Abstract
In this work CsPbIBr2 is doped with rubidium, where up to 12% of caesium atoms are replaced with those of rubidium. The obtained Cs1 − xRbxPbIBr2, x= (0, 0.02, 0.04, 0.06, 0.08, 0.10, 0.12), films were characterized by X-ray diffraction (XRD), the scanning electron microscope (SEM), photoluminescence (PL) and UV–visible spectroscopy. The integration of Rb+ ions into the lattice leads to a detectable change in optoelectronic and morphological structure. Substituting 6% of caesium atoms yields the best results, eliminating pinholes and elevating crystallite size and absorption coefficient by 116 and 125%, respectively. Other novel observations, of particular interest, include a slight increase in band-gap energy from 2.1 eV to 2.14 eV and a decrease in stability. Over a period of 15 days, where temperature and relative humidity kept at 23 °C and 20%, respectively, a larger amount of degradation was seen to take place as rubidium content was increased. Therefore, the doping of CsPbIBr2 with rubidium is most useful in the case where specifically film and crystal quality are desired to be targeted.
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1 Introduction
The rise of perovskite solar cells (PSCs) has been accompanied by an unprecedented increase in power conversion efficiency (PCE) from 3.8% to 25.5%, in just over a decade [1, 2]. Perovskites are crystal structures of the composition ABX3. In many cases, they can be predicted using the Goldschmidt tolerance and the octahedral factor [3,4,5]. Furthermore, they tend to have a cubic, tetragonal, or orthorhombic structure corresponding to a high, intermediate and low temperature phase, respectively [6]. Methylammonium-based devices catapulted perovskites into the spotlight, having shown exceptional optoelectronic properties including high absorption coefficients, long-carrier lifetimes, favourable spin–orbit coupling, low exciton binding energy, high proportions of free carriers, high mobilities and large diffusion lengths [7,8,9,10,11]. The combination of these outstanding properties with perovskite’s low cost and high scalability demonstrates why these materials have gained such notoriety in the photovoltaic community [12]. That said, there remains one fundamental property which plagues methylammonium-based devices and that is their inherent instability. This is catalysed by moisture, radiation and temperature, factors which the PSC will unavoidably be exposed to during its working life [13,14,15,16].
Since methylammonium-based devices degrade irreversibly back into the precursor components, one of which is volatile, partial substitution with an inorganic cation such as caesium arose as a way to harness the aforementioned optoelectronic properties whilst increasing stability [16, 17]. Similarly, this idea was taken further and completely inorganic devices were investigated. Whilst CsPbI3-based devices showed desirable band-gaps, they too demonstrated degradation, albeit via a reversible phase change [18]. On the other hand, CsPbBr3 showed exceptional stability; however, this came at the cost of increasing the band-gap. For these reasons, iodine–bromine alloys such as CsPbI2Br and CsPbIBr2 became of interest. These alloys strike a compromise between band-gap and stability, the latter being the subject of this work [19, 20].
To date, the highest obtained PCE for a CsPbIBr2-based device is 10.71%, which is just over half of the Shockley–Queisser limit, thus revealing research opportunities in the field [21, 22]. For tables on device PCEs and an overview of the field, see [22, 23]. Whilst the relatively high band-gap of CsPbIBr2 will limit its use in single-junction cells, its true potential may be harnessed as a top cell in a multi-junction, as highlighted by Oxford PV’s recent breakthrough [24, 25]. Until now, devices have been prepared via one-step spin coating, a gas-assisted method, spray-assisted deposition, dual-source thermal evaporation and two-step spin coating [20, 22, 26,27,28,29,30]. As it stands, one of the biggest problems in the field is the consistent deposition of high-quality films, with many reporting a high number of pinholes and small grain sizes [20, 23, 26, 29]. Some of the methods investigated to improve films include: the use of antisolvent to improve coverage and morphology, guanidinium iodide for surface passivation, adding a small amount of PbCl2 to the precursor solution, light soaking, intermolecular exchange, precursor solution ageing, band alignment via interface engineering and doping with magnesium [22, 23, 26, 30]. The latter being related most closely to this work, where the effects of doping CsPbIBr2 with rubidium is investigated. Whilst doping with Rb+ ions has been shown to have a beneficial effect on the sister materials CsPbIBr2 and CsPbBr3, as of yet, there appears to be a lack of equivalent research carried out on CsPbIBr2 [31,32,33].
2 Methodology
2.1 Materials
All chemicals were purchased from Tokyo Chemical Industry unless otherwise stated in parenthesis. The precursor solution consisted of caesium iodide (CsI), lead bromide (PbBr2) and rubidium iodide (RbI, 99 % from Alfa Aesar) dissolved in dimethyl sulfoxide (DMSO 99.9 %).
