纳米压痕仪接触投影面积标定方法的研究

基于Oliver与Pharr方法的纳米压痕实验以其简单方便获得广泛的应用，但众多因素对压 痕实验结果的影响范围并无明确的结论. 其中压痕接触面积的确定是一个重要环节，该因素 对实验结果，特别是小深度下的实验结果具有重要影响. 仔细分析了Oliver与Pharr 方法并进行了几种材料的纳米压痕实验，针对该方法在接触深度确定、不同深度范围下方法 的适用性进行了说明. 分析结果表明，对所有的材料使用统一的面积公式，只有在大压痕深 度时才是适用的，而在小压痕深度时可能带来较大的误差. 因此，应慎重使用由Oliver与 Pharr方法得到的小压痕深度的硬度数据.     

Variation of the strain rate during CSM nanoindentation of glassy polymers and its implication on indentation size effect

The indentation strain rate is currently assumed to remain unvaried during continuous stiffness measurement (CSM) nanoindentation where is imposed to remain constant. To probe the validity of this assumption for the nanoindentation of glassy polymers, a series of experiments have been performed at different set values on poly(methyl methacrylate) and polycarbonate using CSM technique. It is firstly shown that the actual value changes drastically at shallow indentation depths and it takes a considerable depth, which is material independent, for this parameter to attain a stabilized value. Furthermore, the strain rate is measured directly as the descent rate of the indenter divided by its instantaneous depth ( ), and indirectly via considering the variations of the load and hardness during the test. Both of these approaches reveal that the strain rate is considerably larger at shallow depths, and the depth beyond which it becomes constant is material and ratio dependent. Finally, by considering the relationship between the hardness and strain rate, it is observed that although the strain rate variation alters the hardness, its contribution is not able to justify the observed indentation size effect; hence, other contributing factors for this phenomenon are discussed for their possible effects. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 2179–2187     

Molecular Basis for the Mechanical Response of Sulfa Drug Crystals

Comprehension of the nanomechanical response of crystalline materials requires the understanding of the elastic and plastic deformation mechanisms in terms of the underlying crystal structures. Nanoindentation data were combined with structural and computational inputs to derive a molecular-level understanding of the nanomechanical response in eight prototypical sulfa drug molecular crystals. The magnitude of the modulus, E, was strongly connected to the non-covalent bond features, that is, the bond strength, the relative orientation with the measured crystal facet and their disposition in the crystal lattice. Additional features derived from the current study are the following. Firstly, robust synthons well isolated by weak and dispersive interactions reduce the material stiffness; in contrast, the interweaving of interactions with diverse energetics fortifies the crystal packing. Secondly, mere observation of layered structures with orthogonal distribution of strong and weak interactions is a prerequisite, but inadequate, to attain higher plasticity. Thirdly, interlocked molecular arrangements prevent long-range sliding of molecular planes and, hence, lead to enhanced E values. In a broader perspective, the observations are remarkable in deriving a molecular basis of the mechanical properties of crystalline solids, which can be exploited through crystal engineering for the purposeful design of materials with specific properties.     

掺杂对GaN晶体力学性能影响的研究

对GaN单晶力学性能的研究有助于解决其在生长、加工和器件应用中的开裂问题。本文围绕掺杂对GaN单晶力学性能的影响，通过纳米压痕法测试了不同掺杂类型(非掺、Si掺和Fe掺)GaN单晶的弹性模量和硬度，测试结果表明掺杂对GaN单晶的硬度有重要影响。Si掺、Fe掺GaN较非掺样品硬度有所提升，用重掺杂的氨热GaN单晶作为对照，也证明了这一结论。通过高分辨X射线衍射分析和原子力显微镜表征实验发现，晶体结晶质量、接触面积等因素对GaN单晶硬度的影响较小。对GaN表面纳米压痕滑移带长度和晶体晶格常数进行测试，结果表明，掺杂影响GaN单晶硬度的主要原因是缺陷对GaN位错增殖、滑移的阻碍作用和掺杂引起的GaN晶格常数的变化。     

Elastic–plastic deformation of Pb(Zn1/3Nb2/3)O3–(6–7)% PbTiO3 single crystals during nanoindentation

The elastic–plastic deformation behavior of (001)- and (011)-oriented single crystal solid solutions of Pb(Zn_1/3Nb_2/3)O₃–(6–7)% PbTiO₃ (PZN–PT) have been studied using a nanoindentation technique. A procedure is presented here to isolate the elastic, elastic–plastic and plastic contributions to the deformation using the unloading data, and a parameter, referred to as relaxation, is defined to characterize the elastic–plastic deformation during nanoindentations. This relaxation parameter increases with the maximum indentation load due to the higher indentation stress induced, and it also causes less recovery of the material upon indentation unloading compared to predicted pure elastic recovery. For a (001) surface, the relaxation value remains virtually unchanged within the range of the maximum indentation load of 10–50 mN, possibly due to a complete localized depoling of the non-180° domain switching. It is also found that the unpoled surface is more prone to stress-induced depolarization compared to the poled surfaces. Furthermore, by applying the continuous stiffness measurement (CSM) technique, the effects of multiple loading/unloading are studied for both (001)- and (011)-oriented PZN–PTs using the maximum indentation loads of 20 and 50 mN. With more loading/unloading cycles at higher CSM frequencies, stress-induced depolarization becomes prevalent and the contribution of the domain reorientation towards elastic recovery is significantly reduced. As a consequence, the relaxation value is increased, indicating more elastic–plastic deformation. This CSM effect is especially pronounced for poled (011) surfaces.     

