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Temperature-dependent morphology-electron mobility correlations of naphthalene diimide-indacenodithiophene copolymers prepared via direct arylation polymerization

Desiree Adamczak a, Bianca Passarella bc, Hartmut Komber d, David Becker-Koch e, Oleksandr Dolynchuk f, Simon B. Schmidt a, Yana Vaynzof e, Mario Caironi b and Michael Sommer *a
aTechnische Universität Chemnitz Polymerchemie, Straße der Nationen 62, 09111 Chemnitz, Germany. E-mail: michael.sommer@chemie.tu-chemnitz.de; Web: https://www.tu-chemnitz.de/chemie/polymer/
bCenter for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia, Via Pascoli 70/3, 20133 Milano, Italy
cDipartimento di Elettronica, Informazione e Bioingegneria, Politecnico di Milano, 20133, Milan, Italy
dLeibniz-Institut für Polymerforschung Dresden e.V. Hohe Straße 6, 01069 Dresden, Germany
eIntegrated Centre for Applied Physics and Photonic Materials and Centre for Advancing Electronics Dresden (cfaed), Technische Universität Dresden, Nöthnitzer Str. 61, 01187 Dresden, Germany
fExperimental Polymer Physics, Martin Luther University Halle-Wittenberg, 06120 Halle, Germany

Received 21st July 2021 , Accepted 3rd October 2021

First published on 4th October 2021


Abstract

A series of defect-free n-type copolymers poly(naphthalene diimide-alt-indacenodithiophene) P(NDI-IDT) comprising alternating naphthalene diimide (NDI) and indacenodithiophene (IDT) units is prepared using atom-economic direct arylation polycondensation (DAP). Copolymers with varying molecular weights up to Mn,SEC = 113 kg mol−1 are obtained in high yield and used to investigate the optical, thermal and electrical properties as a function of chain length. Two weak endotherms are seen in differential scanning calorimetry experiments at 68 °C and 180–220 °C, depending on molecular weight, which are ascribed to side chain (Tm,1) and main chain (Tm,2) melting, respectively. Thin-film morphologies are weakly crystalline for annealing temperatures below Tm,2, with organic field-effect (OFET) mobilities being on the order of 10−3 cm2 V−1 s−1. Under these conditions very low Urbach energies (EU) between 28 and 30 meV are found. However, thermal annealing above Tm,2 results in amorphous morphologies with hypsochromically shifted optical spectra, strongly increased EU and complete loss of mobility. In comparison to the well-investigated bithiophene analogue PNDIT2, P(NDI-IDT) thin films are significantly less crystalline, and solutions lack the typical features of aggregation. This is ascribed to the additional bulky hexylphenyl side chains of P(NDI-IDT) that hamper main chain ordering and aggregate formation and thus, interchain charge hopping. With intrachain transport being limited as well, field-effect electron mobilities are limited to ∼10−3 cm2 V−1 s−1 and mostly independent of chain length. These results demonstrate the importance of both intra- and interchain transport to electron mobility for NDI main chain copolymers.


Introduction

Conjugated polymers are useful materials for high-performance organic electronic devices1–3 such as organic solar cells (OSCs)4,5 or organic field-effect transistors (OFETs).4,6 Especially donor–acceptor copolymers have emerged as modular systems due to versatile tailoring of their structural and electronic properties by suitable selection of donor and acceptor blocks.7–9 In the last decade, one focus has been the development of new n-type polymers for OSCs and OFETs.10–14 Many of these n-type conjugated polymers are based on naphthalene diimide (NDI), perylene diimide (PDI) or bithiophene imide (BTI).10,15–17 A prominent and well-known representative is the naphthalene diimide bithiophene copolymer P(NDIT2), which exhibits intriguing optical and electrical properties.16,18,19 Thus, it has been widely employed in all-polymer solar cells (all-PSCs) yielding power conversion efficiencies (PCEs) up to 10%.20–22 Moreover, derivatization of P(NDIT2) as lead structure upon variation of the NDI monomer,23–25 the donor comonomer,15,16,26,27 or the side chains28–31 has been the subject of many reports. While performance of n-type polymers is rapidly catching up in the area of organic photovoltaics (OPVs),10,32,33 progress in other domains such as organic thermoelectrics and energy storage systems may still profit from further development.34,35 The replacement of bithiophene with the fused donor indacenodithiophene (IDT) has opened up further possibilities for n-type copolymers.28,36–38 IDT building blocks are highly rigid and coplanar and can be easily modified by, for example, side chain variation and backbone extension.39–41 Thereby, polymers such as PIDTBT were designed with low degree of energetic disorder leading to superior charge transport properties.39,42–44 Copolymerisation of IDT with NDI yields low band gap copolymers with n-type transistor characteristics and typical dual band absorption in the red and blue region of visible light. First fabrications of all-PSC devices in combination with common donor materials such as J51,36 PBDB-T38 and PBZ-C628 has led to PCEs of >5%. Another possible application are flexible n-channel organic phototransistors (OTPRs) which can be used in skin therapy systems yielding mobilities in the range from 10−5 to 10−4 cm2 V−1 s−1.37

Next to the choice of building blocks, control over molecular weight (MW) and defects are prime prerequisites for optimizing performance and achieving reproducibility. Syntheses of copolymers based on NDI and/or IDT mostly employ Stille polycondensation,36–38 a technique that comes along with several well-known drawbacks.45–50 The use of direct arylation polycondensation (DAP) is not only more atom-economic, cost-efficient and faster as less reaction steps are involved,47,51,52 but also ideally suited for virtually all combinations of NDIBr2 and thiophene-based comonomers.21,26,53–55 Thus, DAP has been successfully applied to the synthesis of defect-free NDI-based copolymers.26,53,54 However, few reports on IDT-based copolymers made by DAP exist, and little is known about defects.28,56–58 Recently, we reported synthesis of well-defined IDT homo- and copolymers via DAP.59,60 However, in order to optimize the performance of the material it is essential to understand its structure–property relationships. The influence of MW, end groups, processing solvents and post-temperature treatments are important factors that govern morphology and need to be optimized to understand the performance of new materials for organic electronics.

