Formamidinium iodide: crystal structure and phase transitions

Crystal structure, thermal behaviour and phase transitions of formamidinium iodide were studied by DTG, DSC, powder diffraction and X-ray crystallography.

Abstract

At a temperature of 100 K, CH₅N₂ ⁺·I⁻ (I), crystallizes in the monoclinic space group P2₁/c. The formamidinium cation adopts a planar symmetrical structure [the r.m.s. deviation is 0.002 Å, and the C—N bond lengths are 1.301 (7) and 1.309 (8) Å]. The iodide anion does not lie within the cation plane, but deviates from it by 0.643 (10) Å. The cation and anion of I form a tight ionic pair by a strong N—H⋯I hydrogen bond. In the crystal of I, the tight ionic pairs form hydrogen-bonded zigzag-like chains propagating toward [20-1] via strong N—H⋯I hydrogen bonds. The hydrogen-bonded chains are further packed in stacks along [100]. The thermal behaviour of I was studied by different physicochemical methods (thermogravimetry, differential scanning calorimetry and powder diffraction). Differential scanning calorimetry revealed three narrow endothermic peaks at 346, 387 and 525 K, and one broad endothermic peak at ∼605 K. The first and second peaks are related to solid–solid phase transitions, while the third and fourth peaks are attributed to the melting and decomposition of I. The enthalpies of the phase transitions at 346 and 387 K are estimated as 2.60 and 2.75 kJ mol⁻¹, respectively. The X-ray powder diffraction data collected at different temperatures indicate the existence of I as the monoclinic (100–346 K), ortho­rhom­bic (346–387 K) and cubic (387–525 K) polymorphic modifications.

Chemical context  

Compounds with the general formula ABX ₃ [where A denotes an organic cation e.g. methylammonium (MA, CH₃NH₃ ⁺) or formamidinium [FA = CH(NH₂)₂, CH₃NH₃]; B = Pb, Sn; X = I, Br, Cl] belong to a class of hybrid organic–inorganic perovskites and perform as outstanding light harvesters. These compounds gave birth to a new field of photovoltaics – perovskite solar cells – when Kojima and co-authors used (MA)PbI₃ as a light sensitizer for the first time in dye-sensitized solar cells (DSSCs) in 2009 and showed 3.8% efficiency (Kojima et al., 2009 ▸). Since then, a revolutionary breakthrough has occured in this area and the highest efficiency now has reached 22.1%.

In 2014, the formamidinium cation was proposed to replace methyl­ammonium and the further investigation of (FA)PbI₃ disclosed its superiority to (MA)PbI₃ (Koh et al., 2014 ▸; Pang et al., 2014 ▸). In particular, it was found that (FA)PbI₃ exhibits higher thermal and moisture stability and has a lower bandgap than (MA)PbI₃ which gives a greater capacity for sunlight absorption (Koh et al., 2014 ▸; Han et al., 2016 ▸). Recently, it was shown that the properties of the compounds may be further optimized by tuning the MA/FA ratio and an efficiency of 20.5% has been reached for a mixed compound (Li et al., 2016 ▸; Jeon et al., 2015 ▸).

The main precursors to obtain (FA)PbI₃ are PbI₂ and formamidinium iodide (FA)I. Several methods of perovskite synthesis include steps where it can be obtained directly from (FA)I in a crystalline form (Zhou et al., 2015 ▸; Leyden et al., 2015 ▸). It also appears in a crystalline form and leads to a formation of low-dimensional phases when an excess of it is taken (Xi et al., 2016 ▸; Ma et al., 2017 ▸). Thus, the understanding of the (FA)I crystal structure gives valuable information for understanding the crystallization of formamidinium-based lead halide perovskites. Knowledge of the (FA)I crystal structure may also be of particular inter­est for computer simulations of the processes related to the crystallization of these perovskites. Surprisingly, despite the hundreds of papers published over the last several years that have mentioned (FA)I as a major precursor for hybrid lead halide perovskites, its crystal structure has remained unknown so far.

In this work, we investigated the structure of (FA)I (I) and its thermal behaviour by different physico-chemical methods.

Structural commentary  

At a temperature of 100 K, compound I crystallizes in the monoclinic space group P2₁/c. The formamidinium cation adopts a planar symmetrical structure [r.m.s. deviation is 0.002 Å, and the C—N bond lengths are 1.301 (7) and 1.309 (8) Å; Fig. 1 ▸]. The iodide anion does not lie within the cation plane, but deviates from it by 0.643 (10) Å. The cation and anion in I form a tight ionic pair by the strong N1—H1A⋯I1 hydrogen bond (Table 1 ▸ and Fig. 1 ▸).

