WO2007106788A2

WO2007106788A2 - Precursor compositions for atomic layer deposition and chemical vapor deposition of titanate, lanthanate, and tantalate dielectric films

Info

Publication number: WO2007106788A2
Application number: PCT/US2007/063825
Authority: WO
Inventors: Chongying Xu; Tianniu Chen; Thomas M. Cameron; Jeffrey F. Roeder; Thomas H. Baum
Original assignee: Advanced Technology Materials, Inc.
Priority date: 2006-03-10
Filing date: 2007-03-12
Publication date: 2007-09-20
Also published as: KR20140139636A; EP1994555A4; US8784936B2; EP1994555A2; US8206784B2; WO2007106788A3; TW200801229A; US20120141675A1; JP2009529579A; US7638074B2; US20140295071A1; US20090074965A1; TWI421366B; KR20080113053A; KR20160027244A; US20100062150A1; JP2013093606A; US9534285B2; KR101488855B1

Abstract

Barium, strontium, tantalum and lanthanum precursor compositions useful for atomic layer deposition (ALD) and chemical vapor deposition (CVD) of titanate thin films. The precursors have the formula M(Cp)2, wherein M is strontium, barium, tantalum or lanthanum, and Cp is cyclopentadienyl, of the formula (I), wherein each of R1-R5 is the same as or different from one another, with each being independently selected from among hydrogen, C1-C12 alkyl, C1-C12 amino, C6-C10 aryl, C1-C12 alkoxy, C3-C6 alkylsilyl, C2-C12 alkenyl, R1R2R3NNR3, wherein R1, R2 and R3 may be the same as or different from one another and each is independently selected from hydrogen and C1-C6 alkyl, and pendant ligands including functional group(s) providing further coordination to the metal center M. The precursors of the above formula are useful to achieve uniform coating of high dielectric constant materials in the manufacture of flash memory and other microelectronic devices.

Description

PRECURSOR COMPOSITIONS FOR ATOMIC LAYER DEPOSITION AND

CHEMICAL VAPOR DEPOSITION OF TITANATE, LANTHANATE, AND

TANTALATE DIELECTRIC FILMS

BACKGROUND OF THE INVENTION Field of the Invention

[0001] The present invention relates to precursor compositions having utility for atomic layer deposition and chemical vapor deposition of titanate, lanthanate, and tantalate thin films, e.g., in the manufacture of microelectronic devices, as well as to processes of making and using such precursors, to products formed using such precursor compositions, and to precursor supply systems comprising such precursor compositions in packaged form.

Description of the Related Art

[0002] Strontium titanate (SrTiO₃), barium titanate (BaTiO₃) and barium strontium titanates (Ba_xSr^_xTiO₃ where 0 < x < 1) are high dielectric constant materials that are potentially useful in future generation flash memories as well as other microelectronic products. Lanthanum oxides (La₂O₃), lanthanum tantalates (La_xTa_yO_z where x, y, and z denote oxides of varying composition), and lanthanum titanates (e.g. LaTiO₃) represent another class of high dielectric constant materials potentially useful on future generation microelectronic devices. Uniform coating involving greater than 90% step coverage on high aspect ratio structures is required for such titanate materials to achieve requisite high capacity in flash memory device applications.

[0003] Atomic layer deposition (ALD) is currently being explored as a technique for achieving such step coverage, using strontium β-diketonates and titanium β-diketonates as precursors. It is difficult, however, to achieve satisfactory uniform coating of strontium titanate thin films using the β-diketonate precursors that have been developed to date. Similar deficiencies are encountered when chemical vapor deposition (CVD) is used as a deposition technique to form such titanate films. [0004] The art continues to seek new precursors for deposition of thin film titanates, lanthanates and tantalates such as strontium titanate, barium titanate, barium strontium titanate, lanthanum oxide, lanthanum tantalate, and lanthanum titanate.

SUMMARY OF THE INVENTION

[0005] The present invention relates to barium, strontium, tantalum and lanthanum precursors having utility for atomic layer deposition of titanate films useful in the manufacture of microelectronic devices such as flash memories. The invention further relates to methods of making and using such precursors, to supply systems for selective dispensing of such precursors, and to microelectronic device products fabricated with the use of such precursors. [0006] In one aspect, the present invention relates to precursors having the formula M(Cp)₂, wherein M is strontium or barium, precursors having the formula X₃M(Cp)₂ wherein M is tantalum and X is H or Si(R_a)₃, wherein each R_a can be the same as or different from the other(s), and each is independently selected from among Ci-C₆ alkyl and C₆-Ci₀ aryl; and precursors having the formula M(Cp)₃ wherein M is lanthanum, and wherein Cp is cyclopentadienyl, of the formula

wherein each of Ri-R₅ is the same as or different from one another, with each being independently selected from among hydrogen, C₁-C₁₂ alkyl, C₁-C₁₂ amino, C₆-Ci_O aryl, C₁-C₁₂ alkoxy, C₃-C₆ alkylsilyl, C₂-Ci₂ alkenyl (such term being intended to be broadly construed to include substituents containing linear, branched, and/or cyclic moieties containing ethylenic unsaturation, e.g., vinyl, allyl, cyclic -ene species, etc., and substituents containing various types of such moieties therein, e.g., tetramethylpentadienylvinyl), R¹R²R³NNR³, wherein R¹, R² and R³ may be the same as or different from one another and each is independently selected from hydrogen and Ci-C₆ alkyl, and pendant ligands including functional group(s) providing further coordination to the metal center, such as, for example, alkoxyalkyl, aryloxyalkyl, imidoalkyl, and acetylalkyl, wherein suitable groups in these classes include those of the following formulae:

aminoalkyls wherein: the methylene (-CH₂-) moiety could alternatively be another divalent hydrocarbyl moiety; each of R₁-R₄ is the same as or different from one another, with each being independently selected from among hydrogen and Ci-C₆ alkyl and C₆-Ci₀ aryl; each of R₅and R₆ is the same as or different from the other, with each being independently selected from among Ci-C₆ alkyl; n and m are each selected independently from 0 to 4 with the proviso that m and n cannot be 0 at the same time, and x is selected from 1 to 5;

alkoxyalkyls and aryloxyalkyls wherein each of R₁-R₄ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-C₆ alkyl, and C₆-Ci₀ aryl; R₅ is selected from among Ci-C₆ alkyl, and C₆-Ci₀ aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time;

imidoalkyl wherein each of Ri-R₆ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-C₆ alkyl, and C₆-Ci₀ aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time;

acetylalkyls wherein each of Ri-R₄ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-C₆ alkyl, and C₆-Ci₀ aryl; R₅ is selected from among Ci-C₆ alkyl, and C₆-Ci₀ aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time.

