Template-assisted synthesis of 2D nanosheets using nanoparticle templates

Abstract

A template-assisted method for the synthesis of 2D nanosheets comprises growing a 2D material on the surface of a nanoparticle substrate that acts as a template for nanosheet growth. The 2D nanosheets may then be released from the template surface, e.g. via chemical intercalation and exfoliation, purified, and the templates may be reused.

Claims

1. A composition of matter comprising: a nanoparticle template comprising a material having a first crystal structure; and a two-dimensional (2D) transition metal dichalcogenide nanosheet at least partially covering a surface of the nanoparticle template, the two-dimensional (2D) transition metal dichalcogenide nanosheet comprising a material having a second crystal structure, wherein the first crystal structure and the second crystal structure exhibit therebetween a lattice mismatch of around 5% or less.

2. The composition recited in claim 1, wherein the lattice mismatch between the first crystal structure and the second crystal structure is around 3% or less.

3. The composition recited in claim 1, wherein the first crystal structure is hexagonal.

4. The composition recited in claim 1, wherein the nanoparticle template is a nanopyramid.

5. The composition recited in claim 1, wherein the nanoparticle template is a quantum dot.

6. The composition recited in claim 1, wherein the nanoparticle template is a ZnO nanoparticle.

7. The composition recited in claim 1, wherein the material of the two-dimensional (2D) transition metal dichalcogenide nanosheet is MoS.sub.2, MoSe.sub.2 or WS.sub.2.

8. The composition recited in claim 1, wherein the two-dimensional (2D) transition metal dichalcogenide nanosheet is a two-dimensional (2D) transition metal dichalcogenide quantum dot.

9. The composition recited in claim 1, wherein the nanoparticle template is a metal nanoparticle or a polymer nanoparticle.

10. A composition of matter comprising: a nanoparticle template, the nanoparticle template being a nanopyramid; and a two-dimensional (2D) transition metal dichalcogenide nanosheet at least partially covering a surface of the nanoparticle template.

11. The composition recited in claim 10, wherein: the nanoparticle template comprises a material having a first crystal structure; the two-dimensional (2D) transition metal dichalcogenide nanosheet comprises a material having a second crystal structure; and the first crystal structure and the second crystal structure exhibit therebetween a lattice mismatch of around 5% or less.

12. The composition recited in claim 11, wherein the lattice mismatch between the first crystal structure and the second crystal structure is around 3% or less.

13. The composition recited in claim 11, wherein the first crystal structure is hexagonal.

14. The composition recited in claim 10, wherein the nanoparticle template is a quantum dot.

15. The composition recited in claim 10, wherein the nanoparticle template is a ZnO nanoparticle.

16. The composition recited in claim 10, wherein the two-dimensional (2D) transition metal dichalcogenide nanosheet comprises MoS.sub.2, MoSe.sub.2 or WS.sub.2.

17. The composition recited in claim 10, wherein the two-dimensional (2D) transition metal dichalcogenide nanosheet is a two-dimensional (2D) transition metal dichalcogenide quantum dot.

18. The composition recited in claim 10, wherein the nanoparticle template is a metal nanoparticle or a polymer nanoparticle.

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING(S)

(1) FIG. 1 is a schematic diagram illustrating a process of template-assisted growth of 2D nanosheets according to one embodiment.

(2) FIG. 2 is a UV-vis absorption spectrum of ZnO nanoparticle templates (solid line) and of the substrate-bound MoS.sub.2 material of Example 1 (dashed line).

(3) FIG. 3 is a high-resolution transmission electron micrograph of ZnO templates.

(4) FIG. 4 is a Raman spectrum of the substrate-bound MoS.sub.2 material of Example 1 (grey line) and of the water-purified MoS.sub.2 material prepared in Example 1 (solid line).

(5) FIG. 5 is a high-resolution transmission electron micrograph of the substrate-bound MoS.sub.2 nanosheets prepared in Example 1.

(6) FIG. 6 is a UV-vis absorption spectrum and a photoluminescence (PL) spectrum of the crude exfoliated material of Example 1.

