A folded π-system with supramolecularly oriented dipoles: single-component piezoelectric relaxor with NLO activity

Organic molecules with an active dipole moment have a natural propensity to align in an antiparallel fashion in the solid state, resulting in zero macroscopic polarization. This primary limitation makes the material unresponsive to switching with electric fields, mechanical forces, and to intense laser light. A single-component organic material that bestows macroscopic dipole-driven electro-mechanical and optical functions, e.g., piezoelectric, ferroelectric and nonlinear optical (NLO) activity, is unprecedented due to the design challenges imparted by crystal symmetry and dipole orientations. Herein we report a crystalline organic material that self-assembles with a polar order (P1), and is endowed with a high piezoelectric coefficient (d33–47 pm V−1), as well as ferroelectric and Debye-type relaxor properties. In addition, it shows second harmonic generation (SHG) activity, which is more than five times that of the benchmark potassium dihydrogen phosphate. Piezoelectric force microscopy (PFM) images validated electro-mechanical deformations. Piezoresponse force spectroscopy (PFS) studies confirmed a signature butterfly-like amplitude and a phase loop. To the best of our knowledge, this is the first report of a folded supramolecular π-system that manifests unidirectionally oriented dipoles and exhibits piezoelectricity, ferroelectricity, and has excellent ability to generate second harmonic light. These findings can herald new design possibilities based on folded architectures to explore opto-, electro- and mechano-responsive multifaceted functions.

Understanding the structural and mechanical behaviour of biomolecules and polymers under a physiological electric eld provides insight for designing dipole-active organic materials. The complexity of the hierarchy and folding of biomolecular structures greatly controls their physical properties. Dipolar molecular materials with oriented dipoles can confer nonlinear optical (NLO) activity, as well as piezo and ferroelectricity. 1 Synthetic aromatic oligoamides are one of the potential candidates for mimicking the folded structure of biopolymers. 2 A molecule is driven into a folded geometry depending upon the exibility and bulkiness of its backbone, H-bonding prociency, p-p stacking interactions, and local dielectric environments. 3 Therefore, it has been suggested to utilize non-covalent interactions in designing novel organic materials to unravel functions that are founded on certain symmetry-restricted properties and oriented dipoles. 4 The ease of tuning the solubility, low temperature processability, and lesser toxicity compared to inorganic materials are key advantages to strive towards new organic systems with multifaceted electro-mechanical and NLO response. 5 This has been nicely illustrated by the groups of Tokura, Stupp, Reddy, Ghosh and others. 1,4,5,14,15 Recent reports by the groups of Xiong, Boomishankar, Yang and others majorly focus on pioneering systems based on inorganic and hybrid materials. 6 These are mostly based on two-component ionic systems. However, studies on switchable electrical, mechanical and NLO activity integrated within an all-organic single-component system remain in their infancy.
We envisaged that exible built-in p-conjugated folded conformations can enable a system to function like a molecular spring by enhancing low-energy controlled reversible mechanical deformations. 7-9 Along with this, introducing a chiral backbone in the dipolar molecule is anticipated to attain the desired electro-mechanical and NLO functions, which are restricted by the crystal symmetry and hierarchical ordering of the molecules.
In this work, we have successfully tested this hypothesis using a simplistic design approach. Our design involves two aromatic p-units: p a bearing a carbonyl functionality and p b comprising an elementary polarizable p-nitroaniline unit, in addition to a exible chain and L-alanine amino acid as the chirality-inducing element that acts as a chiral spacer (Scheme 1). Intriguingly, molecule 1 forms a polar, highly oriented dipolar assembly, as validated from its single-crystal X-ray structure. Further, piezoresponse force microscopy (PFM) and piezoresponse force spectroscopy (PFS) studies conrmed piezoelectricity in the nano-regime with a high converse piezoelectric coefficient (d 33 ). Polarization vs. electric eld (P-E) loop measurements corroborated ferroelectric properties. Dielectric measurements of this material revealed Debye-type relaxor properties. Furthermore, the noncentrosymmetric crystalline platform and the supramolecularly oriented dipoles led to high second harmonic generation (SHG) activity. To the best of our knowledge, this is the rst report of an organic singlecomponent material with a dipolar folded architecture that is electro-mechanically responsive as well as SHG active.