[0007] As used herein, the identification of a carbon number range, e.g., in Ci-C₆ alkyl or C₆-Ci₀ aryl, is intended to include each of the component carbon number moieties within such range. Accordingly, Ci-C₆ alkyl is intended to include methyl, ethyl, propyl, butyl, pentyl and hexyl, including a straight chain as well as branched groups of such types. It therefore is to be appreciated that identification of a carbon number range, e.g., Ci-C₆, as broadly applicable to a substituent moiety, enables, in specific embodiments of the invention, the carbon number range to be further restricted, as a sub-group of moieties having a carbon number range within the broader specification of the substituent moiety. By way of example, the carbon number range e.g., Ci-C₆ alkyl, maybe more restrictively specified, in particular embodiments of the invention, to encompass sub-ranges such as C₁-C₄ alkyl, C₂-C₆ alkyl, C₂-C₄ alkyl, C₃-C₅ alkyl, or any other sub-range within the broad carbon number range.

[0008] In another aspect, the invention relates to precursor composition, comprising such precursor in a solvent medium.

[0009] A further aspect of the invention relates to a method of forming a barium-, lanthanum- and/or strontium-containing material on a substrate, comprising contacting the substrate with a vapor of a precursor as described above, to deposit barium, lanthanum and/or strontium on the substrate from said vapor.

[0010] A still further aspect of the invention relates to an atomic layer deposition process for forming a barium, lanthanum and/or strontium titanate on a substrate, comprising:

(a) contacting the substrate with a titanium source under conditions producing a coating of titanium on the substrate;

(b) contacting the titanium-coated substrate with an oxidant or water to form a hydroxylated surface;

(c) contacting the hydroxylated surface with a barium, lanthanum and/or strontium precursor of the present invention, under conditions producing a coating of barium and/or strontium thereon;

(d) contacting the barium, lanthanum and/or strontium-coated substrate with an oxidant or water to form a hydroxylated surface; and

(e) repeating steps (a) through (d) for sufficient number of repetitions to produce a barium, lanthanum and/or strontium titanate film of predetermined thickness.

[0011] In another aspect, the invention relates to a barium, lanthanum and/or strontium supply package, comprising a vessel enclosing an interior volume holding a barium, lanthanum and/or strontium precursor as described above. [0012] A further aspect of the invention relates to an atomic layer deposition process, comprising pulsing of a vapor of a titanium precursor into a deposition reactor, purging the reactor to remove excess titanium precursor, pulsing water vapor into the reactor, optionally with an oxidant, pulsing a barium, lanthanum and/or strontium source into the reactor, purging the reactor to remove excess barium, lanthanum and/or strontium precursor, and pulsing water vapor into the reactor, optionally with an oxidant.

[0013] Additional aspects of the invention relate to forming strontium-, lanthanum- and/or barium-containing films on substrates using the precursors described above, involving the use of chemical vapor deposition or atomic layer deposition, e.g., contacting of a microelectronic device substrate with a vapor of a precursor of the invention.

[0014] Other aspects, features and embodiments of the invention will be more fully apparent from the ensuing disclosure and appended claims.

BRIEF DESCRIPTION OF THE DRAWINGS

[0015] Figure 1 is a schematic representation of an atomic layer deposition process utilizing a precursor of the present invention.

[0016] Figure 2 is a graph of thermal analysis data including thermogravimetric (TG) analysis and differential scanning calorimetry (DSC) data as a function of temperature, for

Ba[(N-Pr)Me₄Cp]₂ exhibiting a melting endotherm at 85.5°C and a residue of 10.88%.

[0017] Figure 3 is a graph of thermal analysis data of Sr(Cp*)₂ including TG and DSC data as a function of temperature, wherein Cp* is pentamethylcyclopentadienyl.

[0018] Figure 4 is a schematic representation of a material storage and dispensing package containing a barium, strontium or lanthanum precursor according to the present invention, in one embodiment thereof.

DETAILED DESCRIPTION OF THE INVENTION, AND PREFERRED EMBODIMENTS THEREOF [0019] The present invention relates to barium, strontium, tantalum and lanthanum precursors having utility for atomic layer deposition of titanate films useful in the manufacture of microelectronic devices such as flash memories. The invention further relates to methods of making and using such precursors, to supply systems for selective dispensing of such precursors, and to microelectronic device products fabricated with the use of such precursors. [0020] In a specific aspect, the present invention relates to precursors having the formula M(Cp)₂, wherein M is strontium or barium, precursors having the formula X₃M(Cp)₂ wherein M is tantalum and X is H or Si(R_a)₃, wherein each R_a can be the same as or different from the other(s), and each is independently selected from among Ci-C₆ alkyl and C₆-Ci₀ aryl; and precursors having the formula M(Cp)₃ wherein M is lanthanum, and wherein Cp is cyclopentadienyl of the formula

wherein each of Ri-R₅ is the same as or different from one another, with each being independently selected from among hydrogen, C₁-C₁₂ alkyl, C₁-C₁₂ amino, C₆-Ci_O aryl, C₁-C₁₂ alkoxy, C₃-C₆ alkylsilyl, C₂-Ci₂ alkenyl, R¹R²R³NNR³, wherein R¹, R² and R³ may be the same as or different from one another and each is independently selected from hydrogen and Ci-C₆ alkyl, and pendant ligands including functional group(s) providing further coordination to the metal center, such as, for example, aminoalkyl, alkoxyalkyl, aryloxyalkyl, imidoalkyl, and acetylalkyl, wherein suitable groups in these classes may for example include those of the following formulae:

aminoalkyls wherein each of R₁-R₄ is the same as or different from one another, with each being independently selected from among hydrogen and Ci-C₆ alkyl and C₆-Ci₀ aryl; each of R₅ and R₆ is the same as or different from the other, with each being independently selected from among Ci-C₆ alkyl; n and m are each selected independently from 0 to 4 with the proviso that m and n cannot be 0 at the same time, and x is selected from 1 to 5;

alkoxyalkyls and aryloxyalkyls wherein each of Ri-R₄ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-C₆ alkyl, and C₆-Ci_O aryl; Rs is selected from among Ci-C₆ alkyl, and C₆-Ci₀ aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time;

[0021] The foregoing precursors can be usefully employed with a suitable titanium precursor to form titanate films of barium, strontium, tantalum and/or lanthanum, e.g. by ALD, CVD or other suitable deposition process.

