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Open Access

Peer-reviewed

Research Article

MoS2 nanosheets direct supported on reduced graphene oxide: An advanced electrocatalyst for hydrogen evolution reaction

  • Jiamu Cao,

    Affiliation MEMS Center, School of Astronautics, Harbin Institute of Technology, Harbin, P. R. China

    ⨯
  • Jing Zhou,

    Affiliation MEMS Center, School of Astronautics, Harbin Institute of Technology, Harbin, P. R. China

    ⨯
  • Yufeng Zhang ,

    yufeng_zhang@hit.edu.cn

    Affiliations MEMS Center, School of Astronautics, Harbin Institute of Technology, Harbin, P. R. China, Key Laboratory of Micro-systems and Micro-structures Manufacturing, Ministry of Education, Harbin, P. R. China

    ⨯
  • Yuezhang Zou,

    Affiliation MEMS Center, School of Astronautics, Harbin Institute of Technology, Harbin, P. R. China

    ⨯
  • Xiaowei Liu

    Affiliations MEMS Center, School of Astronautics, Harbin Institute of Technology, Harbin, P. R. China, Key Laboratory of Micro-systems and Micro-structures Manufacturing, Ministry of Education, Harbin, P. R. China

    ⨯

Abstract

Molybdenum disulfide nanosheets/reduced graphene oxide (MoS2 NSs/rGO) nanohybrid as a highly effective catalyst for hydrogen evolution reaction (HER) have been successfully synthesized by a facile microwave-assisted method. The results clearly reveal that direct grown of MoS2 NSs on rGO have been achieved. Electrochemical tests show that the as-prepared hybrid material exhibited excellent HER activity, with a small Tafel slope of 57 mV dec-1, an overpotential of 130 mV and remarkable cycling stability. After analysis, the observed outstanding catalytic performance can be attributed to the uniform distribution of the MoS2 NSs, which are characterized by the presence of multiple active sites as well as the effective electron transport route provided by the conductive rGO substrate. Moreover, according to the classic theory, the mechanism governing of the catalytic HER on the MoS2 NSs/rGO nanohybrid has been clarified.

Citation: Cao J, Zhou J, Zhang Y, Zou Y, Liu X (2017) MoS2 nanosheets direct supported on reduced graphene oxide: An advanced electrocatalyst for hydrogen evolution reaction. PLoS ONE 12(5): e0177258. https://doi.org/10.1371/journal.pone.0177258

Editor: Jun Xu, Beihang University, CHINA

Received: March 15, 2017; Accepted: April 25, 2017; Published: May 8, 2017

Copyright: © 2017 Cao et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: All relevant data are within the paper and its Supporting Information files.

Funding: The work described in this paper was financially supported by the National Natural Science Foundation of China (No.61404037).

Competing interests: The authors have declared that no competing interests exist.

Introduction

Hydrogen, a scalable and renewable energy, once produced are environmentally and climatically clean over the entire length of its respective conversion chains, from production to utilization [1]. These advantages are enough to make it be one of the most important energy sources which people rely on after fossil energy [2]. In particular, sustainable hydrogen production from water splitting has attracted growing attention [3]. During hydrogen evolution reaction (HER), advanced catalyst plays an indispensable role, which reducing the overpotential of electrodes and producing a high current density and consequently increasing the yield of this important electrochemical process [4]. Up to now, Pt-group metals still have been enrolled as catalysts in HER. However, the high material costs and limited resource of these catalysts hinder the hydrogen economy [5–7]. Consequently, the ongoing search for efficient alternatives composed of low-cost materials is crucial for a sustainable “hydrogen economy” [8–13].

Molybdenum disulfide is a typical member of transition metal sulfide with a layered structure held together by weak van der Waals forces [14–16]. Recent theoretical calculations and experimental results showed that MoS2 to be a competitive electrocatalyst for HER and both computational and experimental date figured the edge sites of MoS2 nanoparticles (NPs) are the active sites so that the interest in using MoS2 as water-splitting electrocatalysts has intensified [17–20]. However, MoS2 exhibits a poor intrinsic conductivity, which severely suppresses charge transport and thus the electrocatalysis efficiency [21,22].

