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      KCI등재 SCOPUS SCIE

      Theoretical probe on modified organic dyes for high-performance dye-sensitised solar cell

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      https://www.riss.kr/link?id=A105894414

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      다국어 초록 (Multilingual Abstract)

      We have proposed newly designed organic sensitizers, which could potentially be the best performing organic dyes for Dye Sensitised Solar Cell applications (DSSC). The designed sensitizers are derivatives of “Triphenylamine (TPA) - Tetrathienoacene (TTA) - Thiophene (T) - cyanoacrylic acid (A)” (TPA-TTAR-T-A) sensitizer. Our conclusions were based on calculations performed using Density Functional Theory (DFT) and Time Dependent Density Functional Theory (TD-DFT) methods, on various theoretical parameters of sensitizers that are pertinent to the Power Conversion Efficiency (PCE) of the solar cell. We strategically incorporated substitutions on the spacer located between the π- bridge and the anchoring group, where the thiophene was inserted in previous study. We found that strengthening the electron withdrawing ability around thiophene spacer by fluorination and cyano substitution, and replacement of thiophene spacer with fluorinated and cyano substituted benzodithiophene complexes results in improved opto-electronic properties of the sensitizers.
      Thereby, we identified six new derivatives and for each derivative we have studied the parameters concerning short circuit current (Jsc), such as molecular geometry, absorption spectrum, frontier molecular orbital patterns, electronic energy levels and excited state life time. Also, we have analysed the intramolecular charge transport characteristics of the designed dyes. By considering the overall computed parameters we were able to sort out two new sensitizers TPA-TTAR-2FT-A and TPA-TTAR-2F2CNBDT-A that delivered the needed characteristics and thereby brings in confidence that these sensitizers could challenge TPA-TTA-T-A as the best performing organic sensitizer.
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      We have proposed newly designed organic sensitizers, which could potentially be the best performing organic dyes for Dye Sensitised Solar Cell applications (DSSC). The designed sensitizers are derivatives of “Triphenylamine (TPA) - Tetrathienoacene ...

      We have proposed newly designed organic sensitizers, which could potentially be the best performing organic dyes for Dye Sensitised Solar Cell applications (DSSC). The designed sensitizers are derivatives of “Triphenylamine (TPA) - Tetrathienoacene (TTA) - Thiophene (T) - cyanoacrylic acid (A)” (TPA-TTAR-T-A) sensitizer. Our conclusions were based on calculations performed using Density Functional Theory (DFT) and Time Dependent Density Functional Theory (TD-DFT) methods, on various theoretical parameters of sensitizers that are pertinent to the Power Conversion Efficiency (PCE) of the solar cell. We strategically incorporated substitutions on the spacer located between the π- bridge and the anchoring group, where the thiophene was inserted in previous study. We found that strengthening the electron withdrawing ability around thiophene spacer by fluorination and cyano substitution, and replacement of thiophene spacer with fluorinated and cyano substituted benzodithiophene complexes results in improved opto-electronic properties of the sensitizers.
      Thereby, we identified six new derivatives and for each derivative we have studied the parameters concerning short circuit current (Jsc), such as molecular geometry, absorption spectrum, frontier molecular orbital patterns, electronic energy levels and excited state life time. Also, we have analysed the intramolecular charge transport characteristics of the designed dyes. By considering the overall computed parameters we were able to sort out two new sensitizers TPA-TTAR-2FT-A and TPA-TTAR-2F2CNBDT-A that delivered the needed characteristics and thereby brings in confidence that these sensitizers could challenge TPA-TTA-T-A as the best performing organic sensitizer.

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      참고문헌 (Reference)

      1 K. Do, 115 : 52-57, 2013

      2 A.S. Shalbi, 76 : 22-53, 2009

      3 M. Gratzel, 414 : 338-334, 2001

      4 A. Hagfeldt, 110 : 6595-6663, 2010

      5 M.C. Hwang, 125 : 39-46, 2016

      6 H.B. Li, 108 : 106-114, 2014

      7 M. Li, 119 : 3299-3309, 2015

      8 N. Lu, 41 : 294-300, 2017

      9 X. Lu, 24 : 3179-3187, 2012

      10 K. Navamani, 5 : 38722-, 2015

      1 K. Do, 115 : 52-57, 2013

      2 A.S. Shalbi, 76 : 22-53, 2009

      3 M. Gratzel, 414 : 338-334, 2001

      4 A. Hagfeldt, 110 : 6595-6663, 2010

      5 M.C. Hwang, 125 : 39-46, 2016

      6 H.B. Li, 108 : 106-114, 2014

      7 M. Li, 119 : 3299-3309, 2015

      8 N. Lu, 41 : 294-300, 2017

      9 X. Lu, 24 : 3179-3187, 2012

      10 K. Navamani, 5 : 38722-, 2015

      11 K. Navamani, 17 : 17729-, 2015

      12 R. Nithya, 15 : 1607-1623, 2014

      13 R. Nithya, 16 : 21496-, 2014

      14 B. Schmatz, 3 : 961-967, 2017

      15 J. Yang, 136 : 5722-5730, 2014

      16 G.H. Rao, 18 : 14279-14285, 2016

      17 T. Shanmugavadivu, 111 : 82-94, 2017

      18 M. Sowmiya, 346 : 372-381, 2017

      19 A. Kathiravan, 19 : 3125-, 2017

      20 P. Naik, 345 : 63-73, 2017

      21 V. Srinivasan, 332 : 453-464, 2017

      22 C. Wang, 2015 : 231-237, 2015

      23 D. Seo, 1081 : 30-37, 2016

      24 X. Zarate, 120 : 1613-1624, 2016

      25 X. Jia, 2 : 19515-19525, 2014

      26 Min-Woo-Lee, 5 : 7711-, 2015

      27 M. Qiu, 119 : 8501-8511, 2015

      28 N. Zhou, 137 : 4414-4423, 2015

      29 M.R. Narayan, 16 : 208-215, 2012

      30 J. Zhang, 119 : 568-576, 2012

      31 R. Katoh, 108 : 4818-4822, 2004

      32 S.I. Gorelsky, 635 : 187-196, 2001

      33 D. Gendron, 4 : 1225-1237, 2011

      34 A. Fitri, 124 : 646-654, 2014

      35 C. Adamo, 304-305 : 166-178, 2015

      36 T.L. Bahers, 7 : 2498-2506, 2011

      37 I. Ciofini, 116 : 11946-11955, 2012

      38 R.Y.-Y. Lin, 2 : 3092-3101, 2014

      39 J. Jun-Ling, 13 : 3714-3722, 2012

      40 N.M. Francesco Ambrosio, 116 : 8-, 2012

      41 N.M. Francesco Ambrosio, 3 : 5-, 2012

      42 T. Lu, "Version 3.6, a Multifunctional Wavefunction Analyzer"

      43 S.I. Gorelsky, "Revision 5.0"

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2008-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2007-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2003-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.8 0.18 1.17
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.92 0.77 0.297 0.1
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