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Photonics
, Volume 8 (7) – Jun 25, 2021

/lp/multidisciplinary-digital-publishing-institute/characterizing-quantum-effects-in-optically-induced-nanowire-self-UnwkQu4PGj

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hv photonics Article Characterizing Quantum Effects in Optically Induced Nanowire Self-Oscillations: Coherent Properties Jeong-Ryeol Choi Department of Nanoengineering, Kyonggi University, Yeongtong-gu, Suwon 16227, Gyeonggi-do, Korea; choiardor@hanmail.net Abstract: Mechanical properties of metallic-nanowire self-oscillations are investigated through a coherent-state analysis. We focus on elucidating the time behavior of quantum energy in such oscillations, in addition to the analysis of ﬂuctuations, evolution of eigenstates, and oscillatory trajectories. The quantum energy varies somewhat randomly at ﬁrst, but, at a later time, it undergoes a stable periodical oscillation; the mean energy in the stabilized motion is large when the frequency of the driving force is resonated with that of the intrinsic oscillation of the nanowire. We conﬁrmed that when the oscillatory amplitude is sufﬁciently low, the quantum energy is quite different from the classical one due to zero-point energy which appears in the quantum regime. Because the power in such an oscillation is typically ultra low, quantum effects in the nanowire oscillations are non- negligible. Detailed analysis for the evolution of the probability densities and their relation with the oscillation trajectories of the nanowire are also carried out. Characterizing quantum effects in the actual oscillatory motions and clarifying their difference from the classical ones are important in understanding nanowire self-oscillations. Keywords: nanowire; nanoelectromechanical system; quantum energy; coherent state Citation: Choi, J.-R. Characterizing 1. Introduction Quantum Effects in Optically The achievement of technological breakthroughs in next-generation nanoelectrome- Induced Nanowire Self-Oscillations: chanical systems (NEMSs) may be possible only when we can efﬁciently control light– Coherent Properties. Photonics 2021, 8, matter interactions [1]. It is highly required to develop high-speed autonomous nanoelec- 237. https://doi.org/10.3390/ tronic devices such as nanoresonators and signal generators through advanced NEMS photonics8070237 technologies. As a consequence, the mechanism of nanoelectromechanical oscillations in nano and photonic devices has been extensively investigated during the past several Received: 16 May 2021 decades. Nanoelectromechanical systems that adopt nanowire resonances have become Accepted: 23 June 2021 important in nanomechanics on account of their potential applicability in diverse ﬁelds of Published: 25 June 2021 the state-of-the-art nanotechnology, such as timing/switching [2,3], ultrasensitive mechani- cal detection and resolution [4,5], single electron resonance tuning [6,7], and radio-wave Publisher’s Note: MDPI stays neutral receptors [8,9]. with regard to jurisdictional claims in In particular, self-oscillating nanowires [10–20] are noticeable because of their use- published maps and institutional afﬁl- fulness as a tool for on-chip controllable electronic actuations [10] and producing ﬁeld iations. emissions [11,12]. Self-oscillation of nano and micromechanical resonators can be produced by feedback from external ampliﬁers [13,14]. Alba et al. recently suggested self-oscillations of nanowires operated by photothermal forces prepared using a laser beam [13]. They achieved nanowire self-oscillations at low power thresholds of incident driving light less Copyright: © 2021 by the author. than 1 W. Because the power in such an oscillation is ultra low, it is desired to treat the Licensee MDPI, Basel, Switzerland. system quantum mechanically in general, instead of the classical analysis [20,21]. This article is an open access article Self-oscillations of nanowires occur due to the periodical electrostatic force acting on distributed under the terms and them, which compensates for air damping. The incident laser beam and a reﬂecting Si conditions of the Creative Commons mirror will produce the standing wave, which acts as the origin of the driving force for Attribution (CC BY) license (https:// the nanowire deposited between them. The setup of this system requires less stringent creativecommons.org/licenses/by/ criterion for the degree of the ambient vacuum, leading to new ﬂexible device applications 4.0/). Photonics 2021, 8, 237. https://doi.org/10.3390/photonics8070237 https://www.mdpi.com/journal/photonics Photonics 2021, 8, 237 2 of 14 with