Here we present a detailed study of the synthesis, the characterization and the effect of annealing temperature on the morphology and optoelectronic properties of P(NDI-IDT) made by DAP. Polycondensation of n-hexylphenyl-substituted IDT with NDIBr2 yields defect-free P(NDI-IDT) in high yields and varying molecular weights up to Mn,SEC = 113 kg mol−1. The polymers show a broad CT band around 728 nm with a band gap of 1.5 eV. While in solution the CT band is highly affected by MW, thin film absorption is mostly dependent on thermal annealing. For annealing below main chain melting, P(NDI-IDT) thin films show weakly crystalline behavior and very low Urbach energies below 30 meV. However, field-effect mobilities are at a modest level, on the order of 10−3 cm2 V−1 s−1. Upon thermal annealing above main chain melting, thin film morphologies become amorphous, resulting in blue-shifted absorption, significantly increased Urbach energies and loss of mobilities. Compared to P(NDIT2), thin films show much weaker crystallinity and lower field-effect mobilities, mainly owing to the additional bulky hexylphenyl side chains in P(NDI-IDT) that hinder aggregation and interchain charge transport.

Results and discussion

Synthesis and characterization

Copolymerization of n-hexylphenyl-substituted indaceno-dithiophene (Ph6-IDT) and 2,6-dibromonaphthalene diimide with 2-octyldodecyl side chains (NDIBr2) via DAP yielded P(NDI-IDT) copolymers with high molar masses Mn,SEC up to 113 kg mol−1 (Scheme 1 and Table 1). These rather high values were achieved as a result of appropriately chosen reaction conditions as well as high solubility, which in turn is caused by side chains being present at both comonomers. Control over molecular weight could be achieved by regulation of reaction temperature and monomer concentration. A reduction of either one of these parameters led to an increase in molar mass (entries P4–P6). We assume that lowering monomer concentration allow longer chains to build up before gelation of the reaction mixture sets in. A reduction of the reaction temperature may suppress degradation of NDI-Br chain ends, similar to previously reported IDT copolymers with benzodiathiazole.60 Interestingly, all polymerizations stopped following gelation of the mixture after a few hours, indicating a rapid build-up of MW. An exception is entry P1, where the low concentration and higher catalyst loading in combination with the addition of a phosphine–ligand facilitates nucleophilic substitution of NDI-Br chain ends by pivalate, leading to NDI-OH end groups (after hydrolysis) and accordingly low molar mass.18,26,53
image file: d1ma00633a-s1.tif
Scheme 1 Synthesis of P(NDI-IDT) via direct arylation polycondensation.
Table 1 Reaction conditions of P(NDI-IDT)a
Entry Solvent [IDT] (M) T (°C) Cat/P-ligand (mol%) M n/Mwb (kg mol−1) Đ Yieldc (%)
a NDIBr2 (1.0 eq.), Ph6-IDT (1.0 eq.), PivOH (1 eq.) and K2CO3 (3 eq.) were used in all entries. b From size exclusion chromatography (SEC) in CHCl3. c Isolated yield after Soxhlet extraction with acetone, ethyl acetate and chloroform.
P1 Mesitylene 0.1 100 5/20 18/25 1.4 60
P2 Mesitylene 0.25 100 5/20 43/86 2.0 91
P3 Toluene 0.25 100 2/— 61/113 1.9 85
P4 Mesitylene 0.1 100 2/— 103/516 5.0 79
P5 Mesitylene 0.25 100 2/— 76/188 2.5 90
P6 Mesitylene 0.25 80 2/— 113/295 2.6 90
P7 Mesitylene 0.5 100 2/— 64/140 2.2 86


High temperature 1H NMR measurements at 120 °C in C2D2Cl4 allow to prove this end group by a characteristic signal53 at 8.38 ppm for the proton ortho to the OH group (Fig. 1a). Without the usage of the P-ligand the polymers contain predominantly – IDT-H end groups (Fig. 1b and Fig. S2, ESI). Ph8-PIDT is a model compound for IDT-IDT homocouplings. The signals from the phenyl rings do not overlap with P(NDI-IDT) signals and their appearance in the P(NDI-IDT) spectrum should indicate such defects. Fortunately, the 1H NMR signals of the P(NDI-IDT) backbone are well separated, but apart from end group signals, additional signals that indicate structural defects are absent. We therefore conclude that P(NDI-IDT) is defect-free, which is in accordance with similar NDI copolymers made by DAP.18,26,53,54 Detailed 1H and 13C NMR analyses are provided in the ESI (Fig. S1–S4).


image file: d1ma00633a-f1.tif
Fig. 1 1H NMR spectra of (a) P7 and (b) P6. (c) depicts the 1H NMR spectrum of model compound Ph8-PIDT. Squares and dots mark signals of the –NDI-OH and the –IDT-H end groups, respectively.

Optoelectronic and thermal properties

The UV-vis spectra of P(NDI-IDT) in dependence of molecular weight are shown in Fig. 2a and b.
image file: d1ma00633a-f2.tif
Fig. 2 Molar extinction coefficient (a) and normalized (b) UV-vis spectra of P(NDI-IDT) of different MW (Mn in g mol−1) in chloroform solution at room temperature. Solvent dependent (c) and film (d) UV-vis spectra of P3 (Mn = 61 kg mol−1).

