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. 2022 Feb 25;14(1):67.
doi: 10.1007/s40820-022-00809-5.

Architecture Design and Interface Engineering of Self-assembly VS4/rGO Heterostructures for Ultrathin Absorbent

Affiliations

Architecture Design and Interface Engineering of Self-assembly VS4/rGO Heterostructures for Ultrathin Absorbent

Qi Li et al. Nanomicro Lett. .

Abstract

The employment of microwave absorbents is highly desirable to address the increasing threats of electromagnetic pollution. Importantly, developing ultrathin absorbent is acknowledged as a linchpin in the design of lightweight and flexible electronic devices, but there are remaining unprecedented challenges. Herein, the self-assembly VS4/rGO heterostructure is constructed to be engineered as ultrathin microwave absorbent through the strategies of architecture design and interface engineering. The microarchitecture and heterointerface of VS4/rGO heterostructure can be regulated by the generation of VS4 nanorods anchored on rGO, which can effectively modulate the impedance matching and attenuation constant. The maximum reflection loss of 2VS4/rGO40 heterostructure can reach - 43.5 dB at 14 GHz with the impedance matching and attenuation constant approaching 0.98 and 187, respectively. The effective absorption bandwidth of 4.8 GHz can be achieved with an ultrathin thickness of 1.4 mm. The far-reaching comprehension of the heterointerface on microwave absorption performance is explicitly unveiled by experimental results and theoretical calculations. Microarchitecture and heterointerface synergistically inspire multi-dimensional advantages to enhance dipole polarization, interfacial polarization, and multiple reflections and scatterings of microwaves. Overall, the strategies of architecture design and interface engineering pave the way for achieving ultrathin and enhanced microwave absorption materials.

Keywords: Architecture design; Interface; Microwave absorption; Self-assembly.

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Figures

Fig. 1
Fig. 1
a Schematic illustration of the synthesis processes for self-assembly VS4/rGO heterostructure. SEM image of b VS4 nanorods, c rGO architecture, and d VS4/rGO heterostructure. e, f TEM images of VS4/rGO heterostructure with different magnification. g HRTEM images of VS4 nanorods showing the d-spacing of 0.56 nm in the (110) plane and rGO showing the d-spacing of 0.37 nm in (0 0 2) plane
Fig. 2
Fig. 2
a TEM image of VS4/rGO heterostructure for the EDS mapping. b EDS spectra and the table of elemental composition. c TEM image corresponding to EDS elemental mappings: V, S, C and O. d XRD patterns of VS4 nanorods and VS4/rGO heterostructures. e Raman spectra of VS4 nanorods, rGO and VS4/rGO heterostructure
Fig. 3
Fig. 3
XPS spectra of VS4/rGO heterostructures: a V 2p, b S 2p, c C 1s. d TGA curves of VS4/rGO heterostructures. e Nitrogen adsorption–desorption isotherms. f Different BET surface areas of VS4/rGO heterostructures
Fig. 4
Fig. 4
Permittivity and dielectric loss tangent of VS4/rGO heterostructures in the frequency range of 2–18 GHz: a ε′, b ε", c Tan δε. d Cole–Cole semicircles for VS4/rGO heterostructure
Fig. 5
Fig. 5
RL curves and 3D presentations of VS4/rGO heterostructures at the thicknesses of 1 to 6 mm in the frequency range of 2–18 GHz: a, b 2VS4/rGO20-30%; c, d 2VS4/rGO40-30%; e, f 2VS4/rGO60-40%
Fig. 6
Fig. 6
a 3D RL presentations of rGO, VS4 nanorods, VS4/rGO nanocomposite, and VS4/rGO heterostructure (2VS4/rGO40-30%). b Attenuation constant α of rGO, VS4 nanorods, VS4/rGO nanocomposite, and VS4/rGO heterostructures (2VS4/rGO40-30%). c Frequency dependence of RL, attenuation constant α and |Zin/Z0| at 1.5 mm for 2VS4/rGO40-30%. d RL of different VS4/rGO heterostructures at 1.4 mm. Comparison of some typical graphene-based absorbents for e EAB and f RLmax at different thickness. g Charge density of the interfaces (I) VS4(-2 0 4)/rGO (1 0 0) interface, (II) VS4(0 2 0)/rGO (1 0 0) interface, (III) VS4(1 1 0)/rGO (1 0 0) interface. h Charge density difference of (I) VS4(-2 0 4)/rGO (1 0 0) and (II) VS4(1 1 0)/rGO (1 0 0) interface
Fig. 7
Fig. 7
Schematic illustration for the microwave absorption mechanism of VS4/rGO heterostructure

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