Electrochemical Exfoliation to Produce High-Quality Black Phosphorus

Payam Hashemi; Davood Sabaghi; Sheng Yang; Ali Shaygan Nia; Xinliang Feng

doi:10.3791/64109

JoVE Journal > Chemistry

Chimica

Electrochemical Exfoliation to Produce High-Quality Black Phosphorus

Published: October 06, 2022

doi:

10.3791/64109

Payam Hashemi^1,2, Davood Sabaghi¹, Sheng Yang¹, Ali Shaygan Nia^1,2, Xinliang Feng^1,2

¹Center for Advancing Electronics Dresden (cfaed) and Department of Chemistry and Food Chemistry,Technische Universität Dresden, ²Department of Synthetic Materials and Functional Devices,Max Planck Institute of Microstructure Physics

Summary

We present a step-by-step procedure for electrochemical exfoliation of black phosphorus (BP), one of the most promising emerging 2D materials with applications in (opto)electronics, from its bulk crystals, as well as the morphological characterization by scanning electron microscopy, atomic force microscopy, and transmission electron microscopy.

Abstract

To obtain high-quality two-dimensional (2D) materials from the bulky crystals, delamination under an externally controlled stimulus is crucial. Electrochemical exfoliation of layered materials requires simple instrumentation yet offers high-quality exfoliated 2D materials with high yields and features straightforward upscalability; therefore, it represents a key technology for advancing fundamental studies and industrial applications. Moreover, the solution processability of functionalized 2D materials enables the fabrication of (opto)electronic and energy devices via different printing technologies such as inkjet printing and 3D printing. This paper presents the electrochemical exfoliation protocol for the synthesis of black phosphorus (BP), one of the most promising emerging 2D materials, from its bulk crystals in a step-by-step manner, namely, cathodic electrochemical exfoliation of BP in the presence of N(C₄H₉)₄∙HSO₄ in propylene carbonate, dispersion preparation by sonication and subsequent centrifugation for the separation of flakes, and morphological characterization by scanning electron microscopy (SEM), atomic force microscopy (AFM), and transmission electron microscopy (TEM).

Introduction

Due to their superior mechanical, electrical, and optical properties in comparison to their layered bulk analogs, 2D materials have attracted considerable attention among the scientific community. Being the predecessor and the most studied of all 2D materials for several decades, graphene is still in the spotlight of cutting-edge discoveries such as membranes¹, sensors², catalysts³, energy technologies⁴, topological spintronic devices⁵, and condensed matter physics⁶. Inspired by that, numerous other 2D materials have been synthesized and investigated, such as metal chalcogenides⁷, layered double hydroxides⁸, and boron nitride⁹. Including the newest additions to the family of 2D materials (i.e., phosphorene¹⁰), MXenes (2D metal carbides or nitrides)¹¹, and 2D polymers (single/few-layer 2D metal/covalent organic frameworks)¹²^,¹³, the family of 2D materials has grown to consist of more than 150 members featuring intrinsic insulators, semiconductors, semimetals, and metals¹⁴.

The emerging 2D materials, such as BP¹⁵^,¹⁶^,¹⁷^,¹⁸^,¹⁹^,²⁰^,²¹^,²², molybdenum disulfide (MoS₂)²³^,²⁴^,²⁵^,²⁶, and indium(III) selenide (In₂Se₃)²⁷^,²⁸^,²⁹, have shown considerable potential in scientific discoveries; however, to extend their excellent physiochemical properties to a macroscopic scale, efficient, reproducible, and low-cost methods are urgently needed. Electrochemical exfoliation is a promising approach for the upscale production of such 2D materials³⁰^,³¹, mainly due to the fact that it can provide gram scales of high-quality and dispersible exfoliated materials in minutes to a few hours due to the efficient intercalation of ions under the electric force.

The accompanying video demonstrates the step-by-step production of dispersions of BP, one of the most promising emerging 2D materials with applications in (opto)electronics, using electrochemical exfoliation, followed by sonication and centrifugation for the separation of flakes from unexfoliated particles, the preparation of dispersions of exfoliated BP flakes in various solvents, and morphological characterization by SEM, AFM, and TEM.

Protocol

NOTE: See the Table of Materials for details related to the materials and equipment used in this protocol.