The synthesis of compound 1 was achieved in three steps (see ESI † for details). Firstly, N ′ -(4-nitrophenyl)ethane-1,2diamine (1a) was synthesized by reacting 4-nitrochlorobenzene with ethylenediamine, and was used in excess in the presence of CuCl 2 . Next, 2-benzamidopropanoic acid (1b) was synthesized by reacting benzoyl chloride with L-alanine in a basic medium. Finally, 1a and 1b were coupled together using DCC (N,N ′ -dicyclohexylcarbodiimide) and HOBt (1-hydroxybenzotriazole) to form the desired peptide linkage in 1. Compound 1 was puried by column chromatography and isolated in 45% yield.
Manifestation of piezoelectricity and ferroelectricity as well as NLO activity from a crystalline system involves satisfying stringent crystallographic symmetry constraints. Gratifyingly, we grew good quality single crystals by slow evaporation of a solution of 1 in ethanol. Single-crystal X-ray crystallographic data validated a triclinic polar space group P 1 , which signies the absence of any rotation axes (other than the identity rotation axis of order 1), rotary-inversion axes, screw axes, or planes. 10 Interestingly, 1 adopts a folded or an 'inverted U' shape in the crystal (Fig. 1a). The crystal packing is governed by two sets of mutually perpendicular H-bonds along the a and c axes. There are two distinct interlayer H-bonds along the c axis, between the -N]O/H-Cof the next layer backbone (2.485Å) and the aromatic = C-H/O]C-(2.529Å) along the c axis ( Fig. 1b), which are longer than the intermolecular H-bonded array along the a axis. There is another set of three H-bonds along the a axis, corresponding to O/H distances of 2.072Å, 2.219Å, and 2.255Å (Fig. 1c). These interactions in 1 assist it to adopt a folded structure and a unidirectional molecular arrangement in the crystal. As a result of such a folded structure, the planes containing the two p-units do not interact facially as they form an angle of 69.4° (Fig. 1d).
This implies that the p clouds of the two aromatic rings weakly interact with each other and thus allow exibility of the folded architecture. Notably, such a parallel orientation of dipoles in p-conjugated folded structures is rare. Therefore, control over H-bonds can be useful in designing dipole active supramolecular structures. 11 Since 1 crystallized in a polar noncentrosymmetric space group with supramolecularly oriented dipoles, manifestation of switchable electrical, mechanical and nonlinear optical properties was anticipated. 12 To examine the piezoelectric properties, we performed PFM alongside topographical studies of crystalline thin lms of 1. The morphology of the thin lms was studied by AFM and scanning electron microscopy, which revealed brous structures ( Fig. S4a and b †). Fig. S4 † shows the topography of the crystalline surface and its corresponding powder XRD pattern.
Scheme 1 (a) Schematic representation of molecule 1 with its important structural components: aromatic unit-p a , dipolar unit-p b and the chiral spacer; (b) molecular structure of 1; (c) supramolecular assembly of 1 to form highly oriented dipoles to function as an electromechano and NLO responsive single-component material. PFS of the nano-domains revealed a buttery-shaped amplitude loop and a phase loop of nearly 180°phase difference both within the long range ( Fig. 2a and b) and a narrow range of DC bias voltage (Fig. S5 †). The converse piezoelectric coefficient, d 33 , of 1 was determined as ∼46.7 pm V −1 (ESI, eqn S1 †). The d 33 value was averaged over the values obtained at four different points.