A commonly adopted solution to avoid the above situations is to fabricate nanosized MoS2 on a high conductivity substrate [23,24]. Benefiting from its large-sized surface area, the good electrical conductivity, and its stable chemical properties, graphene plane is calculated for acting as a substrate of a composite catalyst [25]. A hybrid catalyst which used reduced graphene oxide (rGO) as the substrate and supported by the MoS2 NPs was exhibited the HER catalytic activity with an overpotential of 190 mV and a Tafel slope of 95 mV per dec-1 [26]. To further enhance the conductivity of the hybrid catalyst, Cu NPs were incorporated into the MoS2/rGO structure, and a decreased Tafel slope of 90 mV dec-1 was achieved [27]. But it should be noticed that MoS2 NPs are still intended to pile up in quantity as aggregations on rGO. Another potential problem is that a small reduction of rGO will bring a mass of oxygen-containing functional groups on the substrate, leading to decreased of the conductivity. Herein, we report on polymer-free, one-pot, microwave-assisted method for preparing MoS2 NSs/rGO nanohybrid by employing ethylene glycol (EG) as reducing agent. We further investigate that the resulting catalyst exhibit unusual catalytic activity in HER.

Experimental

Preparation of MoS2 NSs

All chemical reagents used in this experiment were analytical grade. The detailed synthesis procedures will be described in the following. Graphene oxide (GO) was prepared following the Hummer's method. A liquid exfoliation technique of ultrasound probe sonication was used to obtain MoS2 NSs. This method is less susceptible to the surrounding environment, simple for operation, and suitable for large-scale production. To begin with, 1 g of powder of MoS2 was dissolved in 100 mL N-Methylpyrrolidone (NMP), which was placed in a glass vial for a 3.5 h ultrasound under the ultrasound power of 300 W maintaining the temperature at 20°C. Then, the mixture was transferred to centrifuge tubes for the first centrifugal, which was at the speed of 1500 rpm for 60 min and under the temperature at 10°C. The top two-thirds of the supernatant liquid were reserved, and ethanol was added thereto to 300 mL of dilution. After that, the dilution was added into an ultrasonic processor, sonicated with an ultrasound probe for 10 min to obtain the up two-thirds of the solution, and then the solution was centrifuged at 2000 rpm for 60 min. Finally, the supernatant was small-sized MoS2 NSs.

Preparation of MoS2 NSs/rGO hybrid material

During the synthesis of the MoS2 NSs/rGO hybrid material, 20 mg of GO and (1mg, 3 mg, 5mg) of MoS2 NSs were added into 60 mL of a mixture solution of isopropanol and ethylene glycol (v/v = 1:4) and sonicated for 90 min. A 1 M NaOH/EG solution was added to the mixture until a pH of 12 was reached, and then argon was blown into the mixture for 20 min. And then, the mixture was microwaved for ca. 30 s to reach 150°C and was allowed to cool naturally. After that, 1 M dilute nitric acid was added until a pH of 2 was reached. The product was collected by vacuum filtration and vacuum-dried at 60°C.

Electrochemical evaluation

4 mg of the synthesized MoS2 NSs/rGO hybrid material and 80 μL of 5 wt% Nafion were dispersed in 1 mL of a water/ethanol mixture (4:1 v/v) followed by sonication for 15 min to obtain a homogeneous slurry. Subsequently, a glassy carbon electrode (GCE) with a diameter of 3 mm, which was polished by alumina suspensions, was treated with 5 mL of the catalytic slurry and dried naturally. Moreover, pure MoS2 NSs and Pt/C modified electrodes were prepared by the same method for comparison purposes. The HER activities of these catalysts were evaluated via linear sweep voltammetry (LSV) in 0.5 M H2SO4 solution at a scan rate of 5 mV s-1 at room temperature (about 26°C). LSV measurements were conducted using an electrochemical workstation (CHI 660D) and a standard three-electrode setup containing a saturated calomel electrode (SCE) as the reference electrode, Pt foil as the counter electrode, and the modified GCEs as working electrodes. Before electrochemical measurements, the polarization curves were corrected for iR losses, the potentials were calibrated using a reversible hydrogen electrode (RHE) at a scan rate of 100 mV/scan, and the utilized electrolytes were degassed by bubbling Ar gas for 1 h. The AC impedance amplitude measured in the frequency range between 105 Hz and 101 Hz with an amplitude of 5 mV. Stable polarization curves were recorded after 2000 cycles.

Material characterization

The morphology and structure of the MoS2 NSs/rGO hybrid catalyst were detected by the transmission electron microscope (TEM) with accelerating voltage at 300 keV. X-ray photoelectron spectroscopy (XPS) was used to record the element composition and the electron binding energy using a K-Alpha (Thermo Fisher Scientific Company) equipment. Energy dispersive spectrometer (EDS) was used to measure the oxygen content with the electron beam being 15 keV. X-ray diffraction (XRD) profiles of the MoS2 NSs/rGO hybrid catalyst with high-intensity Cu Kα radiation (λ = 1.5406 nm)in the range of 10°-90°.

