Abstract
In this review paper, the residual strain of a polycrystalline halide perovskite film is systematically studied based on its structural inhomogeneity, which is closely correlated to the local carrier dynamics caused by a modulated electronic band structure. Long-range collective strain ordering is responsible for the overall structural properties, consequently determining the optoelectronic properties of the perovskite film. Notably, the perovskite phase stability is strongly affected by the internal strain, favoring a lower energy state. The important parameters affecting the residual strain in a real perovskite film, ranging from thermal stress to lattice mismatch and compositional inhomogeneity, are subsequently introduced along with their impacts on the optoelectronic properties and/or the stability of the crystals.
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Introduction
Interest in halide perovskite crystals has exponentially increased since the very first type of solid-state perovskite solar cell (PSC) was released in 20121,2, demonstrating a promising power conversion efficiency (PCE) of approximately 10% with 500-hour-long shelf stability1. Tremendous efforts have been made to raise the performance of PSCs, and the state-of-the-art technology in PSCs drove its PCE into a remarkable value, 25.5% in 20203, making PSCs highly competitive with conventional photovoltaics and one of the most promising next-generation solar cells4,5,6. Most of the dominant progress in PSCs was achieved through the compositional and morphological engineering of halide perovskite crystals via a macroscopic approach7. The composition of perovskite crystals, initially governed by a single cation- and halide-based methylammonium lead iodide (MAPbI3)1,2, evolved into a cutting-edge mixed cation- and halide-based system where formamidinium cation (FA+) and iodide (I–) assume a majority in composition along with cesium cation (Cs+), MA+ and bromide (Br–)8,9,10,11. Furthermore, the morphology of the perovskite was set as the bulk film12,13, complementarily guided by fundamental studies revealing extremely outstanding optoelectronic properties of halide perovskites14,15,16,17. Though the PCE of PSCs has been significantly raised by the aid of recent evolution with 2D/3D hybrid perovskite architectures18,19,20, there is still room for improvement. Sophisticated micro tuning of the lattice strain of the perovskite film deserves attention for PSCs, aiming at a further boost to close to the theoretical limit as well as ensured intrinsic phase stability.
Strain engineering is a very useful strategy in crystals to minutely modulate electronic properties by tuning the band structure. Strain tailoring is frequently performed on various crystals, such as germanium21, WSe222, and GaAs23, to manipulate their optoelectronic properties. Halide perovskite also provides substantial room for the strain to be involved as a key parameter to alter its electronic band and thus affect the resulting properties. The halide perovskite film shows a residual strain caused by inhomogeneity mainly due to its polycrystalline nature24,25. Any strain in the lattice accordingly has an impact on the electronic band structure by interfering with the bonding strength of the PbI6-coner sharing octahedral frame26,27. Importantly, strain tuning can play a key role in determining the intrinsic stability of the photoactive perovskite phase from a thermodynamic point of view28. Therefore, strain engineering would be a demanding approach for current PSCs toward the next breakthrough. In this review paper, the effect of lattice strain on the relevant optoelectronic properties of halide perovskites is discussed from the electronic band structure to the carrier dynamics and the crystal phase stability as well. Subsequently, methods to perform strain engineering are proposed for halide perovskites by addressing the affecting parameters. Finally, the effective scope of the strain-induced benefits and the expected limits are examined from a practical point of view to provide an overall perspective.
Effect of the lattice strain on optoelectronic properties
The halide perovskite in PSCs shows polycrystallinity due to its film growth at low temperature based on the solution process29. Therefore, the inhomogeneity is necessarily inherent in the perovskite film, where distinctive electronic properties are observed even in the same grain30, which is indicative of the underlying lattice mismatch. The strain induced by local lattice mismatch tends to be relieved by a relaxation mechanism. As the thickness of the perovskite film increases, the increased elastic energy helps the perovskite film dissipate the induced strain31. On the other hand, structural dislocation may occur by generating defects to relieve the strain when the film thickness is thinner than the threshold for elastic relaxation31. The effect of elastic relaxation across the film is negligible in real devices when considering that the threshold thickness of the halide perovskite is far beyond 3 μm32, compared to the ca. 500 nm thick perovskite film in PSCs. Accordingly, the polycrystalline perovskite film is likely to exhibit residual strain and to be involved in bonding hybridization33. The electronic properties of the polycrystalline halide perovskite film are highly subject to macroscopic internal strain, which is determined by the overall localized residual strains on the microscale33,34,35.
Electronic band structure
Perovskite crystals in the form of the bulk film can be exposed to relatively in-plane or out-of-plane strains, indicating strains parallel or perpendicular to the substrate, respectively. In halide lead perovskites, the valence band edge is governed by the antibonding between Pb-6s and halide (X)-p orbitals, while the conduction band edge is mostly determined by nonbonding localized Pb-6p orbitals26,27. The strain-induced lattice expansion/contraction modulates the bond strength in the lattice, leading to a change in the electronic band structure, particularly in the valence band edge. Figure 1a–c shows schematic illustrations of the lattice structure bearing concentrated in-plane strain, implying tensile strain at the bottom surface in Fig. 1a, a strain-free state in Fig. 1b, and compressive strain at the bottom surface in Fig. 1c. Grazing incidence X-ray diffraction (GIXRD) is a well-established tool to characterize the residual strain existing within a material36,37. GIXRD adopts a small incidence angle of ψ over a fixed 2θ corresponding to (hkl) and detects the resulting diffraction intensity from different orientations of the scattering vector (Nk)35, which is not parallel to the substrate normal, as illustrated in Fig. 1d. The GIXRD patterns in Fig. 1e–g effectively reflect the in-plane lattice change by tilting a substrate-loaded instrument with an angle, ψ. In other words, the X-ray diffraction (XRD) peak at ψ = 0 (no tilting) is directly determined by the distance between lattice planes parallel to the substrate, which thus involve no information about the in-plane lattice expansion or contraction. As the tilting angle ψ increases, however, the in-plane lattice distance starts contributing to the beam path and consequently affects the XRD peak position. The residual strain, ε(hkl), can therefore be determined by the difference in the interplanar spacing of d between Nk and N0, ε(hkl) = (dψ – d0)/d0. The tensile strain-induced film shows a gradual peak shift toward a lower 2θ as ψ increases (Fig. 1e), implying lattice expansion, whereas the strain-free film shows constant peak positions regardless of ψ (Fig. 1f). A peak shift to a higher 2θ is observed with increasing ψ in Fig. 1g, which is in accordance with the expected lattice contraction by the compressive strain. Under tensile strain, lattice expansion occurs, resulting in a downshift of the valence band edge as a consequence of weakened antibonding26,27. On the other hand, the lattice contraction by compressive strain strengthens the overlap of the antibonding and thus lifts the valence band edge up compared to the strain-free film.
The tendency is well described in Fig. 2, showing the effect of strains on the calculated band structure (Fig. 2a) and the estimated band gap (Vg) by experimental results (Fig. 2c). A narrower band gap (Vg) is observed from the compressive strain compared to the case of the strain-free film. On the other hand, the tensile strain induces an opposite effect on the band structures, leading to a wider Vg with increasing strain (Fig. 2b). As expected, the effect of strain on the valence band edge is more pronounced than that of the conduction band edge26,27.
Furthermore, the observed difference in the band energy level and Vg by varying the strain is dependent on the composition of the perovskite films. Nevertheless, it is found that a strain within ±2.5% (negative value for the compressive strain and positive value for the tensile strain) has been generally used as a feasible strain window in various studies, providing a controllable margin of Vg within 50 meV25,32,35,38. Notably, the beneficial effect is mostly observed when the inherent strain of the perovskite film ranges from a slight compressive strain (−1.5%) to a strain-free condition (0%)25,32,35.
The effect of spin–orbit coupling (SOC) on the electronic band structure can be reversed when a phase transition is accompanied by intense strain, particularly under high pressure in the GPa range39,40,41. The halide perovskite crystals close to the cubic phase and pseudocubic phase represent Pb-X-Pb with a bond angle of 180° as in the α-phase lattice. Therefore, the tensile strain effectively weakens the orbital coupling between Pb-6s and X-p, while the compressive strain readily strengthens the orbital overlap, as discussed earlier. On the other hand, the intense strain can cause a phase transition from the cubic (α) to the orthorhombic (δ) phase. A stark distortion of the corner-sharing octahedral structure of PbI6 occurs under the δ-phase due to the Jahn–Teller effect40. The distortion makes the Pb-X-Pb bond angle deviate from 180°, where the induced strain exerts more influence on the bond angle than on the bond distance. Consequently, the compressive strain reduces the Pb-X-Pb bond angle, leading to a blueshift in the electronic bandgap based on the reduced SOC39,40,41.
Carrier dynamics
Strain-induced lattice deformation can modulate the electronic band structure and thus consequently affect the carrier dynamics. Figure 3 simulates the effective mass (m*) as a function of strain with corresponding band curvature from first-principle calculation of α-FAPbI332, taking majority components in the most recent mixed-perovskite systems8,9,10,11,18,19,20. The E-k dispersion of the valence band of α-FAPbI3 varies with changing strain, showing a more dispersed configuration for the tensile strain and less curvature for the compressive strain. Therefore, a reduced hole effective mass (mh*) is expected from the compressive strain, implying a better hole-transfer characteristic in the perovskite layer. The electron effective mass (me*) is comparably constant based on the small curvature change observed from the conduction band structure. It is notable that the strain exerts an effect on the overall carrier dynamics mostly by altering the hole-related properties.
The hole mobility is increased under compressive strain owing to the reduced mh* until the intense strain causes considerable dislocations16. A compromise between the lower mh* and the higher trap density due to the compressive strain leads to the highest hole mobility at −1.2% strain for α-FAPbI3 (Fig. 4a)32. The hole mobility tendency is well in accordance with the transient photocurrent results, showing the best performance at −1.2% strain for α-FAPbI3 (Fig. 4b)32. The carrier dynamics observed from (FAPbI3)0.85(MAPbBr3)0.15, one of the most widely used mixed-perovskite compositions, also correspond to the strain effect shown in α-FAPbI3. The (FAPbI3)0.85(MAPbBr3)0.15 under tensile strain demonstrates lower hole mobility than the strain-free film (Fig. 4c), as expected from the increased mh* of α-FAPbI3 with tensile strain. The substantial difference in the measured hole mobility between α-FAPbI3 and (FAPbI3)0.85(MAPbBr3)0.15, even after considering the compositional difference, may arise from the different film qualities and more significantly from the different analysis methods42. Nonetheless, the observed tendencies of the strain-induced hole mobility are well in line with each other. In Fig. 4d, the transient photocurrent of (FAPbI3)0.85(MAPbBr3)0.15 under tensile strain shows a 12.96 μs decay time, while it is highly reduced to 1 μs in the strain-free film35, indicating that the tensile strain effectively impedes hole extraction. Similarly, time-resolved photoluminescence (TR-PL) results demonstrate retarded hole extraction at the interface of (FAPbI3)0.85(MAPbBr3)0.15 with a longer quenching time under tensile strain35.
The enhanced charge extraction is readily reflected in the improved photovoltaic parameters, especially in the fill factor (FF) and open-circuit voltage (VOC). The ideality factor, n, is estimated by the slope of the VOC-light intensity curve to evaluate the recombination behavior, where n approaches 2 as trap-assisted recombination prevails over ideal radiative recombination (n ≈ 1)43. n is decreased from 1.55 to 1.05 when the tensile strain is removed, which is responsible for the improved FF and VOC in the device with the tensile strain-alleviated perovskite film35. It is noted that the component variation in each perovskite film and its singularity in the experimental process should be considered with care for interpretation of the results. The compressive strain in the MAPbBr3 film leads to an increased carrier lifetime with reduced trap density38, in accordance with the above interpretation. In contrast, the MAPbI3 film and the triple cation-based film (MA0.15FA0.79Cs0.06Pb(I0.85Br0.15)3) show a decreased PL intensity under compressive residual strain due to the predominant trap density30. The strain effect from the perspective of defect generation will be intensively discussed in the following section (“Crystallinity”) as closely related to nonradiative recombination.
Crystallinity
The local strain is naturally expected from the polycrystalline perovskite film, where the strain-induced structural defects readily govern the nonradiative recombination44,45. The local structural properties on the microscale can be studied by using micro-XRD (μXRD). Figure 5 shows the spatial maps of the peak scattering vector, q, of the azimuthally integrated <220> planes (Fig. 5a) and <222> plane (Fig. 5b) of the MAPbI3 film with a grain size of 0.5~1 μm. The q mapping apparently confirms the local structural heterogeneity in the MAPbI3 film. The two horizontal slices (indicated as d and e) taken from <220> show subtle shifts in the peak position accompanied by irregular peak broadening, indicating a microscale structural inhomogeneity of ~0.15% in the local q vector for <220>. The μXRD patterns from the two horizontal lines exhibit parallel coupling over a long range (~10 μm), while the two lines from <222> represent antiparallel coupling, which suggests the presence of a long-range region across several grains, sharing similar structural properties across subtle q variations.
The locally oriented strain feature over the long range is more specifically studied by performing nanofocus XRD (nXRD) on the nanoscale. A quiver plot of the <110> orientation of the MAPbI3 film is shown in Fig. 6a, where the diffraction information is represented as a colored arrow in the spatial position. The blue and red parts in the quiver plot indicate supergrains sharing similar crystallographic properties. Figure 6b, c, corresponding to the blue and red supergrains, respectively, reveal a similar strain feature over the large supergrains, though a subtle strain inhomogeneity still exists, as observed from the μXRD results. Remarkably, the largest supergrain for <210> of the MA0.15FA0.79Cs0.06Pb(I0.85Br0.15)3 film is as large as ~25 μm2, far beyond a single grain size of ~1 μm2, overlaid with the SEM image in Fig. 6d. Consequently, the supergrain concept based on a similarity in crystallinity is more important than other concepts in determining the local collective strain boundaries to evaluate structural properties.
The residual strain in the crystal is responsible for defect formation. Confocal PL measurements in the same μXRD region help directly correlate the local strain with the local radiative recombination behavior. Figure 7(a) represents the (compressive) strain mapping estimated from the μXRD map of the MAPbI3 film, where the indicated correlation region in the map matches the confocal PL mapping in Fig. 7b. Importantly, the monitored local PL heterogeneity is subjected to local strain distributions over the map. The comparably high compressive strain results in a low PL intensity (red open circle), while a high PL intensity is measured at the local point with negligible strain (blue open circle). The correlation between the carrier lifetime from TR-PL and the local strain is plotted in Fig. 7c, where the PL lifetime is seen to gradually decrease as the compressive strain is increased, suggesting structural defects with the compressive strain. Figure 7d depicts the local defect concentration as a function of the compressive <110> strain by using a first-principle atomic model. It is assumed that the charged iodide vacancy (VI+) concentration is increased by applying compressive strain30, indicative of pronounced nonradiative recombination assisted by generated defects under the high compressive strain level in the crystal.
It is worth noting that the collective structural/strain properties should be considered to correlate with the bulk properties over the local crystalline heterogeneity with a subtle variation, as discussed earlier. A peak broadening in PL and XRD is usually expected with residual strain owing to a reduced crystallinity on the macroscale. The α-FAPbI3 film under compressive strain results in PL peak broadening32, which is attributed to the reduced crystallinity coupled with the enhanced carrier-phonon coupling, as confirmed by temperature-dependent PL studies32. Similarly, peak broadening in high-resolution XRD patterns is also observed for α-FAPbI3 with increasing compressive strain and with reducing film thickness32. When a film is thinner than a critical thickness for plastic relaxation, the compressive strain level is directly reflected in the reduced crystallinity. After passing through the critical thickness, however, plastic relaxation occurs to relieve the compressive strain by generating dislocations16. Therefore, the increased PL intensity and the increased Vg are observed from a thick film whose thickness allows the compressive strain to be relieved by dislocations32. In the meantime, the increased trap density results from the increased compressive strain level as a consequence of defect propagation into the α-FAPbI3 film by plastic dislocations32, which is in accordance with the microscale defect tendency under compressive strain for the MAPbI3 film.
Crystal phase stability
One of the most important merits in tailoring lattice strain lies in ensuring the phase stability of the metastable perovskite film. The composition of recent perovskites has converged toward α-FAPbI3 as a major component in mixed-perovskite crystals8,9,10,11,18,19,20. The α-FAPbI3 phase shows a spontaneous transition to the nonperovskite δ phase (photoinactive yellow phase) at room temperature46. The instability of the α-FAPbI3 phase, therefore, promotes the incorporation of foreign ions (e.g., MA+, Cs+, Br-) to inhibit the transition to the δ phase by establishing an energetically stable α phase of the perovskite crystals with mixed components47. Notably, the residual strain in the lattice significantly influences the phase stability of α-FAPbI3, leading to superb phase stability under compressive strain even in the absence of foreign ions32. Two α-FAPbI3 films with the internal compressive strain (pink lines) and without strain (black lines) are prepared, and their long-term stabilities are monitored by XRD (Fig. 8a), PL (Fig. 8b), and Raman (Fig. 8c). The compressive strain is induced by using a lattice-mismatched substrate with a lower lattice parameter (please see section “Heteroepitaxial interface”. Heteroepitaxial interface for details), while the strain-free property is simply acquired by increasing the film thickness above the critical thickness for elastic relaxation. The critical thickness of the perovskite film for elastic relaxation is approximately 3 μm. Therefore, the 10 μm-thick film is suitable to be used as a strain-free film through elastic relaxation. In Fig. 8a, the XRD patterns of the α phase, <001> and <002 > , consistently remain even after 360 d under −2.4% (compressive) residual strain. On the other hand, the strain-free α phase immediately turns into the δ phase only after one day. The outstanding phase stability of α-FAPbI3 with compressive strain is confirmed by the PL and Raman results. The stable α phase under compressive strain can be understood in terms of the removal of the driving force for the phase transition. The residual tensile strain in α-FAPbI3, inherited from the film annealing process32, acts as a driving force and thus strongly drives the α phase to transform into the δ phase48. The compressive strain nullifies the driving force and inhibits the structural deformation for the phase transition from occurring32,48. Furthermore, the lower interface energy between the same α phases may also contribute to phase stabilization to some extent. The interface energy between the cubic substrate and the cubic α phase is lower than that with the δ phase, energetically favoring the phase. Interestingly, the improved stability of the MAPbI3 film is also observed under strain in a certain direction25. Figure 8d shows schematic illustrations of the strained MAPbI3 films in different ways by using bendable substrates. The strained films on the convex, flat, and concave substrates are exposed to ~50 mW/cm2 at 65 °C with encapsulation. After 500 h of stress, the strained film on concave substrates demonstrates outstanding phase stability, while decomposition into PbI2 is observed for the flat film as well as (to a more pronounced extent) for the convex film (Fig. 8e). The underlying mechanism is closely correlated to the ion migration energy (Ea). The Ea values of the convex, flat, and concave MAPbI3 films are 0.29, 0.39, and 0.53 eV, respectively, in the dark and 0.046, 0.074, and 0.083 eV, respectively, under 25 mW/cm2 illumination, as plotted in Fig. 8f. Therefore, the reduced Ea of the convex MAPbI3 film accelerates ion migration, facilitating decomposition as well as strain relaxation, whereas the increased Ea of the concave MAPbI3 film effectively suppresses ion migration. Indeed, the strain-involved MAPbI3 stability behavior is closely in line with the strain effect on α-FAPbI3 phase stability from the perspective of the strain tendency itself. The bending process for the MAPbI3 film varies the strain, particularly along the in-plane direction. The perovskite film typically has a tensile strain, emerging from the annealing process followed by cooling (see “Annealing process” for discussion)25,32,35. The compressive strain applied by concave bending hence effectively cancels the residual tensile strain in the flat MAPbI3 film, while convex bending aggravates the existing strain by intensifying the tensile strain. In conclusion, the in-plane compressive strain is beneficial for the phase stability of the overall halide perovskite films.
Notably, the tensile strain formed at the interface enables the black γ-phase of CsPbI3 to be energetically preferred over the yellow δ-phase at room temperature49. When α-CsPbI3, formed at 300 °C, is cooled to room temperature, free-standing isotropic α-CsPbI3 crystals turn into the photoinactive δ-phase because the unstrained yellow δ-phase is thermodynamically more stable than the γ-phase, showing Eγ–Eδ = 85 meV. However, a more pronounced volume reduction is required for the δ-phase (229 Å3 at 0 K) than for the γ-phase (241 Å3 at 0 K), which introduces different energy penalties for the strained films. The anisotropic (in-plane tensile) strain effectively hinders the black γ-CsPbI3 from converting to the δ-phase, ensuring the phase stability of the black CsPbI349.
Affecting parameters
The residual strain existing in the perovskite film is significantly determined by experimental conditions, including the perovskite material composition35, a substrate for film growth32, and external stimuli50,51,52 during the process and the measurement. In this regard, various affecting parameters during the experiments are discussed in the following paragraphs to understand their effect on the crystal and establish a strategy for deriving the most beneficial optoelectronic properties from halide perovskite films by tailoring the strain.
Annealing process (thermal stress)
As shown in Fig. 9a, various forms of MAPbI3 perovskite crystals are prepared based on different methods to modulate the lattice strain and subsequently studied by XRD. It is apparent that the annealed perovskite film (indicated as AF), prepared by a routine annealing process at 100 °C, exhibits a strain, leading to a slight XRD peak shift compared to the case of the single-crystal powder (SCP), which is a standard control sample for the strain-free crystal. The residual strain is formed by the annealing process because the nonannealed film (NAF) shows peak positions consistent with those of the single-crystal powder (SCP). The strain in the annealed film is readily removable by scraping the film to a powder form (SP), implying that the residual strain is maintained by adhesion to the substrate. It is notable that the XRD patterns of films mostly represent out-of-plane diffraction, as shown in Fig. 9c, which mainly reflects the plane distance parallel to the substrate. On the other hand, the in-plane information can be obtained as illustrated in Fig. 9d. A strain in a certain direction usually brings about an opposite strain component in the other direction for overall relaxation25. The tensile (compressive) in-plane (out-of-plane) strain induces a minor compressive (tensile) out-of-plane (in-plane) strain or vice versa. Therefore, the increased in-plane lattice distance (d⊥), indicative of tensile strain, is accompanied by the reduced out-of-plane lattice distance (d∥), indicating compressive strain, as evidenced by the opposite XRD peak shift feature in Fig. 9b.
A gradual peak shift to a higher 2θ angle is observed from the free-standing MAPbI3 crystals during the cooling process from 100 °C to 25 °C, owing to lattice shrinkage (Fig. 10a, c). Remarkably, the out-of-plane lattice contraction during cooling is more prominent in the perovskite film (Fig. 10b, d), which is accordingly ascribed to the lattice strain induced by film adhesion to the substrate. The shrinkage in the out-of-plane interplanar distance is more pronounced, resulting in a significant Δd∥, to compensate for the restrained in-plane contraction, leading to substantial in-plane tensile strain with negligible Δd⊥. In other words, the induced strain in the perovskite film is greatly governed by a difference in the thermal expansion coefficient (α) between the perovskite and the substrate. The α of MAPbI3 is 6.1 × 10−5 ~ 1.57 × 10−4 K−1 25,53, which is approximately one order of magnitude higher than that of common substrates (e.g., αglass = 3.7 × 10−6 K−1, αITO = 8.5 × 10−6 K−1)54. The perovskite film crystallized at high temperature should be cooled down to room temperature. Consequently, it is reasonable to expect the residual tensile strain along the in-plane direction of the annealed perovskite. The greater strain is induced not only by a larger difference in αT between the perovskite and the substrate but also by a higher temperature used for perovskite annealing, regardless of the perovskite composition (MAPbI3, α-FAPbI3, or any mixed composition) and the fabrication method (one-step, two-step, or antisolvent)25. Otherwise, a low-temperature-based process for perovskite crystallization can be another option to form a perovskite film with negligible strain dominated by the interface.
Heteroepitaxial interface
The residual tensile strain induced during the cooling process after annealing is unfavorable, especially for the phase stability of the perovskite film. Furthermore, the optoelectronic properties of the perovskite film are tunable in a sophisticated manner by modulating its internal strain. To take advantage of strain engineering for perovskite-based electronics, the induced strain should remain at the device operating conditions, usually room temperature and ambient pressure. In this regard, tuning the strain of the perovskite is attempted by the lattice mismatch at the interface with a substrate, which has a significant impact on the crystal growth of the epilayer (the perovskite film)32. Single-crystalline MAPbClxBr3−x crystals with cubic phase, synthesized by the inverse temperature growth method55, are used as substrates for α-FAPbI3. The lattice parameter of the single-crystalline substrate (dsub) is controlled by the ratio between Cl and Br in MAPbClxBr3−x, where the increase in x results in the XRD peak shifting toward a higher 2θ angle, indicating a reduction in the lattice parameter of the substrate (Fig. 11a). The α-FAPbI3 film grown on the single-crystalline substrate shows a gradual peak shift as a function of dsub. The lattice mismatch between α-FAPbI3 and the substrate is increased by decreasing dsub based on lattice parameters of 6.35 Å for strain-free α-FAPbI3 and 5.83–5.95 Å for MAPbClxBr3−x32. The increase in lattice mismatch leads to a α-FAPbI3 (001) peak shift to a lower 2θ angle (Fig. 11a), implying an increased lattice parameter along the out-of-phase direction as the in-plane compressive strain is applied by the lattice mismatch. The lattice strain level of α-FAPbI3 ranging from −0.8% to −2.4% is determined by the compositional variation of MAPbClxBr3-x (0 ≤ x ≤ 1.5). Qx and Qz shown in Fig. 11b correspond to the in-plane and out-of-plane reciprocal space coordinates, respectively. The reciprocal space mapping shows a decreased in-plane lattice parameter as well as an increased out-of-plane lattice parameter under the high strain level. A pronounced tetragonality of α-FAPbI3 is therefore estimated by increasing the lattice mismatch from 0% (strain-free) to −1.2% and −2.4% due to lattice deformation by epitaxial compressive strain. Thus, epitaxial crystal growth for strain-engineered perovskite films seems very effective and intuitive. The limit of this approach is the difficulty in acquiring a feasible highly crystalline substrate with the required lattice parameter for perovskite-based electronics.
Compositional material inhomogeneity
The chemical pressure induced by employing foreign ions is represented as lattice strain in crystals56,57. The inhomogeneity in a mixed perovskite film occasionally leads to a vertical gradient in residual strain35. The crystal structure of the (FAPbI3)0.85(MAPbBr3)0.15 perovskite film is investigated by measuring depth-dependent nanobeam electron diffraction patterns. Depths of 50 nm (b), 200 nm (c), and 500 nm (d) from the top surface are chosen for the probe, as indicated in Fig. 12a. The nanobeam electron diffraction patterns reveal that the lattice distance, d, is increased from 1.60 Å to 1.64 Å and 1.67 Å as the probe spot varies from 50 nm to 100 nm and 500 nm deep, respectively (Fig. 12b–d). Furthermore, the depth-dependent GIXRD also confirms the microscopic crystal inhomogeneity, where a peak shift to a lower 2θ, indicative of the increased d along the out-of-plane direction, is monitored as the probe depth is increased. The slope and the sign of the linear plot, 2θ as a function of sin2φ, correspond to the residual strain level and its direction, respectively36,37. In Fig. 12e, the fitted lines have a negative slope regardless of the probe depth, which indicates that d starts increasing by reflecting the in-plane strain component, corresponding to an in-plane tensile strain across the entire film. On the other hand, the strain level is highly governed by the probe depth, showing a higher absolute value of the slope near the top surface (50 nm deep) and a lower absolute value of the slope near the substrate (500 nm deep). The gradient in the in-plane tensile strain emerges vertically in the (FAPbI3)0.85(MAPbBr3)0.15 film, where the intense strain at the top surface is gradually relaxed with increasing depth to the bottom substrate. The observed gradient in the residual strain is well matched with the PL depth profile in Fig. 12f, where a gradual PL peak shift reflects the gradually decreasing tensile strain from the top to the bottom, leading to a lower Vg toward the bottom due to the increased antibonding overlap by relaxing the tensile strain. It is quite unusual for the in-plane tensile strain to be more intense at the top than at the bottom. The induced tensile strain usually prevails at the interface adjacent to the substrate because the tensile strain is highly governed by the α difference between the perovskite and the substrate, which typically results in the opposite trend25,32. This distinctive strain gradient, particularly in the mixed perovskite film, seems to originate from the evolution of the different perovskite compositions depending on the depth, as evidenced by the time-of-flight secondary ion mass spectrometry (TOF-SIMS) results shown in the inset of Fig. 12f. These results show an inconsistent depth profile of MA+ with an MA+-deficient region near the bottom substrate, in accordance with the decreased d along the out-of-plane direction near the top surface by employing a higher concentration of MA+. Therefore, the estimation of the residual strain should be carried out with care, especially in mixed perovskites, after considering the compositional inhomogeneity and distribution.
Summary and perspective
Halide perovskite films based on polycrystalline crystals exhibit strain inhomogeneity, which readily interferes with the bonding strength and thus changes the optoelectronic properties as well as the phase stability. The tensile strain along the in-plane direction arises in the perovskite film during cooling after the film is annealed. The residual tensile strain is mostly responsible for the unfavorable carrier dynamics and the phase stability as well. The overall characteristics of the perovskite crystals are improved by relieving the internal in-plane tensile strain and even further enhanced by inducing the residual compressive strain along the in-plane direction. Inability to control the residual strain would be a great barrier for perovskite-based electronics, whereas strain engineering is a powerful strategy for a sophisticatedly tailored lattice structure to derive demanding properties. Therefore, it is highly necessary to develop a strain tailoring method that is practically compatible with the process conditions for real devices where the intended residual strain remains intact under the device operating conditions. A low-temperature process, epilayer growth on a pre-expanded substrate, or lattice-mismatched substrate compatible with carrier extraction can be an option to fully control the residual strain and thus tune the optoelectronic properties with the ensured stability.
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Acknowledgements
This work was supported by National Research Foundation of Korea (NRF) grants funded by the Ministry of Science, ICT Future Planning (MSIP) of Korea under contracts NRF-2012M3A6A7054861 (Global Frontier R&D Program on Center for Multiscale Energy System), NRF-2016M3D1A1027663, NRF-2016M3D1A1027664 (Future Materials Discovery Program), NRF-2015M1A2A2053004 (Climate Change Management Program) and NRF-2020R1F1A1075558.
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Kim, HS., Park, NG. Importance of tailoring lattice strain in halide perovskite crystals. NPG Asia Mater 12, 78 (2020). https://doi.org/10.1038/s41427-020-00265-w
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DOI: https://doi.org/10.1038/s41427-020-00265-w
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