Abstract
A high throughput method of synthesizing and characterizing a multiplicity of ternary compositions is provided, the method comprising: selecting three components; depositing a gradient of a first component along a first axis; depositing a gradient of a second component along a second axis which is normal to the first axis, such that the gradient is thickest at a first end and thinnest at a second end; and depositing a gradient of a third component along the second axis such that the gradient is thickest at the second end and thinnest at the first end to provide a compositional distribution of the multiplicity of ternary compositions; mapping the compositional distribution of each of the multiplicity of ternary compositions; and analyzing each of the multiplicity of ternary compositions, thereby synthesizing and characterizing the multiplicity of ternary compositions.
Claims
1. A method of synthesizing and characterizing a multiplicity of ternary compositions, the method comprising: selecting three components; depositing a gradient of a first component along a first axis; depositing a gradient of a second component along a second axis which is normal to the first axis, such that the gradient is thickest at a first end and thinnest at a second end; and depositing a gradient of a third component along the second axis such that the gradient is thickest at the second end and thinnest at the first end to provide a compositional distribution of the multiplicity of ternary compositions; mapping the compositional distribution of each of the multiplicity of ternary compositions; and analyzing each of the multiplicity of ternary compositions, thereby synthesizing and characterizing the multiplicity of ternary compositions.
2. The method of claim 1, further comprising alloying the three components.
3. The method of claim 2, wherein the multiplicity of ternary compositions are perovskites.
4. The method of claim 3, wherein the perovskites are Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 perovskites.
5. The method of claim 4, wherein mapping is effected by one or more of nuclear magnetic resonance, powder X-ray diffraction and energy dispersive X-rays.
6. The method of claim 1, wherein the analyzing is in situ analyzing.
7. A ternary perovskite comprising Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3, wherein y is between 0.09 and 0.25, z is between 0.89 and 0.75 and x is non-zero and is no greater than 0.1.
8. A ternary perovskite comprising Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3, wherein x is between 0.001 and 0.1, y is between 0.006 and 0.125 and z is between 0.9 and 0.95.
9. The method of claim 5, wherein the analyzing is in situ analyzing.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0016] The patent or application file contains at least one drawing executed in color. As the color drawings are being filed electronically via EFS-Web, only one set of the drawings is submitted.
[0017] FIG. 1 is a photograph of computing effective tolerance factor of triple cation perovskites. FIG. 1a, Schematic of perovskite cubic unit cell with ABX.sub.3 composition; FIG. 1b, 1D superlattice of ABX.sub.3 with triple A-cations showcasing accumulated offset (=|.sub.2.sub.1|); FIG. 1c, Computed effective Goldschmidt tolerance factor for triple cation perovskites for 0.88<t.sub.eff<1.
[0018] FIG. 2 is a photograph of fabrication of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 t-CGF. FIG. 2a, Schematic of sequential deposition of three layers by slot-die coating, and robotized high-throughput screening by an optical spectrometer. FIG. 2b, Three steps of synthesizing ternary compositionally graded films (t-CGFs); the first layer is made by tilting the slot-die head with one pump profile to form a gradient of CsPbI.sub.3 across the width of the substrate; the second and third layers are deposited by the straight slot-die head with two pump profiles to deposit gradient films of Methylammonium Lead Iodide (MAPbI.sub.3) and formamidinium lead iodide (FAPbI.sub.3), respectively, across the length of the substrate; coating of subsequent layers dissolve previous one(s) and recrystallize into new perovskite compositions. FIG. 2c, Absorption spectra after each step of fabrication. FIG. 2d. Variation of normalized absorbance as a function of wavelength across the film for three sequential layers. FIG. 2e, Normalized absorbance to global maximum showcasing gradient thickness; the gray color of the surface shows standard deviation across the film.
