Data from: Electrostatic complexation of conjugated and bottlebrush polyelectrolytes forms printable conductive inks
Data files
Dec 29, 2025 version files 9.32 MB
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Figure_4a-1_1BPE_1SP3HT_densephase.csv
358 B
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Figure_4a-2_1BPE_2PEDOT-3S-Na_densephase.csv
424 B
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Figure_4b-1_1BPE_1SP3HT_densephase_viscosity.csv
340 B
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Figure_4b-2_1BPE_2PEDOT-3S-Na_densephase_viscosity.csv
337 B
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Figure_6-1_SAXS_1PEDOT-3S-Na-2BPE_Solid.csv
13.70 KB
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Figure_6-2_SAXS_1SP3HT-1BPE_Solid.csv
13.65 KB
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Figure_7_Example_IV_Curve_SP3HT-BPE_Printed_Doped_DoubleLine_1to2_1Vsweep.csv
903 B
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Figure_7_Example_IV_Curve_SP3HT-BPE_Printed_Doped_DoubleLine_2to3_0p5Vsweep.csv
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Figure_7a_Electronic_Conductivity_Single_and_Double_Printed_Lines.csv
271 B
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Figure_8_Example_IV_Curve_PEDOT-3S-Na-BPE_Printed_Doped_1_L1_0p5Vsweep.csv
487 B
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Figure_8_Example_IV_Curve_SP3HT-BPE_Printed_Doped_1_L0_0p5Vsweep.csv
490 B
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Figure_8_Normalized_Resistance_Under_Strain.csv
470 B
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Figure_S1-S8_NMR.zip
8.57 MB
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Figure_S10_Uvvis_PEDOT-3S-Na_Solution.csv
11.89 KB
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Figure_S11_Uvvis_SP3HT_Solution.csv
20.62 KB
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Figure_S12_Uvvis_BPE_Solution.csv
21.08 KB
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Figure_S13-1_Uvvis_PEDOT-3S-Na_Solution_SolventRatio.csv
18.30 KB
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Figure_S13-2_Uvvis_PEDOT-3S-Na_Solution_SolventRatio.csv
2.50 KB
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Figure_S14_Uvvis_1PEDOT-3S-Na-2BPE_Supernatant.csv
11.70 KB
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Figure_S15-1_UvvisNIR_PEDOT-3S-Na_Film.csv
34.29 KB
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Figure_S15-2_UvvisNIR_1PEDOT-3S-Na-2BPE_Film.csv
112.13 KB
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Figure_S16_Amp_sweep_BPE_solid.csv
589 B
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Figure_S17_Amp_sweep_1PEDOT-3S-Na-1BPE_complex.csv
441 B
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Figure_S17_Amp_sweep_1PEDOT-3S-Na-2BPE_complex.csv
430 B
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Figure_S17_Amp_sweep_1SP3HT-1BPE_complex.csv
358 B
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Figure_S17_Amp_sweep_1SP3HT-2BPE_complex.csv
409 B
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Figure_S18_Viscosity_1PEDOT-3S-Na-2BPE_complex.csv
337 B
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Figure_S18_Viscosity_1SP3HT-1BPE_complex.csv
340 B
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Figure_S19_Thixotropic_1PEDOT-3S-Na-2BPE_complex.csv
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Figure_S20_Oscillation_1SP3HT-1BPE_complex_0min.csv
358 B
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Figure_S20_Oscillation_1SP3HT-1BPE_complex_15min.csv
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Figure_S20_Oscillation_1SP3HT-1BPE_complex_45min.csv
589 B
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Figure_S20_Oscillation_1SP3HT-1BPE_complex_5min.csv
588 B
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Figure_S25-1_GIWAXS_SP3HT_Film.csv
82.34 KB
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Figure_S25-2_GIWAXS_PEDOT-3S-Na_Film.csv
118.18 KB
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Figure_S25-3_GIWAXS_BPE_Film.csv
82.33 KB
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Figure_S25-4_GIWAXS_1SP3HT-1BPE-undoped_Film.csv
44.86 KB
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Figure_S25-5_GIWAXS_1SP3HT-1BPE-immersed-doped_Film.csv
44.86 KB
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Figure_S25-6_GIWAXS_1SP3HT-1BPE-vapor-doped_Film.csv
82.34 KB
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Figure_S25-7_GIWAXS_1PEDOT-3S-Na-2BPE_Film.csv
17.89 KB
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Figure_S26_Conductivity_Complexes.csv
434 B
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Figure_S27_Normalized_Resistance_Complexes.csv
570 B
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Figure_S30_Resistance_PEDOT-3S-Na-BPE.csv
418 B
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Figure_S31_Resistance_SP3HT-BPE.csv
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Figure_S35_Resistance_PEDOT-3S-Na-BPE.csv
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README.md
5.03 KB
Abstract
Electrostatic complexation enables blending of otherwise immiscible polymers by liquid–liquid phase separation, forming a polymer-rich phase suitable for processing. We explored design rules for processable complexes using electrically conductive conjugated polyelectrolytes (CPEs) and mechanically tunable bottlebrush polyelectrolytes (BPEs). Sulfonated polythiophene and self-doped sulfonated PEDOT were examined to study how charge fraction influences compatibilization, printability, and properties. The resulting CPE: BPE complexes exhibited rheology suitable for direct ink writing into thick patterned structures. Upon drying, they combined electrical conductivity with elasticity and adhesiveness, enabling applications in soft, thick, semiconducting materials.
