2010
DOI: 10.1016/j.apsusc.2010.08.024
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Enhancement of surface mechanical properties by using TiN[BCN/BN]n/c-BN multilayer system

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Cited by 21 publications
(8 citation statements)
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“…According to this model, each interface in the multilayer system works like a grain boundary, such that dislocations pile-up at the interfaces and harden the layer by strain [12,33,34]. The enhancement of mechanical properties for TiN/TiAlN multilayers is in accordance with the increase in hardness as it has been shown in multilayer-type coatings for diverse material systems (e.g., TiCN/TiNbCN [12], CrN/AlN [35], TiN/VN, TiN/TiAlN and TiN[BCN/BN]n/c-BN [34,36,37]. Furthermore, a dependence of the elasticity with the bilayer number (n) or bilayer period (Λ) was observed, the highest bilayer number corresponds to the highest elastic modulus.…”
Section: Hardness and Elastic Modulussupporting
confidence: 52%
“…According to this model, each interface in the multilayer system works like a grain boundary, such that dislocations pile-up at the interfaces and harden the layer by strain [12,33,34]. The enhancement of mechanical properties for TiN/TiAlN multilayers is in accordance with the increase in hardness as it has been shown in multilayer-type coatings for diverse material systems (e.g., TiCN/TiNbCN [12], CrN/AlN [35], TiN/VN, TiN/TiAlN and TiN[BCN/BN]n/c-BN [34,36,37]. Furthermore, a dependence of the elasticity with the bilayer number (n) or bilayer period (Λ) was observed, the highest bilayer number corresponds to the highest elastic modulus.…”
Section: Hardness and Elastic Modulussupporting
confidence: 52%
“…Two characteristics peak at ∼1391 and ∼815 cm –1 are due to the in-plane B–N and out-of-plane B–N–B bending bond vibration of h-BN, respectively. The IR spectrum shows a prominent wide band absorption around 2800–3600 cm –1 due to the N–H bond . The stretching vibrations of the tetrahedral iron–oxygen bond and nickel–oxygen bond vibration in the octahedral sites of nickel ferrite are responsible for the IR absorption peak at 563 and 420 cm –1 , respectively (Figure a) .…”
Section: Resultsmentioning
confidence: 99%
“…The IR spectrum shows a prominent wide band absorption around 2800−3600 cm −1 due to the N−H bond. 47 The stretching vibrations of the tetrahedral iron−oxygen bond and nickel− oxygen bond vibration in the octahedral sites of nickel ferrite are responsible for the IR absorption peak at 563 and 420 cm −1 , respectively (Figure 3a). 48 According to the IR spectra in Figure 3a, as there is no shifting of the FTIR spectrum, we can conclude that there is no bonding between h-BN and nickel ferrite.…”
Section: Ftir Analysismentioning
confidence: 99%
“…No clear signals are recorded for duty cycles lower than 45% of P. Some peaks appear as the nitrogen injection time increases and become more significant when the duty cycle exceeds 55% of P. A broad asymmetric band appears close to 1390 cm −1 and clearly develops as dc reaches 90% of P, which is mainly assigned to the characteristic absorption of hexagonal BN (in-plane B-N bond stretching) in a Ti-B-N single layer [43,44]. Similarly, a broad and significant signal is measured around 738 cm −1 related to the B-N-B bending mode occurring in the amorphous boron nitride [37], and a second signal is associated with the transverse optical mode of the cubic BN phase at 1108 cm −1 [45,46]. A narrow and intense peak can also be noticed at 610 cm −1 , with a few weak peaks between 500 and 600 cm −1 .…”
Section: Composition and Structurementioning
confidence: 96%