Ultrafast Nonlinear Optical Excitation Behaviors of Mono- and Few-Layer Two Dimensional MoS2

The layered MoS2 has recently attracted significant attention for its excellent nonlinear optical properties. Here, the ultrafast nonlinear optical (NLO) absorption and excited carrier dynamics of layered MoS2 (monolayer, 3–4 layers, and 6–8 layers) are investigated via Z-scan and transient absorption spectra. Our experimental results reveal that NLO absorption coefficients of these MoS2 increase from–27 × 103 cm/GW to–11 × 103 cm/GW with more layers at 400-nm laser excitation, while the values decrease from 2.0 × 103 cm/GW to 0.8 × 103 cm/GW at 800 nm. In addition, at high pump fluence, when the NLO response occurs, the results show that not only the reformation of the excitonic bands, but also the recovery time of NLO response decreases from 150 ps to 100 ps with an increasing number of layers, while the reductive energy of A excitonic band decreases from 191.7 meV to 51.1 meV. The intriguing NLO response of MoS2 provides excellent potentials for the next-generation optoelectronic and photonic devices.


Introduction
Recently, the layered properties of transition metal chalcogenides (TMDCs) have attracted a number of attentions and opened up new possibilities for many optoelectronic applications. There is a transition from an indirect bandgap of the multilayer to a direct gap of the monolayer for TMDCs, which may lead to significant changes in the photoconductivity and the absorption spectra, as well as the photoluminescence (PL) [1]. Importantly, the study of the layer-dependent broadband tunable optical-response-wavelength of TMDCs, which ranges from the near-infrared to the visible region, is promising to provide a fertile playground to explore new applications in optical switching, mode-locking, and optical limiting devices [2][3][4][5][6][7][8][9][10][11][12][13]. Thus, a clear understanding of the layer-dependent nonlinear absorption properties and carrier dynamics is in great need, in order to fulfill the above goals.
In fact, the layer-dependent optical properties of TMDCs have already attracted intensive research efforts. Jun Wang et al. [11]. In particular, the two-photon absorption (TPA) and the saturation absorption (SA) are both observed, along with the characterization of the layer-dependent nonlinear optical parameters. The relevant electronic properties and carrier dynamics are measured by the optical spectroscopy, a systematic study of the evolution of the optical properties and electronic structure of ultrathin MoS 2 crystals as a function of layer numbers [12][13][14][15][16][17], indicating that the physical properties including the relaxation process and nonlinear susceptibility would change significantly with a decrease in the layer number, less than 7. For instance, the decay time, such as the interband electron-hole combination time, increases with more layers [13,16]. However, the dependence of the optical absorption nonlinearity on the layer number of 1 -10, including the saturable absorption and the change of the excitonic band renormalization, remains to further study, which is of great importance for developing ultrafast and high performance optoelectrical devices.

Methods
In this work, we experimentally study the nonlinear optical (NLO) response of MoS 2 , considering both cases of mono-and few-layer. Specifically, MoS 2 films are prepared by using the same chemical vapor deposition (CVD) process [18]. The NLO absorption and carrier dynamics are characterized by employing open aperture (OA) Z-scan and pump-probe techniques under a femtosecond laser excitation (400 nm and 800 nm). The NLO parameters change accordingly with layer numbers. Moreover, the decay time can be extracted from the pump probe experiments, which shows excellent potential for ultrafast Q-switched picosecond lasers. Furthermore, the fast recovery time of excitonic bands and the fast decay of energy of A exciton in layered MoS 2 opens up new applications in ultrafast photonic devices.

Morphology characterization of MoS 2 films
The mono-and few-layer MoS 2 samples are grown on the sapphire substrate by using the chemical vapor deposition (CVD) method. The thickness is measured with white-light interferometer measurements, and the results are illustrated in Fig. 1. Specifically, the average thickness of each layer is 0.8 nm -0.9 nm, which is in good agreement with the previous report [19]. As shown in Fig. 1(d), with more layers, the color of the MoS 2 samples turns darker. The Raman spectroscopy is employed to examine the crystallinity and layer number. As shown in Fig. 1(e), the frequency difference between the in-plane optical model 1 2 g E and out-plane vibration 1 g A varies from 21.1 cm -1 to 24.6 cm -1 , confirming that MoS 2 films change from monolayer to 6-8 layers [20]. Furthermore, the measured PL intensities under identical excitation at 3.06 eV (405 nm) for monolayer and few layer samples are strikingly different, as illustrated in Fig. 1(f). A very strong PL peak at 658 nm (~1.9 eV) is observed in monolayer MoS 2 , which is viewed as a direct transition [21]. In contrast, the PL signals of 3-4 layers and 6-8 layers samples are weak and show a red shift with the large layer number. These spectroscopic methods allow us to trace the evolution of both direct and indirect band gaps of the mono-and few-layer MoS 2 .

