Enhanced Electromagnetic Wave Interference by Nanoscale Mixed

Oct 5, 2018 - Enhanced Electromagnetic Wave Interference by Nanoscale Mixed-Dimensional C-MoS2 Magnetic van der Waals Heterostructures...
0 downloads 0 Views 4MB Size
Subscriber access provided by UNIV OF NEW ENGLAND ARMIDALE

Article

Enhanced Electromagnetic Wave Interference by Nanoscale MixedDimensional C-MoS2 Magnetic van der Waals Heterostructures Erqi Yang, Xiaosi Qi, Guohui Zheng, Ren Xie, Zhongchen Bai, Yang Jiang, Shuijie Qin, and Wei Zhong ACS Appl. Nano Mater., Just Accepted Manuscript • DOI: 10.1021/acsanm.8b01448 • Publication Date (Web): 05 Oct 2018 Downloaded from http://pubs.acs.org on October 8, 2018

Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.

is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

Page 1 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

Figure 1. FE-SEM and TEM images of (a,b) Fe3O4-MoS2, (c,d) S400, and (e,f) S500, respectively. 80x84mm (300 x 300 DPI)

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Figure 2. (a-c) XRD patterns, and (d) Raman spectra of the catalyst precursor, S400 and S500, respectively. 80x60mm (300 x 300 DPI)

ACS Paragon Plus Environment

Page 2 of 43

Page 3 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

Figure 3. Schematic diagram for the formation mechanism of “3-0-2” type C-Fe3O4-MoS2 and “1-0-2” type CNTs-Fe@Fe3C-MoS2 vdWHs, respectively. 80x58mm (300 x 300 DPI)

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Figure 4. Magnetic hysteresis loops for (a) S400, and (b) S500 at 300 K (inset is the enlarged part close to the origin). 80x30mm (300 x 300 DPI)

ACS Paragon Plus Environment

Page 4 of 43

Page 5 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

Figure 5. EM parameters of the obtained samples: (a,b) real and imaginary parts of permittivity, and (c,d) real and imaginary parts of permeability. 80x56mm (300 x 300 DPI)

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Figure 6. Three-dimensional RL curves of (a) Fe3O4-MoS2, (b) S400, and (c) S500; (d) RL versus frequency of the as-prepared samples with the thicknesses of 4.9 mm. 80x59mm (300 x 300 DPI)

ACS Paragon Plus Environment

Page 6 of 43

Page 7 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

Figure 7. Comparison of dm for (a,c) S400, and (b,d) S500 under the quarter-wavelength matching model at fm. 80x57mm (300 x 300 DPI)

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Figure 8. (a,b) Loss tangent, and (c) attenuation loss of the obtained samples. 80x60mm (300 x 300 DPI)

ACS Paragon Plus Environment

Page 8 of 43

Page 9 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

Figure 9. Schematic illustration of possible microwave absorption mechanism of (a) S400, and (b) S500.

80x25mm (300 x 300 DPI)

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 10 of 43

Enhanced Electromagnetic Wave Interference by Nanoscale Mixed-Dimensional

C-MoS2

Magnetic

van

der

Waals

Heterostructures Er-qi Yang,† Xiao-si Qi,†,‡,* Guo-hui Zheng,† Ren Xie,† Yang Jiang,† Zhong-chen Bai,† Shui-jie Qin,† Wei Zhong,‡,* †