Figure 1.

The mol­ecular structure of salt I. Displacement ellipsoids are shown at the 50% probability level. H atoms are presented as small spheres of arbitrary radius. Dashed line indicates the inter­molecular N—H⋯I hydrogen bond.

Table 1. Hydrogen-bond geometry (Å, °).

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1A⋯I1	0.90	2.77	3.612 (5)	156
N2—H2A⋯I1i	0.90	2.74	3.622 (4)	166

Symmetry code: (i) .

In order to understand the thermal behaviour of I at elevated temperatures, the sample was investigated by TG and DSC methods in the temperature region from 293 to 750 K at a rate of 5 K min⁻¹. The mass loss started from ∼520 K (Fig. 2 ▸). Differential scanning calorimetry revealed three narrow endothermic peaks at 346, 387 and 525 K, and one broad endothermic peak at ∼605 K. The first and the second peaks are related to solid–solid phase transitions, while the third and the fourth peaks are attributed to the melting and decomposition of I. Enthalpy of the phase transitions at 346 and 387 K are estimated as 2.24 and 2.87 kJ mol⁻¹, respectively.

Figure 2.

Thermogravimetry and differential scanning calorimetry analyses for I.

The X-ray powder diffraction data collected at different temperatures confirm the existence of different phases (Fig. 3 ▸). At low temperatures, salt I exists in a monoclinic phase and exhibits a significant change of the parameters with a rise in temperature (100 → 195 → 293 K, Fig. 3 ▸). A phase existing at 358 K is indexed in an ortho­rhom­bic crystal system [a = 7.3915 (8) Å, b = 6.3358 (8) Å, c = 5.2391 (9) Å; M(20) = 25, F(20) = 45]. Another high-temperature phase is cubic, exhibiting only a few reflections at 400 K [a = 5.0571 (5) Å; M(13) = 126, F(13) = 109]. It seems to be a plastic phase similar to a plastic phase for methyl­ammonium iodide (Ishida et al., 1995 ▸; Yamamuro et al., 1992 ▸).

Figure 3.

X-ray powder diffraction data for I at different temperatures.

Supra­molecular features  

In the crystal of I, the tight ionic pairs form hydrogen-bonded zigzag-like chains propagating toward [20] by the strong inter­molecular N2—H2A⋯I1ⁱ hydrogen bonds (Table 1 ▸ and Fig. 4 ▸). The hydrogen-bonded chains are further packed in stacks along [100] (Fig. 4 ▸) [symmetry code: (i) x − 1, −y + , z + ].

Figure 4.

The crystal structure of I demonstrating the hydrogen-bonded zigzag-like chains propagating toward [20]. Dashed lines indicate the inter­molecular N—H⋯I hydrogen bonds.

Synthesis and crystallization  

Polycrystalline powder of I was purchased from Dyesol and used without further purification. Single crystals suitable for X-ray structural study were obtained by recrystallization from an anhydrous ethanol solution by slow cooling.

Refinement  

Crystal data, data collection and structure refinement details are summarized in Table 2 ▸. X-ray diffraction study of I was carried out on the ‘Belok’ beamline of the National Research Center ‘Kurchatov Institute’ (Moscow, Russian Federation) using a Rayonix SX165 CCD detector. Reflection intensities measured were corrected for absorption using the Scala (Evans, 2006 ▸) program.

Table 2. Experimental details.

Crystal data
Chemical formula	CH5N2 +·I−
M r	171.97
Crystal system, space group	Monoclinic, P21/c
Temperature (K)	100
a, b, c (Å)	4.8211 (6), 13.776 (3), 7.0113 (10)
β (°)	98.06 (3)
V (Å3)	461.06 (14)
Z	4
Radiation type	Synchrotron, λ = 0.96990 Å
μ (mm−1)	15.38
Crystal size (mm)	0.06 × 0.05 × 0.03
Data collection
Diffractometer	Rayonix SX165 CCD
Absorption correction	Multi-scan (SCALA; Evans, 2006 ▸)
T min, T max	0.400, 0.600
No. of measured, independent and observed [I > 2σ(I)] reflections	5111, 949, 894
R int	0.070
(sin θ/λ)max (Å−1)	0.642
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S	0.039, 0.093, 1.06
No. of reflections	949
No. of parameters	38
H-atom treatment	H-atom parameters constrained
Δρmax, Δρmin (e Å−3)	0.87, −0.91

Computer programs: Marccd (Doyle, 2011 ▸), iMosflm (Battye et al., 2011 ▸), SHELXT (Sheldrick, 2015a ▸), SHELXL2014 (Sheldrick, 2015b ▸) and SHELXTL (Sheldrick, 2008 ▸).