smaller device footprints. For more details of the mechanism of nanowire self- oscillations, including the enhancement of the quality factor and the photothermal effects on the oscillatory motion, refer to Reference [13] and references therein. The theoretical understanding of the oscillatory behavior of the system and the proper analysis of their underlying features may be crucial in order to support the interpretation of associated experimental outcomes. The purpose of this work is to investigate quantum effects in nanowire self-oscillations by introducing a coherent-state model for their quantum description [22]. To this end, we regard nanowire oscillations induced by periodically varying external forces. Especially, we focus on elucidating the characteristics of the resultant quantum energy. The coherent states heavily resemble classically oscillating states, allowing quantum-classical correspondence for a certain situation, i.e., in the classical limit. However, the differences in the evolution of quantum observables with the classical counterparts are important, especially in the low oscillation-energy limit because of the prominence of quantum effects in that situation. In this regard, the analysis in our research may provide a deeper insight for characterizing the oscillatory motion of nanowires. The nanowire oscillations are actually described by time-dependent Hamiltonians due to the periodic external force and the damping factor. Such Hamiltonian systems will be described with the annihilation and the creation operators associated with the harmonic oscillator (HO). Based on this description, we will analyze the evolution of the system in detail and will compare the consequences with those of the classical analysis. 2. Methods To analyze temporal evolution of nanowire self-oscillations, we ﬁrst need to describe their oscillatory motion. We consider an optically absorbing bimetallic nanowire of which the substance is SiN-Nb for convenience, which was used in reference [13]. The size of the sample nanowire reported in reference [13] is 40 m 55 nm 25 nm (length width thickness). However, without difﬁculty, our study can also be extended to other cases of nanowire self-oscillations of which material and its size are different. In principle, it is possible to describe nanowire oscillations quantum mechanically regardless of the size of a nanowire. However, such a description may especially be useful when the mechanical description of the oscillation cannot be covered by classical mechanics. From an experimentally supported theory of quantum mechanics, it is known that quantum effects are non-negligible when the dimension of material is less than the Fermi wavelength [23]. The type of material may also affect the measure of quantum effects. Regarding this, quantum effects in the oscillation are relatively prominent when the stiffness (spring constant) of the material is large; this is due to the fact that quantum zero-point energy is proportional to the oscillatory frequency, i.e., square root of the spring constant. The oscillation of the nanowire is driven by a standing wave that is prepared by an incident laser beam and a reﬂecting mirror. A sinusoidal photothermal force induces a self-oscillation of the nanowire of which either side is clamped. The classical equation of motion for such an oscillation can be written as [13] x ¨ + g x ˙ + w x = f cos(wt), (1) e d where g is the effective damping factor, w is the effective angular frequency, and f is the e e amplitude of the photothermal force divided by the nanowire mass and w is the driving frequency. For detailed formulae of g and w , see, for example, reference [13]. e e The quantum Hamiltonian of the system is represented as p 1 g t g t 2 2 e e H = e + e m[w x ˆ 2 f cos(wt)x ˆ]. (2) 2m 2 Photonics 2021, 8, 237 3 of 14 This is obtained by replacing canonical variables x and p in the classical Hamiltonian ˆ ˆ ˆ ˆ with quantum operators x and p, respectively. In other words, if we replace x and p with x and p from Equation (2), we have the classical Hamiltonian. Based on Hamilton’s equations ¶H ¶H x ˙ = , p ˙ = , (3) ¶p ¶x we can easily conﬁrm that such a classical Hamiltonian yields Equation (1). p p Using the annihilation operator a ˆ = mw /(2h ¯ )x ˆ + (i/ 2mw h ¯ )p ˆ and its hermitian e e adjoint a ˆ (creation operator), this Hamiltonian can be rewritten in the form h ¯ w † 2 †2 H = [cosh(g t)(2a ˆ a ˆ + 1) + sinh(g t)(a ˆ + a ˆ )] e e mh ¯ g t † e f cos(wt)(a ˆ + a ˆ ). (4) 2w We can express the eigenvalue equation of the annihilation operator as a ˆjai = ajai, (5) where a is the eigenvalue and jai is the eigenstate. Notice that the eigenstate in this case is the well-known Glauber coherent state [22]. The expectation value of the Hamiltonian in the coherent state is given by H = hajHjai. (6) From the use of Equation (4) together with the relations haja ˆjai = a, haja ˆ jai = a , (7) we readily have h ¯ w 2 2 2 H = [cosh(g t)(2jaj + 1) + sinh(g t)(a + a )] a e e mh ¯ g t e f cos(wt)(a + a ). (8) 2w In the next section, this formula will be used in order to study the time behavior of the system in the coherent state. 