Physical college, Guizhou University, Guiyang 550025, China



Collaborative Innovation Center of Advanced Microstructures and Jiangsu Province

Key Laboratory for Nanotechnology, Nanjing University, Nanjing 210093, China

1

ACS Paragon Plus Environment

Page 11 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

Abstract: It is generally believed that the matching of electromagnetic (EM) impedance or making the best of the interface polarization is an efficient way to achieve a good EM wave absorbing capability. Herein, the mixed-dimensional C-MoS2 based magnetic van der Waals heterostructures (vdWHs) were elaborately designed and successfully synthesized through the catalytic decomposition of C2H2 over Fe3O4-MoS2. By controlling the pyrolysis temperature, “3-0-2” type heterostructured C-Fe3O4-MoS2 ternary nanohybrid consisting of three-dimensional (3-D) carbon layers, zero dimensional (0-D) magnetite particles, two-dimensional (2-D) MoS2 nanosheets (NSs), and “1-0-2” type CNTs-Fe@Fe3C-MoS2 vdWHs consisting of 1-D carbon nanotubes (CNTs), 0-D Fe and Fe3C nanoparticles, and 2-D MoS2 NSs were selectively synthesized. Compared to “0-2” type Fe3O4-MoS2, the obtained results demonstrated clearly that the introduction of carbon to form the mixed-dimensional C-MoS2 based magnetic vdWHs could greatly enhanced the EM wave absorption properties. Owing to the better optimization between magnetic loss and dielectric loss, more defect dipole and interface polarizations, the obtained “1-0-2” type CNTs-Fe@Fe3C-MoS2 nanohybrid displayed enhanced microwave absorption property.

Consequently,

mixed-dimensional

a

C-MoS2

versatile based

way vdWHs

was

provided

to

produce

the

for

designing

high-performance

microwave absorption materials. Keywords: chemical vapor deposition, interface polarization, mixed-dimensional C-MoS2 based nanohybrids, carbon nanotubes, EM wave absorption capabilities

2

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 12 of 43

Introduction In the past decades, great efforts have been devoted to develop electromagnetic (EM) absorbers owing to the rapid development of wireless techniques, expansive problems of EM radiation and interference.1,2 High performance microwave absorption materials (MAMs) are required to possess a broad absorption frequency bandwidth, excellent EM attenuation capability, low density and good thermal stability features.3 Therefore, the applications of the traditional strong absorption MAMs such as ferrite, metals and their composites, 4,5 are greatly limited by their high density and large loading ratio.6 It is known that the EM loss characteristics can be well evaluated by the EM parameters ( µ and ε ) of MAMs. The optimization of EM parameters, namely EM impedance match, is important to improve microwave absorption performances (MAPs). And a good matching of EM impedance is able to achieve by modulating the categories and contents of nanohybrids.7,8 Accordingly, different categories of high-effective absorbents have been developed. For example, Fe@carbon nanotubes (CNTs) and Fe@ZnO were proved to exhibit excellent MAPs.9,10 Very recently, graphene (G), reduced graphene oxide (RGO), and MXenes have been thought as a the representatives of novel MAMs because of their unique two-dimensional

(2-D)

structures

and

outstanding

chemical

and

physical

properties,11,12 and similar results were also obtained over MoS2 nanosheets (NSs).13,14 However, due to the deficiency of their intrinsical characteristics (relatively low conductivity loss and high density), magnetic nanoparticles (NPs)-MoS2 NSs are very difficult to be used as the efficient MAMs. Moreover, the mixed-dimensional van der Waals heterostructures (vdWHs) based on 2-D layered nanohybrids have been extensively studied owing to their multiple interfaces, interlayer polarization and synergistic effects.15,16 Therefore, building the 3