The H atoms of the NH₂ groups were localized in the difference Fourier map and refined with fixed positional and isotropic displacement parameters [U _iso(H) = 1.2U _eq(N)]. The CH hydrogen was placed in a calculated position, with C—H = 0.95 Å, and refined in the riding model with a fixed isotropic displacement parameter [U _iso(H) = 1.2U _eq(C)].

Supplementary Material

CCDC reference: 1538402

Additional supporting information: crystallographic information; 3D view; checkCIF report

supplementary crystallographic information

Crystal data

CH5N2+·I−	F(000) = 312
Mr = 171.97	Dx = 2.477 Mg m−3
Monoclinic, P21/c	Synchrotron radiation, λ = 0.96990 Å
a = 4.8211 (6) Å	Cell parameters from 600 reflections
b = 13.776 (3) Å	θ = 4.0–36.0°
c = 7.0113 (10) Å	µ = 15.38 mm−1
β = 98.06 (3)°	T = 100 K
V = 461.06 (14) Å3	Prism, colourless
Z = 4	0.06 × 0.05 × 0.03 mm

Data collection

Rayonix SX165 CCD diffractometer	894 reflections with I > 2σ(I)
φ scan	Rint = 0.070
Absorption correction: multi-scan (Scala; Evans, 2006)	θmax = 38.5°, θmin = 4.0°
Tmin = 0.400, Tmax = 0.600	h = −6→6
5111 measured reflections	k = −17→17
949 independent reflections	l = −8→7

Refinement

Refinement on F2	Secondary atom site location: difference Fourier map
Least-squares matrix: full	Hydrogen site location: mixed
R[F2 > 2σ(F2)] = 0.039	H-atom parameters constrained
wR(F2) = 0.093	w = 1/[σ2(Fo2) + 0.7865P] where P = (Fo2 + 2Fc2)/3
S = 1.06	(Δ/σ)max < 0.001
949 reflections	Δρmax = 0.87 e Å−3
38 parameters	Δρmin = −0.91 e Å−3
0 restraints	Extinction correction: SHELXL2014 (Sheldrick, 2015b), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4
Primary atom site location: difference Fourier map	Extinction coefficient: 0.0064 (11)

Special details

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Ų)

	x	y	z	Uiso*/Ueq
I1	0.86658 (6)	0.38577 (2)	0.20022 (5)	0.0218 (2)
N1	0.6120 (9)	0.4171 (3)	0.6569 (7)	0.0250 (10)
H1A	0.7250	0.4174	0.5650	0.030*
H1B	0.6251	0.4648	0.7454	0.030*
N2	0.2540 (9)	0.3389 (3)	0.7860 (7)	0.0254 (11)
H2A	0.1352	0.2882	0.7776	0.030*
H2B	0.2515	0.3832	0.8801	0.030*
C1	0.4296 (11)	0.3478 (4)	0.6606 (8)	0.0227 (11)
H1	0.4233	0.2994	0.5637	0.027*

Atomic displacement parameters (Ų)

	U11	U22	U33	U12	U13	U23
I1	0.0230 (3)	0.0215 (3)	0.0217 (4)	0.00012 (9)	0.0054 (2)	−0.00041 (10)
N1	0.022 (2)	0.030 (2)	0.023 (3)	−0.0030 (18)	0.0030 (19)	0.000 (2)
N2	0.021 (2)	0.022 (2)	0.034 (3)	−0.0020 (17)	0.008 (2)	0.0011 (19)
C1	0.023 (2)	0.026 (3)	0.019 (3)	0.002 (2)	0.001 (2)	0.000 (2)

Geometric parameters (Å, º)

N1—C1	1.301 (7)	N2—H2A	0.8999
N1—H1A	0.9001	N2—H2B	0.9000
N1—H1B	0.9001	C1—H1	0.9500
N2—C1	1.309 (8)
C1—N1—H1A	119.7	H2A—N2—H2B	120.0
C1—N1—H1B	120.3	N1—C1—N2	125.8 (5)
H1A—N1—H1B	120.0	N1—C1—H1	117.1
C1—N2—H2A	119.7	N2—C1—H1	117.1
C1—N2—H2B	120.3

Hydrogen-bond geometry (Å, º)

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1A···I1	0.90	2.77	3.612 (5)	156
N2—H2A···I1i	0.90	2.74	3.622 (4)	166

Symmetry code: (i) x−1, −y+1/2, z+1/2.