(7) FIG. 7 is UV-vis absorption (solid line) and PL (dashed line) spectra of the fraction of material extracted in Example 1 in water (bottom), acetonitrile (middle) and toluene (top).

(8) FIG. 8 is a transmission electron micrograph of the water-purified MoS.sub.2 material prepared in Example 1.

(9) FIG. 9 is a scatter graph of the quantum yield (QY) of the fraction of material of Example 1 extracted in water versus time when stored under N.sub.2 (circles), and with acidification (triangles).

(10) FIG. 10 is a single exponential fit of the time-resolved PL spectrum of acid-treated nanosheets, used to measure the PL lifetime.

(11) FIG. 11 presents a comparison of the UV-vis absorption spectra of fresh (as-extracted) and acidified nanosheets.

DETAILED DESCRIPTION OF THE INVENTION

(12) Herein, a template-assisted method of synthesis of 2D nanosheets is described wherein 2D nanosheets are grown on the surface of a substrate that acts as a template for nanosheet growth. The 2D nanosheets may then be released from the template surface, for example via chemical intercalation and exfoliation, and the templates may be reused. A process of template-assisted growth of 2D nanosheets according to certain embodiments is illustrated in FIG. 1.

(13) As used herein, the term 2D nanosheet is used to describe a particle having a thickness between 1 to 10 atomic or molecular monolayers, and wherein the lateral dimensions are greater than the thickness. The term nanoparticle is used to describe a particle with dimensions on the order of approximately 1 to 100 nm. The term quantum dot (QD) is used to describe a semiconductor nanoparticle displaying quantum confinement effects. The dimensions of QDs are typically, but not exclusively, between 1 to 20 nm. The terms nanoparticle and quantum dot are not intended to imply any restrictions on the shape of the particle. The term 2D nanoparticle is used to describe a particle with lateral dimensions on the order of approximately 1 to 100 nm and a thickness between 1 to 10 atomic or molecular layers, and wherein the lateral dimensions are greater than the thickness. The term 2D nanoflake is used to describe a particle with lateral dimensions on the order of approximately 1 to 100 nm and a thickness between 1 to 5 atomic or molecular monolayers.

(14) The shape and composition of the nanoparticle template are unrestricted. In one embodiment, the nanoparticle template comprises a semiconductor nanoparticle. In another embodiment, the nanoparticle template comprises a metal oxide nanoparticle. In another embodiment, the nanoparticle template comprises a metal nanoparticle. In another embodiment, the nanoparticle template comprises a polymer nanoparticle. In a particular embodiment, the nanoparticle template comprises a QD.

(15) Suitable template materials may include:

(16) semiconductor materials, such as, but not restricted to:

(17) Group 12-16 (II-VI) semiconductor materials, for example, ZnO, ZnS, ZnSe, ZnTe, CdS, CdSe, CdTe, HgS, HgSe, and HgTe;

(18) Group 13-15 (III-V) semiconductor materials, for example, BP, AlP, AlAs, AlSb, GaN, GaP, GaAs, GaSb, InN, InP, InAs, InSb, AlN, and BN;

(19) Group 13-14 (III-IV) semiconductor materials, for example, B.sub.4C, Al.sub.4C.sub.3, and Ga.sub.4C;

(20) Group 13-16 (III-VI) semiconductor materials, for example, Al.sub.2S.sub.3, Al.sub.2Se.sub.3, Al.sub.2Te.sub.3, Ga.sub.2S.sub.3, Ga.sub.2Se.sub.3, In.sub.2S.sub.3, In.sub.2Se.sub.3, Ga.sub.2Te.sub.3, and In.sub.2Te.sub.3; and

(21) Group 14-16 (IV-VI) semiconductor materials, for example, SnS, SnS.sub.2, SnSe, SnTe, PbS, PbSe, and PbTe;

(22) I-III-VI semiconductor materials, for example, CuInS.sub.2, CuInSe.sub.2, CuGaS.sub.2, CuGaSe.sub.2, AgInS.sub.2, and AgInSe.sub.2;

(23) and including doped derivatives and alloys thereof;

(24) metal nanoparticles, for example, Cu, Au, Ag, and Pt;

(25) oxide nanoparticles, for example, TiO.sub.2, SiO.sub.2, and ZrO.sub.2; and

(26) polymer nanoparticles, for example polytetrafluoroethylene (PTFE).