ACS Paragon Plus Environment

Page 13 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

mixed-dimensional 2-D materials based vdWHs can promote the attenuation of EM wave, which may be good candidates of high efficient MAMs.12 For example, 2-D G/zero-dimensional (0-D) metal oxide NPs, 2-D MoS2/one-dimensional (1-D) CNTs, and 2-D MoS2/three-dimensional (3-D) carbon layers were found to show excellent MAPs.17-19 However, the application of vdWHs in MAMs is subject to great restriction since the difficulty in their large-scale production at present. Based on the previously reported work,20,21 the optimization of permeability and permittivity and making full use of the interface polarization are primary strategies to achieve good MAPs. In order to utilize these two aspects effectively and develop high performance MAMs, in this paper, we elaborately designed and successfully synthesized the mixed-dimensional C-MoS2 based magnetic vdWHs by means of a combined hydrothermal process and chemical vapor deposition (CVD) method. By regulating the pyrolysis temperature, “3-0-2” type C-Fe3O4-MoS2 consisting of 3-D carbon layers, 0-D Fe3O4 NPs and 2-D MoS2 NSs, and “1-0-2” type MoS2-Fe@Fe3C-CNTs composing of 1-D CNTs, 0-D α-Fe and Fe3C NPs and 2-D MoS2 NSs could be selectively synthesized, respectively. The advantage of designing the nanohybrids can be mainly summed up five points: (i) the introduction of carbon can enhance the interface polarization and reduce the density of nanohybrids effectively; (ii) the EM parameters may be optimized through regulating the contents of Fe3O4/Fe NPs (magnetic loss substances) and C/CNTs/MoS2 (dielectric loss materials); (iii) CNTs and 2-D MoS2 with large-surface may enhance the interface polarization greatly, which can elevate their MAPs in theory; (iv) the construction of heteronanostructure may provide the synergetic effect, which can strengthen their MAPs greatly; and (v) the proposed strategy for the production of mixed dimensional magnetic C-MoS2 based vdWHs is simple and practical applied. 4

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Experimental Synthesis of “0-2” Type Fe3O4-MoS2 Nanohybrid. Single layered MoS2 NSs were purchased from Xianfeng Nanomaterials Technology Co., Ltd (Nanjing, China). According to the work of Song et al., heterostructured “0-2” type Fe3O4-MoS2 nanohybrid was fabricated by a hydrothermal method.22 As illustrated in the I part of Figure S1 (Supporting Information), firstly, the transparent solution was obtained through ultrasonic mixing 30 mL ethanol with 30 mL deionized water, and MoS2 powder (50 mg) was dispersed in this mixture. 183.8 mg of FeCl3·6H2O and 70.3 g of FeCl2·4H2O were added in 10 mL deionized water under stirring. Subsequently, the configured Fe2+ and Fe3+ solution was mixed with the formed MoS2 liquid under stirred at 80 °C for 30 min. After that, 3 mL of NH4OH was dropwise added into the obtained solution. Finally, the formed solution was transferred to a autoclave (200 mL) and maintained at 120 °C for 120 minutes. And “0-2” type Fe3O4-MoS2 nanohybrid could be obtained after the washing and dry processes. Synthesis of Mixed-Dimensional C-MoS2 Based Magnetic vdWHs. As shown in the II part of Figure S1, similar to our previous work,23 the mixed-dimensional C-MoS2 based magnetic vdWHs were fabricated by means of the CVD method. Typically, 0.1 g of “0-2” type Fe3O4-MoS2 was used as the catalyst precursor, which was put into a tube furnace. And the furnace was heated to 400 °C in N2. Then, N2 was shut off and C2H2 was immediately introduced into the tube at atmospheric pressure. After C2H2 catalytically decomposed at 400 °C for 30 min and cooled to room temperature (RT) in N2, the black sample (denoted as S400) could be obtained. With the other experimental condition unchangeable, the decomposition of C2H2 was conducted at 500 °C. After cooling to RT in N2, much larger quantities of the as-prepared sample at this case (labeled as S500) could be obtained than S400. 5