Results and discussions

The microstructure of the MoS2 NSs/rGO hybrid prepared by microwave assisted method was characterized by TEM, as shown in Fig 1. The micro-sized rGO substrate has a large surface area (Fig 1A). In the magnified image, it can be clearly seen that rGO is very thin and the MoS2 NSs with the sizes of 50–90 nm were deposited uniformly on the surface of rGO substrate, remaining isolated from each other (Fig 1B and 1C). The smaller MoS2 NS with the length of 23.8 nm and the interlayer spacing of 0.64 nm has plenty edge positions (Fig 1D).

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Fig 1. TEM images of MoS2 NSs/rGO.

https://doi.org/10.1371/journal.pone.0177258.g001

Fig 2A shows the XRD pattern of the MoS2 NSs/rGO hybrid. For the pattern of the sample, the peaks at 2θ = 14.2°, 33.0°, 39.7°, and 59.1° are attributed to the (002), (100), (103) and (110) planes of MoS2 [28–29]. Furthermore, we can detect the weak (002) diffraction peaks of the graphene at 2θ = 24.5° in the XRD patterns of the hybrids, which indicates that the graphene nanosheets seldom stack during the microwave-assisted process [27]. XPS were used to characterize the chemical states and electronic states of Mo and S in MoS2 NSs/rGO hybrid catalyst. As shown in Fig 2B and 2C, the binding energies of Mo 3d5/2, Mo 3d3/2 peaks at 229.3 eV and 229.3 eV, S 2p3/2 and S 2p1/2 peaks at 162.2 eV and 163.4 eV indicate that Mo4+ and S2- are the dominant oxidation states. It is obviously to see that there is a slight shift to all the binding energies compared with the reports of pristine MoS2 [30]. It is demonstrated that MoS2 NSs and rGO substrate was not only simply mixed but also have the interaction which improved its conductivity [31]. Fig 2D shows the XPS spectrum of carbon. The highest peak at 284.8eV represents C−C binding energy. The binding energies of C−O and C = O oxygenated functional groups are located at 286.4eV and 288.9eV.

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Fig 2.

XRD pattern of MoS2 NSs/rGO hybrid (a). XPS images of Mo 3d (b) S 2p (c) and C (d).

https://doi.org/10.1371/journal.pone.0177258.g002

The relative content of carbon and oxygen indicate the good degree of reduction. The deoxygenating of GO is estimated by C/O radio, which is about 4.9, much higher than that of GO (S1 Table). The C/O ratio was also measured by EDS, as shown in S1 and S2 Figs. The average atomic percent of carbon is about 81.23% and oxygen is about 18.77%. From Chen’s study, the C/O ratio changed from 2.09 to 5.46 after reduction and the reduced GO showed better performance on conductivity, which indicated a high reduction degree [32].

The electrocatalytic HER activities of MoS2 NSs/rGO hybrid catalyst (the content of MoS2 NSs is identified by atomic absorption spectroscopy as 5 wt.%, 13 wt.% and 20 wt.%) were investigated by polarization curves as shown in Fig 3A, where a commercial Pt catalyst (20 wt.% Pt on Vulcan carbon black) was also included for comparison. It can be seen that the Pt catalyst exhibits very high HER catalytic performance with a near zero overpotential. The as-prepared MoS2 NSs/rGO (13 wt.%) hybrid has an overpotential of 130 mV. In sharp contrast, both the rGO and the pure MoS2 NSs are exhibited no or poor HER electrocatalytic activities due to their low current densities and large overpotential. The linear segments of the Tafel plots (Fig 3B) were fit to the Tafel equation (η = b∙lg j + a, where j is the current density and b is the Tafel slope), yielding Tafel slopes of 91, 63, 57, 71 and 36 mV dec-1 for the MoS2 NSs, MoS2 NSs/rGO (5 wt.%, 13 wt.% and 20 wt.%.) hybrid and Pt/C. The properties of the as-prepared MoS2 NSs/rGO (13 wt.%) hybrid with a Tafel slope of 57 mV dec-1 and an overpotential of 130 mV were better than MoS2 NSs and those of the MoS2/rGO hybrid prepared by previous reports (Tafel slopes of 95 mV dec-1 and 90 mV dec-1) by the same test method [26, 27].

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Fig 3.

