Name: preparation of liquid-exfoliated transition metal dichalcogenide nanosheets with controlled size and thickness: a state of the art protocol
Uploaded: 2016-12-20T12:00:00
Description: Watch this Scientific Journal Video about Preparation of Liquid-exfoliated Transition Metal Dichalcogenide Nanosheets with Controlled Size and Thickness: A State of the Art Protocol at JoVE.com

The research leading to these results has received funding from the European Union Seventh Framework Program under grant agreement n&#176;604391 Graphene Flagship. C.B. acknowledges the German Research Foundation, DFG, under grant BA 4856/2-1.

1. Liquid Exfoliation &#8212; Preparation of Suitable Stock Dispersions
<ol>
	<li>Mount a metal cup underneath a sonotrode in an ice bath.</li>
	<li>Immerse 1.6 g of the TMD powder in 80 mL aqueous solution of sodium cholate (SC) surfactant (sodium cholate concentration, CSC= 6 g L-1) in the metal cup.</li>
	<li>Move the sonic tip to the bottom of the metal cup and then up by ~ 1 cm. Wrap aluminum foil around the sonic probe to avoid spillage.</li>
	<li>Sonicate the mixture under ice-cooling by pr...

<ol>
	<li>Zhang, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ultrathin+Two-Dimensional+Nanomaterials.">Ultrathin Two-Dimensional Nanomaterials.</a> ACS Nano. 9, 9451-9469 (2015).</li><li>Yi, M., Shen, Z. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+review+on+mechanical+exfoliation+for+the+scalable+production+of+graphene.">A review on mechanical exfoliation for the scalable production of graphene.</a> J. Mat. Chem. A. 3, 11700-11715 (2015).</li><li>Jariwala, D., Sangwan, V. K., Lauhon, L. J., Marks, T. J., Hersam, M. 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Z., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Progress,+Challenges,+and+Opportunities+in+Two-Dimensional+Materials+Beyond+Graphene.">Progress, Challenges, and Opportunities in Two-Dimensional Materials Beyond Graphene.</a> ACS Nano. 7, 2898-2926 (2013).</li><li>Bonaccorso, F., Bartolotta, A., Coleman, J. N., Backes, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Two-dimensional+crystals-based+functional+inks.">Two-dimensional crystals-based functional inks.</a> Adv. Mater. , (2016).</li><li>Torrisi, F., Coleman, J. N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Electrifying+inks+with+2D+materials.">Electrifying inks with 2D materials.</a> Nat. Nanotechnol. 9, 738-739 (2014).</li><li>Coleman, J. 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Commun. 5, 5478 (2014).</li><li>Backes, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Edge+and+Confinement+Effects+Allow+in+situ+Measurement+of+Size+and+Thickness+of+Liquid-Exfoliated+Nanosheets.">Edge and Confinement Effects Allow in situ Measurement of Size and Thickness of Liquid-Exfoliated Nanosheets.</a> Nat. Commun. 5, 4576 (2014).</li><li>Backes, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Production+of+Highly+Monolayer+Enriched+Dispersions+of+Liquid-Exfoliated+Nanosheets+by+Liquid+Cascade+Centrifugation.">Production of Highly Monolayer Enriched Dispersions of Liquid-Exfoliated Nanosheets by Liquid Cascade Centrifugation.</a> ACS Nano. 10, 1589-1601 (2016).</li><li>Green, A. A., Hersam, M. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Solution+Phase+Production+of+Graphene+with+Controlled+Thickness+via+Density+Differentiation.">Solution Phase Production of Graphene with Controlled Thickness via Density Differentiation.