In chloroform solution, the polymers are characterized by a pronounced π–π* band at 395 nm and a broad charge transfer (CT) band at 728 nm with an absorption edge at 818 nm and a slight vibronic shoulder around 650 nm. Neither molecular weight nor the nature of the end groups influence the shape of the absorption spectra. In contrast, the molar extinction coefficients are strongly dependent on molecular weight (Table 2).61 Compared to P(NDIT2), the absorption maximum of the low energy band exhibits a bathochromic shift of 35 nm (Fig. 2b), that can be attributed to the stronger donor strength of the IDT building block compared to bithiophene. However, the relative intensity of the CT band is lower, pointing to a reduced electronic interaction between NDI and IDT.23,26 To investigate the optical properties in more detail we chose polymer P3 with a medium molar mass of ∼60 kg mol−1 (Fig. 2c and d). The solvent has a moderate impact on absorbance. The vibronic shoulder of the CT band is most pronounced in the non-polar solvent toluene. In polar solvents such as tetrahydrofurane (THF) and dichloromethane (DCM) the CT band is slightly blueshifted (Fig. 2c). High-temperature UV-vis spectra do not show significantly altered spectra (Fig. S6, ESI). All these results are consistent with highly soluble copolymers that feature weak aggregation in solution. This is different to the optical behavior of P(NDIT2) and is caused by the additional side chains of P(NDI-IDT) located at IDT which hamper ordering processes.62

Table 2 Summary of optical and thermal properties of selected samples
Entry M n/Mwa (kg mol−1) λ abs,max (nm) ε abs,max (103 L mol−1 cm−1) T m1 (°C) T m2 (°C) T c (°C) ΔHm2c (J g−1) ΔHcc (J g−1)
a From SEC in CHCl3. b Measured in chloroform at room temperature; molar extinction coefficient was calculated from maximum wavelength of the low-energy band (see non-italic values). c DSC measured with 20 K min−1 under N2.
P1 18/25 394/726 21 68 183 178 4.03 4.58
P2 43/86 395/731 27 65 202 191 1.90 1.76
P3 61/113 395/728 29 66 207 196 0.79 0.72
P4 103/516 394/726 56 69 213 201 0.64 0.84


Thin film absorption and the influence of the annealing temperature is displayed in Fig. 2d. As spun films show spectra qualitatively similar to those of toluene solutions but with bathochromic shifts of around 40 nm. The spectral shift and the increased intensity of the CT band is attributed to conformational changes/planarization of the polymer backbone as well as chain–chain interactions during film formation. Thermal annealing below main chain melting (cf. Fig. 4) at temperatures of 100–150 °C slightly changes CT band intensity. Annealing at 250 °C, which is above Tm2, however, reduces CT band intensity as well as causes a hypsochromic shift of 16 nm. Additionally, a new band with low intensity and of unknown nature around 850 nm appears. The onset of the absorption band is used to determine the optical bandgap of P1–P4. The spectra reveal an optical bandgap for P(NDI-IDT) of 1.57 eV in solution and a slightly smaller band gap of 1.50 eV in film. The electrical band gaps extracted from cyclic voltammetry (CV), are about 1.85 eV in film and 1.69 eV in solution, respectively (Fig. 3 and Table 3).


image file: d1ma00633a-f3.tif
Fig. 3 Cyclic voltammograms of P(NDI-IDT) as film deposited on an ITO substrate in a 0.1 M NBu4PF6 acetonitrile solution (black) and in a 0.1 M NBu4PF6o-DCB solution (red) at a scan rate of 50 mV s−1.
Table 3 Summary of electrochemical properties
λ onsetabs (nm) E g,opt (eV) E g,el (eV) E ox (V) E red (V) E red 1/2 (V) HOMOd (eV) LUMOd (eV)
a Films were spin coated on ITO substrate (1000 rpm, 60 s) from o-DCB solutions. b In o-DCB solution at r.t. c Determined from absorption onset. d Calculated as followed HOMO = [Eox + 4.8] eV and LUMO = [−E1/2red − 4.8] eV.
Filma 824 1.50 1.85 0.76 −1.09 −1.10 −5.56 −3.71
Solutionb 789 1.57 1.69 0.53 −1.12 −1.17 −5.32 −3.63


Compared to CV measurements in solution with a calculated HOMO of −5.32 eV, the determination from film CV results in a lower lying HOMO energy level of −5.56 eV (Table 3 and Fig. 3). However, the reduction onset E(Red) in solution and film are similar yielding comparable LUMO energy levels of −3.63 eV and −3.71 eV, respectively. The calculated LUMOs are slightly less negative than reported values for P(NDIT2)23,26,38 and reflect the stronger donor character of IDT in comparison to bithiophene.

P(NDI-IDT) shows excellent thermal stability with a degradation temperature greater than 440 °C (Fig. S7, ESI). The thermal properties were further investigated by differential scanning calorimetry (DSC) as a function of molecular weight (Table 2 and Fig. S8, ESI). P1–P4 exhibit weakly semicrystalline behavior seen by two broad and weak endothermic transitions during heating around Tm1 = 68 °C and Tm2 = 178–223 °C depending on molecular weight. Both transitions are most distinct in P1 with lowest MW (Fig. 4a and Fig. S8, ESI). Tm1 around 68 °C vanishes in the second heating cycle and reappears in the first heating cycle after the sample was stored at room temperature for several weeks. In analogy to P3HT,63 we hypothesize that Tm1 arises from side chain melting and Tm2 from main chain melting (Fig. 4b). Apparently the rather high density of side chains of P(NDI-IDT) allows for some ordering, and thus, for the appearance of an endothermic peak in the DSC traces not seen with P(NDIT2). The mixed structure of side chains and their rather random orientation may cause the slow crystallization over a time scale much larger than that of the DSC experiment.


image file: d1ma00633a-f4.tif
Fig. 4 (a) DSC curves of P1 (Mn = 18 kg mol−1). First and second cycles were measured under N2 with 10 K min−1 before and with 20 K min−1 after room temperature aging; (b) side chain Tm1 and main chain Tm2 melting transitions in dependence of MW.