ACS Paragon Plus Environment

Page 14 of 43

Page 15 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

Characterization and Measurement. The as-prepared Fe3O4-MoS2 and C-MoS2 based nanohybrids were characterized by X-ray powder diffractometer (XRD) (model D/Max-RA, Rigaku), transmission electron microscope (TEM) (model Tecnai-G20), field-emission scanning electron microscope (FE-SEM) (model ZEISS SUPRA-40), Raman spectroscopy (Jobin-Yvon Labram HR800 instrument), X-ray photoelectron spectroscopy (XPS) (PHI Quantera system), and Quantum Design MPMS SQUID magnetometer (Quantum Design MPMS-XL), respectively. For microwave measurement, 10 wt% and 30 wt% of Fe3O4-MoS2, C-Fe3O4-MoS2 and CNTs-Fe@Fe3C-MoS2 were mixed with paraffin and compacted into toroidal shaped samples (Rout: 7.0 mm, Rin: 3.0 mm), respectively. The measurement of complex permittivity ( ε = ε ′ − jε ′′ ) and complex permeability ( µ = µ ′ − jµ ′′ ) of the as-prepared composites were carried out by a vector network analyzer (Agilent E8363B). Results and discussion Microstructures and Components. Figure 1 presents the typical morphologies of the catalyst precursor, S400 and S500. As displayed in Figures 1a and 1b, large number of Fe3O4 NPs (as indicated by the black arrow) distribute on the surface of MoS2 NSs (as indicated by the red arrow), and the MoS2 NSs can effectively suppress the aggregation of Fe3O4 NPs. Similar to the previously reported Fe3O4 NPs-MoS2 and MoS2-Ni NPs,22,24 it can be seen clearly that the “0-2” vdWHs between the 0-D Fe3O4 NPs and 2-D MoS2 NSs are well established. Figures 1c and 1d display the microstructure of S400. Typical TEM images of S400 show that different sizes of Fe3O4 NPs are deposited on the surface of MoS2 NSs. Compared to that of the catalyst precursor (as shown in Figure 1b), the closer TEM investigation (as shown in Figures 1d and S2b) reveals that 0-D Fe3O4 NPs are fully encapsulated and joined together by 6

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

3-D layered carbon (as marked by the yellow square in Figure 1d and the blue ellipse in Figure S2b). The high resolution TEM (HRTEM) investigation (Figures S2c and S2d) obviously reveals the lattice fringe of graphite and Fe3O4 (311) plane, and their lattice distance are ca. 0.34 and 0.25 nm, respectively. Similar to the recently reported “201” type nanohybrid obtained over MoS2-Ni NPs,24 the “3-0-2” type C-Fe3O4-MoS2 vdWHs consisting of 3-D carbon layers, 0-D Fe3O4 NPs and 2-D MoS2 NSs can also be produced in large scale. Moreover, On basis of the previous results,23 it is understandable that “3-0-2” type C-Fe3O4-MoS2 vdWHs can grow over Fe3O4 NPs-MoS2. Figures 1e and 1f show the microstructure of S500. As provided in Figure 1e, large scale of flexible 2-D MoS2 NSs and CNTs are found throughout the S500. And the TEM images in the Figures 1f and S3b shows that Fe NPs are encapsulated tightly in turn by Fe3C and CNTs. And the HRTEM investigation (Figure S3c) illustrates that the lattice distance is about 0.61 nm, which corresponds to the (002) plane lattice fringe of MoS2.19 The obtained morphology of S500 is similar to the recently reported heterostructured “201” type MoS2-Ni-CNTs and G-Co-CNTs.23,24 In light of the obtained results, unlike that of S400, one can find that the obtained S500 is “1-0-2” type CNTs-Fe@Fe3C-MoS2 vdWHs. To confirm the phases of the as-prepared samples, their XRD patterns are presented. The obtained catalyst precursor (Figure 2a) exhibits nine evident diffraction peaks, in which the diffraction peaks centered at 14.4 and 39.5° are well-indexed to the hexagonal phase of MoS2 (JCPDS No.24-0513). And a weak and broad peak (centered at ca. 14.4°) corresponding to (002) plane of MoS2, which can be ascribed to the few-layer MoS2 NSs used in our experiment,25 can also be observed. And the other labeled peaks located at the ca.18.3, 30.1, 35.4, 37.1, 43.1, 57.0 and 62.5° match well with the face-center cubic structure of Fe3O4 (JCPDS No.74-0748). There are no other 7