1. Synthesis of black phosphorus (BP) by electrochemical exfoliation

Chop the large pieces of BP crystal into small pieces of ~1-2 mm (≤5 mg) and confine them inside a platinum gauze to serve as the cathode.
Cut a piece of platinum foil with dimensions ~2 cm² to serve as the anode and fix it in a way that it faces the cathode and is 2 cm away from it.
To prepare the electrolyte, prepare a fresh solution of 0.1 M tetra-n-butyl-ammonium bisulfate (TBA·HSO₄) in propylene carbonate (use anhydrous and degassed solvent). Fill the electrochemical cell until the solvent level reaches at least 5 mm above the top of the electrodes (Figure 1C).
Apply a DC potential of −8.0 V to start the delamination. To prevent degradation during the exfoliation, carry out the whole process under an inert atmosphere (e.g., inside a glove box under argon or nitrogen).
NOTE: There is no need for continuous purging of the electrolyte by inert gases.
Upon completion of the delamination (ensure there is no more visible generation of expanded BP), transfer the whole electrolyte, including the exfoliated BP flakes and the larger unexfoliated particles, into a 50 mL centrifuge tube.
Centrifuge at 5,292 × g at 15 °C for 10 min. Discard the electrolyte, add 35 mL of fresh propylene carbonate to the precipitate, and shake it gently. Repeat the centrifugation and washing process 2x with propylene carbonate and 2x with the final solvent of choice (e.g., 2-propanol, N,N-dimethylformamide [DMF], or N-methyl-2-pyrrolidone [NMP]).
Add 5-50 mL of the desired solvent to the precipitated products (depending on the required concentration range) and sonicate the resulting product mixture in an ice-cooled sonication bath for 10 min.
Centrifuge the mixture at 5,292 × g at 15 °C for 10 min to remove the thick-layered BP flakes.
Decant the supernatant containing the monolayer and few-layer (<10 layers) BP flakes into a clean container and keep it in the glove box for further characterization or device fabrication.
Calculate the delamination yield (η) using the gravimetric yield formula represented by equation (1):
η = m₁/m₂ × 100% (1)
where m₂ represents the mass of the starting BP crystal and m₁ the weight of the dispersed BP flakes.
To determine m₁, measure the weight of the BP collected from the vacuum filtration of a certain volume of the BP dispersion (e.g., 0.5 mL). Use polytetrafluoroethylene (PTFE) membrane (0.2 µm pore size) for vacuum filtration.
For long-term storage, close the cap of the container bottle and keep it inside the glovebox (up to 3 months).

2. Sample preparation for characterization by SEM, SEM-EDS, AFM, and TEM

NOTE: To explore the quality and morphological aspects of the synthesized BP flakes, it is necessary to perform characterizations such as SEM³² (for studying the surface morphology of the BP flakes), SEM-EDS³³ (for elemental analysis of the flakes), AFM³⁴^,³⁵ (for analysis of the thickness and lateral size of the flakes), and TEM³⁶^,³⁷ (for detection of the structural defects, shape, and size of the BP flakes). Sample preparation protocols for the abovementioned characterization techniques are explained below (sections 2.1-2.4). For operational procedures of the abovementioned characterization techniques, refer to the cited references³²^,³³^,³⁴^,³⁵^,³⁶^,³⁷.

Sample preparation for characterization by SEM
1. Cut out a small piece (with dimensions around 5−7 mm) of a silicon wafer.
2. Clean the silicon wafer piece using acetone, methanol, and water successively. Then, dry the substrate by blowing compressed air or nitrogen over it.
3. Prepare a 0.5 mL diluted dispersion of the BP dispersion prepared in section 1 by the addition of anhydrous iso-propanol to reach a concentration of ~0.01 mg/mL.
4. Spin coat 1−2 droplets of the prepared diluted dispersion on the clean and dry substrate in the glovebox and let it dry on a hotplate at 100 °C for 6 h (in the glovebox). After cooling to room temperature, use the sample for characterization.
Sample preparation for characterization by SEM-EDS
1. Follow the procedure mentioned in section 2.1; however, prepare a more concentrated dispersion of ~0.1 mg/mL instead of the one mentioned in step 2.1.3.
Sample preparation for characterization by AFM
1. Follow the procedure mentioned in section 2.1; however, use a silicon oxide wafer instead of the silicon wafer mentioned in step 2.1.1.
Sample preparation for characterization by TEM
1. Prepare the diluted dispersion of BP as explained in section 2.1.3.
2. Drop cast one droplet of the dispersion on the carbon microgrids. Use the sample for characterization by TEM after drying it in the glovebox argon-atmosphere (without additional heating) for 24 h.

Representative Results

Figure 1 demonstrates the electrochemical exfoliation of BP crystals, the mechanism of intercalation of TBA·HSO₄ and subsequent delamination, and the reaction cell setup.