Charge transport properties

Organic field-effect transistor (OFET) devices with a top-gate bottom-contact configuration were fabricated to investigate the electron transport properties of P(NDI-IDT). The devices show n-channel behaviour and were optimized by screening the solvent for spin coating, annealing temperature, contact engineering and channel length (Fig. 5 and Fig. S9, S10, ESI). While the solvent seems to have a minor influence on the transfer characteristic curves, the annealing temperature has a greater impact (Fig. 5a and b). Annealing of the devices at moderate temperatures, up to 150 °C, is necessary to enhance their performance, but is deleterious for annealing temperatures that approach Tm2 (Fig. 5b and Table 4).
image file: d1ma00633a-f5.tif
Fig. 5 Optimization of OFET devices. Effect of solvent for spin coating (a) and annealing temperature for P3 (b). Transfer curves of optimized devices as a function of MW (g mol−1) and channel length (c and d).
Table 4 OFET data of P3 devices at different annealing temperaturesa
T anneal (°C) V th (V) On/off ratio μ sat (cm2 V−1 s−1)
a Devices with L = 20 μm were used in all entries. b Calculated at Vd = 5 V in linear scale. c Calculated at Vd = 40 V. d No mobilities could be extracted due to noise in the measurements.
Not annealed 2.8 ∼103 1.5 × 10−3
120 1.9 ∼104 3.9 × 10−3
150 1.7 ∼104 4.2 × 10−3
180 2.5 ∼103 5.3 × 10−4
250d


The charge mobilities of the optimized OFET devices in the saturation regime (Vd = 40 V) are in the order of 10−3 cm2 V−1 s−1 (Table 5). The reduction of the channel length from 20 to 5 μm resulted in a correct scaling of currents, suggesting that contact resistance is not a limiting factor for the estimated field-effect mobility. The current as well as electron mobility increases with increasing molecular weight up to Mn = 61 kg mol−1 and afterwards slightly decreases for the highest MW sample P4 (Fig. 5c and d).

Table 5 OFET characteristics of optimized devices (Tanneal = 150 °C) in dependence of MWa
Entry M n/Mw (kg mol−1) V th (V) On/off ratioc μ sat (cm2 V−1 s−1)
a Devices with L = 20 μm were used in all entries. b Calculated at Vd = 5 V in linear scale. c Values are similar for Vd = 5 V and Vd = 40 V. d Calculated at Vd = 40 V.
P1 18/25 1.8 ∼103 1.1 × 10−3
P2 43/86 2.8 ∼102 4.4 × 10−3
P3 61/113 1.9 ∼103 3.9 × 10−3
P4 103/516 3.4 ∼104 1.7 × 10−3


Overall, the MW dependence of mobility is rather limited. In general, electron mobilities are up to three orders of magnitude lower than the reported values for P(NDIT2).26

In order to better understand the OFET behaviour as a function of the annealing temperature, we first carried out photothermal deflection spectroscopy (PDS) on thin films of P3 and P(NDIT2) as reference. This sensitive technique provides insight into the electronic order of polymer thin films. Thereby, the bandgap edge absorption of polymer films is measured to extract the so-called Urbach energy UE. UE is known to be related to the degree of energetic disorder of the material and hence is typically associated with the charge transport properties.41,42,64,65 The thin films were prepared analogously to the OFET fabrication process. P(NDI-IDT) P3 exhibits a sharp sub-band gap absorption and an extracted value UE = (29.3 ± 0.9) meV (Tanneal = 120 °C). The value is comparable to P(NDIT2) which exhibits UE = (30.6 ± 0.9) meV (Fig. 6 and Table 6). Further experiments in which the influence of annealing temperature on the energetic disorder were investigated, show that annealing at temperature higher than 150 °C is detrimental for the energetic order of the material (Table 6). Interestingly, the lowest Urbach energy (28.2 ± 1.0 meV) could be extracted from the absorption of the P3 as spun thin film, which is one of the lowest reported values for conjugated polymers (Fig. 6).42,66 These observations clearly show that UE alone cannot grasp the complexity of charge transport process in a polymer thin film. While UE can help to understand the relation between thin film morphology and energetic order of optically probed states, the accessibility of such states along the channel of a transistors through an efficient percolative path is a requirement for high carrier mobility. The presence of bulky hexylphenyl side chains at the IDT unit, hindering solution aggregation, as well as crystallization and overall interconnectivity in thin films, can have a drastic effect on morphology and interchain transport. The latter plays a dominant role in the case of highly localized states, as is typical of NDI-based co-polymers, where intrachain transport is not effective.67,68


image file: d1ma00633a-f6.tif
Fig. 6 Comparison between the absorption of P3 (Mn = 61 kg mol−1) and P(NDIT2) (Mn = 62 kg mol−1) thin films in dependence of the annealing temperature; measured by photothermal deflection spectroscopy. The solid line displays the corresponding exponential fits for extraction of the Urbach energy UE. Films were spin-coated (1000 rpm, 60 s) from o-DCB solutions.
Table 6 Urbach energy of P3 and P(NDIT2) in dependence of annealing temperaturea
Entry T anneal (°C) U E (meV)
a Films were spin-coated (1000 rpm, 60 s) from o-DCB solutions and annealed at the given temperature for 30 min under argon.
P3 Not annealed 28.2 ± 1.0
P3 120 29.3 ± 0.9
P3 250 41.7 ± 2.9
P(NDIT2) 120 30.6 ± 2.0


