Influence of external load on friction coefficient of Fe-polytetrafluoroethylene

A coarse-grained molecular dynamics simulation model was developed in this study to investigate the friction process occurring between Fe and polytetrafluoroethylene(PTFE).We investigated the effect of an external load on the friction coefficient of Fe–PTFE using the molecular dynamics simulations and experimental methods.The simulation results show that the friction coefficient decreases with the external load increasing,which is in a good agreement with the experimental results.The high external load could result in a larger contact area between the Fe and PTFE layers,severer springback as a consequence of the deformed PTFE molecules,and faster motion of the PTFE molecules,thereby affecting the friction force and normal force during friction and consequently varying the friction coefficient.     

Ring Airy-Like Beams along Predesigned Parabolic Trajectories

By phase-modulating ring Airy Gaussian beams, ring Airy-like beams propagating along predesigned parabolic trajectories are presented which combine the properties of accelerating beams and abruptly autofocusing beams analytically and numerically for the first time. The enhancement of the quadratic term ratio α shortens the autofocus distance and increases the slope of the beams after autofocusing. Interestingly, the main lobe tends to break into pieces as α increases and the possible reasons have been discussed. Furthermore, the distribution factor β and the radius of the primary r₀ can prominently affect the autofocus distance and the intensity at the focal point but do not change the slope of the beams after the autofocusing. In addition, the self-healing properties are validated to be retainable while RAiG beams via predesigned parabolic trajectories with various α.     

Optimal spectral phase control of femtosecond laser-induced up-conversion luminescence in Sm3+:NaYF4 glass

The spectral phase of the femtosecond laser field is an important parameter that affects the up-conversion(UC)luminescence efficiency of dopant lanthanide ions.In this work,we report an experi-mental study on controlling the UC lmiiinescence efficiency in Sm^3+:NaYF4 glass by 800-nm femtosec-ond laser pulse shaping using spectral phase modulation.The optimal phase control strategy efficiently enhances or suppresses the UC luminescence intensity.Based on the laser-power dependence of the UC luminescence intensity and its comparison with the luminescence spectrum under direct 266-nm fem-tosecond lciser irradiation,we propose herein an excitation model combining non-resonant two-photon absorption with resonance-media ted three-photon absorption to explain the experimental observations.     

Double Andreev reflections at surface states of the topological insulators with hexagonal warping

We study the Andreev reflection(AR)at the interface of the topological insulator with hexagonal warping and superconductor junction.Due to the hexagonal warping effect,the double ARs are found in a certain range of the incident angle,where for one incident electron beam,two beams of holes are reflected back.Interestingly,both the beams of holes are reflected as retro-AR on the same side of the normal line of the interface but with different reflection angles,different from the previously reported double AR with one retro-AR and one specular-AR.The double reflections owing to the warping effect show the optics-like property of the Dirac fermion and can stimulate the double reflections of light in anisotropic crystals.In addition,we find that the double ARs are dependent on the hexagonal warping parameter nonmonotonically,and in an intermediate strength the double AR phenomenon is prominent,providing a possibility to explore the warping parameter of topological insulators.     

用浓度调制光谱法测量水汽辉光放电中OH和H2O的布居数变化

本文使用波长为2.8 μm的分布式反馈激光器来测量水汽辉光放电产生的物种. 使用浓度调制光谱仅观察到OH自由基和瞬态H₂O分子的吸收光谱. 吸收峰的强度和方向随解调相位而变化,但是H₂O的一个吸收峰的方向始终与其它峰相反. OH和H₂O的不同光谱取向反映了能级中粒子数量的增加或减少. 如果在放电过程中可以检测到更多的瞬态物种,则可以更好地研究H₂O的激发、电离和分解动力学. 研究表明,浓度调制光谱的解调相位关系可以用来研究分子能级的布居数变化.     

A solvent-governed surface state strategy for rational synthesis of N and S co-doped carbon dots with multicolour fluorescence

ABSTRACT

Multicolour emissive carbon dots (CDs) are widely investigated by virtue of their merits on fluorescent properties. Method on heteroatom doping assisted with various solvents has been proved efficient in achieving multiple-colour-emissive CDs, especially long-wavelength emission. Herein, a synthesis of multicolour-emissive CDs by controlled surface function is reported. By tuning the thermal-pyrolysis temperature and molar ratio of reactants, optimal emission of the resulted CDs gradually shifts from blue to yellow light with the assistance of different solvents. According to the emissive relationship dependent on excitation, fluorescence lifetimes, and FT-IR of these CDs, the different surface states participated with S and N elements on the surface of carbogenic core govern fluorescent colours of the CDs. In terms of the applications, blue CDs (B-CDs) exhibits high sensitivity for ion detections of Ag⁺ and Fe³⁺, which is further illustrated to have different quenching mechanisms each other because that these ions have the affinity interaction with different surface groups of the CDs. Moreover, blue and yellow CDs solutions are mixed with PVP water solution to fabricate white-light CDs/PVP film, which exhibits stable fluorescence with a CIE coordinate of (0.32, 0.33) and endows these CDs as potentially fluorescent nanomaterial in the solid state lighting field.     

Can (H2O) n (n = 1–2) as effective catalysts in the CH2OO + H2S reaction under tropospheric conditions?

The addition reaction of CH₂OO?+?H₂S → HSCH₂OOH without and with catalyst X (X?=?H₂O and (H₂O)₂) has been investigated by CCSD(T)-F12a/VTZ-F12//B3LYP/aug-cc-pVTZ method and canonical variational transition state theory with small curvature tunneling correction. When H₂O was introduced in the CH₂OO?+?H₂S reaction, it not only acts as a catalyst for producing HSCH₂OOH, but also plays as a reactant to forming HOCH₂OOH. The formation channel of HSCH₂OOH is more important than the formation channel of HOCH₂OOH with its calculated rate constant larger by 11.0–43.2 times within the temperature 280–320?K. Then, (H₂O)₂ catalysed CH₂OO?+?H₂S → HSCH₂OOH reaction has been taken into account with its rate lower 1.9–4.2 times than the reaction of CH₂OO?+?H₂S → HSCH₂OOH with water. Also, CH₂OO?+?H₂S with H₂O cannot compete with the CH₂OO?+?H₂S reaction without water. This is different from CH₂OO?+?(H₂O)₂ reaction, which is about 4 orders of magnitude larger than the rate constant for CH₂OO?+?H₂O reaction. Such discrepancy is possible because C(CH₂OO)···O(H₂O) interaction has been enhanced more obviously by H₂O as compared to that of C(CH₂OO)···O(H₂S) interaction.     

轮背空腔-密封气对CAES向心涡轮变工况流动损失的影响

本文以国内首套MW级压缩空气储能(CAES)系统末级向心涡轮为研究对象,通过数值模拟分析了变工况条件下轮背空腔-密封气对等熵效率和流场结构的影响.结果表明:在求解中考虑轮背空腔-密封气结构能够使等熵效率数值解的偏差减小0.7%;随涡轮进口压力增加,轮背空腔泄漏流由叶片吸力面中部叶高区域逐渐向轮毂转移,流动损失先增加后减小;合理降低轮背空腔泄漏气体的轴向速度,能够减弱轮背空腔-密封气结构对等熵效率的负面影响,使向心涡轮在较宽的变工况范围内都保持高效运行.