Poly(ethylene-co-acrylic acid)-g-poly(ethylene glycol) graft copolymer templated synthesis of mesoporous TiO2 thin films for quasi-solid-state dye sensitized solar cells

Rajkumar Patel, Ye Eun Jung, Dong Jun Kim, Sang Jin Kim, Jong Hak Kim

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

An amphiphilic graft copolymer, poly(ethylene-co-acrylic acid)-graft-poly(ethylene glycol) (PEAA-g-PEG), consisting of a PEAA backbone and PEG side chains was synthesized via an esterification reaction. 1H nuclear magnetic resonance and Fourier-transformed infrared analysis demonstrated esterification between carboxylic acid of PEAA and hydroxyl group of PEG. Small angle X-ray scattering results revealed that the crystalline domain spacing of PEAA increased from 11.3 to 12.8 nm upon using a more polar solvent with a higher affinity for poly(acrylic acid), while the crystalline domain spacing of PEAA disappeared with PEG grafting, indicating structural change to an amorphous state. Mesoporous TiO2 thin films were synthesized via a sol-gel reaction using PEAA-g-PEG graft copolymer as a structure-directing agent. The hydrophilically-preformed TiO2 nanoparticles were selectively confined in the hydrophilic PEG domains of the graft copolymer, and mesoporous TiO2 thin films were formed, as confirmed by scanning electron microscopy. The morphology of TiO2 films was tunable by varying the concentrations of polymer solutions and the amount of preformed TiO2. A quasi-solid-state dye-sensitized solar cell fabricated with PEAA-g-PEG templated TiO2 film exhibited an energy conversion efficiency of 3.8% at 100 mW/cm2, which was greater than that of commercially-available paste (2.6%) at a similar film thickness (3 μm). The improved performance was due to the larger surface area for high dye loading and organized structure with good interconnectivity.

Original languageEnglish
Pages (from-to)68-74
Number of pages7
JournalThin Solid Films
Volume552
DOIs
Publication statusPublished - 2014 Feb 3

Fingerprint

Graft copolymers
acrylic acid
Polyethylene glycols
Acrylics
glycols
copolymers
Ethylene
ethylene
solar cells
dyes
solid state
Thin films
Acids
synthesis
thin films
Grafts
carbopol 940
Esterification
spacing
Crystalline materials

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Surfaces and Interfaces
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Cite this

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title = "Poly(ethylene-co-acrylic acid)-g-poly(ethylene glycol) graft copolymer templated synthesis of mesoporous TiO2 thin films for quasi-solid-state dye sensitized solar cells",
abstract = "An amphiphilic graft copolymer, poly(ethylene-co-acrylic acid)-graft-poly(ethylene glycol) (PEAA-g-PEG), consisting of a PEAA backbone and PEG side chains was synthesized via an esterification reaction. 1H nuclear magnetic resonance and Fourier-transformed infrared analysis demonstrated esterification between carboxylic acid of PEAA and hydroxyl group of PEG. Small angle X-ray scattering results revealed that the crystalline domain spacing of PEAA increased from 11.3 to 12.8 nm upon using a more polar solvent with a higher affinity for poly(acrylic acid), while the crystalline domain spacing of PEAA disappeared with PEG grafting, indicating structural change to an amorphous state. Mesoporous TiO2 thin films were synthesized via a sol-gel reaction using PEAA-g-PEG graft copolymer as a structure-directing agent. The hydrophilically-preformed TiO2 nanoparticles were selectively confined in the hydrophilic PEG domains of the graft copolymer, and mesoporous TiO2 thin films were formed, as confirmed by scanning electron microscopy. The morphology of TiO2 films was tunable by varying the concentrations of polymer solutions and the amount of preformed TiO2. A quasi-solid-state dye-sensitized solar cell fabricated with PEAA-g-PEG templated TiO2 film exhibited an energy conversion efficiency of 3.8{\%} at 100 mW/cm2, which was greater than that of commercially-available paste (2.6{\%}) at a similar film thickness (3 μm). The improved performance was due to the larger surface area for high dye loading and organized structure with good interconnectivity.",
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Poly(ethylene-co-acrylic acid)-g-poly(ethylene glycol) graft copolymer templated synthesis of mesoporous TiO2 thin films for quasi-solid-state dye sensitized solar cells. / Patel, Rajkumar; Jung, Ye Eun; Kim, Dong Jun; Kim, Sang Jin; Kim, Jong Hak.

In: Thin Solid Films, Vol. 552, 03.02.2014, p. 68-74.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Poly(ethylene-co-acrylic acid)-g-poly(ethylene glycol) graft copolymer templated synthesis of mesoporous TiO2 thin films for quasi-solid-state dye sensitized solar cells

AU - Patel, Rajkumar

AU - Jung, Ye Eun

AU - Kim, Dong Jun

AU - Kim, Sang Jin

AU - Kim, Jong Hak

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AB - An amphiphilic graft copolymer, poly(ethylene-co-acrylic acid)-graft-poly(ethylene glycol) (PEAA-g-PEG), consisting of a PEAA backbone and PEG side chains was synthesized via an esterification reaction. 1H nuclear magnetic resonance and Fourier-transformed infrared analysis demonstrated esterification between carboxylic acid of PEAA and hydroxyl group of PEG. Small angle X-ray scattering results revealed that the crystalline domain spacing of PEAA increased from 11.3 to 12.8 nm upon using a more polar solvent with a higher affinity for poly(acrylic acid), while the crystalline domain spacing of PEAA disappeared with PEG grafting, indicating structural change to an amorphous state. Mesoporous TiO2 thin films were synthesized via a sol-gel reaction using PEAA-g-PEG graft copolymer as a structure-directing agent. The hydrophilically-preformed TiO2 nanoparticles were selectively confined in the hydrophilic PEG domains of the graft copolymer, and mesoporous TiO2 thin films were formed, as confirmed by scanning electron microscopy. The morphology of TiO2 films was tunable by varying the concentrations of polymer solutions and the amount of preformed TiO2. A quasi-solid-state dye-sensitized solar cell fabricated with PEAA-g-PEG templated TiO2 film exhibited an energy conversion efficiency of 3.8% at 100 mW/cm2, which was greater than that of commercially-available paste (2.6%) at a similar film thickness (3 μm). The improved performance was due to the larger surface area for high dye loading and organized structure with good interconnectivity.

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