(27) Where an ALD coating is applied to the surface of the nanoparticles, the surface coating may be an inorganic material (e.g. Al.sub.2O.sub.3), an organic material (e.g. polyethylene glycol), or an inorganic-organic hybrid material (e.g. an aluminium alkoxide alucone polymer).

(28) In one embodiment, the nanosheet material to be made comprises a 2D layered material. Suitable examples include, but are not restricted to:

(29) graphene;

(30) graphene oxide, and reduced graphene oxide;

(31) transition metal dichalcogenides, for example, WO.sub.2, WS.sub.2, WSe.sub.2, WTe.sub.2, MnO.sub.2, MoO.sub.2, MoS.sub.2, MoSe.sub.2, MoTe.sub.2, NiO.sub.2, NiTe.sub.2, NiSe.sub.2, VO.sub.2, VS.sub.2, VSe.sub.2, TaS.sub.2, TaSe.sub.2, RuO.sub.2, RhTe.sub.2, PdTe.sub.2, HfS.sub.2, NbS.sub.2, NbSe.sub.2, NbTe.sub.2, FeS.sub.2, TiO.sub.2, TiS.sub.2, TiSe.sub.2, and ZrS.sub.2;

(32) transition metal trichalcogenides such as, for example, TaO.sub.3, MnO.sub.3, WO.sub.3, ZrS.sub.3, ZrSe.sub.3, HfS.sub.3, and HfSe.sub.3;

(33) Group 13-16 (III-VI) compounds such as, for example, InS, InSe, GaS, GaSe, and GaTe;

(34) Group 15-16 (IV-VI) compounds such as, for example, Bi.sub.2Se.sub.3, and Bi.sub.2Te.sub.3;

(35) nitrides, for example, h-BN;

(36) oxides, for example, LaVO.sub.3, LaMnO.sub.3, TiO.sub.2, MnO.sub.2, V.sub.2O.sub.5, TaO.sub.3, RuO.sub.2, MnO.sub.3, WO.sub.3, LaNbO.sub.7, Ca.sub.2Nb.sub.3O.sub.10, Ni(OH).sub.2, and Eu(OH).sub.2;

(37) layered copper oxides; micas; and bismuth strontium calcium copper oxide (BSCCO);

(38) phosphides, for example, Li.sub.7MnP.sub.4, and MnP.sub.4;

(39) silicene; germanene; and stanene.

(40) Within these materials, adjacent layers are held together by van der Waals interactions, which may readily be broken by techniques such as intercalation and exfoliation to remove the nanosheets from the template surface.

(41) A particular embodiment includes a method of synthesizing a 2D TMDC nanosheet on a nanoparticle template. In one embodiment, the nanoparticle template material has a hexagonal crystal structure and a low lattice mismatch to the nanosheet material so as to enable uniform monolayer growth of a nanosheet shell to proceed. Otherwise, excessive strain may give rise to defects or even entirely separate particle growth.

(42) In the case of MoS.sub.2, the lattice mismatch to hexagonal ZnO is about 3%. By controlling conditions carefully, monodisperse, wide band gap, ZnO nanoparticle core templates may be made and a monolayer of MoS.sub.2 epitaxially grown thereon providing luminescence due to the MoS.sub.2. By controlling the ZnO nanoparticle core size, the outer MoS.sub.2 size (and hence band gap) may consequently be controlled, thus providing a range of photoluminescence- (PL-) emitting core/shell structures. The as-formed nanosheets may be removed from the ZnO nanoparticle surface, leaving the ZnO nanoparticle templates to be reused.