Nonlinear optical properties of MoS 2 films
The OA Z-scan technique is one of the most researched approaches to study the NLO response. Typical Z-scan curves of mono-and few-layer MoS 2 under the excitation of 400 nm laser are illustrated in Fig. 2. All three types of MoS 2 exhibit saturable absorption, since all used samples have a bandgap smaller than 1.9 eV (bulk MoS 2 ), and the energy of the incident photon is about 3.1 eV, above all the bandgaps of samples. However, different situation phenomena occur in the MoS 2 films under an 800-nm excitation (please see Fig. 3). In particular, the strong TPA response is the dominant effect when determining the absorption in both the monolayer and 3 -4 layers MoS 2 films, whereas in the 6 -8 layers MoS 2 film, the SA response plays the key role. In addition, the 3-4 layers MoS 2 exhibits a strong TPA response rather than saturable absorption as reported in [3], which can be concluded that the defected state may exit in the 3-4 layers MoS 2 , so that the 3-4 layers MoS 2 can absorb two photons, during the Z-scan process [4].  According to the Z-scan theory [3,4] . Here, α 0 and α NL are the linear and nonlinear absorption coefficients. The normalized power transmission is given as [3,11] NL 0 eff open 2 where L eff is the effective thickness of a sample, I 0 is the on-axis peak irradiance at the position of focus, z is the longitudinal displacement from the focus, and z 0 is the beam's diffraction length.
By combining the experimental data with (1), the NLO absorption coefficient (α NL ) in the MoS 2 films can be calculated. The giant SA phenomenon is observed in our investigated MoS 2 films, which turns stronger with higher incident irradiance. Particularly, in the monolayer MoS 2 , the value of α NL changes gradually from (-1.53 ± 0.25) × 10 -5 cm/GW at 8.8 GW/cm 2 to (-2.79 ± 0.65) × 10 4 cm/GW at 180 GW/cm 2 . On the other hand, when under an 800-nm excitation, the values of α NL in these MoS 2 films confirm the existence of the TPA effect, which are presented in Fig. 3(d). Compared with Fig. 2(d) and Fig. 3(d), the values of α NL in these MoS 2 films grow, with an increase in the layers, at 400-nm laser excitation with the same intensity, while the values of α NL decrease at 800 nm. In addition, at 400 nm, the values of α NL in the same MoS 2 films all present a linear increase first and then remain stable with the growth of incident irradiance, due to the saturation of saturable absorption [11], while α NL of the same sample has an approximately constant with an increase in the incident irradiance.
Aiming at quantifying the dependence of the NLO response on the layers, we extract the linear and NLO absorption coefficients of MoS 2 films from Z-scan measurements. Additionally, the imaginary part of the third-order NLO susceptibility, Imχ 3 , can be computed by using the following approximation as [3,11] where c is the light speed, λ is the wavelength of incident light, and n is the index of refraction. The nonlinear parameters become stable with an increase in the incident irradiance, which reflects the saturation of the nonlinear optical response. Thus, the relevant stable parameters, for both types of excitation, are summarized in Table 1.
where A represents the linear coefficient, δT is the saturable modulation depth, and Is is the saturable irradiance. Here, δT can be changed from 23% to 46% while Is can be altered from 15.63 GW/cm 2 to 26.04 GW/cm 2 with more layers. By calculating the linear and NLO parameters, it is clear that these parameters are closely related to the number of layers. With an increase in the layers, the transmission decreases, while the value of α NL increases at 400 nm and drops at 800 nm, which suggests that the MoS 2 is a promising material for layer-dependent optoelectronic devices. These parameters make it possible that MoS 2 is an appealing alternative in applications of Q-switched and mode locked pulsed lasers.