Figure 1: Schematic demonstration of the mechanism of electrochemical exfoliation of black phosphorus crystals and the reaction setup. (A) Electrochemical exfoliation of BP crystals, (B) the mechanism of intercalation of TBA·HSO₄ and subsequent delamination, and (C) the reaction cell setup. This figure has been modified from Yang et al.¹⁵. Copyright 2018, John Wiley and Sons. Abbreviations: BP = black phosphorus; TBA·HSO₄ = tetra-n-butyl-ammonium bisulfate. Please click here to view a larger version of this figure.

Quaternary ammonium cations, such as tetramethylammonium cation (TMA⁺ 0.56 nm), tetraethylammonium cation (TEA⁺ 0.67 nm), and tetrabutylammonium cation (TBA⁺ 0.83 nm)³⁸, have larger diameters than the interplanar spacing of BP (d = 0.53 nm). As a result, when a potential of -8.0 V is applied, the BP crystals confined within the Pt gauze expand and start to find their way out of the Pt gauze and into the electrolyte solution along with mild bubble formation within a short time of 15 min in the solution of TBA·HSO₄ (Figure 2). By contrast, TMA·HSO₄ and TEA·HSO₄ result in less expansion lasting over more than 1 h.

Figure 2: Electrochemical exfoliation of BP crystals. Electrochemical exfoliation of BP crystals in 0.1 M TBA·HSO₄ in propylene carbonate at -8.0 V over a course of 60 min. This figure has been adapted from Yang et al.¹⁵. Copyright 2018, John Wiley and Sons. Abbreviations: BP = black phosphorus; TBA·HSO₄ = tetra-n-butyl-ammonium bisulfate. Please click here to view a larger version of this figure.

Without applying the electric potential, TBA⁺ cations, which are larger than TMA·HSO₄ and TEA·HSO₄ and have lower charge density cannot intercalate into BP crystals¹⁵. The yields of delamination of BP in a solution of TBA·HSO₄ in propylene carbonate, as the electrolyte, at various potentials and molarities are demonstrated in Figure 3.

Figure 3: The yield of delamination in TBA·HSO₄ in propylene carbonate solution. Yields at various (A) applied potentials and (B) concentrations of the electrolyte. This figure has been modified from Yang et al.¹⁵. Copyright 2018, John Wiley and Sons. Abbreviation: TBA·HSO₄ = tetra-n-butyl-ammonium bisulfate Please click here to view a larger version of this figure.

One of the advantages of the presented electrochemical exfoliation is the possibility of the production of dispersions of BP flakes in a series of desired solvents (e.g., 2-propanol, DMF, NMP) at the desired concentrations (10-100 µg mL^─1), depending on the targeted application. By the addition of less solvent in the sonication step, it is possible to obtain more concentrated dispersions (refer to protocol section 1.7). Due to the chemical instability of exfoliated BP, low-boiling point solvents, such as 2-propanol (which facilitates the removal of solvent at lower temperatures), are recommended. A dispersion of BP in 2-propanol is stable for up to 3 days.

Figure 4A,B demonstrates the SEM images of BP flakes with irregular shapes and broad size distribution (≥2 µm on average, and in some cases, 20.6 µm). Statistical analysis of more than 300 flakes (Figure 4H) revealed a bimodal size distribution with modes correlated to 1.2 µm² and 3.9 µm². This can be assigned to the side fragmentation process when larger flakes break into smaller fragments. More than 70% of the flakes are around 10 µm² in size; whereas in the case of liquid-phase exfoliation, the average dimensions of BP flakes are less than 1.0 µm² as a consequence of the fragmentation that occurs during long and harsh sonication processes (e.g., for 4 h)³⁹.

Figure 4: Microscopy of BP flakes. (A,B) SEM images of BP flakes obtained by electrochemical exfoliation. (C,D) TEM images of BP flakes, and (E) their diffraction pattern. (F) High-resolution TEM and (G) AFM images of BP flakes. The measured thicknesses of three random flakes (2.3 nm, 3.8 nm, and 4.5 nm) are demonstrated. (H) Analysis of the lateral size of randomly selected individual BP flakes. (I) Statistical calculation of the average thickness of BP flakes according to AFM data. This figure has been modified from Yang et al.¹⁵. Copyright 2018, John Wiley and Sons. Scale bars = (F) 1 nm, (D) 0.5 µm, (C) 1 µm, (A,G) 2 µm. Abbreviations: BP = black phosphorus; SEM = scanning electron microscopy; TEM = transmission electron microscopy; AFM = atomic force microscopy. Please click here to view a larger version of this figure.

TEM was used to investigate the crystal structure of BP sheets. TEM images show BP flakes that are thin and large (Figure 4C,D). Figure 4E illustrates the diffraction pattern with 002 facet (corresponding to 0.44 nm lattice constant) and 200 facet (corresponding to 0.34 nm lattice constant). The high-resolution TEM image demonstrates a defect-free lattice with a symmetric orthogonal structure (Figure 4F), which is in agreement with the intrinsic crystal features of pristine BP. As determined by AFM (Figure 4G), BP flakes have a thickness of 1.3-9.5 nm. The estimated average thickness of flakes obtained by counting more than 100 random flakes is 3.7 nm ± 1.3 nm (corresponding to 4-10 layers; Figure 4I)¹⁵. It is noteworthy that, for solution-processed BP flakes, there is usually a high possibility of overestimation of the heights measured by AFM due to trace amounts of solvents and the likelihood of capillary adhesion⁴⁰. Nonetheless, the coverage of delaminated BP flakes by a thin layer of solvent reduces its ambient oxidation and prolongs their stability for up to 5 days¹⁵.

Elemental mapping of P and C using SEM-energy dispersive spectroscopy (SEM-EDS) was carried out on a BP thin film (obtained from vacuum filtration) attached to a conductive carbon tape (Figure 5). Figure 5E,F clearly shows the high intensity of P in the BP thin film and C in the conductive carbon tape.

Figure 5: BP film. (A) Thin film of BP obtained by vacuum filtration. (B–D) Morphology of the surface and edges of the BP film (attached to conductive carbon tape for SEM imaging). (E,F) Elemental P and C mapping of the BP film (on conductive carbon tape), respectively. This figure has been modified from Yang et al.¹⁵. Copyright 2018, John Wiley and Sons. Scale bars = (B) 1 µm, (C) 10 µm, (D) 250 µm. Abbreviations: BP = black phosphorus; SEM = scanning electron microscopy. Please click here to view a larger version of this figure.

Discussion

BP has a valence shell configuration of 3s² 3p³, and each phosphorus atom possesses a lone electron pair, which makes the phosphorus atoms vulnerable to fast oxidative degradation in the presence of oxygen, water, and light⁴¹. To prevent degradation, it is recommended to use degassed and anhydrous solvents and reagents and carry out the production process under an inert atmosphere.

During the exfoliation of BP crystals, part of the produced H⁺ (equation 1 and equation 2) is reduced at the BP interfaces, forming H₂ bubbles (equation 3) that increase the interlayer spacing and promote the intercalation of larger cations of TBA⁺ in the BP layers (Figure 1B).

TBA·HSO₄ TBA⁺ + HSO₄^─ (1)

HSO₄^─ SO₄^2─ + H⁺ (2)

2 H⁺ + 2e^─ → H₂ (3)

At the same time, part of the H⁺ undergoes catalytic reduction at the surface of the Pt gauze, forming small bubbles (equation 4 and equation 5). This latter part of the gas release does not contribute to the overall exfoliation efficiency. At voltages more negative than -8.0 V, particularly more negative than -12 V, this bubble formation becomes more and more dominant and results in the reduction of the delamination yield (Figure 3A).

H⁺ + e^─ → H_ads (4)

2 H⁺ + 2e^─ → H₂ (5)

The maximum yield of exfoliation (78 wt%) was observed when 0.1 M of TBA·HSO₄ in propylene carbonate was used. Concentrations of TBA·HSO₄ more than 0.2 M had an adverse effect on the yield of exfoliated product (Figure 3B)¹⁵.

As a polar aprotic solvent, propylene carbonate has high stability against cathodic reduction⁴². It has a moderate surface tension (40.8 dyne·cm^-1)⁴³, comparable to that of BP flakes (~40 dyne·cm^-1)⁴⁴, which brings about a proper dispersibility of BP flakes. The solvated protons arise from the dissociation of HSO₄ anions. This shows the important role of bisulfate anions in the exfoliation process. Replacing bisulfate anions with ClO₄^– or PF₆^– did not result in satisfactory results¹⁵.

The key advantage of electrochemical exfoliation of BP compared to other methods is that it allows milligram- to gram-scale production of high-quality and stable dispersions of BP in various solvents. The main reason for this is that the applied electric current drives the intercalation forward without applying strong mechanical force by long and harsh ultrasonication steps; therefore, the obtained BP flakes have larger lateral size compared to those obtained by liquid-phase exfoliation methods. Running the whole electrochemical exfoliation and dispersion steps under an anhydrous and oxygen-free atmosphere prevents the undesired oxidation and results in high-quality and defect-free BP flakes. Moreover, the high-quality BP dispersions obtained by electrochemical exfoliation can be further functionalized to improve their ambient stability and electrical properties¹⁶.