</a> Nano Lett. 9, 4031-4036 (2009).</li><li>Harvey, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Preparation+of+Gallium+Sulfide+Nanosheets+by+Liquid+Exfoliation+and+Their+Application+As+Hydrogen+Evolution+Catalysts.">Preparation of Gallium Sulfide Nanosheets by Liquid Exfoliation and Their Application As Hydrogen Evolution Catalysts.</a> Chem. Mater. 27, 3483-3493 (2015).</li><li>Hanlon, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Liquid+Exfoliation+of+Solvent-Stabilised+Few-Layer+Black+Phosphorus+for+Applications+Beyond+Electronics.">Liquid Exfoliation of Solvent-Stabilised Few-Layer Black Phosphorus for Applications Beyond Electronics.</a> Nat. Commun. 6, 8563 (2015).</li><li>Backes, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Spectroscopic+metrics+allow+in-situ+measurement+of+mean+size+and+thickness+of+liquid-exfoliated+few-layered+graphene+nanosheets.">Spectroscopic metrics allow in-situ measurement of mean size and thickness of liquid-exfoliated few-layered graphene nanosheets.</a> Nanoscale. 8, 4311-4323 (2016).</li><li>Ridings, C., Warr, G. G., Andersson, G. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Composition+of+the+outermost+layer+and+concentration+depth+profiles+of+ammonium+nitrate+ionic+liquid+surfaces.">Composition of the outermost layer and concentration depth profiles of ammonium nitrate ionic liquid surfaces.</a> Phys. Chem. Chem. Phys. 14, 16088-16095 (2012).</li><li>Nemes-Incze, P., Osv&#225;th, Z., Kamar&#225;s, K., Bir&#243;, L. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Anomalies+in+thickness+measurements+of+graphene+and+few+layer+graphite+crystals+by+tapping+mode+atomic+force+microscopy.">Anomalies in thickness measurements of graphene and few layer graphite crystals by tapping mode atomic force microscopy.</a> Carbon. 46, 1435-1442 (2008).</li><li>Paton, K. R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Scalable+production+of+large+quantities+of+defect-free+few-layer+graphene+by+shear+exfoliation+in+liquids.">Scalable production of large quantities of defect-free few-layer graphene by shear exfoliation in liquids.</a> Nat. Mater. 13, 624-630 (2014).</li><li>Novoselov, K. S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Two-dimensional+atomic+crystals.">Two-dimensional atomic crystals.</a> Proc. Nat. Ac. Sci. U. S. 102, 10451-10453 (2005).</li><li>Kouroupis-Agalou, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Nanoscale. 6, 5926-5933 (2014).</li><li>Hanlon, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Production+of+Molybdenum+Trioxide+Nanosheets+by+Liquid+Exfoliation+and+Their+Application+in+High-Performance+Supercapacitors.">Production of Molybdenum Trioxide Nanosheets by Liquid Exfoliation and Their Application in High-Performance Supercapacitors.</a> Chem. 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Sample preparation
The samples described here are produced by tip sonication. Alternative exfoliation procedures can be used, but will lead to different concentrations, lateral sizes and degrees of exfoliation. Higher amplitudes and longer on pulses during the sonication should be avoided to prevent damaging of the sonicator. Similar results were obtained using 500 W processors. However, sonication time and amplitude has an impact on the nanosheet exfoliation and variations from this protocol may...

