Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) has been studied for a wide range of applications due to its potential as a transparent electrode. Herein, the use of imidazole and its derivatives as a neutralizing additive for PEDOT:PSS dispersion and in-depth studies of their effects in terms of electrical properties and stability is reported. Although the neutralization in general reduces the electrical conductivity of PEDOT:PSS, the conductivity after imidazole treatment (685.2 S cm 21 ) is higher than that after treatment of other derivatives. Spectroscopic and thermoelectric studies show that the de-doping effect resulted in the conductivity reduction. As a trade-off of the conductivity reduction, greatly enhanced long-term stability and noncorrosive characteristics are obtained after neutralization. The change in sheet resistance of imidazole-treated PEDOT:PSS after 500 h under harsh conditions (85 8C and 85% humidity) is half that of the untreated samples, demonstrating the great enhancement of the stability.
Poly(3,4-ethyldioxythiophene):poly(styrene sulfonate) (PEDOT:PSS), as an thermoelectric(TE) material, exhibits a high electrical conductivity and ZT value (10 À1 -10 0 ). Nevertheless, a low thermovoltage of the organic thermoelectric materials must be overcome, in comparison to that of semi metals. Recently, to address these challenges, several researchers have investigated PEDOT:PSS/carbon material composites.Herein, a transparent and flexible hybrid film made up of rapid thermal chemical vapor deposition (RTCVD) graphene and PEDOT:PSS results in enhanced TE performance. The PEDOT:PSS was synthesized by oxidative polymerization, and the hybrid process of the graphene film and PEDOT:PSS film was conducted using the layer-by-layer method. The results of AFM and Raman spectroscopy revealed that the synergistic effect through composite films improved the electrical properties. The maximum electrical conductivity and power factor of the RTCVD graphene/PEDOT:PSS (RCG/P) hybrid film were 1096 S cm À1 and 57.9 mW m À1 K
À2, respectively. In addition, the RCG/P hybrid film exhibited excellent mechanical flexibility and stability.
For the first time, the 3 dimensionally stacked NAND Flash memory, is developed by implementing S 3 ( Single-crystal Si layer Stacking ) technology, which was used to develop S 3 SRAM previously. The NAND cell arrays are formed on the ILD as well as on the bulk to double the memory density without increasing the chip size. The feasibility of the technology was proven by the successful operation of 32 bit NAND Flash memory cell strings with 63nm dimension and TANOS structures. The novel NAND cell operational scheme, so called SBT ( Source-Body Tied) scheme, is presented to maximize the advantages of 3 dimensionally stacked NAND cell structures.
Even though poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) has been commonly used as a hole extraction layer (HEL) for p-i-n perovskite solar cells (PSCs), the cells' photovoltaic performance deteriorates because of the low and unstable work functions (WFs) of PEDOT:PSS versus those of a perovskite layer. To overcome this drawback, we synthesized a copolymer (P(SS- co-TFPMA)) ionomer consisting of PSS and tetrafluoropropylmethacrylate (TFPMA) as an alternative to conventional PEDOT:PSS. The PEDOT:P(SS- co-TFPMA) copolymer solution and its film exhibited excellent homogeneity and high phase stability compared with a physical mixture of TFPMA with PEDOT:PSS solution. During spin coating, a self-organized conducting PEDOT:P(SS- co-TFPMA) HEL evolved and the topmost PEDOT:P(SS- co-TFPMA) film showed a hydrophobic surface with a higher WF compared to that of the pristine PEDOT:PSS film because of its chemically bonded electron-withdrawing fluorinated functional groups. Interestingly, the WF of the conventional PEDOT:PSS film dramatically deteriorated after being coated with a perovskite layer, whereas the PEDOT:P(SS- co-TFPMA) film represented a relatively small influence. Because of the superior energy-level alignment between the HEL and a perovskite layer even after the contact, the open-circuit voltage, short-circuit current, and fill factor of the inverted planar p-i-n PSCs (IP-PSCs) with PEDOT:P(SS- co-TFPMA) were improved from 0.92 to 0.98 V, 18.96 to 19.66 mA/cm, and 78.96 to 82.43%, respectively, resulting in a 15% improvement in the power conversion efficiency vs that of IP-PSCs with conventional PEDOT:PSS. Moreover, the IP-PSCs with PEDOT:P(SS- co-TFPMA) layer showed not only improved photovoltaic performance but also enhanced device stability due to hydrophobic surface of PEDOT:P(SS- co-TFPMA) film.
Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is a promising conducting polymer in terms of its applicability to transparent and flexible electronic devices. Generally, a negatively charged PSS chain can interact with alkali metal cations like sodium and potassium. During polymerization, these ions, especially sodium ions, remain in an aqueous state and affect particle formation. This paper describes the effect of residual sodium ions on the synthesis of PEDOT:PSS and its electrical and optical properties. Removing the sodium ions weakens the coulombic interaction between the PEDOT and PSS chains, which leads to a linear conformation. This conformational change enhances the electrical conductivity and work function. Furthermore, transmittance in the visible region increased remarkably because the intrinsic electrical properties of the PEDOT:PSS particles were improved. Moreover, the colloidal stability was enhanced because the particle coagulation caused by residual sodium ions was reduced. In summary, we determined that sodium ions in PEDOT:PSS have a considerable influence on its electrical and optical properties and colloidal stability for practical applications.
(3,4-Ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), a representative conducting polymer, is environment-friendly and offers easy processing and flexibility owing to its hydro-dispersive properties.
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