Polarization curves for the catalysts of MoS2 NSs, MoS2 NSs/rGO (5 wt.%, 13 wt.% and 20 wt.%.), and Pt/C (a) and their corresponding Tafel plots (b). Impedance spectroscopy at an overpotential of 120 mV (c). Durability test for MoS2 NSs/rGO hybrid catalyst (d). The inset is TEM image of the MoS2 NSs/rGO hybrid after 2000 cycles.

https://doi.org/10.1371/journal.pone.0177258.g003

As a result, the excellent HER performance of the MoS2 NSs/rGO (13 wt.%) hybrid catalyst can be attributed to the strong electronic coupling between the MoS2 NSs and rGO. To reap this effect, we performed impedance measurements at an overpotential of η = 130 mV. As is shown in Fig 3C, in the same amount of catalyst, the MoS2 NSs/rGO (13 wt.%) hybrid material exhibits a lower alternating-current impedance of ~180 Ω which very close to that of the Pt/C (alternating-current impedance of ~40 Ω) and much lower than that of the MoS2 NSs (alternating-current impedance of~1200 Ω). Another important standard for an excellent electrocatalyst is the high durability. To further evaluate the long-term stability, the MoS2 NSs/rGO (13 wt.%) catalyst was cycled continuously for 2000 cycles in an acidic environment. Then, the nanohybrid catalyst afforded similar i-V curves just like before, with negligible loss of the cathodic current (Fig 3D). Next, we use TEM to observe that the original morphology of the hybrid was well-maintained (the insert of Fig 3D).

Remarkably, Tafel slopes are one of the most significant factors that can discern the HER mechanism. According to the classic theory [33], Tafel slopes for the typical Volmer, Heyrovsky, and Tafel reactions are around of 120 mV dec-1, 40 mV dec-1, and 30 mV dec-1, respectively (1–3). The following are the now accepted steps by which HER in acidic aqueous media described, where MHads represents a hydrogen atom chemically adsorbed on an active site of various material (M). In view of the Tafel slope of 57 mV dec-1 for the MoS2 NSs/rGO (13 wt.%) hybrid in the current work, a combination of the Volmer reaction, involving an electrochemical desorption step that converts protons into absorbed hydrogen atoms on the catalyst surface, and the Heyrovsky reaction, involving the formation of surface scope hydrogen molecules, should dominate the HER on the catalytic process of the MoS2 NSs/rGO catalyst. In other words, the rate determining step is the electrochemical desorption of Hads and H3O+ to form hydrogen, and the HER occurs through a Volmer-Heyrovsky mechanism.

(1)(2)(3)

According to the results of our research, the rate-limiting step on the MoS2 NSs/rGO catalyst is electrochemical desorption. Fig 4 gives a simple model to demonstrate that synergistic effect of MoS2 NSs and rGO in the HER catalytic process are existence. With the rGO functions as substrates, the electrons can be rapidly transferred from C to the active edges of S under an external electric field through the heterojunction. Consequently, the MoS2 NSs/rGO hybrid structure can promptly and more efficiently promote the reaction that reduces dissociated H+ and produces H2 on a fairly large number of active sites.

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Fig 4. Schematic illustration of the mechanism governing the catalytic HER on the MoS2 NSs/rGO structure.

https://doi.org/10.1371/journal.pone.0177258.g004

Conclusions

In summary, a facile microwave-assisted method has been used to synthesize MoS2 NSs/rGO hybrid catalyst for HER. TEM images show that MoS2 can disperse better on rGO, which suggests more active sites for HER. Moreover, the MoS2 NSs/rGO hybrid catalyst exhibits excellent properties for HER, which may be attributed to the high specific surface area and the uniform distribution of MoS2 NSs loaded on rGO. Besides, the distinguished conductivity of rGO and the firm interaction between MoS2 NSs and rGO can lead to the parasitic Ohmic losses of the hybrid less than that of original MoS2 NSs in HER. Therefore, this work describes an environmentally friendly and low-cost approach to synthesize the effective MoS2 NSs/rGO hybrid catalyst, suggesting the great potential applications in HER.

Supporting information

S1 Fig. SEM image of MoS2 NSs/rGO (13 wt.%).

https://doi.org/10.1371/journal.pone.0177258.s001

(DOCX)

S2 Fig. The EDS pattern of C and O in MoS2 NSs/rGO hybrid catalyst.

https://doi.org/10.1371/journal.pone.0177258.s002

(DOCX)

S1 Table. The test details of XPS (C1s and O1s).

https://doi.org/10.1371/journal.pone.0177258.s003

(DOC)

Acknowledgments

The work described in this paper was financially supported by the National Natural Science Foundation of China (No.61404037).

Author Contributions

  1. Conceptualization: JC.
  2. Data curation: JC.
  3. Formal analysis: JC JZ.
  4. Funding acquisition: Y. Zhang.
  5. Investigation: JC Y. Zou.
  6. Methodology: JC JZ.
  7. Project administration: JC JZ.
  8. Resources: XL.
  9. Software: JC JZ.
  10. Supervision: JC JZ.
  11. Validation: JC JZ.
  12. Visualization: JC JZ.
  13. Writing – original draft: JC JZ.
  14. Writing – review & editing: JC JZ.

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