2.2 Thin film preparation
The Cs1 − xRbxPbIBr2 thin films were deposited on top of fluorine-doped tin oxide (FTO) substrates (TEC 15 A) by one-step spin coating technique, with an area of 2.5cm2, purchased from XOP Glass. Substrates were cleaned for 15 min in detergent, ethanol (LabKem), acetone (VWR Chemicals) and isopropanol (VWR Chemicals) in an ultrasonic bath before a further 15 min in the UV-Ozone, manufactured by Ossila. The CsPbIBr2 precursor solution was prepared by allowing CsI and PbBr2 to dissolve completely in DMSO (1 mL), at room temperature. To dope CsPbIBr2 with RbI, 0.5 M solutions with molar ratios of \(100-\text{x}: \text{x} : 100\)(CsI:RbI:PbBr2) were prepared, where \(\text{x}\) is the rubidium doping percentage. After the solution was mixed at 85 °C temperature and solutions were left to heat overnight in the glovebox. Samples were statically spin coated at 3500 RPM for 30 s, after which they were annealed for 5 min at 50 °C and then 250 °C. Samples were stored in inert N2 atmosphere until used.
2.3 Characterization techniques
Thin films of Cs1 − xRbxPbIBr2, where = 0 %, 2 %, 4 %, 6 %, 8 %, 10 and 12 %, were characterized by X-ray diffraction (XRD) using the RIGAKU Ultima IV with Cu kα radiation (λ = 1.5418 Å). Morphology images were taken using the scanning electron microscope (SEM) Quanta 200-FEI with an applied voltage of 1.5 kV. Optical properties were performed with an Ocean Optics HR4000 spectrophotometer and photoluminescence (PL) emission was driven by a He–Cd laser with a wavelength of λ = 405 nm (Fig. 1).
3 Results and discussion
To characterize the X-ray diffraction (XRD) peaks, a Rietveld Refinement was carried out. The refinement itself was found to be exceptionally precise, with Rwp = 5.94% and Rp = 4.30% (Fig. 1b). These values reflect the accordance between the predicted and measured spectra, with 0% corresponding to identical curves. The crystals were found to be strongly oriented in the (100) plane, with the bright peaks at 14.9° and 30.1° corresponding to the (100) and (200) indices. A small peak at 22° is believed to be attributed to the (110) plane. These results are in accordance with the literature [22, 26, 33], except for one study that found an orthorhombic structure with the primary peak at 30° belonging to the (220) plane [29]. The lattice was found to be tetragonal and belonging to the Pm-3 m space group, with a = b = 5.93278 ± 0.00030 and c = 5.88519 ± 0.00842. These results are in accordance with those found elsewhere [23, 34] (see Fig. S1 in supplementary materials) (Table 1; Fig. 2).
Interestingly, it seems that the full width at half maximum (FWHM) of the main diffraction peaks reaches its narrowest when 6 of caesium atoms are substituted with rubidium (see Fig. S2 in supplementary materials). Application of the Scherrer equation reveals that crystallite sizes take an approximately parabolic form, with a maximum at 6 [35, 36]. This maximum corresponds to an increase in crystallite size of 117% and 116%, corresponding to the (100) and (200) peaks, respectively, when compared to the non-doped sample. As the concentration of rubidium ions in the precursor solution was increased, all the peaks in the sample were systematically shifted. This can be seen for the (200) and (100) plane (Fig. 1d). This is likely attributable to the fact that Rb+ (1.52 A) has a smaller ionic radius than Cs+ (1.67 A), therefore a shift to higher angles correspond to a contraction of the unit cell [33]. Moreover, the contraction of the unit cell suggests that rubidium ions are substituting caesium rather than occupying interstitial sites.
To independently confirm the insertion of rubidium into the lattice, energy-dispersive X-ray spectroscopy (EDS) was performed (see Fig. S2 in supplementary materials). Given that Rb+ ions substitute Cs+ ions as A-site cations, it is possible to determine their population as
where \(R{b}^{+}\%\) and \(C{s}^{+}\%\) are the atomic percentages measured. Plotting this against precursor concentration yields a linear relationship with \(R{b}_{population}^{+}\approx R{b}_{precursor}^{+}\), suggesting that all the rubidium precursor is fully integrated into the structure (Fig. 3b).
Using the focused ion beam (FIB) it was possible to design a cut in the sample, allowing the thickness of the sample to be measured (Fig. 3a). Carrying out this process for all samples, an average thickness of 195nm was found, with a standard deviation of 13nm.