[0022] In one embodiment, wherein the precursor is Ba(Cp)₂, the precursor is used in a form that is not coordinated with any Lewis bases or other complexation agents, that is, without complexation with adduct-forming groups such as tetrahydrofuran, dienes, trienes, glymes, diglymes, triglymes, tetraglymes, etc.

[0023] Additionally, or alternatively, the R groups on the cyclopentadienyl rings of such Ba(Cp)₂ precursor may in specific embodiments be constituted to exclude the following substituent combinations as being identically present on each of the two cyclopentadienyl rings: (i) wherein R₁-R₅ are all methyl, (ii) wherein three of such R₁-R₅ substituents are isopropyl and the remaining two of such substituents are H, (iii) wherein three of such Ri-R₅ substituents are t-butyl and the remaining two of such substituents are H, (iv) wherein four of such R₁-R₅ substituents are methyl and the remaining substituent is (Me)₂NCH₂CH₂- , and (v) wherein four of such R₁-R₅ substituents are methyl and the remaining substituent is EtOCH₂CH₂- where Et is ethyl.

[0024] Correspondingly, the Sr(Cp)₂ precursor may be selected in specific embodiments wherein at least one of the following criteria are met: (a) the precursor is not coordinated with tetrahydrofuran, and (b) Ri-R₅ are selected to exclude the following substituent combinations as being identically present on each of the two cyclopentadienyl rings: (i) wherein R₁-R₅ are all methyl, and (ii) wherein three of such Ri-R₅ substituents are isopropyl and the remaining two of such substituents are H.

[0025] In another embodiment, the invention contemplates Sr(Cp)₂ compounds that are uncoordinated with any complexation agents.

[0026] In yet another embodiment, the precursor compounds of the invention may be stabilized with Lewis base ligands, subject to the exceptions stated in the preceding paragraphs.

Lewis bases suitable for such purpose include, without limitation, alkenes, dienes, cycloalkenes, cyclooctatetraenes, alkynes, substituted alkynes (symmetrical or asymmetrical), amines, diamines, triamines, tetraamines, polyamines, ethers, diglymes, triglymes, tetraglymes, tetramethyl sulfides, dialkylsulfides, ethylenediamine, vinyltrimethylsilane, allyltrimethylsilane, and pentamethyl diethylenetriamine.

[0027] In one embodiment, the cyclopentadienyl ligand includes a ligand formed according to the following reaction (wherein the second reactant and final ligand are represented with kappa (K) donor notation):

[0028] The precursors of the invention may be supplied in any suitable form for volatilization to produce the precursor vapor for deposition contacting with the substrate, e.g., in a liquid form that is vaporized or as a solid that is dissolved or suspended in a solvent medium for flash vaporization, as a sublimable solid, or as a solid having sufficient vapor pressure to render it suitable for vapor delivery to the deposition chamber, or in any other suitable form.

[0029] When solvents are employed for delivery of the precursors of the invention, any suitable solvent media can be employed in which the precursor can be dissolved or dispersed for delivery. By way of example, the solvent medium may be a single-component solvent or a multicomponent solvent mixture, including solvent species such as C₃-Ci₂ alkanes, C₂-Ci₂ ethers, Cβ-Ci₂ aromatics, C₇-C₁₆ arylalkanes, Cio-C₂₅ arylcyloalkanes, and further alkyl- substituted forms of aromatic, arylalkane and arylcyloalkane species, wherein the further alkyl substituents in the case of multiple alkyl substituents may be the same as or different from one another and wherein each is independently selected from Ci-C₈ alkyl. Particularly preferred solvents include alkanes, alkyl-substituted benzene compounds, benzocyclohexane (tetralin), alkyl-substituted benzocyclohexane and ethers, with tetrahydrofuran, xylene, 1,4- tertbutyl toluene, 1,3-diisopropylbenzene, tetralin, dimethyl tetralin, octane and decane being particularly preferred solvent species.

[0030] In instances where liquid delivery is employed in deposition processes of the invention to form deposited metal films, it may be preferable to utilize high boiling point solvents in order to avoid metal precursor deposits in the delivery system, such as in flow circuitry, and in vaporizers that are utilized to volatilize the metal precursor to form a corresponding precursor vapor, where the system is otherwise susceptible to solids deposition and clogging. For example, in delivery systems utilizing low boiling solvents for delivery of the precursor, e.g., a strontium precursor for liquid delivery atomic layer deposition, residual precursor of solution in the vaporizer and delivery lines will evaporate leaving behind solid precursor. Eventually such precursor builds up and clogs the delivery system. [0031] Accordingly, in various embodiments of the invention, it may be desirable to utilize high boiling aromatic solvents, e.g., aromatic solvents having a boiling point at 1 atmosphere pressure in a range of from about 140⁰C to about 250⁰C. For example, in liquid delivery strontium precursor applications for atomic layer deposition processes, suitable solvents may include xylene, 1,4-tertbutyltoluene, 1,3-diisopropylbenzene, tetralin, dimethyltetralin and other alkyl-substituted aromatic solvents.

[0032] In general, the precursor compositions of the invention may alternatively comprise, consist, or consist essentially of any of the components and functional moieties discloses herein, in specific embodiments of the invention.

[0033] The titanium precursors useful with the barium, strontium, tantalum and/or lanthanum precursors of the invention include those of the formula X₂TiCp₂, where Cp is the same as described above, and each X is independently selected from among chlorine, bromine, iodine, Ci-C₄ alkyl and Ci-C₄ alkoxy, dialkylamido (such as those of the formula RiR₂N-, where Ri and R₂ are independently selected from Ci-C₄ alkyls,) and cyclic alkylamido (such as those of the formula (CH₂)_yN-, where y is an integer selected from among 2, 3, 4, 5 and 6). [0034] Because both MCp₂ and X₂TiCp₂ are highly sensitive to hydroxyl-terminated surfaces, such precursors react readily to form respective self-limiting monolayers on substrate surfaces such as semiconductor wafers having free hydroxyl functionality thereon. MO and TiO₂ can be deposited sequentially from these precursors, and post-annealed to achieve various dielectrics, e.g., strontium titanate (STO) dielectrics, lanthanum titanate (LTO) dielectrics, barium titanate (BTO) dielectrics and barium strontium titanate (BSTO) dielectrics. [0035] The cyclopentadienyl precursors of the invention are particularly useful in atomic deposition layer processes, such as the illustrative process schematically represented in Figure 1.