(43) For the growth of MoS.sub.2, it is believed that curvature in the crystal lattice may lead to an indirect band gap. Therefore, in one embodiment, the 2D nanosheets are grown on nanopyramid-shaped nanoparticles, providing a flat surface for nanosheet growth. The growth of ZnO nanopyramids has previously been described by Chen et al. [Y. Chen, M. Kim, G. Lian, M. Johnson and X. Peng, J. Am. Chem. Soc., 2005, 127, 13331]

(44) Other 2D shell materials may be used in place of MoS.sub.2. Particular materials of interest are those with monolayer luminescence such as MoSe.sub.2, WS.sub.2 and WSe.sub.2. Other core structures or alloys may be chosen that have a similar crystal structure and low lattice mismatch such as GaN to MoS.sub.2.

(45) However, the shape of the template is not restricted to nanopyramids. In other embodiments, 2D nanosheets are grown on a template with a curved surface. Examples of suitable templates include spherical nanoparticles of semiconductor materials, or spherical nanoparticles of polymers such as polytetrafluoroethylene (PTFE). The use of a spherical template may assist in the lifting and removal of the as-formed nanosheet from the surface of the template.

(46) In a further embodiment, 2D nanosheets are grown on the surface of a template wherein the template comprises a layer of material deposited by atomic layer deposition (ALD). ALD provides highly conformal coatings, therefore a template with an ALD-coated surface may provide a highly uniform substrate for 2D nanosheet growth, leading to the synthesis of highly uniform, defect-free nanosheets.

(47) In one embodiment, the nanoparticle template comprises a material having a first crystal structure and the nanosheet comprises a material having a second crystal structure, wherein the first crystal structure and the second crystal structure have a small lattice mismatch. In one embodiment the lattice mismatch between the first crystal structure and the second crystal structure is around 5% or lower, for example, around 3% or lower. A small lattice mismatch may be desirable as this may help to facilitate epitaxial growth of the nanosheet on a surface of the template, and to prevent strain at the interface between the template and the 2D nanosheet.

(48) In one embodiment, the 2D nanosheets are 2D nanoflakes. In one embodiment, the 2D nanosheets are 2D QDs. QDs have widely been investigated for their unique optical, electronic and chemical properties, which originate from quantum confinement effects; as the dimensions of a semiconductor nanoparticle are reduced below twice the Bohr radius, the energy levels become quantized, giving rise to discrete energy levels. The band gap increases with decreasing particle size, leading to size-tunable optical, electronic and chemical properties, such as size-dependent photoluminescence. Moreover, it has been found that reducing the lateral dimensions of a 2D nanoflake into the quantum confinement regime may give rise to yet further unique properties, depending on both the lateral dimensions and the number of layers of the 2D nanoflake. In one embodiment, the lateral dimensions of the 2D nanoflakes may be in the quantum confinement regime, wherein the optical, electronic and chemical properties of the nanoflakes may be manipulated by changing their lateral dimensions. For example, metal chalcogenide monolayer nanoflakes of materials such as MoSe.sub.2 and WSe.sub.2 with lateral dimensions of approximately 10 nm or less may display properties such as size-tunable emission when excited. This can enable the electroluminescence maximum (EL.sub.max) or photoluminescence (PL.sub.max) of the 2D nanoflakes to be tuned by manipulating the lateral dimensions of the nanoflakes. As used herein, a 2D quantum dot or 2D QD refers to a semiconductor nanoparticle with lateral dimensions in the quantum confinement regime and a thickness between 1-5 atomic or molecular monolayers. As used herein, a single-layered quantum dot or single-layered QD refers to a semiconductor nanoparticle with lateral dimensions in the quantum confinement regime and a thickness of a single monolayer. Compared with conventional QDs, 2D QDs have a much higher surface area-to-volume ratio, which increases as the number of monolayers is decreased. The highest surface area-to-volume ratio is seen for single-layered QDs. This may lead to 2D QDs having very different surface chemistry from conventional QDs, which may be exploited for applications such as catalysis.

(49) By changing the dimensions of the template, the lateral dimensions of the nanosheet grown on the surface may be modified, thus allowing control over the emission wavelength of the nanosheets.