Nonlinear ultrafast optical dynamics of MoS 2 films
Pump-probe experiments are performed to evaluate the excited-state dynamics in the MoS 2 films. Firstly, under the pulsed pump radiation, the carries are thermalized within few tens of femtoseconds. During the hot-carrier cooling process, weaker probe pulses are incident into the sample with a certain time delay and then collected by the detector. In order to explore the carrier relaxation, differential transmission trace is analyzed as a function of time delay and wavelength. We start our analysis by investigating the relaxation time in the MoS 2 films under different low-influence photoexcitations, using 400-nm laser excitation and supercontinum white light probe, as shown in Figs. 4(a) to 4(c). Note that here and in what follows the experiments are carried out at the temperature of T = 300 K, unless otherwise specified.
As shown in Figs. 4(a) to 4(c), the dynamic relaxation curves exhibit an exponential decay, which can be simulated by using an exponential model [16]: where τ 1 , τ 2 , and τ 3 stand for the fast, intermediate, and slow relaxation time, respectively. Precisely, the relaxation time is extracted to be 0.44 ± 0.02 ps and 127 ± 12.5 ps for monolayer MoS 2 , 0.59 ± 0.03 ps and 136.7 ± 9.1 ps for 3 -4 layers MoS 2 , and 0.7 ± 0.02 ps, 12 ± 2.6 ps, and 314 ± 23 ps for 6 -8 layers MoS 2 . Note that the measured τ 1 has a relatively good agreement with the reported results for MoS 2 films [16,17], while τ 2 and τ 3 seem a little longer than what were reported in [16,17], and this may be due to the defect of the sample. Thus the decay time, including different materials, is summarized in Table  2. Due to different wavelengths of the pump and probe laser, the same layer MoS 2 flakes behave differently. In the meanwhile, compared with the black phosphorus (BP) nanosheets and graphene, the decay time of MoS 2 is longer. This is because that the bandgap of MoS 2 is larger than BP nanosheets and graphene.
Another significant aspect of dynamic relaxation exploration is to characterize the correlation between transient absorption (TA) spectra and time delay. Taking the excitation fluence of the NLO response into consideration, under a higher influence (665 μJ/cm 2 ), indicating that the injected electron-hole pair density is around 1.4 × 10 15 cm -2 , the three types of MoS 2 show NLO response rather than the optical response at a relatively low laser fluence [13][14][15]16,17].  Graphene 0.13-0.33 3.5-4.9 -- [5] As for the three MoS 2 films, the photo-induced absorption (PA, positive) features of A exciton show the red shift while the other three peaks exhibit blue shifts, as illustrated in Figs. 4(d) to 4(f). The spectra characteristics of the three MoS 2 films are similar.
To be more specific, as Fig. 5 illustrates, the process with regard to PA peaks and time delay can be roughly divided into four parts. Firstly, when the time delay is within 0.5 ps, the red shift occurs at PA peaks of A exciton, which is due to an increase in the excitonic band energy, whereas PA features of B exciton decline which is caused by the intensification of the state filling effect [3]. Then, with the time delay in the range of 0.5 ps -5 ps, both A and B excitons reach a quasi-equilibrium state, where the densities of these two excitons stop growing.
In particular, the density of A exciton starts to decrease while for B exciton it is assumed to be constant, since the recombination process of A exciton is faster than that of B exciton. Thus, a resulting decrease in the excitonic band energy leads to the blue shift of PA peaks at A exciton resonances [22], whereas the state filling effect seems to have little effect on the growth of photo-induced bleaching (PB, negative) peaks at B exciton resonances [22]. Next, when the time delay is around 5 ps -150 ps, PA features of both A and B excitons exhibit blue-shift behaviors, which can be attributed to a decrease in the excitonic band energy. Finally, with the time delay larger than 150 ps, the TA spectra recover to four features configuration, which indicates that A and B excitons reach an equilibrium state. Because of high pump influence, the renormalization of the excitonic band begins within 5 ps, faster than 20 ps in the previous work [17]. Furthermore, the energy of A excitonic band decreases greater than that at a lower pump fluence. Our work also emphasizes on the dependence of the recovery time and the reductive energy of the excitonic band, which remains unclear before. We obtain the shifts of the PA and PB features of A and B excitons, according to the method reported by Tian Jiang et al. [23], and the recovery time of excitonic band decreases from 150 ps to 100 ps, with an increase in the layers, while the reduction energy of A exciton at the high pump fluence within 5 ps decreases from 191.7 meV to 51.1 meV.

Conclusions
In conclusion, we have investigated the ultrafast NLO properties and excited carrier dynamics in the monolayer and few-layer MoS 2 by conducting the femtosecond OA Z-scan experiments and pump-probe experiments. Two excitation wavelengths are utilized in this work, which leads to a layer-dependent NLO response in the layered MoS 2 films: (1) the values of α NL in these MoS 2 films grow, with an increase in the layers, at 400-nm laser excitation with the same intensity, while the values of α NL decrease at 800-nm laser excitation; (2) the modulation depth can be changed from 23% to 46% while saturable irradiance can be altered from 15.63 GW/cm 2 to 26.04 GW/cm 2 with an increase in layers. Based on the data from the pump-probe experiments, the characterized relaxation time is extracted to be 0.44 ps and 127 ps for monolayer MoS 2 , 0.59 ps and 136.7 ps for 3 -4 layers MoS 2 , and 0.7 ps, 12 ps, and 314 ps for 6 -8 layers MoS 2 . Furthermore, we have also presented an analysis of TA spectra in the layered MoS 2 films, accounting for various values of time delay. To be more specific, the recovery time of excitonic band decreases from 150 ps to 100 ps, with an increase in the layers, and another significant result, which is rarely reported, is that the reductive energy of A exciton at the high pump fluence within 5 ps decreases from 191.7 meV to 51.1 meV with an increase in layers. The remarkable nonlinear absorption and excited carrier dynamics achievable in the layered MoS 2 films can facilitate high-performance optical modulators and switches, as well as other ultrafast photonics devices. It should be noted that the experimental and theoretical techniques introduced in this work can be applied to types of TMDCs in which the nonlinearity can become significant.