The influence of grain size and texture on the Young's modulus of nanocrystalline nickel and nickel–iron alloys

Hardness and Young's modulus were measured by nanoindentation on a series of electrodeposited nanocrystalline nickel and nickel–iron alloys. Hardness values showed a transition from regular to inverse Hall–Petch behaviour, consistent with previous studies. There was no significant influence of grain size on the Young's modulus of nanocrystalline nickel and nickel–iron alloys with grain sizes greater than 20?nm. The Young's modulus values for nanocrystalline nickel and nickel–iron alloys for grain sizes less than 20?nm were slightly reduced when compared to their conventional (randomly oriented) polycrystalline counterparts. The observed trend with decreasing grain size was found to be consistent with composite model predictions that consider the influence of intercrystalline defects. However, there was some notable variability of the measured values when compared to the model predictions. Three theoretical relationships were used to characterise the anisotropic elastic behaviour of these materials. As a result, texture was also considered to have an influence on the measured Young's modulus and used to explain some of the observed variability for the entire grain size range (9.8–81?nm).     

Critical review of claims for ultra-hardness in nanocomposite coatings

Claims for ultra-hardness (H?≈?100?GPa) in nanocomposite coatings are critically examined in terms of the experimental evidence first presented in 1999 and theoretical support published over the past 10 years. It is shown that the results of experimental work cannot be validated, and that there are many unresolved issues associated with the supporting theoretical arguments. Using the methods outlined by the authors, whose work is reviewed here, but with more precise application of the equations involved, and reading directly from their reported relationships between Y and H, the best estimate of the hardness for the materials under consideration appears to be of the order of ≈55?GPa. This estimate is validated by actual measurements on a diamond sample and super-hard coatings, and finite element computations in comparison with experimental results for ultra-hard coatings. It is shown that the conclusions of the work being reviewed do not stand up to scrutiny and that the hardness of the ultra-hard coatings is most likely over-estimated by a factor of ≈2.     

Influence of free volume and medium-range order on the deformation response of rapidly solidified and bulk Zr-based (Zr52Ti6Al10Cu18Ni14) metallic glass

Free volume and medium-range order (MRO) present in rapidly solidified ribbons (RSRs) and bulk metallic glasses (BMGs) of Zr₅₂Ti₆Al₁₀Cu₁₈Ni₁₄ have been probed by high resolution electron microscopy, fluctuation microscopy, positron annihilation and differential scanning calorimetry. In the as-solidified condition, RSRs showed higher free volume and lower MRO in comparison to BMGs. Within BMGs, the central regions showed higher MRO and lower free volume than the peripheral regions. Uniform deformation of BMGs and RSRs modified their structures, where in, free volume increased in the former and reduced in the latter. These changes in structures led to work hardening in RSRs and work softening in BMGs. Such behaviour could be explained by invoking a concept of critical free volume in the glass phase. For samples (in as-solidified condition) having free volume higher than the critical value, free volume decreased with deformation and showed work-hardening behaviour. In contrast, the work softening behaviour was noticed in samples having free volume lower than the critical free volume.     

NANOINDENTATION SIMULATION OF PE/POSS UNDER DIFFERENT SHAPES OF INDENTERS

In this paper,the nanoindentation simulation on the two models of neat polyethylene(PE) and the polyethylene incorporated with 25wt% POSS(POSS-PE) is performed to reveal the reinforcing mechanism of the mechanical properties.The influence of the indenter shapes on nanoindentation is researched by using three different shapes of diamond indenters(cube-corner indenter,cylindrical indenter with spherical tip and cylindrical indenter with flat tip).The molecular mechanics method is adopted to eliminate the temp...     

Effect of adhesive and cohesive strength on the tribological behaviour of non‐reactively sputtered TiC thin films

Titanium carbide (TiC) thin films were deposited on D9 steel substrates at room temperature (RT), 200 °C and 400 °C. A compound TiC target was sputtered to deposit films in a non‐reactive argon atmosphere. As‐deposited films were characterised for structural, chemical and mechanical properties. Nanoindentation and scratch tests were performed to evaluate the cohesive and adhesive strength of the films, respectively. Tribological properties of the films were investigated using a tribometer. An increase in nano‐hardness from 7.2 to 10.5 GPa was observed as deposition temperature was increased. The films deposited at RT and 200 °C showed poor adhesion leading to the inferior tribological performance. In contrast, films deposited at 400 °C showed better adhesion which improved the wear resistance. Tribological behaviour of TiC thin films was correlated with contact deformation modes of coatings. These modes revealed significant role of adhesive and cohesive strength associated with the coatings. Copyright © 2009 John Wiley & Sons, Ltd.