(50) The method of preparing the nanoparticle templates is unrestricted. The method of preparing the nanosheets on the template surface is unrestricted. In one embodiment, one or more nanosheet precursors are added to a solution of the templates under conditions to effect the conversion of the one or more nanosheet precursors to nanosheets on a surface of the templates. The as-formed nanosheets may subsequently be removed from the template surface and separated from the templates.

(51) The as-formed nanosheets may be removed from the template surface by any suitable technique. In one embodiment, the nanosheets are removed from the template surface by an intercalation and exfoliation process. Intercalation and exfoliation processes are well-known in the art and are described in Applicant's co-pending U.S. patent application Ser. No. 15/631,323, filed Jun. 23, 2017, which is hereby incorporated by reference in its entirety. An intercalation and exfoliation process typically involves the addition of an intercalating agent to a layered material to expand the inter-layer distance, followed by an exfoliation process to prize the layers apart. In one embodiment, the intercalation process comprises stirring the substrate-bound (template-nanosheet) material in the presence of one or more primary amines, for example, hexylamine and/or propylamine. In a further embodiment, the exfoliation process comprises stirring the intercalated substrate-bound (template-nanosheet) material in a solvent such as, but not restricted to, acetonitrile. In another embodiment, the nanosheets are removed from the template surface via ultrasonication.

(52) The nanosheets may be subsequently purified to separate them from the templates. Optionally, size-selective separation techniques may be used to isolate nanosheets having similar dimensions (and thus similar emissive properties). Non-limiting examples of size-selective separation techniques include: solvent polarity purification; size-selective precipitation; column chromatography; and dialysis.

(53) Surprisingly, it has been found that a post-treatment comprising an acidification step may increase the photoluminescence quantum yield (PLQY) of the nanosheets.

(54) Applications of nanosheets may include, but are not restricted to: photoluminescence applications; electroluminescence applications; photovoltaic applications; catalysis; sensors; heterostructure devices; and use in devices such as field-effect transistors and photodetectors. The nanosheets may also be surface-functionalized for use in biological applications, such as biological imaging.

Example 1: Template-Assisted Growth of MoS.SUB.2 .Nanosheets on ZnO Templates

(55) ZnO Template Synthesis

(56) 16 g octadecane and 0.506 g (0.8 mmol) zinc stearate were mixed and degassed at 105 C. for 1 hr. 4 g octadecane and 1.082 g (4 mmol) octadecanol were mixed in a vial and degassed for 1 hr at 100 C. In another vial 2 g octadecane and 0.2275 g (0.8 mmol) steric acid were mixed and degassed at 100 C. for 1 hr. Under nitrogen, the zinc stearate/octadecane mixture was heated to 280 C. The octadecanol/octadecane mixture was loaded into a syringe and quickly injected. The solution was left for 8 minutes. The steric acid/octadecane mixture was loaded into a syringe and injected after 8 minutes. The reaction was left for a further 2 hrs and then cooled to 80 C. 100 mL ethylacetate were added and the reaction centrifuged. 10 mL toluene were added and warmed to dissolve the solid. 20 mL methanol were added and the flocculate was collected by centrifugation. The solid was re-dissolved in toluene with warming and passed through a 0.2 m Teflon syringe filter.

(57) The UV-visible (UV-vis) absorption spectrum of the ZnO nanoparticle templates is shown in FIG. 2 (solid line). High-resolution transmission electron microscopy (FIG. 3) shows triangular-shaped nanoparticles suggestive of nanopyramids.

(58) Ligand Exchange

(59) 1 g hexadecylamine, 10 mL hexadecane and all of the ZnO cores were added to a freshly cleaned round-bottomed flask and degassed at 100 C. for 1 hr. The reaction was left at 110 C. overnight to enable ligand exchange. The next day the reaction was degassed a further 1 hr at 100 C.