GIWAXS measurements

To gain further information about the molecular packing of P(NDI-IDT), grazing incidence wide-angle X-ray scattering (GIWAXS) measurements were performed on thin films of P3. The films were prepared using the conditions for the best OFET device with Tanneal = 120 °C (below main chain melting) and, in comparison, for annealing above main chain melting at Tanneal = 250 °C. The results are illustrated in Fig. 7a–d. The sample annealed at 120 °C shows a low degree order suggesting a liquid crystalline organization rather than a crystalline one. The observed (100) and (200) peaks at q = 0.334 Å−1 and q = 0.668 Å−1 allowed determining the interchain d100-spacing along the side chain direction being 18.81 Å. The azimuthal distribution of the (100) peak clearly indicates a preferential edge-on orientation (Fig. 7a and b). Furthermore, the 2D GIWAXS image and the 1D scattering curves extracted from it along meridian and equator do not show any prominent π–π stacking peaks (Fig. 7a and b). Such observation confirms the drastic effect of the molecular structure on the π–π stacking disorder, introducing energetic barriers to interchain transport of electrons through the films. Upon annealing at 250 °C (Fig. 7c and d) the material evidences a solely edge-on orientation and a significantly reduced molecular ordering, as the area below the (100) peak decreased by about 20 times (see ESI, Figure S11), with a slightly decreased d100-spacing. The dependence of the annealing temperature on the molecular ordering complies with the previously discussed reduction of the CT absorption band and can partly explain the diminished mobilities for annealing above 150 °C.
image file: d1ma00633a-f7.tif
Fig. 7 GIWAXS patterns and 1D GIWAXS profiles of P3 thin films annealed at 120 °C (a and b) and at 250 °C (c and d) as well as of P(NDIT2) thin film annealed at 120 °C (e and f).

In order to investigate the difference of ordering between P(NDI-IDT) and P(NDIT2), the GIWAXS measurements of a P(NDIT2) film annealed at 120 °C were carried out (Fig. 7e and f). In contrast to the edge-on orientation of P(NDI-IDT), P(NDIT2) exhibits a predominant face-on orientation. In addition, a (020) diffraction peak corresponding to the π–π stacking distance of 3.94 Å can be monitored suggesting a significantly higher crystalline order than that in P(NDI-IDT).

Experimental

Materials and methods

All starting materials were purchased from commercial sources and used without further purification unless otherwise specified. All reactions were carried out in flame dried glassware and under dry inert gas atmosphere. Compounds Ph6IDT, NDIBr2 and the model compound Ph8-PIDT were synthesized according to published protocols.59,60,69

Detailed information about instrumentation and experimental procedures are described in the ESI. SEC curves of the samples P1–P7 are shown in Fig. S5.

Synthetic procedures

General synthetic procedure for synthesis of P(NDI-IDT) via DAP (P6). Ph6IDT (141.1 mg, 155.5 μmol, 1 eq.), NDIBr2 (153.2 mg, 155.5 μmol, 1 eq.), pivalic acid (15.9 mg, 155.5 μmol, 1 eq.) and potassium carbonate (64.5 mg, 466.6 μmol, 3 eq.) were placed in a vial and dissolved in 0.62 mL degassed mesitylene. Then Pd2dba3 (2.8 mg, 2 mol%) were added under argon and stirred for 48 h at 80 °C. After cooling to room temperature, the mixture was diluted with chloroform, precipitated into methanol and purified by Soxhlet extraction with acetone, ethyl acetate and chloroform. The chloroform fraction was filtered through a silica gel plug and dried overnight in a vacuum oven at 50 °C to afford a dark green solid. Yield: 243 mg (90%).

Conclusions

We have presented a robust and atom-economic friendly protocol to prepare highly soluble alternating copolymers made from naphthalene diimide (NDI) and indacenodithiophene (IDT) via direct arylation polycondensation. Detailed molecular characterizations indicate that P(NDI-IDT) is defect-free. Molecular weights (MWs) up to Mn,SEC = 113 kg mol−1 can be tuned by an appropriate adjustment of reaction conditions. The optical behaviour of the polymers indicate weakly aggregated chains. In solution, the absorption spectra are almost independent of temperature and moderately influenced by the type of solvent. Thermal annealing of thin films above 150 °C results in hypsochromically shifted spectra and reduced intensity of the CT band. While molar extinction coefficients and thermal properties do depend on MW, absorption onset and maximum of the charge transfer band are not affected by MW. DSC shows two weak and broad endothermic transitions which are ascribed to side chain and main chain melting. Optimization of the OFET devices reveal that annealing is important to boost performance, but it is deleterious at temperatures above 150 °C, where films lose their weak crystallinity. Electron mobilities are moderate and mostly independent of MW for as spun films and entirely vanish for thermal annealing above main chain melting. Urbach energies are very low for as spun films but rather higher after thermal annealing above main chain melting. GIWAXS reveals a very weakly crystalline morphology of films after spin coating and an almost entirely amorphous morphology after thermal annealing above main chain melting. Taken together, both low Urbach energies as well as a semicrystalline morphology with chain–chain contacts are required for efficient charge transport. The latter is not possible in P(NDI-IDT) films, as the additional and bulky hexylphenyl side chains do not allow for significant solution aggregation and crystallization in thin films. These results emphasize the importance of interchain transport for high carrier mobility, especially if intrachain transport alone is not efficient as is the case with P(NDIT2). Side chain variation at the IDT monomer may allow control over aggregation for P(NDI-IDT) to capitalize on its very low Urbach energies as well as on fibrillar morphologies commonly seen with P(NDIT2).