From the PFM studies, the piezo-responses were phase and amplitude images collected at room temperature. Green to paleyellow contrast in the amplitude images signied the extent of electro-mechanical deformation vertically and horizontally ( Fig. 3a and b). Brighter yellow regions in the lateral amplitude image suggested favourable lateral deformation over vertical. Fig. 3c and d highlight the macromolecular insight of the phase of oriented dipoles in the thin lm. The blue to red color contrast implies anti-parallel to parallel orientation of the polaraxis induced by the applied electric eld. We attempted to record domain switching images at reverse voltages to address the ferroelectric behaviour. However, a thin lm of 1 did not show reversible switching characteristics within ± 15 V. Consequently, crystalline thin lm surface imaging helped to understand the responsible vectorial component for brighter lateral amplitude.
Further, vertical and lateral amplitude PFM images were collected in mutually perpendicular X and Y scanning directions (Fig. 4). In the X-scanning, dened as '00', the cantilever long-axis is perpendicular to the scan direction, whereas in the Y-direction, dened as '90 ′ , the cantilever long-axis is parallel to the scan direction. If the dipoles are oriented perpendicular (out-of-plane) to the X-Y surface plane, then the tip always deects vertically in both the X and Y scans in vertical mode as induced by the vertical oscillation of the dipoles. Here, in the vertical mode of the X-and Y-scanning images ( Fig. 4a-b), the most occurring amplitude values are nearly the same, but the maximum number of pixels are nearly two times more in Y scanning than for X scanning. This indicates that the vertical deection of the tip is not purely coupled with the out-of-plane oscillation.
While the dipoles are aligned in parallel to the long-axis of the cantilever, fully or partially, the vertical deection of the cantilever gets affected due to the buckling motion of the tip and appeared in vertical imaging. 13 However, lateral mode images produced the most occurring deection amplitude (64 mV) in the X scan and maximum pixels (3300) in the Y scan with comparable amplitude value (Fig. 4c-d). These results suggest   that better electro-mechanical coupling occurs in the X-Y plane of the crystalline surface of 1. In addition, bulk piezoelectric studies on a crystalline pellet of 1 at 300 K revealed characteristic strain vs. E loops, conrming the feature of a piezoelectric material (Fig. 5a).
We calculated the spontaneous polarization in the bulk along the three-axes by using a vd-DF2 functional in the Berry phase method. The computed values of the crystal lattice parameters were in good agreement with the experimental ones (ESI, Table S5 †). We obtained nearly equal values of polarization, i.e., 32 and 30 along the b-and c-axes, respectively, and 20 along the a-axis. Therefore, these calculated results validated that 1 has signicantly high polarization for piezo-response in all directions. Comparatively weak and long H-bonds along the c-axis are easily polarizable in an applied electric eld than the shorter H-bonds along the a-axis. This explanation is in line with the theoretically predicted polarization value along the c axis and the analysis of the PFM amplitude images.
Ordered networks of donor-acceptor type systems have been shown to be potential candidates towards all-organic ferroelectric materials. 14 It is noteworthy that hydrogen bonded molecules undergo reversible polarisation switching that enables the system to exhibit ferroelectric properties and can be an effective strategy to create organic ferroelectric analogues of potassium dihydrogen phosphate (KDP). 15 For ferroelectricity to transpire, it is crucial to have aligned dipoles in these H-bonded systems. 16 In our case, single-crystal X-ray data of molecule 1 revealed a fully oriented molecular arrangement in the bulk, and a polar space group, which led us to examine its ferroelectric properties. P-E loop measurements were performed in pellet form at 300 K. Distinct saturation of polarization in both sides of the P-E hysteresis loops was not observed (Fig. 5b). The gradual increase in AC voltage amplitude at a constant frequency retained the shape of the asymmetric loop. The asymmetric nature in the P-E and the strain vs. applied eld loops suggest non-ideal or leaky ferroelectric characteristics for 1.
One of the reasons for the asymmetric P-E loop could be the intrinsic characteristic of the folded dipoles. As revealed from the single-crystal XRD studies, 1 exhibits weak intramolecular p-interactions that hold the molecules in the folded form and the intermolecular H-bonds hold the dipoles in an organized, dipole-oriented fashion. Therefore, improper reorientation of the initially oriented dipoles can occur while applying the reverse electric eld, resulting in an asymmetric loop. The other possible reason could be the evolution of defects generated during the sample preparation or difference in charge trapping in the crystalline interface between the two electrode regions during the application of external elds, which builds up an internal eld, leading to an asymmetric loop. This aspect has been seen in other ferroelectric materials. 17 We measured the leakage current of 1 and found it to make a negligible contribution as the magnitude of current remained very low, in the order of ∼10 −7 (Fig. S6 †).