The possibility to produce and process graphene, related two-dimensional (2D) crystals in the liquid phase makes them promising materials for an ever growing range of applications as composite materials, sensors, in energy storage and conversion and flexible (opto) electronics.1-6 To exploit 2D nanomaterials within applications such as these will require inexpensive and reliable functional inks with on-demand lateral size and thickness of the nanoscale constituents, as well as controlled rheological and morphological properties amenable to industrial-scale printing/coating processes.7 In this regard, liquid phase exfoliation has become an important production technique giving access to a whole host of nanostructures in large quantities.6,8,9 This method involves the sonication or shearing of layered crystals in liquids. If the liquid is appropriately chosen (i.e., suitable solvents or surfactant) the nanosheets will be stabilized against reaggregation. Numerous applications and proof-of-principle devices have been demonstrated by such techniques.6 Probably the greatest strength of this strategy is its versatility, as numerous layered parent crystals can be exfoliated and processed in a similar way, providing access to a broad palette of materials which can be tailored to the desired application.
However, despite this recent progress, the resultant polydispersity that arises due to these liquid-phase production methods (in terms of nanosheet length and thickness) still presents a bottleneck in the realization of high performance devices. This is mostly because the development of novel and innovative size selection techniques has thus far required nanosheets length and thickness characterization using tedious statistical microscopy (atomic force microscopy, AFM and/or transmission electron microscopy, TEM).
Despite these challenges, several centrifugation techniques have been reported to achieve length and thickness sorting.6,10-13 The simplest scenario is homogeneous centrifugation, where the dispersion is centrifuged at a given centrifugal acceleration and the supernatant is decanted for analysis. The centrifugation speed sets the size cut-off, whereby the higher the speed, the smaller are the nanosheets in the supernatant. However, this technique suffers from two major disadvantages; firstly, when larger nanosheets are to be selected (i.e., the dispersion is centrifuged at low speeds and the supernatant is decanted) all smaller nanosheets will also remain in the sample. Secondly, regardless of the centrifugation speed, a significant proportion of the material tends to be wasted in the sediment.
An alternative strategy for size selection is density gradient (or isopycnic) centrifugation.11,14 In this case, the dispersion is injected into a centrifuge tube containing a density gradient medium. During ultracentrifugation (typically &#62; 200,000 x g), a density gradient is formed and the nanosheets move to the point in the centrifuge where their buoyant density (density including the stabilizer and solvent shell) matches the density of the gradient. Note that the nanomaterial can also move upward during this process (depending on where it was injected). In such a way, the nanosheets are effectively sorted by thickness rather than mass (opposed to homogeneous centrifugation). While this procedure offers a unique opportunity to sort nanosheets by thickness, it suffers from notable disadvantages. For example, the yields are very low and at present do not allow for the mass production of separated nanosheets. This is partly related to low contents of monolayers in stock dispersions after liquid-exfoliation and can potentially be improved by optimizing exfoliation procedures in the future. In addition, it is typically a time-consuming multi-step ultracentrifugation process involving multiple iterations to achieve efficient size selection. Furthermore, in the case of inorganic nanomaterials, it is restricted to polymer-stabilized dispersions to obtain the required buoyant densities and the gradient medium in the dispersion may interfere with further processing.
We have recently shown that a procedure we term liquid cascade centrifugation (LCC) offers an exciting alternative,13 as we will also detail in this manuscript. This is a multi-step procedure which is extremely versatile allowing various cascades to be designed according to the desired outcome. To demonstrate this process, a standard cascade is portrayed in Figure 1 and involves multiple centrifugation steps whereby each features a higher speed than the last. After each step, the sediment is retained and the supernatant is then used in the proceeding stage. As a result, each sediment contains nanosheets in a given size range which have been &#34;trapped&#34; between two centrifugations with different speeds; the lower one removing larger nanosheets into the previous sediment while the higher speed removes the smaller nanosheets into the supernatant. Critical to LCC, the resulting sediment can be redispersed completely by mild sonication in the respective medium, which in this case is aqueous sodium cholate H2O-SC (at SC concentrations as low as 0.1 g L-1). The result is dispersions with virtually any chosen concentration. Importantly, virtually no material is wasted in LCC, resulting in the collection of relatively large masses of size-selected nanosheets. As shown here, we have applied this procedure to a number of liquid-exfoliated nanosheets including MoS2 and WS2 as well as GaS,15 black phosphorus16 and graphene17 in both solvent and surfactant systems.
This unique centrifugation procedure enables the efficient size-selection of liquid exfoliated nanosheets and has subsequently enabled a significant advancement in terms of their size and thickness determination. In particular, through this approach we demonstrated previously that optical extinction (and absorbance) spectra of the nanosheets change systematically as function of both nanosheets lateral dimensions and nanosheets thickness. As we summarize here, this has allowed us to link the nanosheet spectral profile (specifically the intensity ratio at two positions of the extinction spectrum) to the mean nanosheet length as a result of nanosheet edge effects.12,13 Importantly, the same equation can be used to quantify the size of MoS2 and WS2. Furthermore, we show that the A-exciton position shifts towards lower wavelengths as a function of mean nanosheet thickness due to confinement effects. Even though exfoliation, as well as size selection and determination are in general rather robust procedures, the quantitative outcome depends on subtleties in the protocol. However, especially for newcomers to the field, it is difficult to judge which process parameters are most relevant. This comes down to the fact that experimental sections of research papers only provide a rough protocol, without discussing what outcome is to be expected when modifying the procedure or giving a rational behind the protocol. In this contribution, we intend to address this as well as provide a detailed guide and discussion to the production of liquid-exfoliated nanosheets of controlled size and to the accurate determination of size by either statistical microscopy or analysis of the extinction spectra. We are convinced that this will help to improve reproducibility and hope it will be a useful guide for other experimentalists in this research area.
<img alt="Figure 1" src="/files/ftp_upload/54806/54806fig1.jpg" /> 
Figure 1: Schematic of the size selection by liquid cascade centrifugation. Size-selected nanosheets are collected as sediments. Each sediment is collected or &#34;trapped&#34; between two centrifugation speeds (&#969;) starting from low speeds and going to higher ones from step to step. The sediment discarded after the first centrifugation contains unexfoliated layered crystallites while the supernatant discarded after the last centrifugation step contains extremely small nanosheets. Size-selected dispersions are prepared by re-dispersing the collected sediments in the same medium (here aqueous surfactant solution) at reduced volumes. Adapted with permission from 13. <a href="http://cloudflare.jove.com/files/ftp_upload/54806/54806fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