Author contributions

D. Adamczak synthesized the polymers and characterized them by SEC, UV-vis and PL spectroscopy, cyclic voltammetry, TGA as well as DSC analyses. D. Adamczak wrote the first draft of the manuscript. B. Passarella and M. Caironi characterized the polymers in organic field-effect transistors. H. Komber performed high-temperature NMR spectroscopy and evaluated the data. D. Becker-Koch and Y. Vaynzof performed PDS experiments. O. Dolynchuk carried out the GIWAXS measurements and evaluated the data. S. Schmidt synthesized P(NDIT2). M. Sommer designed and supervised the work. All authors were involved in revising the manuscript.

Conflicts of interest

There are no conflicts to declare.

Acknowledgements

The authors thank M. Raisch and R. Hertel for DSC measurements and D. Stegerer for TGA measurements. M. S. acknowledges the DFG for funding (project SO1213/8-2). O. D. acknowledges financial support from the European Union (EFRE). Y. V. thanks the Fulbright Commission for support (Fulbright-Cottrell Award 2018). The OFETs fabrication of this work was partially carried out at Polifab, the micro- and nanotechnology center of the Politecnico di Milano.

Notes and references

  1. Y. J. Wang and G. Yu, J. Polym. Sci., Part B: Polym. Phys., 2019, 57, 1557–1558 CrossRef CAS.
  2. J. de Mello, J. Anthony and S. Lee, ChemPhysChem, 2015, 16, 1099–1100 CrossRef CAS PubMed.
  3. R. M. Pankow and B. C. Thompson, Polymer, 2020, 207, 122874 CrossRef CAS.
  4. A. Facchetti, Chem. Mater., 2011, 23, 733–758 CrossRef CAS.
  5. S. Holliday, Y. Li and C. K. Luscombe, Prog. Polym. Sci., 2017, 70, 34–51 CrossRef CAS.
  6. M. Kim, S. U. Ryu, S. A. Park, K. Choi, T. Kim, D. Chung and T. Park, Adv. Funct. Mater., 2019, 1904545 Search PubMed.
  7. S. E. Root, S. Savagatrup, A. D. Printz, D. Rodriquez and D. J. Lipomi, Chem. Rev., 2017, 117, 6467–6499 CrossRef CAS PubMed.
  8. Y. Huang, D. L. Elder, A. L. Kwiram, S. A. Jenekhe, A. K. Y. Jen, L. R. Dalton and C. K. Luscombe, Adv. Mater., 2019, 1904239 Search PubMed.
  9. M. Goel, C. D. Heinrich, G. Krauss and M. Thelakkat, Macromol. Rapid Commun., 2019, 40, 1800915 CrossRef PubMed.
  10. Z. Genene, W. Mammo, E. Wang and M. R. Andersson, Adv. Mater., 2019, 31, 1807275 CrossRef PubMed.
  11. A. F. Paterson, S. Singh, K. J. Fallon, T. Hodsden, Y. Han, B. C. Schroeder, H. Bronstein, M. Heeney, I. McCulloch and T. D. Anthopoulos, Adv. Mater., 2018, 30, 1801079 CrossRef PubMed.
  12. H. Sun, X. Guo and A. Facchetti, Chem, 2020, 6, 1310–1326 CAS.
  13. K.-J. Baeg, M. Caironi and Y.-Y. Noh, Adv. Mater., 2013, 25, 4210–4244 CrossRef CAS PubMed.
  14. T. L. D. Tam and J. Xu, J. Mater. Chem. A, 2021, 9, 5149–5163 RSC.
  15. N. Zhou and A. Facchetti, Mater. Today, 2018, 21, 377–390 CrossRef CAS.
  16. M. Sommer, J. Mater. Chem. C, 2014, 2, 3088–3098 RSC.
  17. X. Guo, A. Facchetti and T. J. Marks, Chem. Rev., 2014, 114, 8943–9021 CrossRef CAS PubMed.
  18. R. Matsidik, A. Luzio, S. Hameury, H. Komber, C. R. McNeill, M. Caironi and M. Sommer, J. Mater. Chem. C, 2016, 4, 10371–10380 RSC.
  19. H. Yan, Z. Chen, Y. Zheng, C. Newman, J. R. Quinn, F. Dötz, M. Kastler and A. Facchetti, Nature, 2009, 457, 679–686 CrossRef CAS PubMed.
  20. B. Fan, L. Ying, P. Zhu, F. Pan, F. Liu, J. Chen, F. Huang and Y. Cao, Adv. Mater., 2017, 29, 1703906 CrossRef PubMed.
  21. K. D. Deshmukh, R. Matsidik, S. K. K. Prasad, N. Chandrasekaran, A. Welford, L. A. Connal, A. C. Y. Liu, E. Gann, L. Thomsen, D. Kabra, J. M. Hodgkiss, M. Sommer and C. R. McNeill, ACS Appl. Mater. Interfaces, 2018, 10, 955–969 CrossRef CAS PubMed.
  22. N. Zhou, A. S. Dudnik, T. I. N. G. Li, E. F. Manley, T. J. Aldrich, P. Guo, H.-C. Liao, Z. Chen, L. X. Chen, R. P. H. Chang, A. Facchetti, M. Olvera de la Cruz and T. J. Marks, J. Am. Chem. Soc., 2016, 138, 1240–1251 CrossRef CAS PubMed.