3. Results and Discussion 3.1. Solution for the Eigenvalue To see time evolution of observables in the coherent state, it is necessary to know how a evolves in time. The time evolution of a can be analyzed from the Euler–Lagrange equation, which is given by a ˙ = [a, H ], (9) ih ¯ where [X, Y] is a Poisson bracket of the form [24] ¶X ¶Y ¶X ¶Y [X, Y] = . (10) ¶a ¶a ¶a ¶a A simple evaluation after substituting Equation (8) into Equation (9) leads to g t a ˙ = iw [cosh(g t)a + sinh(g t)a ] + ie f cos(wt). (11) e e e 2h ¯ w e Photonics 2021, 8, 237 4 of 14 To solve this differential equation, we divide a into real and imaginary parts such that a(t) = a (t) + ia (t), (12) 1 2 where a and a are real. Then, we easily conﬁrm that the real and imaginary parts of 1 2 Equation (11) are given respectively by g t a ˙ = w e a , (13) e 2 g t g t e e a = w e a + e f cos(wt). (14) 2 e 1 2h ¯ w We conﬁrm, using these two equations, that a (t) satisﬁes the differential equation of the form mw ¨ ˙ a + g a + w a = f cos(wt). (15) 1 e 1 1 e d 2h ¯ On the other hand, a can be directly identiﬁed from Equation (13) once a is determined 2 1 from Equation (15). From basic mechanics, the solution of a in Equation (15) (and consequently, a ) 1 2 is composed of a complementary solution a (a ) and a particular solution a (a ), 1,c 2,c 1,p 2,p such that a = a + a , (16) 1 1,c 1,p a = a + a . (17) 2 2,c 2,p A minor evaluation using Equation (15) together with Equation (13) gives the complemen- tary and the particular solutions as a = a exp(g t/2) cos(w t + j), (18) 1,c 0 e M cos(wt d ) mw e p a = f , (19) 1,p d 2 2 2 2 2 1/2 2h ¯ [(w w ) + g w ] e e a = a exp(g t/2) cos(w t + j d ), (20) 2,c 0 e M c sin(wt d ) a = w f exp(g t) , (21) 2,p e 2 2 2 2 2 1/2 2h ¯ w [(w w ) + g w ] e e 2 2 2 2 where w = w g /4, d = atan(w w , g w), d = atan(g , 2w ), a is a constant, M p e c e M 0 e e e and j is an arbitrary phase. Here, d atan(u, v) is an inverse function of tan d = v/u, where the valid range of this function is 0 d < 2p. The complete solution of a given above will be used in estimating the quantum time behavior of the system in the subse- quent subsections. 3.2. Fluctuations Now, we see the ﬂuctuations of canonical variables, which are expressed in terms of the ladder operators as h ¯ x ˆ = (a ˆ + a ˆ ), (22) 2mw mw h ¯ ˆ ˆ ˆ p = i (a a). (23) The ﬂuctuation of an arbitrary operator A in the coherent state can be deﬁned to be 2 2 1/2 ˆ ˆ DA = [hajA jaihajAjai ] . (24) Photonics 2021, 8, 237 5 of 14 For the case of canonical variables given in Equations (22) and (23), we easily have h ¯ Dx = , (25) 2mw mw h ¯ Dp = . (26) Equation (5) has been used in these derivations. We can see that these two ﬂuctuations give the exact minimum uncertainty product DxDp = h ¯ /2. However, if we use the g t ˆ ˆ physical momentum that is deﬁned by p = pe (see Equation (A2) in Appendix A and reference [25]) instead of the canonical momentum, the uncertainty product is given by g t DxDp = (h ¯ /2)e . (27) This vanishes in the long time limit, whereas the value of DxDp does not vary at all times. However, in the HO limit where g ! 0, Equation (27) also becomes a constant value h ¯ /2, which is the minimum uncertainty. 3.3. Evolution of the Quantum Energy We now turn our attention to the quantum mechanical energy. Unlike the classical energy, quantum energy is different depending on given quantum states. For instance, it is well known that quantum energy is discrete and involves a zero-point energy in the Fock state. For the case of the coherent state that we treat now, quantum energy is determined in terms of a. It is well known that the energy operator of a nonstationary system is different from the Hamiltonian. The energy operator in this dissipative system is given by [26,27] p ˆ 1 2g t 2 2 E = e + mw x ˆ . (28) 2m 2 This can be obtained from Equation (A3) in Appendix A via the replacement of x and p by ˆ ˆ operators x and p, respectively. The evaluation for the expectation value of this operator in the coherent state gives the quantum energy: h ¯ w g t 2 2 2 E = e [cosh(g t)(2jaj + 1) + sinh(g t)(a + a )]. (29) a e e In the derivation of this quantity, we have used