[0036] As shown in Figure 1, a silicon substrate 10 is shown as having a noble metal electrode 12 thereon (Step 1). This structure then is subjected to contact with titanium precursor of the formula TiR₂X₂ under suitable deposition conditions to form a structure (Step 2) in which the noble metal electrode 10 is functionalized on its upper surface with titanium moieties. The thus-functionalized structure then is submitted to contact with an oxidant [O] such as oxygen, ozone, etc., or water. A wide variety of oxidants can be used for such purpose.

The surface then reacts with the oxidant to form a hydroxylated surface (Step 3).

[0037] The hydroxylated surface of the device structure next is contacted with the strontium reagent, Sr(Cp)_2, to yield the strontiated (strontium-functionalized) surface (Step 4).

The strontiated surface then is contacted with oxidant or water to form the hydroxylated surface

(Step 5), and the hydroxylated surface thereafter is processed by contact with the titanium precursor, with repetition of the above-described steps (Steps 2-5) any suitable number of times to build up a layer 14 of strontium titanate, SrTiC>₃ (Step 6).

[0038] In this repetitive manner, a dielectric film of strontium titanate is built up over the electrode layer in the device structure, with the deposition process being conducted through multiple steps of titanium functionalization, hydroxylation, strontiation and hydroxylation, to build up the strontium titanate film to a desired thickness.

[0039] Analogous processes can be carried out utilizing alternating layers of Ba, Sr, and

Ti, Ba and Sr mixtures and Ti, La and Ta, and La and Ti.

[0040] In one embodiment of such process, the oxidant is selected from among oxygen, ozone and oxygen plasma. The use of such oxidant may eliminate the need for a final annealing step, such as rapid thermal annealing.

[0041] In general, the thickness of the titanate layer in the practice of the present invention can be of any suitable value. In a specific embodiment of the invention, the thickness of the titanate layer can be in a range of from 5 nm to 500 nm or more.

[0042] The titanium precursors usefully employed in the broad practice of the invention can be of any suitable type, and include, without limitation, the aforementioned Cp₂TiX₂, as well as titanium alkoxides, Ti(OR)₄, such as Ti(OPr-i)₄ and Ti(OBu-t)_4> and titanium beta- diketonate alkoxides, Ti(β-diketonate)₂(OR)₂, such as Ti(thd)₂(OPr-i)₂ and Ti(thd)₂(OBu-t)₂.

[0043] One preferred reagent for forming a titanate film is B a[(n-Pr) Me₄Cp]₂. Figure 2 is a graph of thermal analysis data including thermogravimetric (TG) analysis and differential scanning calorimetry (DSC) data, as a function of temperature, for Ba[(n-Pr)Me₄Cp]₂, exhibiting a melting endotherm at 85.5°C and a residue of 10.88%.

[0044] Another preferred strontium precursor in the practice of the present invention is bis(pentamethylcyclopentadienyl) strontium. Figure 3 is a graph of thermal analysis data including TG and DSC data as a function of temperature, for Sr(Cp*)₂, wherein Cp* is pentamethylcyclopentadienyl.

[0045] The strontium, lanthanum, tantalum and barium precursors of the invention may be provided in any suitable packaged form, as appropriate to storage of the precursor and its subsequent delivery in use. In one embodiment, the precursor package comprises a vessel defining a closed interior volume holding the precursor, with the vessel having a valve head assembly connected thereto. The valve head assembly may include a manual or automatic valve controller, to modulate the position of a valve element in the value head assembly, between a fully opened and a fully closed position, as required for storage and dispensing use of the package.

[0046] In general, the precursor may be provided in a form appropriate for delivery and use, e.g., in a form for liquid delivery or alternatively for solid precursor delivery of vapor.

[0047] Figure 4 is a schematic representation of a material storage and dispensing package

100 containing a barium, strontium, tantalum or lanthanum precursor, according to one embodiment of the present invention.

[0048] The material storage and dispensing package 100 includes a vessel 102 that may for example be of generally cylindrical shape as illustrated, defining an interior volume 104 therein. In this specific embodiment, the barium or strontium precursor is a solid at ambient temperature conditions, and such precursor may be supported on surfaces of the trays 106 disposed in the interior volume 104 of the vessel, with the trays having flow passage conduits

108 associated therewith, for flow of vapor upwardly in the vessel to the valve head assembly, for dispensing in use of the vessel.

[0049] The solid precursor can be coated on interior surfaces in the interior volume of the vessel, e.g., on the surfaces of the trays 106 and conduits 108. Such coating may be effected by introduction of the precursor into the vessel in a vapor form from which the solid precursor is condensed in a film on the surfaces in the vessel. Alternatively, the precursor solid may be dissolved or suspended in a solvent medium and deposited on surfaces in the interior volume of the vessel by solvent evaporation. For such purpose, the vessel may contain substrate articles or elements that provide additional surface area in the vessel for support of the precursor film thereon.

[0050] As a still further alternative, the solid precursor may be provided in granular or finely divided form, which is poured into the vessel to be retained on the top supporting surfaces of the respective trays 106 therein.

[0051] The vessel 102 has a neck portion 109 to which is joined the valve head assembly 110. The valve head assembly is equipped with a hand wheel 112 in the embodiment shown. The valve head assembly 110 includes a dispensing port 114, which may be configured for coupling to a fitting or connection element to join flow circuitry to the vessel. Such flow circuitry is schematically represented by arrow A in Figure 4, and the flow circuitry may be coupled to a downstream ALD or chemical vapor deposition chamber (not shown in Figure 4). [0052] In use, the vessel 102 is heated, such input of heat being schematically shown by the reference arrow Q, so that solid precursor in the vessel is at least partially volatilized to provide precursor vapor. The precursor vapor is discharged from the vessel through the valve passages in the valve head assembly 110 when the hand wheel 112 is translated to an open valve position, whereupon vapor deriving from the precursor is dispensed into the flow circuitry schematically indicated by arrow A.

[0053] In lieu of solid delivery of the precursor, the precursor may be provided in a solvent medium, forming a solution or suspension. Such precursor-containing solvent composition then may be delivered by liquid delivery and flash vaporized to produce a precursor vapor. The precursor vapor is contacted with a substrate under deposition conditions, to deposit the metal, e.g., strontium, barium, tantalum and/or lanthanum, on the substrate as a film thereon. [0054] In one embodiment, the precursor is dissolved in an ionic liquid medium, from which precursor vapor is withdrawn from the ionic liquid solution under dispensing conditions.