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	<tbody>
		<tr height="42">
			<td height="42" style="height:42px;width:233px;">Sodium cholate hydrate, from ox and/or sheep bile</td>
			<td style="width:105px;">Sigma Aldrich</td>
			<td style="width:127px;">C1254-100G</td>
			<td style="width:523px;">Surfactant used as stabilizer in the form of an aqueous solution (i.e. after dissolving the powder in millipore water)</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:233px;">MoS2 powder</td>
			<td style="width:105px;">Sigma Aldrich</td>
			<td style="width:127px;">69860-100G</td>
			<td style="width:523px;">Other distributors available, but exfoliation and outcome of size selection can vary</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:233px;">WS2, powder 2 um</td>
			<td style="width:105px;">Sigma Aldrich</td>
			<td style="width:127px;">243639-50G</td>
			<td style="width:523px;">Other distributors available, but exfoliation and outcome of size selection can vary</td>
		</tr>
		<tr height="84">
			<td height="84" style="height:84px;width:233px;">ImageJ Software</td>
			<td style="width:105px;">Developer: National Insitutes of Health</td>
			<td style="width:127px;">64-bit Java version 2.45 1.6.0_24</td>
			<td style="width:523px;">Image processing software used for TEM analysis, free download</td>
		</tr>
		<tr height="84">
			<td height="84" style="height:84px;width:233px;">Gwyddion Software</td>
			<td style="width:105px;">Developer: Czech Metrology Institute</td>
			<td style="width:127px;">64-bit Java version 2.45</td>
			<td style="width:523px;">Image processing software used for AFM analysis, free download</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:233px;">Origin Pro Software</td>
			<td style="width:105px;">OriginLab</td>
			<td style="width:127px;">Version 2016</td>
			<td style="width:523px;">Software used for data analysis such as differntiation and fitting of the extinction spectra</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:233px;">Centrifuge&#160;</td>
			<td style="width:105px;">HettichLab</td>
			<td style="width:127px;">Mikro 220R</td>
			<td style="width:523px;">any other benchtop centrifuge is suitable</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:233px;">Rotor 1</td>
			<td style="width:105px;">Hettich</td>
			<td style="width:127px;">Rotor 1016</td>
			<td style="width:523px;">for centrifugation &#60; 5000 x g</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:233px;">Rotor 2</td>
			<td style="width:105px;">Hettich</td>
			<td style="width:127px;">Rotor 1195-A</td>
			<td style="width:523px;">for centrifugation &#62; 5000 x g</td>
		</tr>
	</tbody>
</table>

preparation of liquid-exfoliated transition metal dichalcogenide nanosheets with controlled size and thickness: a state of the art protocol