  23. Y. Shin, A. Welford, H. Komber, R. Matsidik, T. Thurn-Albrecht, C. R. McNeill and M. Sommer, Macromolecules, 2018, 51, 984–991 CrossRef CAS.
  24. E. Zhou, M. Nakano, S. Izawa, J. Cong, I. Osaka, K. Takimiya and K. Tajima, ACS Macro Lett., 2014, 3, 872–875 CrossRef CAS.
  25. S. B. Schmidt, M. Hönig, Y. Shin, M. Cassinelli, A. Perinot, M. Caironi, X. Jiao, C. R. McNeill, D. Fazzi, T. Biskup and M. Sommer, ACS Appl. Polym. Mater., 2020, 2, 1954–1963 CrossRef CAS.
  26. R. Matsidik, M. Giorgio, A. Luzio, M. Caironi, H. Komber and M. Sommer, Eur. J. Org. Chem., 2018, 6121–6126 CrossRef CAS.
  27. J. W. Jung, J. W. Jo, C.-C. Chueh, F. Liu, W. H. Jo, T. P. Russell and A. K.-Y. Jen, Adv. Mater., 2015, 27, 3310–3317 CrossRef CAS PubMed.
  28. B. Zhu, L. Guo, P. Deng and S. Liu, J. Mater. Chem. C, 2021, 9, 2198–2204 RSC.
  29. D. Kiefer, A. Giovannitti, H. Sun, T. Biskup, A. Hofmann, M. Koopmans, C. Cendra, S. Weber, L. J. Anton Koster, E. Olsson, J. Rivnay, S. Fabiano, I. McCulloch and C. Müller, ACS Energy Lett., 2018, 3, 278–285 CrossRef CAS PubMed.
  30. Y. Shin, H. Komber, D. Caiola, M. Cassinelli, H. Sun, D. Stegerer, M. Schreiter, K. Horatz, F. Lissel, X. Jiao, C. R. McNeill, S. Cimò, C. Bertarelli, S. Fabiano, M. Caironi and M. Sommer, Macromolecules, 2020, 53, 5158–5168 CrossRef CAS.
  31. H. You, D. Kim, H.-H. Cho, C. Lee, S. Chong, N. Y. Ahn, M. Seo, J. Kim, F. S. Kim and B. J. Kim, Adv. Funct. Mater., 2018, 28, 1803613 CrossRef.
  32. A. Wadsworth, M. Moser, A. Marks, M. S. Little, N. Gasparini, C. J. Brabec, D. Baran and I. McCulloch, Chem. Soc. Rev., 2019, 48, 1596–1625 RSC.
  33. K. Feng, J. Huang, X. Zhang, Z. Wu, S. Shi, L. Thomsen, Y. Tian, H. Y. Woo, C. R. McNeill and X. Guo, Adv. Mater., 2020, 32, 2001476 CrossRef CAS PubMed.
  34. H. Jia and T. Lei, J. Mater. Chem. C, 2019, 7, 12809–12821 RSC.
  35. Y. Lu, J.-Y. Wang and J. Pei, Chem. Mater., 2019, 31, 6412–6423 CrossRef CAS.
  36. L. Xue, Y. Yang, Z.-G. Zhang, X. Dong, L. Gao, H. Bin, J. Zhang, Y. Yang and Y. Li, J. Mater. Chem. A, 2016, 4, 5810–5816 RSC.
  37. S. Lee, C. Lee, H. Kim and Y. Kim, J. Mater. Chem. C, 2020, 8, 15778–15787 RSC.
  38. S. Shi, P. Chen, Y. Chen, K. Feng, B. Liu, J. Chen, Q. Liao, B. Tu, J. Luo, M. Su, H. Guo, M. Kim, A. Facchetti and X. Guo, Adv. Mater., 2019, 31, 1905161 CrossRef CAS PubMed.
  39. Y. Li, M. Gu, Z. Pan, B. Zhang, X. Yang, J. Gu and Y. Chen, J. Mater. Chem. A, 2017, 5, 10798–10814 RSC.
  40. C. Liang and H. Wang, Org. Electron., 2017, 50, 443–457 CrossRef CAS.
  41. A. Wadsworth, H. Chen, K. J. Thorley, C. Cendra, M. Nikolka, H. Bristow, M. Moser, A. Salleo, T. D. Anthopoulos, H. Sirringhaus and I. McCulloch, J. Am. Chem. Soc., 2020, 142, 652–664 CrossRef CAS PubMed.
  42. D. Venkateshvaran, M. Nikolka, A. Sadhanala, V. Lemaur, M. Zelazny, M. Kepa, M. Hurhangee, A. J. Kronemeijer, V. Pecunia, I. Nasrallah, I. Romanov, K. Broch, I. McCulloch, D. Emin, Y. Olivier, J. Cornil, D. Beljonne and H. Sirringhaus, Nature, 2014, 515, 384–388 CrossRef CAS PubMed.
  43. I. McCulloch, R. S. Ashraf, L. Biniek, H. Bronstein, C. Combe, J. E. Donaghey, D. I. James, C. B. Nielsen, B. C. Schroeder and W. Zhang, Acc. Chem. Res., 2012, 45, 714–722 CrossRef CAS PubMed.
  44. X. Zhang, H. Bronstein, A. J. Kronemeijer, J. Smith, Y. Kim, R. J. Kline, L. J. Richter, T. D. Anthopoulos, H. Sirringhaus, K. Song, M. Heeney, W. Zhang, I. McCulloch and D. M. DeLongchamp, Nat. Commun., 2013, 4, 2238 CrossRef PubMed.
  45. C. Cordovilla, C. Bartolomé, J. M. Martínez-Ilarduya and P. Espinet, ACS Catal., 2015, 5, 3040–3053 CrossRef CAS.
  46. L. A. Estrada, J. J. Deininger, G. D. Kamenov and J. R. Reynolds, ACS Macro Lett., 2013, 2, 869–873 CrossRef CAS.