[0019] FIG. 3 is a photograph of slot-die coating profiles and the schematics of two different setups. FIG. 3a. One-pump profile: Filling the reservoir of the head with CsPbI.sub.3 while the speed of the head is zero, and supplying the head with the same ink and a proper speed of pumping while the head is moving. FIG. 3b. The setup for achieving gradient in width: A tilted head setup supplied from one pump. FIG. 3c. Two-pump profile: Filling the reservoir of the head with a perovskite ink while the speed of the head is zero and supplying the head with a proper solvent and a calculated speed. FIG. 3d. The setup for achieving gradient thickness in length: A straight head setup supplied from two pumps to dilute the filled ink by solvent while the head is moving along the substrate.
[0020] FIG. 4 is a photograph of mapping quasi-triple composition of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3. FIG. 4a.
[00001]
values in Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 for the maximum contribution range of Cs equal to 0.2 possessing a small area map. FIG. 4b
[00002]
values in Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 for the maximum contribution range of MA equal to 0.5 possessing a moderate area map with a fast-decaying rate from left to right. FIG. 4c.
[00003]
values in Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 for the contribution range of FA equal to 1 possessing a large area map with a slow decaying rate.
[0021] FIG. 5 is a photograph of high-throughput screening of the ternary t-CGF. FIG. 5a. High-throughput map of two opposite CGFs through the length with FAPbI.sub.3, MAPbI.sub.3, and one t-CGF across the width from the top; FIG. 5b. Details of robotized measurement via robot arm grabbing the probe of the spectrometer and positioning on top of the t-CGF sample; FIG. 5c. High-throughput measurement path for screening the ternary t-CGF via robot arm.
[0022] FIG. 6 is a photograph of validating organic compound ratios along the t-CGF via nuclear magnetic resonance (NMR). FIG. 6a. Normalized raw NMR data; FIG. 6b. the comparison of designed/experiment ratios of MA over FA through the t-CGF in four spots.
[0023] FIG. 7 is a graph quantifying gradient deposition by measuring content of atoms across the width of the t-CGF via Energy Dispersive X-Rays (EDX). FIG. 7a. Cesium (Cs) over lead (Pb). FIG. 7b. Iodine (I) over lead (Pb).
[0024] FIG. 8 is a photograph characterizing Cs-rich and Cs-poor bands via Powder X-ray diffraction (pXRD). FIG. 8a. Four positions from the Cs rich band of the fabricated t-CGF, FIG. 8b. Four positions from the Cs poor band of the fabricated t-CGF, FIG. 8c. Zoomed-in peaks for only (100) crystal plane of perovskite and the PbI.sub.2 peaks to demonstrate the transition of the perovskite peak position and full-width at half-maximum. FIG. 8d. Average grain size transition through the t-CGF from FA rich segment toward the MA-rich segment for two bands. FIG. 8e. Lattice parameter transition through the t-CGF from the FA-rich segment toward MA-rich segment for two bands.
[0025] FIG. 9 is a photograph characterizing two compositions to analyze ternary cations on stabilization of perovskite. FIG. 9a. pXRD; FIG. 9b. Scanning electron microscope (SEM) results for ternary perovskite showing cross-sectional view (up) and top view (bottom) FIG. 9c. SEM image of binary cation perovskite showing cross-sectional view (up) and top view (bottom).
[0026] FIG. 10 is a photograph of high-throughput screening t-CGF with mapping the optoelectronic properties of 520 composition of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 on real location. FIG. 10 a. Bandgaps, FIG. 10b. Urbach energies, FIG. 10c. Absorbance values at 784 nm, FIG. 10d. Ratio of absorbance values of the aged to fresh at the wavelength of 784 nm for 520 locations (compositions).
[0027] FIG. 11 is a photograph showing a stability test of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 t-CGF. FIG. 11a, Image of fresh t-CGF of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3. FIG. 11b, Image of the same t-CGF aged for 92 days under 99% relative humidity; the dashed rectangle shows perovskite compositions that experienced no/little color change. FIG. 11c, Bandgaps, FIG. 11d, Urbach energies, FIG. 11e, Absorbance values, FIG. 11f, Ratio of absorbance values of the aged to fresh at the wavelength of 784 nm for 520 locations (compositions).
[0028] FIG. 12 is a photograph showing re-optimizing t-CGF in three steps. FIG. 12a. Aged t-CGF of large map are of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 with stable region FIG. 12b. Re-synthesizing a fresh t-CGF of the previous shown map; FIG. 12c. Aged t-CGF under 99% relative humidity (RH) for 20 days.
[0029] FIG. 13 is a photograph showing operational stability of ternary perovskite solar cells. FIG. 13a, Evolution of current-voltage characteristics of perovskite solar cells in ambient air at 57% RH at 60 C. without encapsulation. FIG. 13b, Selected compositions from the stable region in the ternary diagram. FIG. 13c, Loss of short circuit current density (J.sub.SC), and FIG. 13d, open circuit voltage (V.sub.OC) as a function of perovskite composition within h of test in ambient air at 57% RH at 60 C. without encapsulation.
[0030] FIG. 14 is a photograph of categorizing degradation mechanism of mixed triple cation Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 from the discovered region by tracking the evolution of current-voltage characteristics of perovskite solar cells in ambient air at 57% RH at 60 C. without encapsulation. The compositions of perovskite solar cells (PSCs) is divided to Cs-rich region (up), and the Cs-poor region for different MA/FA ratios (down).
[0031] FIG. 15 is a photograph of categorizing degradation mechanism of fixed-halide from the discovered region vs. mixed-halide perovskites under high stress (e.g., elevated temperature up to 60 C., RH 57%, without sealing). The mixed-halide perovskite is reported to have at least 500 hours of stability but exhibit only 100 seconds under the given conditions; this represents a factor of 1.8*10.sup.4 in accelerating the degradation.
[0032] FIG. 16 is a photograph comparing the operational stability of two PSCs from the inks including the single-halide perovskites from the discovered ranges including ink 1: Cs.sub.0.09MA.sub.0.12FA.sub.0.79PbI.sub.3 vs. mixed-halide perovskites (ink 2: Cs.sub.0.05MA.sub.0.15FA.sub.0.80PbI.sub.2.55Br.sub.0.45). The maximum power point measurement under no encapsulation and no nitrogen blowing at 45 C. for single-halide including ink 1 (black), the other compositions are from the discovered range reported in this article (red stars), and the mixed halide perovskite (ink 2 with blue stars); Inset: the appearances of two solar cell devices with the given compositions that are exposed to the ambient air after 3 months.
DESCRIPTION
[0033] Except as otherwise expressly provided, the following rules of interpretation apply to this specification (written description and claims): (a) all words used herein shall be construed to be of such gender or number (singular or plural) as the circumstances require; (b) the singular terms a, an, and the, as used in the specification and the appended claims include plural references unless the context clearly dictates otherwise; (c) the antecedent term about applied to a recited range or value denotes an approximation within the deviation in the range or value known or expected in the art from the measurements method; (d) the words herein, hereby, hereof, hereto, hereinbefore, and hereinafter, and words of similar import, refer to this specification in its entirety and not to any particular paragraph, claim or other subdivision, unless otherwise specified; (e) descriptive headings are for convenience only and shall not control or affect the meaning or construction of any part of the specification; and (f) or and any are not exclusive and include and including are not limiting. Further, the terms comprising, having, including, and containing are to be construed as open-ended terms (i.e., meaning including, but not limited to,) unless otherwise noted.
[0034] Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. Where a specific range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range, is included therein. All smaller sub ranges are also included. The upper and lower limits of these smaller ranges are also included therein, subject to any specifically excluded limit in the stated range.
[0035] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the relevant art. Although any methods and materials similar or equivalent to those described herein can also be used, the acceptable methods and materials are now described.
[0036] In a cubic perovskite structure of ABX.sub.3 composition, the lattice parameter can be extracted from two Miller planes (FIG. 1a): from (200) plain in which case the unit cell (.sub.1) is comprised of two radii of B and X; and from (100) plane in which case the unit cell (.sub.2) is comprised of cathetus of the right-angle triangle whose hypotenuse is comprised of two radii of A and X. The ratio of a.sub.2/a.sub.1, known as Goldschmidt tolerance factor (t), should be close to unity to form a stable perovskite with no/little structural distortion.
[0037] Goldschmidt's theory was applied to assess the structural stability of iodide triple-A-cation perovskites, Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3, where x+y+z=1. Mixed halides were not considered, as they are known, also shown below, to be prone to phase segregation. If the ternary perovskite is represented as a 1D superlattice of N=n.sub.1+n.sub.2+n.sub.3 unit cells (FIG. 1b), where n.sub.1, n.sub.2, and n.sub.3 define the ratio of A-site cations (x=n.sub.1/N, y=n.sub.2/N, z=n.sub.3/N), then the effective tolerance factor is t.sub.eff=(n.sub.1.sub.2+n.sub.2.sub.2+n.sub.3.sub.2)/N.sub.1, where .sub.2, .sub.2, .sub.2 are (100) lattice constants with Cs, MA and FA, respectively.
[0038] The effective tolerance factor for a superlattice possessing triple cations with three different lattice constants was derived: r.sub.A, r.sub.B, and r.sub.X are the radii of A, B, and X sites, respectively, of the ABX.sub.3 composition. The lattice constant estimated in (100) and (200) planes, shown in FIG. 1a, are a.sub.1=2 (r.sub.X+r.sub.B) and a.sub.2={square root over (2)} (r.sub.A+r.sub.X), respectively. The tolerance factor is then
[00004]
[0039] The lattice constant for the (100) plane can vary due to dissimilar ionic radii of A in triple-cation perovskite (a.sub.2, a.sub.2, and a.sub.2).
[0040] Assuming a rectangular mapping area of w=5 (cm) and l=26 (cm), the positions in two dimensions (e.g., x.sub.i=[0; 26] and y.sub.j=[0; 5]) to (X.sub.iY.sub.i) were normalize as follow:
[00005]
[0041] Combinatorial contribution of three cations are a, b, and c:
[00006] [0042] and the total combinatorial contribution range of triple compositions is
[00007] [0043] in which a, b, and c are the maximum combinatorial contribution ranges of each cation respectively. For full ternary combinatorial composition, the maximum values of a, b, and c are 1. For a quasi-ternary composition that considers only a limited range of contribution, the a, b, and c vary based on the considered range of optimization. The first, second, and third terms in (4) are related to combinatory indices of FA, MA, and Cs, respectively. Then the optimization composition as a function of space is:
[00008] [0044] with an effective tolerance factor of:
[00009]
[0045] Taking t.sub.eff>0.88 as a criterion to form a stable cubic perovskite structure, the compositional range of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 was 0<x<0.2, 0<y<1, and 0<z<1 (FIG. 1c).
[0046] The ternary alloys were synthesized having the defined compositional range. Making them by traditional fragmentary approach would not only be time-consuming (e.g., 103 compositions only for 10% increments), but would also miss many intermediate compositions.
[0047] Ternary compositionally graded film (t-CGF) was obtained by coating gradient films of three ingredients sequentially, but with varying gradient directions (FIG. 2a). Individual graded films were synthesized by slot-die coating. The slot-die coating was facilitated by two pumps that supply the precursors and/or solvents to the reservoir of the slot-die head. A personal computer mode controller was used to program the volume and speed of injecting inks and/or solvents. The gradient program enables the pumps to provide gradient pressure on syringes and thus changing the combinatorial ratio of ink to be printed on a substrate. Since the substrate is placed on a hot plate, any deposited composition is crystallized due to quick removal of solvents. Two profiles were used for synthesizing gradient thickness in width and length of substrates.
[0048] To achieve a gradient thin film in width for CsPbI.sub.3, one pump profile of the slot-die coater (FIG. 3a) was applied and tilted the slot-die head to fabricate a gradient thickness across the width of the substrate (FIG. 3b). This leads to a gradient thickness across the substrate.
[0049] To achieve a gradient film in length for MAPbI.sub.3, two pump profiles were used (FIG. 3c). The reservoir was filled of the slot-die head with MAPbI.sub.3 and halted it during the deposition and instead supplied solvent from another pump to dilute the ink in situ. FAPbI.sub.3 was deposited in the same way, but in opposite gradient direction.
[0050] The time needed to fill the reservoir from pump A was measured to calculate the optimized speed of pump B for considerable dilution of the stored perovskite ink. A pre-annealing temperature of 70 C. was set for the two first layers to keep the gradient map of thickness constant for the next steps and the last layer was deposited at 140 C.
[0051] To achieve t-CGFs, three layers were deposited sequentially, on top of each other, with varying thicknesses to cover the entire compositional space with asymmetric combinatorial ratios. One of the steps in preparing a t-CGF is to map the position of synthesized compositions, i.e., identifying the unknown values (e.g., x, y, and z) in the Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 as a function of position (X and Y) in the film. The symmetric mapping approach considers a full combinatorial range of the unknown values in a composition with a linear trend in cartesian space. For example, in a binary combinatorial system, two unknown values in A.sub.xB.sub.y composition map x and y values in a linear manner (y=1x) from 0 to 1 in two opposite gradient directions. On the other hand, an asymmetric mapping approach considers a quasi-combinatorial range in which the growth rates of unknown values are not equal in one space length. The asymmetric map enables the investigation of a large map area of one component to be dominant in the combinatorial contribution range. FIG. 4 shows asymmetric mapping ranges for the quasi-ternary composition of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3.
[0052] The t-CGF was fabricated on a substrate of 130 cm.sup.2 area (5 cm width and 26 cm length). FIG. 2b provides the detailed three-step fabrication conditions of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 t-CGFs. First, CsPbI.sub.3 film was deposited by a tilted slot-die head to achieve a thickness gradient across the width of the substrate (FIG. 3a,b). MAPbI.sub.3 was then deposited on top of CsPbI.sub.3 film by an in-situ decrease of ink concentration to achieve a thickness gradient across the length of the substrate, wherein the gradient was thickest at a first end A, decreasing to a second end B (FIG. 3c,d). Finally, FAPbI.sub.3 film was deposited on top of CsPbI.sub.3/MAPbI.sub.3 sandwich film, but its thickness gradient was opposite to MAPbI.sub.3, such that the gradient was thickest at second end B, decreasing to first end A.
[0053] To assess the capability of the approach in the fabrication of thickness-graded films, absorption spectra were measured for every 0.25 cm.sup.2 segment of the substrate, which sums up to 520 locations (130 cm.sup.2/0.25 cm.sup.2 i.e., 52 in length10 in width). The measured absorption spectra were normalized and the variance of S()=A.sub.r-maxA.sub.r-min for 10 lines of measurement was calculated as a function of wavelength. All S() were plotted for quantifying the sensitivity of spectra on the thickness of the deposited thin film. The first set of data is collected from the first layer of depositing CsPbI.sub.3 which exhibits a broader range of sensitivity. The local quantification map was also plotted as shown in the second set of analyses shown in FIG. 2e for validating the quality of t-CGF layers. The maximum S() was picked to normalize all Absorbance values of that specific wavelength in 10 measured lines to the maximum corresponding value. The results were mapped in height to demonstrate the linearity of the gradient deposition direction. Similarly, the Absorption values of the datasets were normalized to the average values across the width of deposition. A robotic arm and a reflection probe of a spectrometer was used to collect all spectra in 10 minutes (FIG. 5). Since absorbance directly depends on the absorber's thickness (Beer-Lambert law), absorbance value (A) was used to estimate the spatial thickness of films for each deposited layer. FIG. 2c shows the spectra for each layer at 520 locations. From the maximum variance of absorbance as a function of wavelength, S(), along the t-CGF photon wavelength that exhibits the highest sensitivity to the absorber's thickness were found (FIG. 2d).
[0054] The S() shows a clear red-shift by adding each layer indicating successful alloying of compositions in each deposition step. The maximum S() value was used to map thickness gradience along and across the fabricated t-CGF in each step (FIG. 2e). All three layers (CsPbI.sub.3, MAPbI.sub.3, and FAPbI.sub.3) were deposited in a gradient with a low standard deviation of <10.sup.2 of relative absorbance (FIG. 2e) that guarantees alloying of all designed combinatorial ratios.
[0055] The exact composition of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 in a specific location of t-CGF can be determined from its spatial coordinates, just like the coordinates can be calculated from the given composition, as discussed above. The compositional distribution of the Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 t-CGF was validated by conventional analytical methods. NMR was used to explore the ratio of organic cations (e.g., MA and FA) through the length since their gradient ratio is designed to change in length. FIG. 6a shows the results of NMR spectra in four positions. The varying peak at 3.32 (ppm) clarifies the variation ratio of organic compounds with different values of FA over MA. FIG. 5b compares the designed and measured data and shows good agreement between those. Lastly, pXRD was used to identify grain size and lattice parameters. The prepared ternary library was divided into two bands with 4 samples starting from the FA-rich region toward the MA-rich segment. Four color plots as blue, red, green, and orange were used for specifying Cs rich band, Cs poor band, FA rich region, and MA rich segment respectively. FIGS. 8a and 8b show the pXRD results for the Cs rich and Cs poor bands having PbI.sub.2 peak around 2=12.6 and peaks corresponding to perovskite of Miller planes of (100), (011), and (111) at around 2=14, 19.81, and 24.29, respectively. Four samples were measured in both Cs rich and poor bands at 1 (cm), 9 (cm), 17 (cm), and 25 (cm) along the fabricated ternary t-CGF. FIG. 7c shows the zoomed-in peaks of PbI.sub.2 and only (100) perovskite peak to demonstrate details of the peak representing a transition in peak positioning and the variation of full-width at half-maximum of the measured pXRD results. The grain size can be also affected by fabrication factors such as annealing duration. The Scherrer equation was used to compute the average grain sizes through the CGF. The analysis shows that the Cs rich band possesses a larger grain size than the Cs poor band region. Similarly, the grain size becomes bigger by reaching the MA-rich segment (FIG. 8).
[0056] The ratios of organic and inorganic ions, identified by NMR and EDX, from multiple locations, were in good agreement with the expected compositions (FIGS. 6 and 7). Powder XRD shows single peaks corresponding to the perovskite phase indicating the successful formation of alloys (FIGS. 8a-c), rather than multi-layered structures in which case one would expect to observe multiple perovskite diffraction peaks. Thus, each subsequent slot-die-coating dissolved the previous layers and crystallized as a new alloy:
##STR00001##
[0057] where I and s stand for the solution and solid, respectively.
[0058] Powder XRD spectra show shrinkage of the crystal lattice parameters from FA-rich perovskite to Cs and MA-rich perovskites, again indicating the successful formation of ternary gradient film (FIG. 8e). In addition, the full-width at half maxima of XRD peaks indicate that the Cs-rich films are made of larger crystallites (FIG. 8d); this observation is further supported by surface SEM-images of Cs-less and Cs-containing perovskite films (FIG. 9).
[0059] The t-CGFs provide an unprecedented dense library to study the properties and stability of alloys, unlike conventional approaches which study only a fragment of possible compositions. The bandgap and Urbach energy of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 alloys was measured at 520 locations. The bandgap, as expected, increased from 1.50 (eV) for FA-rich perovskite to 1.61 (eV) for MA- and Cs-rich perovskite (FIG. 10a). All studied Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 alloys, when fresh, show a relatively small Urbach energy of 203 meV demonstrating low energy disorder and hence can be used to make performing cells.
[0060] FIGS. 11a and 11b show the fresh t-CGF of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3, and the same after it was aged at 99% relative humidity for 92 days, respectively. The humidity stress discolored a major portion of the t-CGF, while only its small area remained black (FIG. 11b). To quantify the stability of ternary alloys, absorbance (FIG. 11e) of the fresh and aged t-CGF was measured, and the ratio of absorbance values at 784 nm was determined: in this analysis, more deviation of this ratio from unity means more change, or instability, of the composition. The stable range shown in FIG. 11b, when decoded to composition is made of Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3 with 0<x<0.1; 0.1<y<0.25; 0.75<z<0.9 (FIG. 11f). FIG. 10 shows the optoelectronic properties of the t-CGF in the real space. This stable range was re-synthesized and this combinational range remained black when exposed to identical humidity stress (FIG. 12). The following provided an excellent result: 0.001<x<0.1, 0.006<y<0.125 and 0.9<z<0.95. The following produced a good result: 1<x<0.125, 0.125<y<0.25, and 0.85<z<0.9.
[0061] The broadest range for Cs.sub.xMA.sub.yFA.sub.zPbI.sub.3, was y between 0.09 and 0.25, z between 0.89 and 0.75 and x being non-zero and no greater than 0.1.
[0062] Solar cells were fabricated in a conventional architecture (Glass/ITO/SnO.sub.2/Perovskite/Spiro-OMeTAD/Au) in ambient air. Three types of mono-halide perovskites from the defined stable range were chosen and entitled FA-, MA-, and Cs-rich regions (exact compositions are shown in FIG. 13 and FIG. 14). The best device showed 22% power conversion efficiency. Mixed-halide perovskite solar cells (Cs.sub.0.05MA.sub.0.15FA.sub.0.8PbI.sub.2.55Br.sub.0.45) were also fabricated which demonstrated over 500 hours of maximum power point operational stability at room temperature when encapsulated.
[0063] To study the stability of PSCs, their current-voltage characteristics was measured in ambient air at 57% RH at 60 C. without encapsulation. These conditions represent accelerated tests by a factor of 10.sup.4 compared to encapsulated devices tested with no heating stress (FIG. 15). Mixed halide perovskites demonstrate rapid degradation of all photovoltaic figures-of-merit when tested in these conditions due to phase segregation at high temperatures (FIG. 13a). This agrees with their rapid loss of efficiency when tested under maximum power point operation unencapsulated at 60 C. (FIG. 16). MA-rich perovskites experience rapid loss of J.sub.SC due to the loss of MA (FIG. 13a), while FA-rich perovskites experience a rapid loss of volatile organic compounds (V.sub.OC) due to polymorphism of FA-rich perovskites (FIG. 13a). Cs-containing perovskites, among all, show the least loss in all photovoltaic parameters likely due to improved morphology of perovskites (FIG. 13a). PSCs from 8 locations of the defined stable region of ternary perovskites were fabricated (FIG. 14). FIG. 13c, 13d, and FIG. 15 show the trends as a function of composition, based on which it was concluded that J.sub.SC loss can be minimized with the increase of FA and Cs components, while the presence of the optimum amount of MA is needed to minimize the V.sub.OC loss.
[0064] In another embodiment, ternary alloys that are not ternary perovskites were synthesized using the same methodology as described herein. In yet another embodiment, ternary compositions were synthesized using three components, each in a solvent that was compatible with the solvent of the other solvents, or all components being in the same solvent.
Materials
[0065] Cesium iodide (CsI, >99.99%) were purchased from MilliporeSigma. Formamidinium iodide (FAI, >99.99%), and methylammonium iodide (MAI, >99.99%) were purchased from Great Cell, lead (II) iodide (PbI2, 99.99%) from TCI chemicals, and lead bromide (PbBr2) was purchased from Alfa Aesar as perovskite precursors. N, N-dimethyl formamide (DMF, 99.5%), dimethylsulfoxide (DMSO, 99.5%), chlorobenzene (99.5%), and acetonitrile (ACN, 99.9%) solvents were parched from Milipore Sigma. Tin (IV) oxide (SnO2) 15% in H2O colloidal dispersion solution was purchased from the Alfa Aesar. Sprio-OMeTAD was purchased from Xi'an Polymer Light Technology Co., Ltd. Bis(trifluoromethane) sulfonimide lithium salt (Li-TFSI 99.95%) and cobalt salt (FK 209 Co (III) TFSI) were purchased from Milipore Sigma.
Ternary CGF Fabrication
[0066] Perovskite inks were made by dissolving MAI, FAI, CsI, and PbI.sub.2 in DMF and DMSO with the ratio of (4:1) to prepare 1.4 M, 0.7 M, and 0.28 M solutions of FAPbI.sub.3, MAPbI.sub.3, and CsPbI.sub.3, respectively.
[0067] Slot-die coating was performed on InfinityPV Research Laboratory Coater (RLC). CsPbI.sub.3 was deposited using one pump with a tilted head: first, the dead volume and the reservoir were filled, and then the film was deposited at a small speed. MAPbI.sub.3 and FAPbI.sub.3 were deposited in gradient thickness using two pumps. The dead volumes (from syringes to the end of the T junction) were filled with inks at a speed of 0.01 ml/min, and then the T junction was attached to the slot-die head. The time required to fill the slot-die head until the appearance of ink at the tip of the head at a speed of 0.3 ml/min was measured to be 56 s. Then the first ink supply was paused, but the second string containing DMF and DMSO with a 4:1 ratio was pumped at the same speed of 0.3 ml/min. The speed of the moving head along the 260 mm was installed to be 260 mm/56 s=4.64 mm/s to be able to linearly dilute the stored ink in the reservoir. MAPbI.sub.3 and FAPbI.sub.3 were deposited in opposite directions. The first and second layers were fabricated at 70 C.; the final layer was deposited at 140 C.
PSC Fabrication
[0068] The UV-Ozone treated glass/ITO substrates were coated with SnO.sub.2 by dropping 60 l of mixed SnO2:H.sub.2O (1:6). Six ml deionized (DI) water and 1 ml of SnO.sub.2 15% in H.sub.2O colloidal dispersion nanoparticles was used and then sonicated for 30 minutes and filtered with 0.45 m polyvinylidene difluoride (PVDF) syringe filter before deposition. The tin oxide layer is dropped and spin coated for 1 minute with 3000 r.p.m. and repeating the process twice. Then the substrate was annealed at 140 C. for 20 minutes and treated with UV-Ozone for 15 minutes. Perovskite solution based was prepared by dissolving 1 molar mass of combinatorial ratios of CsI, MAI, FAI, and PbI.sub.2 on 0.666 ml of DMF: DMSO with the ratio of 1:10. Then 90 l of mixed-cation, single-halide perovskite (1.5 M) in the ambient air was deposited by a spinner at 500 r.p.m. for 5 s, 4500 r.p.m. for the 30 s. During the last step, 500 l of chlorobenzene was dropped on the film at the 30 s, followed by annealing at 140 C. for 10 min. Spiro solution was prepared by dissolving 0.1 mg of spiro-OMeTAD powder in 1.1 ml of chlorobenzene, 0.039 ml of tBP, 0.023 ml of Li-TFSI (dissolved in acetonitrile, 540 mg/mL), and 0.01 ml of Co-complex (dissolved in acetonitrile, 376 mg/mL) solution. Then 60 l Spiro-OMeTAD was dynamically spin-coated for the 30 s. Finally, 70 nm gold was thermally evaporated (Angstrom Engineering). All the solutions i.e. perovskite, and spiro-OMeTAD were filtered with 0.22 m polytetrafluoroethylene (PTEE) syringe filter.
[0069] While example embodiments have been described in connection with what is presently considered to be an example of a possible most practical and/or suitable embodiment, it is to be understood that the descriptions are not to be limited to the disclosed embodiments, but on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the example embodiment. Those skilled in the art will recognize or be able to ascertain using no more than routine experimentation, many equivalents to the specific example embodiments specifically described herein. Such equivalents are intended to be encompassed in the scope of the claims, if appended hereto or subsequently filed.