The only downside to electrochemical exfoliation of BP, compared to the mechanical exfoliation method, is that the electrochemical exfoliation method has several steps, namely, electrochemical exfoliation, successive washing and centrifugation, and finally, a mile bath sonication.

Another advantage of the synthesis of BP dispersions by the electrochemical exfoliation method is the possibility of modification of the obtained BP dispersions, with different average flake sizes in various solvents and at various concentrations for different applications. For general applications, such as the fabrication of electronic devices and the characterizations or further functionalization of BP flakes, dilute dispersions in low-boiling point solvents such as 2-propanol are preferred. However, for the inkjet printing of electronics, more concentrated dispersions in high-boiling point solvents, such as DMF or NMP, are more practical.

For some applications, such as inkjet printing, the average flake size of the electrochemically exfoliated BP dispersions should be reduced to a certain degree by longer bath sonication times (depending on the size of the inkjet printing cartridge nozzle size) to prevent the clogging of the nozzles. However, to obtain efficient overlapping of the BP flakes and the formation of uniform and continuous printed patterns, the average size of the flakes should not be decreased more than necessary (>5.0 µm²). The average flake size of the BP dispersions produced by liquid-phase exfoliation is not large enough for reproducible inkjet printing according to our experience.

Troubleshooting guidelines
In case of no visual sign of exfoliation after 15 min, the electrochemical reaction setup and the electrical connections must be checked. It is better to avoid increasing the suggested applied voltage or the concentration of the electrolyte or decreasing the distance between the electrodes. It is important to ensure that the exfoliated BP products generated on the working electrode do not come in contact with the counter electrode to prevent short-circuiting. In case the exfoliated products approach the counter electrode, the working electrode must be tapped gently to remove the loosely bonded and bulky exfoliated products. This may result in a sudden increase in the electrical current, which is normal and is the result of increased exposure of new BP crystal surfaces to the electrolyte. The increased electrical current will decrease again in a few seconds. It is essential to trace any sign of organic contaminations, shown by the characterization method, back to improper washing and centrifugation, the quality of the used chemicals, or improper handling of the reaction, reaction work-up, sample preparation, or characterization steps.

Black phosphorus (BP) is one of the most promising emerging 2D materials, with applications in photodetectors, field-effect transistors, energy storage (supercapacitor and batteries), and catalysts. Electrochemical exfoliation is a highly versatile method for the production of a wide spectrum of 2D materials from their bulk crystals³⁰, with unique advantages such as obtaining low-defect flakes with average lateral sizes larger than those obtained from liquid-phase exfoliation and the possibility of large-scale and economic production. This article presents a protocol for the production of dispersions of high-quality BP flakes by electrochemical exfoliation, sample preparation methods for the characterization of the synthesized BP flakes, and the corresponding characterization data.

Divulgazioni

The authors have nothing to disclose.

Acknowledgements

The authors acknowledge ERC Consolidator Grant on T2DCP, M-ERA-NET project HYSUCAP, SPES3 project funded by the German Ministry for Education and Research (BMBF) under Forschung für neue Mikroelektronik (ForMikro) program, Graphene Flagship Core 3 881603, and Emerging Printed Electronics Research Infrastructure (EMERGE). The EMERGE project has received funding from the European Union's Horizon 2020 Research and Innovation Programme under grant agreement No. 101008701. The authors thank Dr. Markus Löffler for helpful discussions and characterization and also acknowledge the Center for Advancing Electronics Dresden (cfaed) and the Dresden Center for Nanoanalysis (DCN).

Materials

2-Propanol	Sigma Aldrich	278475	anhydrous, 99.5%
Atomic force microscopy (AFM)	Bruker Multimode 8 system
Black phosphorus	Smart Elements	4504	Black Phosphorus 5.0 g sealed under Argon in ampoule
Centrifuge	Sigma 4-16KS
Propylene carbonate	Sigma Aldrich	310328	anhydrous, 99.7%
Scanning electron microscope (SEM)	Zeiss Gemini 500
Tetra-n-butylammonium hydrogen sulfate	Sigma Aldrich	791784	anhydrous, free-flowing, Redi-Dri, 97%
Transmission electron microscopy (TEM)	Zeiss Libra 120 kV

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