ACS Paragon Plus Environment

Page 16 of 43

Page 17 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

peaks corresponding to ferric oxide such as Fe2O3 and FeO are found. The existence of MoS2 can also be further proved by the XPS (Figure S4). The binding energy peaks of S 2p 3/2, Mo 3d 5/2 and Mo 3d 3/2 can be seen clearly at 161.1, 228.3 and 231.3 eV, respectively. Additionally, the peak at ca. 164.5 eV indicates the existence of bridging disulfides S 2, which confirms further that the existence of MoS2. The 2 results of XRD, XPS and microstructure (Figures 1) confirm the used catalyst precursor is “0-2” type Fe3O4-MoS2 vdWHs. Figure 2b gives the XRD pattern of S400. One can find that the characteristic peaks of MoS2 and Fe3O4 coexist in the obtained XRD results. Additionally, a new broad peak centered at about 26.2° is obviously detected, which should be corresponded to the shell layer of carbon (JCPDS No.03-0401). Based on the aforementioned microstructure images and compared to that of the catalyst precursor, the obtained results demonstrate that the as-prepared S400 is “3-0-2” type C-Fe3O4-MoS2 vdWHs. The similar result was also reported before.26 Unlike that of S400, as displayed in Figure 2c, the aforementioned characteristic peaks of Fe3O4 cannot be seen over the as-prepared S500. And the relative XRD peak intensity ratio of carbon evidently become high, which is attributed to the increasing carbon content with the enhancement of pyrolysis temperature as mentioned in the experimental section. Moreover, as indicated by the symbols, some new obvious diffraction peaks located at ca. 37.8, 41.6, 43.4, 57.3 and 45.1°well corresponds to the standard XRD data of Fe3C (JCPDS No.06-0670) and Fe (JCPDS No.01-1267), respectively. Based on the obtained results of phase and morphology, it can be seen that the obtained S500 is heterostructured “1-0-2” type CNTs-Fe@Fe3C-MoS2 quaternary nanohybrid. In order to further confirm the existence of carbon material in the as-prepared samples, their Raman spectra were 8

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

obtained. As presented in Figure 2d, the obtained S400 and S500 exhibit two strong peaks at 1345 (D band) and 1586 cm−1 (G band), respectively. It is well known that the defects and/or disorder of carbon materials result in the appearance of D band while the G band originates from crystallite graphitic structure.27 Generally, the decomposition temperature plays a great impact on the formation of mixed dimensional C-MoS2 based vdWHs. The similar temperature effect has also been reported before.28 Overall, the obtained results can be summarized as two points: (1) all the nanohybrids obtained by the catalytic decomposition of C2H2 at 400 and 500 °C over Fe3O4-MoS2 are the mixed dimensional magnetic vdWHs; (2) different categories of mixed dimensional C-MoS2 based vdWHs can be selectively synthesized by regulating the decomposition temperature. Therefore, a convenient and effective scheme is designed to produce the mixed dimensional magnetic C-MoS2 based vdWHs. Possible Formation Mechanism for the Mixed Dimensional C-MoS2 Based vdWHs. On the basis of the experimental aim and our acquired results, different categories of C-MoS2 based vdWHs are selectively produced by controlling the experimental temperature. According to the previously related reports,29,30 the interactions between C2H2 and Fe3O4 occur at high temperature, in which C2H2 induces the carbothermic reduction to synthesize Fe, iron oxide and/or Fe will generate crystalline graphite. Similar to that of core@shell Fe3O4@C,30 our obtained results suggest that the chemical reaction between C2H2 and Fe3O4 does not occur under this conditions ( ≤ 400 °C), which is the reason for the formation of “3-0-2” type C-Fe3O4-MoS2 vdWHs. However, the carbothermic reduction will be happen immediately when the temperature rises to 500 °C, and metal Fe will be generated without the residual Fe3O4 phase. And the formation of “1-0-2” type 9

ACS Paragon Plus Environment

Page 18 of 43

Page 19 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

CNTs-Fe@Fe3C-MoS2 quaternary nanohybrid may be explained by the following reaction: 8C 2 H 2 + 2 Fe 3 O4 → 15C + Fe 3 C + 3 Fe + 8 H 2 O

(1)