  47. N. S. Gobalasingham and B. C. Thompson, Prog. Polym. Sci., 2018, 83, 135–201 CrossRef CAS.
  48. N. Snoeij, Toxicol. Appl. Pharmacol., 1985, 81, 274–286 CrossRef CAS PubMed.
  49. D. J. Burke and D. J. Lipomi, Energy Environ. Sci., 2013, 6, 2053 RSC.
  50. T. M. Pappenfus, F. Almyahi, N. A. Cooling, E. W. Culver, S. C. Rasmussen and P. C. Dastoor, Macromol. Chem. Phys., 2018, 219, 1800272 CrossRef.
  51. S.-L. Suraru, J. A. Lee and C. K. Luscombe, ACS Macro Lett., 2016, 5, 724–729 CrossRef CAS.
  52. J.-R. Pouliot, F. Grenier, J. T. Blaskovits, S. Beaupré and M. Leclerc, Chem. Rev., 2016, 116, 14225–14274 CrossRef CAS PubMed.
  53. R. Matsidik, H. Komber, A. Luzio, M. Caironi and M. Sommer, J. Am. Chem. Soc., 2015, 137, 6705–6711 CrossRef CAS PubMed.
  54. R. Matsidik, H. Komber and M. Sommer, ACS Macro Lett., 2015, 4, 1346–1350 CrossRef CAS.
  55. Y. Shin, M. Massetti, H. Komber, T. Biskup, D. Nava, G. Lanzani, M. Caironi and M. Sommer, Adv. Electron. Mater., 2018, 4, 1700581 CrossRef.
  56. S. Chen, K. C. Lee, Z.-G. Zhang, D. S. Kim, Y. Li and C. Yang, Macromolecules, 2016, 49, 527–536 CrossRef CAS.
  57. Y. Li, W. K. Tatum, J. W. Onorato, S. D. Barajas, Y. Y. Yang and C. K. Luscombe, Polym. Chem., 2017, 8, 5185–5193 RSC.
  58. Y. Li, W. K. Tatum, J. W. Onorato, Y. Zhang and C. K. Luscombe, Macromolecules, 2018, 51, 6352–6358 CrossRef CAS.
  59. D. Adamczak, H. Komber, A. Illy, A. D. Scaccabarozzi, M. Caironi and M. Sommer, Macromolecules, 2019, 52, 7251–7259 CrossRef CAS.
  60. D. Adamczak, A. Perinot, H. Komber, A. Illy, S. Hultmark, B. Passarella, W. L. Tan, S. Hutsch, D. Becker-Koch, C. Rapley, A. D. Scaccabarozzi, M. Heeney, Y. Vaynzof, F. Ortmann, C. R. McNeill, C. Müller, M. Caironi and M. Sommer, J. Mater. Chem. C, 2021, 9, 4597–4606 RSC.
  61. M. S. Vezie, S. Few, I. Meager, G. Pieridou, B. Dörling, R. S. Ashraf, A. R. Goñi, H. Bronstein, I. McCulloch, S. C. Hayes, M. Campoy-Quiles and J. Nelson, Nat. Mater., 2016, 15, 746–753 CrossRef CAS PubMed.
  62. R. Steyrleuthner, M. Schubert, I. Howard, B. Klaumünzer, K. Schilling, Z. Chen, P. Saalfrank, F. Laquai, A. Facchetti and D. Neher, J. Am. Chem. Soc., 2012, 134, 18303–18317 CrossRef CAS PubMed.
  63. Z. Wu, A. Petzold, T. Henze, T. Thurn-Albrecht, R. H. Lohwasser, M. Sommer and M. Thelakkat, Macromolecules, 2010, 43, 4646–4653 CrossRef CAS.
  64. A. J. Kronemeijer, V. Pecunia, D. Venkateshvaran, M. Nikolka, A. Sadhanala, J. Moriarty, M. Szumilo and H. Sirringhaus, Adv. Mater., 2014, 26, 728–733 CrossRef CAS PubMed.
  65. H. Chen, A. Wadsworth, C. Ma, A. Nanni, W. Zhang, M. Nikolka, A. M. T. Luci, L. M. A. Perdigão, K. J. Thorley, C. Cendra, B. Larson, G. Rumbles, T. D. Anthopoulos, A. Salleo, G. Costantini, H. Sirringhaus and I. McCulloch, J. Am. Chem. Soc., 2019, 141, 18806–18813 CrossRef CAS PubMed.
  66. T. H. Thomas, D. J. Harkin, A. J. Gillett, V. Lemaur, M. Nikolka, A. Sadhanala, J. M. Richter, J. Armitage, H. Chen, I. McCulloch, S. M. Menke, Y. Olivier, D. Beljonne and H. Sirringhaus, Nat. Commun., 2019, 10, 2614 CrossRef PubMed.
  67. R. Noriega, J. Rivnay, K. Vandewal, F. P. V. Koch, N. Stingelin, P. Smith, M. F. Toney and A. Salleo, Nat. Mater., 2013, 12, 1038–1044 CrossRef CAS PubMed.
  68. A. Onwubiko, W. Yue, C. Jellett, M. Xiao, H.-Y. Chen, M. K. Ravva, D. A. Hanifi, A.-C. Knall, B. Purushothaman, M. Nikolka, J.-C. Flores, A. Salleo, J.-L. Bredas, H. Sirringhaus, P. Hayoz and I. McCulloch, Nat. Commun., 2018, 9, 416 CrossRef PubMed.
  69. X. Guo and M. D. Watson, Org. Lett., 2008, 10, 5333–5336 CrossRef CAS PubMed.

Footnote

Electronic supplementary information (ESI) available: General measurements and characterization; additional NMR, SEC, TGA, DSC and GIWAXS data. See DOI: 10.1039/d1ma00633a

This journal is © The Royal Society of Chemistry 2021