<▼1><P>Herein, a new asymmetric n-type semiconducting molecule (PhITBD) with an indenothiophene core was designed, synthesized using tethering 2-(benzo[<I>c</I>][1,2,5]-thiadiazol-4-ylmethylene)-malononitrile (BM) as terminal...
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https://www.riss.kr/link?id=A107433596
2017
-
SCIE
학술저널
7182-7190(9쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<▼1><P>Herein, a new asymmetric n-type semiconducting molecule (PhITBD) with an indenothiophene core was designed, synthesized using tethering 2-(benzo[<I>c</I>][1,2,5]-thiadiazol-4-ylmethylene)-malononitrile (BM) as terminal...
<▼1><P>Herein, a new asymmetric n-type semiconducting molecule (PhITBD) with an indenothiophene core was designed, synthesized using tethering 2-(benzo[<I>c</I>][1,2,5]-thiadiazol-4-ylmethylene)-malononitrile (BM) as terminal groups, and applied to polymer solar cells (PSCs).</P></▼1><▼2><P>Herein, a new asymmetric n-type semiconducting molecule (PhITBD) with an indenothiophene core was designed, synthesized using tethering 2-(benzo[<I>c</I>][1,2,5]-thiadiazol-4-ylmethylene)-malononitrile (BM) as terminal groups, and applied to polymer solar cells (PSCs). The PSCs with asymmetric PhITBD displayed improved power conversion efficiencies (PCE) of 6.57% as compared to those with the symmetric molecule IDT-2BM. The higher PCE value of the PhITBD-based PSC was mainly attributed to the enhanced photovoltaic properties, the <I>V</I>oc, <I>J</I>sc, FF induced by complementary light absorption (550–600 nm range), morphological improvement, and balanced charge carrier transport in the active layer. Due to the effective morphological control and absorption enhancement, asymmetric structured n-type-conjugated molecules are potential candidates for improving the performance of bulk heterojunction non-fullerene type PSCs.</P></▼2>
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