We summarize recent advances in the production of liquid-exfoliated transition metal dichalcogenide (TMD) nanosheets with controlled size and thickness. Layered crystals of molybdenum disulphide (MoS2) and tungsten disulphide (WS2) are exfoliated in aqueous surfactant solution by sonication. This yields highly polydisperse mixtures containing nanosheets with broad size and thickness distributions. However, for most purposes, specific sizes (in terms of both lateral dimension and thickness) are required. For example, large and thin nanosheets are desired for (opto) electronic applications, while laterally small nanosheets are interesting for catalytic applications. Therefore, post-exfoliation size selection is an important step that we address here. We provide a detailed protocol on the efficient size selection in large quantities by liquid cascade centrifugation and the size and thickness quantification by statistical microscopic analysis (atomic force microscopy and transmission electron microscopy). The comparison of MoS2 and WS2 shows that both materials are size-selected in a similar way by the same procedure. Importantly, the dispersions of size-selected nanosheets show systematic changes in their optical extinction spectra with size due to edge and confinement effects. We show how these optical changes are related quantitatively to the nanosheets dimensions and describe how mean nanosheets length and layer number can be extracted reliably from the extinction spectra. The exfoliation and size selection protocol can be applied to a broad range of layered crystals as we have previously demonstrated for graphene, gallium sulphide (GaS) and black phosphorus.

Liquid cascade centrifugation (Figure 1) is a powerful technique to sort liquid-exfoliated nanosheets by size and thickness as illustrated in Figure 2 for both MoS2 and WS2. Nanosheet lateral sizes and thicknesses can be characterized by statistical TEM and AFM, respectively. A typical AFM image is shown in Figure 2A. The apparent nanosheet thickness is converted to layer number using step height analysis (Fi...

Watch this Scientific Journal Video about Preparation of Liquid-exfoliated Transition Metal Dichalcogenide Nanosheets with Controlled Size and Thickness: A State of the Art Protocol at JoVE.com

Preparation of Liquid-exfoliated Transition Metal Dichalcogenide Nanosheets with Controlled Size and Thickness: A State of the Art Protocol

A protocol for the liquid exfoliation of layered materials to nanosheets, their size selection and size measurement by microscopic and spectroscopic techniques is presented.

与尺寸可控液体剥离的过渡金属二硫属化物纳米片和厚度的制备：艺术议定书的国家

We summarize recent advances in the production of liquid-exfoliated transition metal dichalcogenide (TMD) nanosheets with controlled size and thickness. ...

