilization between 1 and 4. Precipitation results from mixing cationic 1 with the anionic indomethacin, but not with methotrexate, suggesting that the composition of the drug may dictate the scope of delivery applications. Dendrimer 1 solubilizes 10-hydroxycamptothecin and a novel bisindolemethane; approximately four and five molecules of drug per dendrimer are solubilized, respectively. In cell-culture experiments using a luciferase reporter gene assay, the dendrimer:bisindolemethane conjugate shows comparable activity to the bisindolemethane delivered in aqueous DMSO, suggesting that the dendrimer does not preclude delivery of the molecule to an intracellular target. Preliminary toxicology studies of 1 in mice show that this molecule has no adverse toxicity to the kidneys or the liver in single doses delivered intraperitoneally up to 10?mg/kg.     

Thermally crosslinkable hole‐transporting poly(fluorene‐co‐triphenylamine) for multilayer polymer light‐emitting diodes

This article reports the synthesis and characterization of a novel thermally crosslinkable hole‐transporting poly (fluorene‐co‐triphenylamine) (PFO‐TPA) by Suzuki coupling reaction, followed with its application in the fabrication of multilayer light‐emitting diodes by wet processes. The thermal, photophysical, and electrochemical properties of PFO‐TPA were investigated by differential scanning calorimeter, thermogravimetric analysis, optical spectroscopy, and cyclic voltammetry, respectively. Thermally crosslinked PFO‐TPA, through pendant styryl groups, demonstrates excellent thermal stability (T_d > 400 °C, T_g = 152 °C), solvent resistance, and film homogeneity. Its highest occupied molecular orbital level (?5.30 eV) lies between those of PEDOT:PSS (?5.0 ～ ?5.2 eV) and poly(9,9‐dioctylfluorene) (PFO: ?5.70 eV), forming a stepwise energy ladder to facilitate hole injection. Multilayer device with crosslinked PFO‐TPA as hole‐injection layer (HIL) (ITO/PEDOT:PSS/HIL/PFO/LiF/Ca/Al) was readily fabricated by successive spin‐coating processes, its maximum luminance efficiency (3.16 cd/A) were about six times higher than those without PFO‐TPA layer (0.50 cd/A). The result of hole‐only device also confirmed hole‐injection and hole‐transport abilities of crosslinked PFO‐TPA layer. Consequently, the device performance enhancement is attributed to more balanced charges injection in the presence of crosslinked PFO‐TPA layer. The thermally crosslinkable PFO‐TPA is a promising material for the fabrication of efficient multilayer polymer light‐emitting diodes because it is not only a hole‐transporting polymer but also thermally crosslinkable. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Synthesis,characterization, and ethylene (Co)polymerization behavior of trichlorotitanium 2‐(1‐(arylimino)propyl)quinolin‐8‐olates

A series of trichlorotitanium complexes containing 2‐(1‐(arylimino)propyl)quinolin‐8‐olates was synthesized by stoichiometric reaction of titanium tetrachloride with the corresponding potassium 2‐(1‐(arylimino)propyl)quinolin‐8‐olates and was fully characterized by elemental analysis, nuclear magnetic resonance spectroscopy, and by single‐crystal X‐ray diffraction study of representative complexes. All titanium complexes, when activated with methylaluminoxane, exhibited high catalytic activity toward ethylene polymerization [up to 1.15 × 10⁶ g mol^?1(Ti) h^?1] and ethylene/α‐olefin copolymerization [up to 1.54 × 10⁶ g mol^?1 (Ti) h^?1]. The incorporation of comonomer was confirmed to amount up to 2.82 mol % of 1‐hexene or 1.94 mol % of 1‐octene, respectively. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Dual thermo‐ and pH‐sensitive network‐grafted hydrogels formed by macrocrosslinker as drug delivery system

Dual thermo‐ and pH‐sensitive network‐grafted hydrogels made of poly(N,N‐dimethylaminoethyl methacrylate) (PDMAEMA) network and poly(N‐isopropylacrylamide) (PNIPAM) grafting chains were successfully synthesized by the combination of atom transfer radical polymerization (ATRP), reversible addition‐fragmentation chain transfer (RAFT) polymerization, and click chemistry. PNIPAM having two azide groups at one chain end [PNIPAM‐(N₃)₂] was prepared with an azide‐capped ATRP initiator of N,N‐di(β‐azidoethyl) 2‐chloropropionylamide. Alkyne‐pending poly(N,N‐dimethylaminoethyl methacrylate‐co‐propargyl acrylate) [P(DMAEMA‐co‐ProA)] was obtained through RAFT copolymerization using dibenzyltrithiocarbonate as chain transfer agent. The subsequent click reaction led to the formation of the network‐grafted hydrogels. The influences of the chemical composition of P(DMAEMA‐co‐ProA) on the properties of the hydrogels were investigated in terms of morphology and swelling/deswelling kinetics. The dual stimulus‐sensitive hydrogels exhibited fast response, high swelling ratio, and reproducible swelling/deswelling cycles under different temperatures and pH values. The uptake and release of ceftriaxone sodium by these hydrogels showed both thermal and pH dependence, suggesting the feasibility of these hydrogels as thermo‐ and pH‐dependent drug release devices. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011