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1. Complementary design and examination of p- and n-type conjugated polymers and their evaluation as transport materials

2. Polaron spin dynamics in high-mobility polymeric semiconductors

3. Long spin diffusion lengths in doped conjugated polymers due to enhanced exchange coupling

5. Observation of Weak Counterion Size Dependence of Thermoelectric Transport in Ion Exchange Doped Conducting Polymers Across a Wide Range of Conductivities

6. Single Atom Selenium Substitution‐Mediated P‐Type Doping in Polythiophenes toward High‐Performance Organic Electronics and Thermoelectrics

7. Publisher Correction: Long spin diffusion lengths in doped conjugated polymers due to enhanced exchange coupling

11. Charge transport physics of a unique class of rigid-rod conjugated polymers with fused-ring conjugated units linked by double carbon-carbon bonds

12. Fused electron deficient semiconducting polymers for air stable electron transport

13. Acene Ring Size Optimization in Fused Lactam Polymers Enabling High n-Type Organic Thermoelectric Performance

14. Linking Glass‐Transition Behavior to Photophysical and Charge Transport Properties of High‐Mobility Conjugated Polymers

17. Anisotropy of Charge Transport in a Uniaxially Aligned Fused Electron‐Deficient Polymer Processed by Solution Shear Coating

18. Performance Improvements in Conjugated Polymer Devices by Removal of Water Induced Traps

19. Crystal Engineering of Dibenzothiophenothieno[3,2-b]thiophene (DBTTT) Isomers for Organic Field-Effect Transistors

20. Linking Glass‐Transition Behavior to Photophysical and Charge Transport Properties of High‐Mobility Conjugated Polymers.

24. Improved environmental stability of organic lead trihalide perovskite-based photoactive-layers in the presence of mesoporous TiO2

25. Improved environmental stability of organic lead trihalide perovskite-based photoactive-layers in the presence of mesoporous TiO2.

26. Charge transport physics of a unique class of rigid-rod conjugated polymers with fused-ring conjugated units linked by double carbon-carbon bonds.

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