In this reaction, the reduction reaction between C2H2 and Fe3O4 will occur, and the element of Fe will be easily carbonized to produce Fe3C. According to the pervious results,31,32 the metal carbide is very important to form core@shell@shell structured CNT-based hybrids. Therefore, the formation of “1-0-2” type CNTs-Fe@Fe3C-MoS2 quaternary nanohybrid can be attributed to the reduction reaction between C2H2 and Fe3O4-MoS2. In light of our obtained experimental outcomes and the growth models for

carbon

nanomaterials,33

the

formation

mechanism

for

“1-0-2”

type

CNTs-Fe@Fe3C-MoS2 vdWHs can be well interpreted by the mode of tip-growth, and the diagram of the growth process is displayed in Figure 3. The possible pathways to grow “1-0-2” type CNTs-Fe@Fe3C-MoS2 vdWHs are in this manners: (1) the reduction reaction between Fe3O4 and C2H2 to form Fe and Fe3C NPs; (2) the decomposition of C2H2 on the surface of Fe and Fe3C NPs to produce carbon atoms; (3) the dissolution and diffusion of carbon atoms around the catalyst; (4) the growth of carbon film along the surface of catalyst and inducing the generation of CNTs-Fe@Fe3C-MoS2 vdWHs. And the formation of heterostructured “3-0-2” type C-Fe3O4-MoS2 ternary nanohybrid is ascribed to the in situ low-temperature carbonization. Therefore, the designed plan is efficient and applicable for the synthesis of mixed dimensional vdWHs, which can fulfill the simultaneous construction of double attenuation mechanism, synergistic effect and interface engineering to solve EM wave interference issue. Properties of Mixed Dimensional C-MoS2 Based vdWHs. Figure 4 displays 10

ACS Paragon Plus Environment

ACS Applied Nano Materials 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 20 of 43

the RT magnetic hysteresis (M-H) curves of S400 and S500. It can be seen that the Ms and Hc values of S400 and S500 are 44.7 emu/g and 107 Oe, 19.9 emu/g and 202 Oe. Moreover, the comparison results show that: (1) the obtained samples exhibit the typical ferromagnetic properties at RT, which is attributed to the existence of magnetic Fe3O4 and Fe NPs; (2) compared with the Ms value of Fe3O4-MoS2 reported elsewhere,22

the

obtained

Ms

values

of

nanohybrids

are

as

follows:

Fe3O4-MoS2>S400>S500, which proves further that the introduction of carbon material during the CVD process. Based on the obtained experimental results, much more quantities of samples can be collected over the same amount of Fe3O4-MoS2 with a rise of temperature. That is to say, the content of magnetic NPs in the as prepared samples is become lower and lower with the increasing of temperature, which is consistent with their magnetic measurement. Moreover, after being placed in air for thirty days, the C-MoS2 based vdWHs exhibit no changes in phase and magnetic results, which confirms further that the magnetic NPs are well protected by carbon layers or CNTs. In general, although the introduction of carbon material decreases their Ms values, the as-prepared hybrids display good stabilities. Additionally, their complex permittivity should be enhanced evidently and tuned by the temperature, which is propitious to achieve a good EM impedance match and enhance the MAPs. Figure 5 displays the EM parameters of composites with the 30 wt% filler loading. As shown in Figures 5a and 5b, besides weak fluctuations, the ε ′ and ε ′′ values of the obtained mixed dimensional C-MoS2 based vdWHs decrease when the frequency increases, which can be interpreted by the Debye theory.34 And the obtained S500 displays evident fluctuating behaviors of ε ′ and ε ′′ , which is ascribed to a significant lag of displacement current at the ‘core@shell@shell’ interfaces.10,35,36 In 11

ACS Paragon Plus Environment

Page 21 of 43 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

ACS Applied Nano Materials

addition, it can be noticed that the obtained S500 presents the negative permittivity values. Actually, the negative permittivity behaviors have been observed previously in the conductive filler (such as metal NPs, CNTs) when its content exceeds the percolation threshold.37,38 However, the origin for the negative values of permittivity is still not fully established. Combined with the previous result, we think that the transport of more electrons to form CNTs-MoS2 conductive network due to the mass production of CNTs. Large quantities of capacitor networks are changed to conductive paths, which can be considered as an inductor. Therefore, the obtained S500 displays the negative permittivity behaviors, which is similar to the metallic wires reported in previous study.38 By comparison, we can find that the ε values of the obtained samples are as follows: Fe3O4-MoS2