Dataset DOI: 10.5061/dryad.tht76hfcg
Description of the data and file structure
This dataset contains the raw (or preliminarily processed) data of experimental results collected to publish a manuscript: "Electrostatic Complexation of Conjugated and Bottlebrush Polyelectrolytes Forms Printable Conductive Inks", authored by Intanon Lapkriengkri, Alexandra Zele, Hyunki Yeo, Anush Singhal, Rachel A. Segalman, Christopher A. Bates, and Michael L. Chabinyc.
Detailed experimental methods can be accessed through the Supporting Information from the original document.
Characterization methods accompanied to this dataset
Nuclear magnetic resonance (NMR)
All bottlebrush polymer 1H NMR spectra were collected using a Varian Unity Inova AS600 600 MHz equipped with a 5 mm Varian triple resonance 1H/13C/15N inverse detection probe with z-axis pulsed field gradient (PFG). All linear polymer 1H NMR spectra were collected using a 600MHz SB Varian VNMRS equipped with a double resonance Broadband Probe Head 600 DB Auto X. Small molecule 1H, 13C NMR, and 2D-NMR were collected using a Bruker Avance NEO 500 MHz equipped with a CryoProbe Prodigy BBO probe with z-axis PFG.
UV-Vis spectroscopy
Solutions: The targeted concentrations of polyelectrolytes were prepared using molarity defined by mols of charged repeating units (Q = 0.8 for SPEDOT and 0.6 for SP3HT and BPE). Absorbance of the solutions were measured through a Cary UV-Vis spectrophotometer (Agilent).
Solid samples for spectroscopy: PEDOT-3S-Na:BPE was extruded and smeared on top of a quartz substrate. The reflectance of the dried solid was measured through an UV3600 UV-Vis-NIR spectrometer (Shimadzu). The absorbance was calculated by the Kubelka-Munk transformation function of the diffuse reflectance spectra.
Rheology
A strain-controlled ARES-G2 rheometer equipped with an Advanced Peltier System (APS) and a solvent trap from TA Instruments was used to investigate the shear stress relaxation and linear viscoelastic properties of the blend. 8-mm stainless steel plates were used for all measurements. Pieces of paper soaked with water and THF were carefully placed inside the solvent trap to provide a saturated solvent environment to the material during testing to best minimize solvent evaporation. All measurements were done at room temperature using the same geometry and setup.
Grazing-incident wide angle X-ray scattering (GIWAXS)
Identical films for UV-Vis-NIR measurements were brought on beamline 11–3 at the Stanford Synchrotron Radiation Lightsource (SSRL). LaB6 was used as the calibrant for the beam center and a sample-to-detector distance of 315 mm was used. 2-D GIWAXS scattering images were collected using 2D Rayonix MX225 CCD area detector at an incidence angle of 0.10° with 30 s exposure times. The samples were kept under helium during X-ray exposure to minimize sample degradation and scattering from oxygen. The collected data was processed using Nika, a 2-D data reduction macro on Igor Pro using established procedures.
Files and variables
Each file names are associated with the content and description of data, in a format of .csv.
File names are formatted as: "Figure XX_Data Type and variables_Material_Sample type"
Plotted figures and type of variables, materials, and sample type are also defined in original manuscript.
Commonly used variables with abbreviations:
q: q-factor (unit: Å-1) in GIWAXS, WAXS and SAXS raw datafiles
Abs.: Absorbance of (unit: a.u.) of UV-vis and UV-vis-NIR spectroscopy datafiles
C: concentration (unit: mmol L-1) in concentration datafiles
V: voltage (unit: V) in CV and conductivity datafiles
I: current (unit: A) in CV and conductivity datafiles
E: binding energy (unit: eV) in XPS datafiles
G': Storage modulus, G'': Loss modulus (unit: MPa) in Rheology datafiles
Shear rate (unit: s-1) in Rheology datafiles
Viscosity (unit: Pa s) in Rheology datafiles
Code/software
For file: Figure_S1-S8_NMR.zip
Please extract and open each folder with any NMR analyzing software (e.g., MestReNova or Topspin - free for academia)
Other files are in .csv format that can be directly plotted by any graphing software
Access information
Other publicly accessible locations of the data:
- N/A
Data was derived from the following sources:
- The majority of research reported here were collected from the either Chabinyc, Bates, Segalman's lab, and the shared facilities of the Materials Research Science and Engineering Center (MRSEC) at UC Santa Barbara.
- SAXS experiments were supported by the BioPACIFIC Materials Innovation Platform of the National Science Foundation.
- GIWAXS was carried out at Stanford Synchrotron Radiation Lightsource at SLAC National Accelerator Laboratory.