[0055] As a still further alternative, the precursor may be stored in an adsorbed state on a suitable solid-phase physical adsorbent storage medium in the interior volume of the vessel. In use, the precursor vapor is dispensed from the vessel under dispensing conditions involving desorption of the adsorbed precursor from the solid-phase physical adsorbent storage medium.

[0056] Supply vessels for precursor delivery may be of widely varying type, and may employ vessels such as those commercially available from ATMI, Inc. (Danbury, Connecticut) under the trademarks SDS, SAGE, VAC, VACSorb, and ProE-Vap, as may be appropriate in a given storage and dispensing application for a particular precursor of the invention.

[0057] The precursors of the invention thus may be employed to form precursor vapor for contacting with a substrate to deposit a thin film of barium, strontium, tantalum or lanthanum thereon, in connection with concurrent or sequential deposition of titanium from a suitable titanium source reagent, to produce titanate films as barium titanate, lanthanum titanate, tantalum titanate, strontium titanate, and barium strontium titanate.

[0058] In a preferred aspect, the invention utilizes the barium, strontium, tantalum and/or lanthanum precursors to conduct atomic layer deposition in connection with the use of a suitable titanium source reagent, yielding ALD films of superior high dielectric character that are uniformly coated on the substrate with high step coverage even on high aspect ratio structures.

[0059] Accordingly, the barium, strontium, tantalum and lanthanum precursors of the present invention enable a wide variety of microelectronic devices, e.g., semiconductor products, flat panel displays, etc., to be fabricated with high dielectric constant titanate films of superior quality.

[0060] The features and advantages of the invention are more fully shown by the following non-limiting example.

[0061] Example 1 [0062] In the synthesis of bis(pentamethylcyclopentadienyl)strontium ((Cp*)₂Sr), potassium pentamethylcyclopentadiene (KCp*, 5.11 grams, 29.29 mmol) was added to a stirred suspension of strontium diiodide (SrI₂, 5.00 grams, 14.64 mmol) in 300 ml of diethyl ether. The mixture was stirred for 48 hours, filtered, and concentrated in vacuo giving 4.10 grams of the bis(pentamethylcyclopentadienyl)strontium diethyl ether adduct ((Cp*)₂Sr(OEt₂)). The coordinated diethyl ether was removed by a toluene reflux process. In a typical, but non-limiting example, 3.00 grams of (Cp*)₂Sr(OEt₂) were dissolved in 150 ml of toluene. The toluene solution was heated to 110 ⁰C and the toluene/diethyl ether removed slowly in vacuo giving an off yellow solid. This process was repeated three more times to give the ether free (Cp*)₂Sr. High purity (Cp*)₂Sr can be obtained by sublimation at 120-130 ⁰C. [0063] An atomic layer deposition process is carried out as generally schematically shown in Figure 1, in which the process involves pulsing of a titanium source into the deposition reactor, purging the reactor to remove excess titanium precursor, then pulsing water vapor into the reactor, with or without oxidant (such as O₂, O₃ or N₂O,) followed by pulsing the strontium source into the reactor and then purging, followed by introduction of water vapor with or without oxidant. This process is repeated until a desired film thickness of the strontium titanate layer is reached. Deposition temperature is advantageously in a range of from 250⁰C to 500⁰C. Pulse rates can be on the order from 10 milliseconds to 30 seconds or more. After deposition, the film may require rapid thermal annealing (RTA) to obtain a crystalline SrTiO₃ film, by RTA treatment at temperature in a range of from 500⁰C to 900⁰C, for an annealing period of from a few seconds to 30 minutes or more. An oxygen plasma may be used in the reactant step, in addition to or in lieu of the forgoing annealing treatment.

[0064] Corresponding synthesis can be carried out to form other cyclopentadienyl compounds of the invention, e.g., tantalum compounds.

[0065] While the invention has been disclosed herein with respect to particular illustrative embodiments, aspects and features, it will be recognized that the invention is not thus limited, but rather extends to and encompasses other variations, modifications and alternative embodiments, as will readily suggest themselves to those of ordinary skill in the art based on the disclosure herein. Accordingly, the claims set out hereinafter are intended to be construed to encompass all such variations, modifications and alternative embodiments, as being within the spirit and scope of such claims.

Claims

THE CLAIMS What is claimed is:

1. A precursor selected from among precursors having the formula M(Cp)₂, wherein M is strontium or barium, precursors having the formula X₃M(Cp)₂ wherein M is tantalum and X is H or Si(R_a)₃, wherein each R_a can be the same as or different from the other(s), and each is independently selected from among Ci-C₆ alkyl and C₆-Ci_O aryl; and precursors having the formula M(Cp)₃ wherein M is lanthanum, and wherein Cp is cyclopentadienyl of the formula

wherein each of R₁-R₅ is the same as or different from one another, with each being independently selected from among hydrogen, C_rCi₂ alkyl, C_rCi₂ amino, C₆-Ci₀ aryl, C_rCi₂ alkoxy, C₃-C₆ alkylsilyl, C₂-Ci₂ alkenyl, R¹R²R³NNR³, wherein R¹, R² and R³ may be the same as or different from one another and each is independently selected from hydrogen and Ci-C₆ alkyl, and pendant ligands including functional group(s) providing further coordination to the metal center M.

2. The precursor of claim 1, wherein M is barium.

3. The precursor of claim 1, wherein M is strontium.

4. The precursor of claim 1, wherein M is lanthanum.

5. The precursor of claim 1, wherein M is tantalum.

6. The precursor of claim 1, comprising Ba[(n-Pr)Me₄Cp]₂.

7. The precursor of claim 1, comprising bis(pentamethylcyclopentadienyl) strontium.

8. The precursor of claim 1, wherein said pendant ligands include a ligand selected from the group consisting of aminoalkyl, alkoxyalkyl, aryloxyalkyl, imidoalkyl, and acetylalkyl.

9. The precursor of claim 1, wherein said pendant ligands include a ligand selected from the group consisting of:

(A) aminoalkyls of the following formulae:

wherein each of R₁-R₄ is the same as or different from one another, with each being independently selected from among hydrogen and Ci-C₆ alkyl and C₆-Ci_O aryl; each of Rsand R₆ is the same as or different from the other, with each being independently selected from among Ci-C₆ alkyl; n and m are each selected independently from 0 to 4 with the proviso that m and n cannot be 0 at the same time, and x is selected from 1 to 5;

(B) alkoxyalkyls and aryloxyalkyls of the following formulae:

wherein each of R₁-R₄ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-C₆ alkyl, and C₆-Ci_O aryl; R₅ is selected from among Ci-C₆ alkyl, and C₆-Ci₀ aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time;

(C) imidoalkyl of the formula:

wherein each of Ri-R₆ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-C₆ alkyl, and C₆-Ci_O aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time;

(D) acetylalkyls of the formula:

wherein each of R₁-R₄ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-C₆ alkyl, and C₆-Ci₀ aryl; R₅ is selected from among Ci-C₆ alkyl, and C₆-Ci₀ aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time.