(60) Substrate-Bound MoS.sub.2 Synthesis

(61) In a vial, 2 g hexadecylamine and 10 mL hexadecane were mixed and degassed at 100 C. for 1 hr. In a glovebox, a vial was loaded with 0.132 g Mo(CO).sub.6 then capped with a SUBA-SEAL rubber septum [SIGMA-ALDRICH CO., LLC, 3050 Spruce Street St. Louis Mich. 63103] and removed from the glovebox. The hexadecylamine/hexadecane mixture was loaded into a syringe and transferred to the Mo(CO).sub.6 vial. The Mo(CO).sub.6/hexadecylamine/hexadecane mixture was warmed to about 150 C. under nitrogen until a clear, dark yellow/orange solution formed. The ligand-exchanged ZnO cores were heated to 250 C. and 0.5 mL portions of the molybdenum precursor were added every 5 minutes until 5 mL in total were added. Then, 0.75 mL dodecanethiol was added over 40 minutes and left for 1.5 hrs when complete. Three lots of 2 mL portions of the molybdenum precursor were then added at 5 minute intervals to complete the molybdenum addition. 0.75 mL dodecanthiol was then added over 5 minutes and left for 45 minutes. The reaction was cooled to 60 C., then 80 mL acetone were added and centrifuged. The solid was redissolved in 25 mL hexane and stored under N.sub.2.

(62) The UV-vis absorption spectrum of the substrate-bound MoS.sub.2 material is shown in FIG. 2 (dashed line). The change in the UV-vis absorption spectrum compared to that of the ZnO templates is indicative of nanosheet growth on the template. FIG. 4 (grey line) shows the Raman spectrum of the substrate-bound MoS.sub.2 material. The peaks at 375 and 398 cm.sup.1 are in good accordance with the literature values for the E.sup.1.sub.2g and A.sub.1g bands of MoS.sub.2, respectively. High-resolution TEM (FIG. 5) shows the substrate-bound MoS.sub.2. The obscuring of the shape of the ZnO nanopyramids is indicative of nanosheet growth on the ZnO templates.

(63) Intercalation and Exfoliation

(64) The substrate-bound MoS.sub.2 sample was added to an N.sub.2-filled round-bottomed flask and to it was added 2 mL hexylamine and 10 mL propylamine, which was then stirred for 3 days. The mixture was dried using an N.sub.2 flow and to the solid under N.sub.2 was added 200 mL acetonitrile and stirred for 3 days. The supernatant was decanted and centrifuged and any solid discarded. The liquid was reduced to an oil, under reduced pressure at 30 C., on a rotary evaporator and then re-dissolved in 6 mL acetonitrile. The crude, exfoliated material was left in a vial, in air with the lid closed, for 6 days.

(65) The UV-vis absorption spectrum of the crude exfoliated material is shown in FIG. 6 (solid line). The PL spectrum of the crude exfoliated material (at two different excitation wavelengths: 360 nm and 450 nm) is also shown in FIG. 6 (dashed and dotted lines, respectively), revealing excitation wavelength-dependent PL.

(66) Solvent Polarity Purification

(67) The sample was dried back to an oil on a rotary evaporator and then 30 mL water were added. The sample was sonicated briefly and then passed through a 0.45 m polypropylene syringe filter. The water sample was flushed with N.sub.2 and stored in a glass vial. Residual solid retained on the filter and in the rotary evaporator flask was collected with acetonitrile and again passed through the same syringe filter. Residual solid that was not water- or acetonitrile-soluble was collected by the addition of toluene.

(68) The fraction of material extracted in water had a PLQY of 15.5%. The UV-vis and PL spectra of the fraction of material extracted in water are shown in FIG. 7 (bottom) as the solid and dashed lines, respectively. The Raman spectrum is shown in FIG. 4 (black line). The positions of the E.sup.1.sub.2g and A.sub.1g bands are relatively unchanged relative to those of the substrate-bound MoS.sub.2. A TEM image of the water-extracted nanosheets is shown in FIG. 8, which shows round (diameter 5 nm) nanosheets.

(69) The fraction of material extracted in acetonitrile (MeCN) had a PLQY of 3.7%. The UV-vis and PL spectra of the fraction of material extracted in acetonitrile are shown in FIG. 7 (middle) as the solid and dashed lines, respectively.