The goal of this protocol is to produce two dimensional nanosheets stabalized in liquid with controlled lateral size and thickness from bulk crystals. We also demonstrate methods to characterize the morphology and quantitatively determine the nanosheet dimensions from extinction spectra. This method can help answer key questions in nanoscience, such as the influence of nanosheet dimensions on the properties of structures and composites containing these sheets exfoliated in liquid.The main advantage of this technique is that it's applicable to many different true day materials and only requires commonplace laboratory equipment. In particular, the spectroscopic metrics allow rapid assessment of the dispersions that are produced. Demonstrating the procedure will be Farnia Rashvand, a PhD student, and Kevin Synnatschke, a Master's student from my laboratory.To begin this procedure, mount a metal cup underneath a sonotrode in an ice bath. Immerse 0.6 grams of a transition metal dichalcogenide or TMD powder in 80 milliliters of an aqueous solution of sodium cholate surfactant in the metal cup. Move the solid flathead tip to the bottom of the metal cup and then raise it approximately one centimeter.Wrap aluminum foil around the sonic probe to avoid spillage. To sonicate the mixture by probe sonication, set the amplitude to 60%and the pulsing to six seconds on, and two seconds off. Then switch on the sonicator and run the process for one hour.Next, centrifuge the dispersion at 2, 660 times g for 1.5 hours. After discarding the supernatant, add 80 milliliters of fresh surfactant solution to the sediment and agitate the mixture. Then, transfer the mixture back to the metal cup.Now, subject the dispersion to a second, longer sonication using the solid flathead tip for five hours at 60%amplitude under ice cooling. After every two hours, pause the sonication and replace the ice bath. Remove unexfoliated particles by centrifugation at 240 times g for two hours.When finished, discard the sediment. Following this, centrifuge the supernatant at higher centrifugal acceleration. Collect the sediment in three to eight millileters of fresh surfactant solution.Centrifuge the supernatant at an even higher centrifugal acceleration of 950 times g for two hours. Then collect the sediment in three to eight milliliters of fresh surfactant solution. For atomic force microscopy, dilute the dispersion so that it is almost transparent to the human eye.Following this, heat a wafer to approximately 170 degrees Celsius on a hot plate. Then deposit the dispersion on the preheated wafer. Rinse the wafer thoroughly with a minimum of five milliliters of water and three milliliters of 2-Propanol to remove residual surfactant and other impurities.Following this, load the sample in AFM instrument. Scan and save multiple images across the sample with the atomic force microscope in tapping mode. For samples containing larger nanosheets, increase the field of view up to eight by eight micrometers squared and use scan rates of 0.4 to 0.7 hertz.To perform the thickness measurement, open the software and select the relevant AFM image via File and Open. Correct the background using the level data by mean plane subtraction, align rows, and correct horizontal scars in the data process section of the Home menu. Apply the corrections, change the image color for better contrast by right-clicking on the the legend and set the Z plane to zero.Next, zoom into the region of choice by first clicking on the Crop tool in the Home menu. Then drag the cursor over the image to mark the region of choice and press Apply. Check the create new channel to open the selected region in a new window.Select extract profiles from the Tools menu and draw a line across the nanosheet. After the window showing the thickness length profile opens, enter the thickness value in a table. Take the approximate median value of the thickness profile across the nanosheet, taking extreme care to measure only individually deposited and non-aggregated nanosheets.For spectral acquisition, dilute the high concentration sample with the respective medium to yield extinctions below two across the entire spectral range. Set the increments for spectral acquisition to 0.5 nanometers in the instruments setting. Choose subtract baseline in the instruments settings.After placing a cuvette containing the aqueous sodium cholate solution in the spectrometer, run the measurement. Following this, remove the cuvette from the spectrometer and empty it. Add the sample to the cuvette and place the cuvette in the spectrometer.Then run the measurement. Using the data analysis and graphing software, select the column containing the extinction intensity. Click on the Analysis tab, select Mathematics from the dropdown menu, and click on Differentiate.Then select Open Dialog. After the new window opens, set the derivative order to two and press OK.Select the column containing the derivative, click on Analysis and choose Signal Processing. Click on Smooth and then select Open Dialog from the dropdown menu.Next, choose Adjacent Averaging as the smoothing method and set the points to 20. Plot the resultant smoothed spectrum, which is displayed as new columns. Finally, read off the peak position from the second derivative by placing the cursor in the center of the peak.Liquid cascade centrifugation is used to sort liquid-exfoliated nanosheets by size and thickness as demonstrated for molybdenum and tungsten disulfide. A typical AFM image is shown here. And the nanosheet thickness is converted to layer number using step height analysis.Statistical microscopic analysis yields length and number of layer histograms. The mean nanosheet length and layer number plotted as a function of central acceleration shows a similar trend for both materials. The length plotted as a function of nanosheet layer number confirms that smaller, thinner nanosheets are separated from larger, thicker ones.Optical extinction spectra of molybdenum and tungsten disulfide with different mean nanosheet sizes and thicknesses are shown here. The corresponding fitted second derivatives of the A-exciton region illustrate well-defined peak shifts of the transition. Data for both materials collapses on the same curve if appropriate peak positions are chosen and means that the nanosheet size can be quantitatively linked to the nanosheet length via the same equations.The A-exciton extinction coefficient is length dependent except at certain positions, so that the corresponding extinction coefficient can be used as measure for nanosheet concentration. The number of layers can be quantitatively related to the A-exciton peak position. Once mastered, large quantities of liquid-exfoliated nanosheet dispersions with controlled and known dimensions can be produced in only a couple of days.This is enabled by the high throughput size determination based on the optical extinction spectra. Since the nanosheet size determines its properties, the size control is crucial. After the development of the metrics, this technique paved the way for researchers to explore them in a number of applications, from electrocatalysis to electronics to composite reinforcement.After watching this video, you should have a good understanding of how to produce size selected nanosheet dispersions using liquid phase exfoliation and liquid cascade centrifugation procedures. Following the dispersion preparation, it's very important to perform basic characterization using statistical microscopy and optical extinction spectroscopy to confirm the nature of the dispersion constituents. Most excitingly, the resulting size selected nanosheet dispersions can then be subject to various liquid phase processing methods to produce thin films and other nanosheet containing structures for a wide range of potential applications.