10. The precursor of claim 1, wherein said pendant ligands include -CH₂-CH₂-N(CHs)₂.

11. A precursor composition, comprising the precursor of claim 1 in a solvent medium.

12. A solid precursor as claimed in claim 1.

13. A method of forming a metal-containing material on a substrate, wherein the metal is selected from among barium, strontium, tantalum and lanthanum, said method comprising contacting the substrate with a vapor of a precursor as claimed in claim 1, to deposit said metal on the substrate from said vapor.

14. The method of claim 13, comprising atomic layer deposition of barium, strontium and/or lanthanum on the substrate.

15. The method of claim 14, wherein said atomic layer deposition further comprises deposition of titanium or tantalum on said substrate from a titanium or tantalum precursor.

16. The method of claim 15, wherein the titanium or tantalum precursor comprises a precursor of the formula X₂TiCp₂, where Cp is cyclopentadienyl, of the formula

wherein each of Ri-R₅ is the same as or different from one another, with each being independently selected from among hydrogen, C₁-C₁₂ alkyl, C₁-C₁₂ amino, C₆-Ci_O aryl, C₁-C₁₂ alkoxy, C₃-C₆ alkylsilyl, C₂-C_n alkenyl, R¹R²R³NNR³, wherein R¹, R² and R³ may be the same as or different from one another and each is independently selected from hydrogen and Ci-C₆ alkyl, and pendant ligands including functional group(s) providing further coordination to the metal center M, and each X is independently selected from among chlorine, bromine, iodine, Ci-C₄ alkyl, Ci-C₄ alkoxy, dialkylamido and cyclic alkylamido.

17. The method of claim 16, wherein X is selected from among dialkylamido of the formula RiR₂N-, where Ri and R₂ are independently selected from Ci-C₄ alkyls, and cyclic alkylamido of the formula (CH₂)_yN-, where y is an integer selected from among 2, 3, 4, 5 and 6.

18. The method of claim 15, wherein the titanium or tantalum precursor comprises a precursor selected from the group consisting of titanium alkoxides and titanium beta-diketonate alkoxides.

19. The method of claim 15, wherein the titanium or tantalum precursor comprises a titanium precursor selected from the group consisting of Ti(OPr-i)₄, Ti(OBu-t)₄ (Ti(thd)₂(OPr-i)₂ and Ti(thd)₂(OBu-t)₂.

20. The method of claim 15, wherein the titanium or tantalum precursor comprises a tantalum precursor of the formula X₃TaCp₂, where Cp is cyclopentadienyl, of the formula

wherein each of Ri-R₅ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-Ci₂ alkyl, Ci-Ci₂ amino, C₆-Ci₀ aryl, C_rCi₂ alkoxy, C₃-C₆ alkylsilyl, C₂-Ci₂ alkenyl, R¹R²R³NNR³, wherein R¹, R² and R³ may be the same as or different from one another and each is independently selected from hydrogen and Ci-C₆ alkyl, and pendant ligands including functional group(s) providing further coordination to the metal center M, and each X is independently selected from among hydrogen, chlorine, bromine, iodine, Ci-C₄ alkyl, Ci-C₄ alkoxy, dialkylamido and cyclic alkylamido.

21. The method of claim 15, wherein the titanium or tantalum precursor comprises a tantalum precursor having the formula Ta(RiR₂N)₅ wherein Ri and R₂ are independently selected from among Ci-C₄ alkyls, and cyclic alkylamido of the formula (CH₂)_yN-, wherein y is an integer selected from among 2, 3, 4, 5 and 6.

22. The method of claim 15, wherein the titanium or tantalum precursor comprises a tantalum precursor selected from the group consisting of tantalum alkoxides and tantalum beta- diketonate alkoxides.

23. The method of claim 15, wherein the titanium or tantalum precursor comprises a precursor selected from the group consisting of Ta(OPr-i)₅, Ta(OBu-t)₅ Ta(thd)(OPr-i)₄ and Ta(thd)(EtO)₄.

24. The method of claim 15, wherein said substrate comprises hydroxyl functional groups thereon.

25. The method of claim 15, wherein said substrate comprises a semiconductor substrate.

26. The method of claim 15, wherein the metal-containing material on the substrate comprises a barium and/or strontium titanate.

27. The method of claim 26, wherein said barium and/or strontium titanate comprises a titanate selected from the group consisting of strontium titanate, barium titanate and barium strontium titanate.

28. The method of claim 16, wherein said pendant ligands include a ligand selected from the group consisting of aminoalkyl, alkoxyalkyl, aryloxyalkyl, imidoalkyl, and acetylalkyl.

29. The method of claim 16, wherein said pendant ligands include a ligand selected from the group consisting of:

(A) aminoalkyls of the following formulae:

wherein each of R₁-R₄ is the same as or different from one another, with each being independently selected from among hydrogen and Ci-Cβ alkyl and Cβ-Cio aryl; each of Rsand Re is the same as or different from the other, with each being independently selected from among Ci-C₆ alkyl; n and m are each selected independently from 0 to 4 with the proviso that m and n cannot be 0 at the same time, and x is selected from 1 to 5;

(B) alkoxyalkyls and aryloxyalkyls of the following formulae:

- . c i ) A-i4 \-C i -) /—m O R₅ ³

R₂ R₄ wherein each of R₁-R₄ is the same as or different from one another, with each being independently selected from among hydrogen, C₁-C₆ alkyl, and C₆-C₁₀ aryl; R₅ is selected from among C₁-C₆ alkyl, and C₆-C₁₀ aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time;

(C) imidoalkyl of the formula:

wherein each of R₁-R₆ is the same as or different from one another, with each being independently selected from among hydrogen, C₁-C₆ alkyl, and C₆-C₁₀ aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time;

(D) acetylalkyls of the formula:

wherein each of R₁-R₄ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-C₆ alkyl, and C₆-Ci_O aryl; R₅ is selected from among Ci-C₆ alkyl, and C₆-Ci₀ aryl; and n and m are selected independently from 0 to 4, with the proviso that m and n cannot be 0 at the same time.