Observations carried out using the scanning electron microscope (SEM) revealed that the sample doped with 6% rubidium had the best quality overall, with no pinholes and uniform coverage (see Fig. 4). The reference sample showed an abundance of pinholes; however, increasing the rubidium content caused a decrease in the density of pinholes. Once the rubidium concentration was increased past 6 %, the film quality decreased. This can be seen in the 8% sample (Fig. 4d) where small pinholes are beginning to form once more. It is believed that these pinholes form when pockets of solvent remain within the material during the crystallization process [23]. Measuring the absorbance of the freshly prepared samples, it was possible to calculate their absorption spectrum using the thickness values (Fig. 5a). All samples have an absorption coefficient of around 2 × 104 cm−1 above 2.2 eV and show the onset of the optical band edge around 2.07 eV (≈ 600nm), which agrees with values found elsewhere [20, 29]. Whilst most samples had a comparable absorption coefficient to the non-doped sample, the 6% sample increased by 125 %. Intuitively, this makes sense, since the 6 % sample showed no pinholes in SEM (Fig. 4c) and larger crystallite sizes (Fig. 1d), suggesting it would be a more effective absorber. It should be noted, however, that the absorption coefficient scales inversely with layer thickness and as such the precision of these values are limited by the methods employed previously (Fig. 3a) [20, 29]. Employing the Tauc plot to estimate the band-gap, band-gap values increased slightly from 2.1 to 2.14 eV, as rubidium content was increased. Similar parts of the spectra were taken for the linear fit, to minimize any random errors (Fig. 5b).
To model the photoluminescence (PL) spectra taken, a predicted spectrum was constructed by summing two Gaussian functions of the form
where \({y}_{0}\), \(A\), \({x}_{c}\) and \(\omega\) are constants. Using this method, it was possible to discern a primary and secondary component of a given PL spectrum (Fig. 5c). The R2 value is a statistical measure of the similarity between curves, in the case that they are identical it is equal to 1. For these models, all R2 values lay above 0.996, except for the 4 % sample which had significantly more background noise. It is thought that the secondary components of the PL spectra arise, under illumination, due to the formation of iodine-rich phases [28] (see Table S1 in supplementary materials).
Combining the results from PL measurements with those from the absorption coefficient, it can be said that an increase in band-gap is almost certainly taking place as elevated quantities of rubidium are incorporated into the lattice (Fig. 5d). Given the limitations of the Tauc plot, band-gap values are almost perfectly in accordance with those taken from the primary PL component. Moreover, both techniques yield the desired band-gap value for the reference sample [20, 23, 26, 29]. To investigate the effect of rubidium incorporation on the stability of CsPbIBr2, the absorption coefficients were measured after the samples had been stored in ambient conditions (Fig. 6a). A batch of newly synthesized samples were kept in the laboratory for 15 days, during which temperature and relative humidity kept constant, at 23 °C and 20%, respectively.
In general, higher rubidium content is shown to correlate with accelerated degradation, demonstrated by films with larger quantities of Rb experiencing larger shifts in energy (Fig. 6a). Most likely, the absorption coefficient curves shifting to higher energies correspond to a progressive change from the meta-stable high-temperature α-phase towards the intermediate-temperature δ-phase, which is stable at room temperature. The shift is especially pronounced for the 12 % sample, which had changed phase within one day (Fig. 6b). It is possible that due to the decreased ionic radius of rubidium, the volumetric ratio between the PbX6 octahedra and A-site cations decreases, aggravating its thermodynamic instability [18].
4 Conclusion
In this study, the effect of rubidium incorporation in the CsPbIBr2 lattice is investigated via XRD, SEM, EDS and optical measurements. The correct incorporation of rubidium is independently confirmed from XRD peak shifts and EDS results. Grain size is shown to be a function of dopant content, taking its maximum value when 6% of caesium atoms are replaced with rubidium. SEM measurements reveal that the methodology yields layers with an average thickness of 195nm (σ = 13nm). In terms of morphology, the incorporation of rubidium, up to 6%, seems to favourably affect film coverage by decreasing pinholes. Optical measurements reveal that samples have an absorption coefficient around 2 × 104 cm−1 above 2.2 eV, with the 6% sample having a superior absorption coefficient. Absorption coefficient and PL measurements both suggest a slight increase in band-gap as rubidium content is increased. Overall, the sample with 6% rubidium showed the best results. Investigation into the stability of the prepared samples reveals that rubidium incorporation has an adverse effect on stability. Whilst doping CsPbIBr2 with rubidium seems to decrease stability, the technique brings a myriad of improvements to the crystal and film quality. As such it should be considered as a useful tool when developing high-quality thin films.
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Acknowledgements
This work was supported by Ministerio de Economía y Competitividad (Grant Number PID2019-107137RB-C21). One of the authors A.W.S. acknowledges the Generalitat Valenciana and the EU for financial support (ACIF/2020/286).
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Alexander Wyn Stewart, Amal Bouich, Bernabé Marí Soucase have direct or indirect financial interest in the subject matter discussed in the manuscript.
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Stewart, A.W., Bouich, A. & Marí, B. Inorganic perovskites improved film and crystal quality of CsPbIBr2 when doped with rubidium. J Mater Sci: Mater Electron 32, 24825–24833 (2021). https://doi.org/10.1007/s10854-021-06941-z
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DOI: https://doi.org/10.1007/s10854-021-06941-z