(70) The fraction of material extracted in toluene had a PLQY of 2.1%. The UV-vis and PL spectra of the fraction of material extracted in toluene are shown in FIG. 7 (top) as the solid and dashed lines, respectively.

(71) Surprisingly, the QY of the fraction of material extracted in water was found to increase over time when stored under N.sub.2, as shown in FIG. 9 (circles).

(72) Effect of Acidification

(73) A portion of the water-soluble fraction was acidified to a pH of 2-3 using concentrated HCl. The sample was flushed with N.sub.2 and stored inerted in a crimp vial. Surprisingly, the QY of the material was found to increase with acidification and time, as shown in FIG. 9 (triangles).

(74) The PL lifetime of the acidified material was measured using time-resolved photoluminescence. Using a single exponential fit (FIG. 10), the PL lifetime was measured at 9.8 ns. This is very close to the highest PL lifetime for chemically treated MoS.sub.2 reported in the literature (10.8 ns) [M. Amani, D.-H. Lien, D. Kiriya, J. Xiao, A. Azcatl, J. Noh, S. R. Medhvapathy, R. Addou, S. KC, M. Dubey, K. Cho, R. M. Wallace, S.-C. Lee, J. H. He, J. W. Ager III, X. Zhang, E. Yabonovitch and A. Javey, Science, 2015, 350, 1065] and several orders of magnitude longer than that of as-exfoliated MoS.sub.2, which is typically on the order of 100 ps.

(75) The UV-vis absorption profile of the acid-treated nanosheets was also more defined and slightly red-shifted compared to that of the as-extracted nanosheets, as shown in FIG. 11.

Example 2: Template-Assisted Growth of MoSe.SUB.2 .Nanosheets on ZnO Templates

(76) ZnO Template Synthesis

(77) ZnO templates were prepared according to Example 1.

(78) Ligand Exchange

(79) 1 g hexadecylamine, 10 mL hexadecane and all of the ZnO cores (in toluene) were added to a round-bottomed flask and degassed at 80 C. for 1 hr. The reaction was left at 110 C., under nitrogen, overnight to enable ligand exchange. The next day the reaction was degassed for a further 1 hr at 80 C.

(80) Substrate-Bound MoSe.sub.2 Synthesis

(81) In a vial, 2 g hexadecylamine and 10 ml hexadecane were mixed and degassed at 80 C. for 1 hr. In a glovebox, a vial was loaded with 0.132 g Mo(CO).sub.6 then capped with a SUBA-SEAL rubber septum and removed from the glovebox. The hexadecylamine/hexadecane mixture was added to the Mo(CO).sub.6 vial, under nitrogen. The Mo(CO).sub.6/hexadecylamine/hexadecane mixture was warmed to about 150 C., under nitrogen. The ligand-exchanged ZnO cores were heated to 250 C., under nitrogen, and 1 mL portions of the molybdenum precursor were added every 5 minutes until the complete solution had been added. Then, 2 g diphenyl diselenide dissolved in 5 mL toluene were added over 90 minutes, via a syringe pump, and left for 50 minutes at 250 C. when complete. The reaction was cooled to 60 C., then 80 mL acetone were added and centrifuged. The solid was washed with acetone and centrifuged, twice. The brown precipitate was dispersed in 25 mL hexane.

(82) Intercalation and Exfoliation

(83) The process was carried out under anaerobic conditions. The solution of substrate-bound MoSe.sub.2 in hexane was added to a nitrogen-filled flask containing 2 mL hexylamine and 10 mL propylamine. The mixture was stirred for 3 days. The reaction solution was evaporated under vacuum for 20 minutes, leaving a brown oil. 200 mL of degassed acetonitrile were added, then stirred for 3 days. The solution was filtered under nitrogen using a cannula filter, before evacuating under vacuum. The evacuated oil was redispersed in 6 mL acetonitrile, then stored in air for 6 days.

(84) Solvent Polarity Purification

(85) The acetonitrile supernatant was decanted, then water was added to the solids, followed by sonication for 5 minutes.