Unlike normal ferroelectrics that show a sharp transition temperature, a round-shaped hump is observed in the temperature (273 K to 433 K) and frequency dependent dielectric constant (real part, 3 ′ ) measurements of 1 (Fig. 5c). This hump further shis towards a higher temperature and gradually gets attened with increasing frequency (Fig. 5d). These are characteristics of Debye-type dielectric relaxors, whereby dipoles are not able to reorient under the reverse applied eld, and thus fail to exhibit a sharp transition at high frequency. Fig. S7 † shows that the dielectric dispersion at different frequencies obeyed the modied Curie-Weiss law [ESI eqn S1 †]. The slope of this plot determines the diffusion constant (g) value to be ∼1.7, which further suggests that 1 has relaxor properties. 18 Finally, we performed SHG measurements on a crystalline sample of 1, which showed 5.3 times SHG activity with respect to the benchmark potassium dihydrogen phosphate (KDP). The crystalline sample showed high chemical and optical stability with an input laser pulse energy of 3-5 mJ per pulse. This frequency doubling efficiency of 1 is amongst the best within the family of organic single-component systems, as recently exemplied by Seferos and co-workers. 1d The polarizable intermolecular H-bonds have better coupling with the applied eld instead of an individual dipole, which results in NLO and electrical response. 19 Beside these H-bonds, the skewed conformation between the two aromatic rings of 1 brings about exibility in the backbone. Therefore, the vibration of local folding motifs along b axis remarkably adds an effect in the piezo-response. 20

Conclusions
In summary, we have shown for the rst time that organic folded structures can be utilized to elicit piezo-and ferroelectric properties, as well as efficient second harmonic generation, all within a single-component, macroscopically dipole active system. This multi-function generation is unprecedented in a single-component all-organic system. The ability of the material to form supramolecularly oriented dipoles along with the manifestation of the polar crystalline order P 1 (i.e., devoid of any rotation axes, rotary-inversion axes, screw axes, or planes) results in the evolution of a multifaceted electro-, mechano-and nonlinear optical response. PFM imaging of the crystalline thin lms in vertical and lateral modes enabled understanding of the orientation of the dipoles in their immobile phase. PFS studies revealed a high piezoelectric coefficient (d 33 -47 pm V −1 ) as well as a characteristic buttery-like loop, as mandated by a piezoelectric material. Bulk piezoelectric studies on a crystalline pellet revealed characteristic strain vs. E loops, while bulk ferroelectric studies revealed characteristic P-E loops. Dielectric studies conrmed Debye-type relaxor properties. In addition, SHG activity was observed, which was more than ve times that of the benchmark potassium dihydrogen phosphate. Thus, single-component supramolecular systems with special molecular architectures can be conceptualized in preference to bicomponent organic systems to elicit piezo-, electro-or other stimuli-based responses. 21 These systems can be further engineered for exciting energy and light harvesting applications. 22 We believe these ndings will stimulate new design possibilities based on folded architectures and new dipole active p-systems 23 to explore opto, electro and mechano-responsive multifaceted functions.

Data availability
The datasets supporting this article have been uploaded as part of the ESI. †

Author contributions
The molecular design was conceived by D. A. and P. M. Synthesis of the molecule was conducted by D. A. S. D carried out the PFM and PFS studies. The ferroelectric studies were carried out by C. T, S. D., and R. K. in the supervision of R. C., and S. S. G. H. helped in the crystal data collection and analysis with contributions from D. A. Computational studies were completed by S. K. K. and R. K. G. The manuscript was written by S. D. with contributions from D. A. All the authors agreed on the nal version of the manuscript.

Conflicts of interest
There are no conicts to declare.