Research

JoVE Journal

Engineering

Controlling the Size, Shape and Stability of Supramolecular Polymers in Water

控制的大小，形状和稳定性超分子聚合物在水

For aqueous based supramolecular polymers, the simultaneous control over shape, size and stability is very difficult1. At the same time, the ability to do ...

科研

工程学

Synthesis of Phase-shift Nanoemulsions with Narrow Size Distributions for Acoustic Droplet Vaporization and Bubble-enhanced Ultrasound-mediated Ablation

相移窄粒度分布的纳米乳液的合成声波液滴蒸发和泡增强的超声介导消融

High-intensity  focused ultrasound (HIFU) is used clinically to thermally ablate tumors. To  enhance localized heating and improve thermal ablation in ...

Fine-tuning the Size and Minimizing the Noise of Solid-state Nanopores

微调尺寸和最小化固态纳米孔的噪音

Solid-state nanopores have emerged as a versatile tool for the characterization of single biomolecules such as nucleic acids and proteins1. However, the ...

Quantum State Engineering of Light with Continuous-wave Optical Parametric Oscillators

光与连续波光学参量振荡器的量子态工程

Engineering non-classical states of the electromagnetic field is a central quest for quantum optics1,2. Beyond their fundamental significance, such states ...

Characterization of Nanocrystal Size Distribution using Raman Spectroscopy with a Multi-particle Phonon Confinement Model

使用拉曼光谱与多颗粒的声子坐月子型号纳米大小分布的特征

Analysis of the size distribution of nanocrystals is a critical requirement for the processing and optimization of their size-dependent properties. The ...

Indirect Fabrication of Lattice Metals with Thin Sections Using Centrifugal Casting

与超薄切片格金属制造间接使用离心铸造

One of the typical methods to manufacture 3D lattice metals is the direct-metal additive manufacturing (AM) process such as Selective Laser Melting (SLM) ...

Electrospray Deposition of Uniform Thickness Ge23Sb7S70 and As40S60 Chalcogenide Glass Films

Electrospray Deposition of Uniform Thickness Ge23Sb7S70 and As40S60 Chalcogenide Glass Films

厚度均匀葛电沉积<sub&gt; 23</sub&gt;锑<sub&gt; 7</sub&gt;取值<sub&gt; 70</sub&gt;和As<sub&gt; 40</sub&gt;取值<sub&gt; 60</sub&gt;硫系玻璃薄膜

Solution-based electrospray film deposition, which is compatible with continuous, roll-to-roll processing, is applied to chalcogenide glasses. Two ...

Hand Controlled Manipulation of Single Molecules via a Scanning Probe Microscope with a 3D Virtual Reality Interface

通过手扫描探针显微镜用三维虚拟现实接口控制单分子的操作

Considering organic molecules as the functional building blocks of future nanoscale technology, the question of how to arrange and assemble such building ...

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets

由界面润湿片的热力学生长触发的液晶中的定向转变

In liquid crystal (LC) physical chemistry, molecules near the surface play a great role in controlling bulk orientation. Thus far, mainly to achieve ...

Preparation of Large-area Vertical 2D Crystal Hetero-structures Through the Sulfurization of Transition Metal Films for Device Fabrication

硫化过渡金属膜制备大面积垂直2D 晶体杂化结构

We have demonstrated that through the sulfurization of transition metal films such as molybdenum (Mo) and tungsten (W), large-area and uniform transition ...