Example 3: Template-Assisted Growth of WS.SUB.2 .Nanosheets on ZnO Templates

(86) ZnO Template Synthesis

(87) ZnO templates were prepared according to Example 1.

(88) Ligand Exchange

(89) Ligand exchange was carried out according to Example 2.

(90) Substrate-Bound WS.sub.2 Synthesis

(91) In a vial, 2 g hexadecylamine and 10 ml hexadecane were mixed and degassed at 80 C. for 1 hr. In a glovebox, a vial was loaded with 0.176 g W(CO).sub.6 then capped with a SUBA-SEAL rubber septum and removed from the glovebox. The hexadecylamine/hexadecane mixture was added to the W(CO).sub.6 vial, under nitrogen. The W(CO).sub.6/hexadecylamine/hexadecane mixture was warmed to about 150 C., under nitrogen, resulting in a pale yellow solution. The ligand-exchanged ZnO cores were heated to 250 C., under nitrogen, while stirring, and 0.5 mL portions of the tungsten precursor were added every 5 minutes for 45 minutes (10 injections). 0.75 mL 1-dodecanthiol was added over 40 minutes using a syringe pump, then left for 90 minutes at 250 C. Three 2-mL portions of the tungsten precursor were then added at 5 minute intervals. 0.75 mL 1-dodecanethiol was added over 5 minutes using a syringe pump, then left at 250 C. for 45 minutes. The reaction was cooled to 60 C., then 80 mL acetone were added, followed by centrifugation. The solids were collected and re-dissolved in 25 mL hexane (bubbled with nitrogen).

(92) Intercalation and Exfoliation

(93) The solution of substrate-bound WS.sub.2 in hexane was added to a nitrogen-filled flask containing 2 mL hexylamine and 10 mL propylamine. The mixture was stirred for 3 days. The reaction solution was evaporated under vacuum for 20 minutes, leaving a brown oil. 200 mL of degassed acetonitrile were added, then stirred for 3 days. The solution was decanted and filtered through a 0.45 m syringe filter, before removing the solvent via rotary evaporation. 6 mL acetonitrile were added, then the solution was transferred to a vial and left in air for 7 days.

(94) Solvent Polarity Purification

(95) The solution in acetonitrile was dried back to an oil using a rotary evaporator. 30 mL water were added, then the sample was sonicated for 5 minutes. The solution was filtered through a 0.45 m syringe filter. The resulting colourless solution was degassed and retained as the water-soluble phase (PL.sub.max=431 nm; QY=15.7%). 15 mL acetonitrile was swirled in the rotary evaporator flask and passed through a syringe filter. The resulting orange solution was retained as the acetonitrile-soluble phase (PL.sub.max=435 nm; QY=6.7%). 15 mL toluene were swirled in the rotary evaporator flask and passed through a syringe filter. The pale yellow solution was retained as the toluene-soluble phase (PL.sub.max=427 nm; QY=2.3%).

(96) Advantages of the above-described method include:

(97) The method is scalable.

(98) The material produced has a high QY compared to 2D nanosheets produced by the methods of the prior art, which suggests a material having fewer defects and a higher degree of crystallinity.

(99) By controlling parameters including the template dimensions and size distribution, a narrow sheet size distribution may be achieved.

(100) Non-exfoliated material may be reused, resulting in a high reaction yield, thus avoiding material waste.

(101) The method provides a simple means colloidal 2D monolayer formation without chemical cutting or mechanical exfoliation. Narrower PL emission becomes possible without the extensive size selection operations that may be required for 2D monolayers made by other means. The nanoparticles may be made to be soluble in a range of different solvents.

(102) The foregoing presents particular embodiments of a system embodying the principles of the invention. Those skilled in the art will be able to devise alternatives and variations which, even if not explicitly disclosed herein, embody those principles and are thus within the scope of the invention. Although particular embodiments of the present invention have been shown and described, they are not intended to limit what this patent covers. One skilled in the art will understand that various changes and modifications may be made without departing from the scope of the present invention as literally and equivalently covered by the following claims.