30. The method of claim 26, wherein said barium and/or strontium titanate is deposited on a silicon substrate.

31. The method of claim 26, wherein said barium and/or strontium titanate is deposited on a semiconductor substrate.

32. The method of claim 26, as conducted in a method of fabricating a semiconductor device.

33. The method of claim 32, wherein said semiconductor device comprises a flash memory device.

34. An atomic layer deposition process for forming a barium, lanthanum and/or strontium titanate on a substrate, comprising:

(b) contacting the titanium-coated substrate with an oxidant or water to form a hydroxylated surface; (c) contacting the hydroxylated surface with a barium, lanthanum and/or strontium precursor as claimed in claim 1, under conditions producing a coating of barium, lanthanum and/or strontium thereon;

35. The process of claim 34, wherein said predetermined thickness is in a range of from 5 nm to 500 nm.

36. A precursor supply package, comprising a vessel enclosing an interior volume holding a precursor as claimed in claim 1.

37. The package of claim 36, wherein the precursor is in a solid form.

38. The package of claim 36, wherein the precursor is in a liquid form.

39. The package of claim 36, wherein the vessel interior volume contains surface-adding structure therein.

40. The package of claim 39, wherein said surface-adding structure includes trays.

41. The package of claim 36, wherein the interior volume of the vessel holds support articles on which the precursor is supported.

42. The package of claim 36, wherein said precursor is contained in the vessel in a particulate form.

43. The package of claim 36, wherein said precursor is contained in the vessel in the form of a coating on a support structure.

44. The package of claim 36, wherein said precursor is contained in the vessel in a solvent solution or suspension.

45. The package of claim 36, wherein said precursor is contained in the vessel in an ionic liquid medium.

46. The package of claim 36, wherein said precursor is contained in the vessel in an adsorbed state on a solid-phase physical adsorbent.

47. An atomic layer deposition process, comprising pulsing of a vapor of a titanium precursor into a deposition reactor, purging the reactor to remove excess titanium precursor, pulsing water vapor into the reactor, optionally with an oxidant, pulsing a barium, lanthanum and/or strontium source into the reactor, purging the reactor to remove excess barium, lanthanum and/or strontium precursor, and pulsing water vapor into the reactor, optionally with an oxidant.

48. The process of claim 47, wherein said pulsing and purging steps are carried out in a repetitive cycle.

49. The process of claim 47, conducted at temperature in a range of from 250⁰C to 500⁰C.

50. The process of claim 47, wherein said pulsing steps are carried out for a period of time in a range of from 10 milliseconds to 30 seconds.

51. The process of claim 47, further comprising rapid thermal annealing at temperature in a range of from 500⁰C to 900⁰C, for an annealing period of up to 30 minutes.

52. The process according to claim 47, wherein said pulsing water vapor is accompanied by said oxidant.

53. The process according to claim 52, wherein said oxidant comprises oxidant selected from the group consisting of oxygen, ozone and oxygen plasma.

54. The process according to claim 47, wherein the barium, lanthanum and/or strontium source comprises a precursor having the formula M(Cp)₂, wherein M is strontium or barium, and Cp is cyclopentadienyl, of the formula

wherein each of R₁-R₅ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-Ci₂ alkyl, Ci-Ci₂ amino, C₆-Ci₀ aryl, C_rCi₂ alkoxy, C₃-C₆ alkylsilyl, C₂-Cj₂ alkenyl, R¹R²R³NNR³, wherein R¹, R² and R³ may be the same as or different from one another and each is independently selected from hydrogen and Ci-C₆ alkyl, and pendant ligands including functional group(s) providing further coordination to the metal center M.

55. A chemical vapor deposition process, comprising contacting a substrate with vapor of a barium and/or strontium precursor, and with vapor of a titanium precursor, under vapor deposition conditions, to form a layer of barium and/or strontium titanate on the substrate, wherein said barium and/or strontium precursor has the formula M(Cp)₂, wherein M is barium or strontium, and Cp is cyclopentadienyl, of the formula

wherein each of Ri-R₅ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-Ci₂ alkyl, Ci-Ci₂ amino, C₆-Ci₀ aryl, C_rCi₂ alkoxy, C₃-C₆ alkylsilyl, C₂-C₁₂ alkenyl, R¹R²R³NNR³, wherein R¹, R² and R³ may be the same as or different from one another and each is independently selected from hydrogen and Ci-C₆ alkyl, and pendant ligands including functional group(s) providing further coordination to the metal center M.

56. The precursor of claim 1, wherein M is barium and the precursor is not coordinated with any complexation agents.

57. The precursor of claim 1, wherein M is barium and the precursor is not coordinated with any Lewis bases.

58. The precursor of claim 1, wherein M is barium and the precursor is uncoordinated with any of tetrahydrofuran, dienes, trienes, glymes, diglymes, triglymes, and tetraglymes.

59. The precursor of claim 1, wherein M is barium and Ri-R₅ are selected to exclude the following substituent combinations as being identically present on each of the two cyclopentadienyl rings: (i) wherein Ri-R₅ are all methyl, (ii) wherein three of such Ri-R₅ substituents are isopropyl and the remaining two of such substituents are H, (iii) wherein three of such Ri-R₅ substituents are t-butyl and the remaining two of such substituents are H, (iv) wherein four of such R₁-R₅ substituents are methyl and the remaining substituent is (Me)₂NCH₂CH₂- , and (v) wherein four of such Ri-R₅ substituents are methyl and the remaining substituent is EtOCH₂CH₂- where Et is ethyl.

60. The precursor of claim 1, wherein M is barium, as complexed with a Lewis base, subject to the proviso that R₁-R₅ are selected to exclude the following substituent combinations as being identically present on each of the two cyclop entadienyl rings: (i) wherein Ri-R₅ are all methyl, (ii) wherein three of such R_rR₅ substituents are isopropyl and the remaining two of such substituents are H, (iii) wherein three of such Ri-R₅ substituents are t-butyl and the remaining two of such substituents are H, (iv) wherein four of such R_rR₅ substituents are methyl and the remaining substituent is (Me)₂NCH₂CH₂- , and (v) wherein four of such Ri-R₅ substituents are methyl and the remaining substituent is EtOCH₂CH₂- where Et is ethyl.