Equations (22) and (23) together with Equation (7). We have illustrated the time evolution of the quantum energy and the corresponding Hamiltonian in Figures 1–3. Figure 1 shows that, while the expectation value of the Hamiltonian increases with time, the quantum energy dissipates. Such a dissipation is more signiﬁcant when g is large. However, the quantum energy cannot be lowered below a certain value because of the existence of the intrinsic uncertainty in quantum observables, including the quantum energy. The magnitude of g is determined by the air pressure in the experimental chamber. Hence, in order to diminish its magnitude, the degree of vacuum in the chamber should be kept high. From Figure 2, we see that both the Hamiltonian and the quantum energy oscillate according to the driving force. Figure 2A,B shows that the Hamiltonian and the quantum energy oscillate rapidly depending on the driving frequency w, provided that w > w . On the other hand, for the case w < w given in Figure 2C, the quantum energy varies with a relatively high amplitude. Figure 2B,C shows that if the amplitude of the external driving force is high (i.e., f is large), the variation of the energy becomes signiﬁcant. An entrain- ment of the self-oscillation occurs if the driving force is sufﬁciently high [13,28,29]. Then, the nanowire oscillates according to the driving frequency rather than its natural frequency. Photonics 2021, 8, 237 6 of 14 Figure 1. The dependence of time evolution of the Hamiltonian expectation value (A) and the quantum energy (B) on g . The values that we have used are w = 1, j = 0, a = 1, w = 5, m = 1, e e 0 h ¯ = 1, and f = 0.5. The reference line (dashed line) in the bottom part of (B) is 0.25, which is the minimum value of the quantum energy in this model; this rule will also be applied in the subsequent ﬁgures of the quantum energy (Figures 2C and 3C). Figure 3 reveals that the driving frequency w is also a critical factor on the evolution pattern of the quantum energy and the Hamiltonian. If w is near w , the increase of the Hamiltonian over time is very rapid (see the green curves in Figure 3A,B). On the other hand, we see from Figure 3C that the quantum energy steadily oscillates over time when t is sufﬁciently large; in this case, the mean energy is relatively high when w is near the resonance one. The frequency of such an energy oscillation increases as w grows. In an extreme case where w = 10 (the violet curve in Figure 3C), the frequency of the energy oscillation is very large while the oscillation does not thoroughly disappear even after a long lapse of time (see the inset in Figure 3C). Because cosh(g t) ' sinh(g t) ' exp(g t)/2 e e e in the limit g t 1, the quantum energy represented in Equation (29) eventually becomes h ¯ w E ' [a (t) + 1/2], (30) after a sufﬁcient long time. However, if we consider that a exponentially dissipates over 1,c time according to Equation (18), the energy expression in Equation (30) can be further simpliﬁed to h ¯ w E ' [a (t) + 1/2]. (31) 1,p 2 Photonics 2021, 8, 237 7 of 14 Hence, in a long time limit, the quantum energy oscillates depending on w which is the oscillation frequency of a . This is the reason why Figure 3C shows the increase of the 1,p oscillation frequency of E in the stabilized situation as w grows. Figure 2. The time evolution of H (A) and E (B,C) depending on f , where w = 8 for (A,B), while a a w = 0.5 for (C). The values that we have used are g = 0.2, w = 1, j = 0, a = 1, m = 1, and h ¯ = 1. e e 0 The difference of (C) from (B) is only the value of the taken w. Photonics 2021, 8, 237 8 of 14 Figure 3. The effects of w on the time evolution of H (A,B) and E (C). (B) is a log-scale graph for a a a relatively long time. The values that we have used are g = 0.2, w = 1, j = 0, a = 1, m = 1, h ¯ = 1, e e and f = 0.5. By comparing Equations (18) and (19), we see that a is involved in a , whereas 0 1,c a does not involve it. For this reason, if the amplitude a grows, E (and hence H ) a a 1,p 0 increases monotonically at ﬁrst. However, when t is sufﬁciently large, the inﬂuence of a on quantum energy is negligible because the right-hand side of Equation (31) is independent of a . For the non-driven case ( f = 0), the quantum energy reduces to the case of a simple dissipative oscillator, which is shown in Equation (A16) of reference [30]. Photonics 2021, 8, 237 9 of 14 Figure 4 is the comparison of the quantum energy with the corresponding classical energy described in Appendix A. For the case that the oscillation amplitude of the nanowire is small, quantum energy is quite different from the classical energy (see Figure 4A). The instantaneous minimum values of the quantum kinetic energy T and the quantum potential energy V are not zero, whereas their classical counter parts are zero. However, we see from Figure 4B that the quantum and the classical energies are very much the same when the oscillation amplitude is sufﬁciently high. The second term in the right-hand side of Equation (31) gives the lowest limit of the quantum energy, which is h ¯ w /4 for a large t. It may be possible to neglect quantum effects in the oscillation if the oscillatory energy is 1000 times larger than this base energy; hence, a rough critical energy that divides the low and high energies is E = 250h ¯ w . For example, for the case that the effective a,critical frequency is given by f = w /(2p) = 10 MHz, the critical energy is estimated to be e e E 2 10 J. a,critical Figure 4. Comparison of the quantum energy with the classical energy for a low (A) and a relatively high (B) amplitude regime. E , T , and V are the total quantum energy, the quantum kinetic energy, a a a and the quantum potential energy, whereas E , T , and V are the total classical energy, the classical cl cl cl kinetic energy, and the classical potential energy, respectively. The taken values of (a , A , f ) are 0 0 d (1, 1.74, 1) for (A) and (10, 14.2, 10) for (B). Other values that we have used are g = 0.2, w = 1, e e j = 0, m = 1, h ¯ = 1, and w = 5. Photonics 2021, 8, 237 10 of 14 3.4. Analysis of the Eigenstate Now we see the evolution of the coherent state hxjai, which is the eigenstate in Equation (5). The solution of Equation (5) in the conﬁguration space is given by mw mw 2mw 1 1 e e e 4 2 2 2 hxjai = exp x + a x jaj a . (32) h ¯ p 2h ¯ h ¯ 2 2 iw t For the case of g ! 0 and f ! 0, we have a(t) = a(0)e ; then, the above eigenstate e d exactly recovers to that of the simple harmonic oscillator, which appeared in reference [31]. The evolution of the probability density jhxjaij can be seen from Figure 5. The position, in which the probability density takes a peak value, oscillates and converges toward the origin over time at ﬁrst. However, it does not totally collapse even after a long lapse of time; in this case, the remained oscillation with a reduced amplitude is due to the external driving force. If the power supplied from the laser beam is suspended, such a residual oscillation will be quenched eventually. However, even in that case, the width of the probability density in the conﬁguration space may not vanish. The probability density left in the non-zero position in this case is intrinsically related to the minimum uncertainty. Figure 5A is for w > w while Figure 5B is the case w < w . A careful observation of e e Figure 5A reveals that the associated probability density exhibits a rapid oscillation with a tiny amplitude due to the relatively high value of the driving-force frequency. On the other hand, the probability density in Figure 5B oscillates with a relatively huge amplitude even when t is sufﬁciently large as a consequence of the smallness of the driving frequency w; recall, from Figure 2C, that the quantum energy also deviates highly when w is small. Figure 5. Time evolution of the probability density jhxjaij for w = 5 (A) and w = 0.5 (B). The values that we have used are g = 0.2, w = 1, j = 0, a = 3, m = 1, h ¯ = 1, and f = 1. e e 0 d Photonics 2021, 8, 237 11 of 14 It may also be noteworthy to analyze the behavior of the probability densities when 2 2 1/2 the driving frequency approaches amplitude resonance frequency, (w g /2) . We e e have depicted the evolution of jhxjaij together with the momentum probability density 2 2 jhpjaij for a nearly resonated system in Figure 6. For the plot of jhpjaij , we used the Fourier transformation of Equation (32). For the plot of jhpjaij , we used the Fourier transformation of Equation (32). Figure 6A,B shows that both the position expectation value x and the classically evaluated position x (the momentum expectation value p and a cl a the classical canonical momentum p ) closely follow the trajectory of the most probable cl 2 2 value of jhxjaij (jhpjaij ). For the case of the resonance or near resonance where f is sufﬁciently large, a and a are dominant compared to a and a , respectively (see 1,p 2,p 1,c 2,c Equations (18)–(21)). Due to this, the probability densityjhxjaij in Figure 6A oscillates with a relatively high amplitude even when t is large. On the other hand, oscillatory amplitudes of jhpjaij and the canonical momenta p and p diverge exponentially over time. In cl addition, the physical momentum p does not diverge but oscillates fairly uniformly. k,a Figure 6. (A): Comparison of the time evolution of the probability densityjhxjaij (density plot) with that of the quantum expectation value x (= hajxjai) and its classical counter part x represented in cl Equation (A4). (B): Comparison of the time evolution of the momentum probability density jhpjaij (density plot) with that of the quantum expectation value p (= hajp ˆjai), p (Equation (A5)), and the cl expectation value of the physical momentum p (= hajp ˆ jai). w = 1.1 is used for both panels (A,B); k k this case corresponds to near resonance like that of the green curves in Figure 3. Other values that we have used are g = 0.2, w = 1, j = 0, a = 3, m = 1, h ¯ = 1, f = 1, and A = 4.2426. e e 0 0 d Photonics 2021, 8, 237 12 of 14 4. Conclusions We have investigated the time evolution of nanowire self-oscillations activated by an incident laser beam in the coherent state. The quantum solution of the system has been obtained from the fundamental Hamiltonian dynamics. We have focused on time behavior of the quantum energy based on its rigorous analytical evaluation. The effects of the variations of several parameters on the evolution of the quantum energy have been analyzed using various relevant illustrations. It turned out that the external driving force gravely affects the nanowire oscillation. Although the quantum energy dissipates over time at ﬁrst, it becomes a steadily oscillating stable value at a later time where the average energy dissipated by damping is entirely compensated by the external driving force. The mean energy in the stabilized oscillation becomes high when the driving frequency approaches the resonance frequency; this means that the resonance is important in order to maintain the nanowire oscillation. We have conﬁrmed that quantum mechanical energy in a weak oscillation is very different from the classical one as a manifestation of quantum effects, especially when the oscillation power is nearly lowest. Apparently, quantum effects are non-negligible in nanowire oscillations as a consequence of the fact that the power in such oscillations is actually extremely low [13]. The analysis for the evolution of the quantum probability densities is also carried out. The position, in which the position probability density takes a peak value, oscillates in time. The amplitude of such an oscillation is especially large when the periodically varying force supplied by the external beam is resonated with the intrinsic nanowire oscillation. As w deviates from the resonance frequency, the oscillation amplitude at a sufﬁciently large t drops. However, in such non-resonated cases, the oscillation amplitude when w < w is quite large compared to that when w > w , provided that the amplitude of the driving force is sufﬁciently large. We showed that the time behaviors of the probability densities match well with the trajectories of the position and momentum variables. The consequence in this work may be useful in understanding the quantum effects of nanowire self-oscillations. The elucidation of fundamental mechanisms for the nanowire oscillations is necessary in order to apply them to NEMSs. The low power consumption of nanowire self-oscillations may admit a new route for self-excited low-loss integrable NEMS devices with an enhanced Q-factor [20,32]. Funding: This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (No.: NRF-2021R1F1A1062849). Institutional Review Board Statement: Not applicable. Informed Consent Statement: Not applicable. Data Availability Statement: Not applicable. Conﬂicts of Interest: The author declares no conﬂict of interest. Appendix A. Classical Energy From the classical point of view, the energy of the system is given by 1 1 2 2 2 E = mx ˙ + mw x . (A1) cl 2 2 This can also be represented in terms of momentum instead of x ˙ . If we insert Equation (2) into the ﬁrst part of Equation (3), we have the expression of the canonical momentum as g t p = p e , (A2) k Photonics 2021, 8, 237 13 of 14 where p is the physical momentum (p = mx ˙ ). Now the classical energy of the system k k can be rewritten in terms of p, such that p 1 2g t 2 2 E = e + mw x . (A3) cl 2m 2 If we denote the classical solutions for canonical coordinate x and momentum p as x and cl p , respectively, they are represented in the form cl cos(wt d ) x = A exp(g t/2) cos(w t + j) + f , (A4) cl 0 e M d 2 2 2 2 2 1/2 [(w w ) + g w ] e e dx cl p = m exp(g t) , (A5) cl dt where A is an amplitude. References 1. 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Photonics – Multidisciplinary Digital Publishing Institute

**Published: ** Jun 25, 2021

**Keywords: **nanowire; nanoelectromechanical system; quantum energy; coherent state

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