61. The precursor of claim 1, wherein M is barium, and at least one of the following conditions is satisfied: (1) the precursor is not coordinated with any Lewis bases, and (2) R_rR₅ are selected to exclude the following substituent combinations as being identically present on each of the two cyclopentadienyl rings: (i) wherein Ri-R₅ are all methyl, (ii) wherein three of such Ri-R₅ substituents are isopropyl and the remaining two of such substituents are H, (iii) wherein three of such R_rR₅ substituents are t-butyl and the remaining two of such substituents are H, (iv) wherein four of such Ri-R₅ substituents are methyl and the remaining substituent is (Me)₂NCH₂CH₂- , and (v) wherein four of such R_rR₅ substituents are methyl and the remaining substituent is EtOCH₂CH₂- where Et is ethyl.

62. The precursor of claim 1, wherein M is strontium, and at least one of the following conditions is satisfied: (a) the precursor is not coordinated with tetrahydrofuran, and (b) Ri-R₅ are selected to exclude the following substituent combinations as being identically present on each of the two cyclopentadienyl rings: (i) wherein Ri-R₅ are all methyl, and (ii) wherein three of such Ri-R₅ substituents are isopropyl and the remaining two of such substituents are H.

63. The precursor of claim 1, wherein M is strontium, and the precursor is stabilized with a Lewis base.

64. The precursor of claim 1, in a solvent medium selected from among alkanes and ethers.

65. The precursor of claim 64, wherein the solvent medium comprises tetrahydrofuran.

66. The precursor of claim 64, wherein the solvent medium comprises octane.

67. The precursor of claim 64, wherein the solvent medium comprises decane.

68. The precursor of claim 1, wherein M is strontium, and the precursor is not coordinated with any complexation agents.

69. The precursor of claim 1, comprising La(Cp)₃, wherein Cp is cyclopentadienyl, of the formula

wherein each of R₁-R₅ is the same as or different from one another, with each being independently selected from among hydrogen, Ci-Ci₂ alkyl, Ci-Ci₂ amino, C₆-Ci₀ aryl, C_rCi₂ alkoxy, C₃-C₆ alkylsilyl, C₂-Ci₂ alkenyl, R¹R²R³NNR³, wherein R¹, R² and R³ may be the same as or different from one another and each is independently selected from hydrogen and Ci -Ce alkyl, and pendant ligands including functional group(s) providing further coordination to La.

70. A method of forming a La-containing material on a substrate, comprising contacting the substrate with vapor of the precursor as claimed in claim 69.

71. The method of claim 70, comprising chemical vapor deposition or atomic layer deposition of said La-containing material on said substrate.

72. The method of claim 70, wherein said La-containing material comprises La titanate.

73. A method of manufacturing a microelectronic device, comprising contacting of a microelectronic device substrate with a precursor as claimed in claim 1.

74. The method of claim 73, wherein the contacting comprises chemical vapor deposition.

75. The method of claim 73, wherein the contacting comprises atomic layer deposition.

76. The precursor composition of claim 11, wherein the solvent medium comprises a solvent species selected from the group consisting of C₃-C₁₂ alkanes, C₂-C₁₂ ethers, Ce-C^ aromatics, C₇-Ci₆ arylalkanes, Ci₀-C_2S arylcyloalkanes, and further alkyl-substituted forms of such aromatic, arylalkane and arylcyloalkane species, wherein the further alkyl substituents in the case of multiple alkyl substituents may be the same as or different from one another and wherein each is independently selected from Ci-C₈ alkyl.

77. The precursor composition of claim 11, wherein the solvent medium comprises a solvent species selected from the group consisting of alkanes, alkyl-substituted benzene compounds, benzocyclohexane (tetralin), alkyl-substituted benzocyclohexane and ethers.

78. The precursor composition of claim 11, wherein the solvent medium comprises a solvent species selected from the group consisting of tetrahydrofuran, xylene, 1,4-tertbutyl toluene, 1,3- diisopropylbenzene, tetralin, dimethyltetralin, octane and decane.

79. The precursor composition of claim 11, wherein the solvent medium comprises a solvent species selected from the group consisting of aromatic solvents having a boiling point at 1 atmosphere pressure in a range of from about 140⁰C to about 250⁰C.

80. The precursor composition of claim 11, wherein the solvent medium comprises a solvent species selected from the group consisting of xylene, 1,4-tertbutyl toluene, 1,3- diisopropylbenzene, tetralin, dimethyltetralin and other alkyl-substituted aromatic solvents.

81. The precursor composition of claim 79, wherein said precursor comprises bis(pentamethylcyclopentadienyl)strontium.

82. The precursor composition of claim 80, wherein said precursor comprises bis(pentamethylcyclopentadienyl)strontium.

83. A method of depositing a metal on a substrate, comprising conducting a liquid delivery deposition process with a precursor composition comprising the precursor as claimed in claim 1, in a solvent medium comprising a solvent species selected from the group consisting of C₃- C₁₂ alkanes, C₂-C₁₂ ethers, Cβ-Ci₂ aromatics, C₇-C₁₆ arylalkanes, C₁₀-C₂₅ arylcyloalkanes, and further alkyl-substituted forms of such aromatic, arylalkane and arylcyloalkane species, wherein the further alkyl substituents in the case of multiple alkyl substituents may be the same as or different from one another and wherein each is independently selected from Ci-C₈ alkyl.

84. The method of claim 83, wherein the solvent medium comprises a solvent species selected from the group consisting of alkanes, alkyl-substituted benzene compounds, benzocyclohexane (tetralin), alkyl-substituted benzocyclohexane and ethers.

85. The method of claim 83, wherein the solvent medium comprises a solvent species selected from the group consisting of tetrahydrofuran, xylene, 1,4-tertbutyltoluene, 1,3- diisopropylbenzene, tetralin, dimethyltetralin, octane and decane.

86. The method of claim 83, wherein the solvent medium comprises a solvent species selected from the group consisting of aromatic solvents having a boiling point at 1 atmosphere pressure in a range of from about 140⁰C to about 250⁰C.

87. The method of claim 83, wherein the solvent medium comprises a solvent species selected from the group consisting of xylene, 1,4-tertbutyltoluene, 1,3-diisopropylbenzene, tetralin, dimethyltetralin and other alkyl-substituted aromatic solvents.

88. The method of claim 83, wherein said precursor comprises bis(pentamethylcyclopentadienyl)strontium.

89. The method of claim 87, wherein said precursor comprises bis(pentamethylcyclopentadienyl)strontium.

90. The method of claim 83, wherein the liquid delivery deposition process comprises atomic layer deposition.

91. The method of claim 89, wherein the liquid delivery deposition process comprises atomic layer deposition.

92. The precursor of claim 1, wherein the cyclopentadienyl ligand includes a ligand formed according to the following reaction: