Effect of Anode Interfacial Modification by Self-Assembled Monolayers on the Organic Solar Cell Performance
A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5′-phenyl-2,2′-bitien-5-yl] benzoic acid (ZE-Ph), 4-[5′-(4-fluorophenyl)-2,2′-bitien-5-yl]benzoic acid (ZE-1F), and 4-[5′-(3,5-difluorophenyl)-2,2′-bitien-5-yl]benzoic acid (ZE-2F) were synthesized to use an inter...
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Published in | ACS omega Vol. 9; no. 7; pp. 7413 - 7423 |
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Abstract | A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5′-phenyl-2,2′-bitien-5-yl] benzoic acid (ZE-Ph), 4-[5′-(4-fluorophenyl)-2,2′-bitien-5-yl]benzoic acid (ZE-1F), and 4-[5′-(3,5-difluorophenyl)-2,2′-bitien-5-yl]benzoic acid (ZE-2F) were synthesized to use an interlayer between an ITO electrode and a MoO3 thin film layer in an organic solar cell (OSC) having poly-3 hexylthiophene (P3HT): [6,6]-phenyl C61 butyric acid methyl ester (PC61BM) blend. The work function and surface wetting properties of the ITO were tuned by SAM molecules. The power conversion efficiency of fabricated OSC devices was improved compared to that of the control device from 1.93 to 2.20% and 2.22% with ZE-Ph and ZE-1F-modified ITO electrodes, respectively. The short-circuit current density (J sc) was increased from 6.16 to 7.10 mA/cm2 and 6.94 mA/cm2 with control, ZE-Ph, and ZE-1F-modified solar cells, respectively. The increase in short-circuit current density (J sc) shows that the hole-transporting properties between ITO and MoO3 were improved by the use of ZE-Ph and ZE-1F compared with that of the ITO/MoO3 electrode configuration. The open-circuit voltage (V oc) of the SAM-modified ITO-based devices was also improved compared with the V oc of unmodified ITO-based devices. These results show that using a monolayer as an interlayer in OSCs is an important strategy to improve the performance of OSCs. All the device parameters were characterized by Kelvin probe force microscopy, cyclic voltammetry, contact angle, and I–V measurements. |
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AbstractList | A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5'-phenyl-2,2'-bitien-5-yl] benzoic acid (ZE-Ph), 4-[5'-(4-fluorophenyl)-2,2'-bitien-5-yl]benzoic acid (ZE-1F), and 4-[5'-(3,5-difluorophenyl)-2,2'-bitien-5-yl]benzoic acid (ZE-2F) were synthesized to use an interlayer between an ITO electrode and a MoO
thin film layer in an organic solar cell (OSC) having poly-3 hexylthiophene (P3HT): [6,6]-phenyl C
butyric acid methyl ester (PC
BM) blend. The work function and surface wetting properties of the ITO were tuned by SAM molecules. The power conversion efficiency of fabricated OSC devices was improved compared to that of the control device from 1.93 to 2.20% and 2.22% with ZE-Ph and ZE-1F-modified ITO electrodes, respectively. The short-circuit current density (
) was increased from 6.16 to 7.10 mA/cm
and 6.94 mA/cm
with control, ZE-Ph, and ZE-1F-modified solar cells, respectively. The increase in short-circuit current density (
) shows that the hole-transporting properties between ITO and MoO
were improved by the use of ZE-Ph and ZE-1F compared with that of the ITO/MoO
electrode configuration. The open-circuit voltage (
) of the SAM-modified ITO-based devices was also improved compared with the
of unmodified ITO-based devices. These results show that using a monolayer as an interlayer in OSCs is an important strategy to improve the performance of OSCs. All the device parameters were characterized by Kelvin probe force microscopy, cyclic voltammetry, contact angle, and
-
measurements. A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5′-phenyl-2,2′-bitien-5-yl] benzoic acid (ZE-Ph), 4-[5′-(4-fluorophenyl)-2,2′-bitien-5-yl]benzoic acid (ZE-1F), and 4-[5′-(3,5-difluorophenyl)-2,2′-bitien-5-yl]benzoic acid (ZE-2F) were synthesized to use an interlayer between an ITO electrode and a MoO 3 thin film layer in an organic solar cell (OSC) having poly-3 hexylthiophene (P3HT): [6,6]-phenyl C 61 butyric acid methyl ester (PC 61 BM) blend. The work function and surface wetting properties of the ITO were tuned by SAM molecules. The power conversion efficiency of fabricated OSC devices was improved compared to that of the control device from 1.93 to 2.20% and 2.22% with ZE-Ph and ZE-1F-modified ITO electrodes, respectively. The short-circuit current density ( J sc ) was increased from 6.16 to 7.10 mA/cm 2 and 6.94 mA/cm 2 with control, ZE-Ph, and ZE-1F-modified solar cells, respectively. The increase in short-circuit current density ( J sc ) shows that the hole-transporting properties between ITO and MoO 3 were improved by the use of ZE-Ph and ZE-1F compared with that of the ITO/MoO 3 electrode configuration. The open-circuit voltage ( V oc ) of the SAM-modified ITO-based devices was also improved compared with the V oc of unmodified ITO-based devices. These results show that using a monolayer as an interlayer in OSCs is an important strategy to improve the performance of OSCs. All the device parameters were characterized by Kelvin probe force microscopy, cyclic voltammetry, contact angle, and I – V measurements. A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5'-phenyl-2,2'-bitien-5-yl] benzoic acid (ZE-Ph), 4-[5'-(4-fluorophenyl)-2,2'-bitien-5-yl]benzoic acid (ZE-1F), and 4-[5'-(3,5-difluorophenyl)-2,2'-bitien-5-yl]benzoic acid (ZE-2F) were synthesized to use an interlayer between an ITO electrode and a MoO3 thin film layer in an organic solar cell (OSC) having poly-3 hexylthiophene (P3HT): [6,6]-phenyl C61 butyric acid methyl ester (PC61BM) blend. The work function and surface wetting properties of the ITO were tuned by SAM molecules. The power conversion efficiency of fabricated OSC devices was improved compared to that of the control device from 1.93 to 2.20% and 2.22% with ZE-Ph and ZE-1F-modified ITO electrodes, respectively. The short-circuit current density (Jsc) was increased from 6.16 to 7.10 mA/cm2 and 6.94 mA/cm2 with control, ZE-Ph, and ZE-1F-modified solar cells, respectively. The increase in short-circuit current density (Jsc) shows that the hole-transporting properties between ITO and MoO3 were improved by the use of ZE-Ph and ZE-1F compared with that of the ITO/MoO3 electrode configuration. The open-circuit voltage (Voc) of the SAM-modified ITO-based devices was also improved compared with the Voc of unmodified ITO-based devices. These results show that using a monolayer as an interlayer in OSCs is an important strategy to improve the performance of OSCs. All the device parameters were characterized by Kelvin probe force microscopy, cyclic voltammetry, contact angle, and I-V measurements. A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5′-phenyl-2,2′-bitien-5-yl] benzoic acid (ZE-Ph), 4-[5′-(4-fluorophenyl)-2,2′-bitien-5-yl]benzoic acid (ZE-1F), and 4-[5′-(3,5-difluorophenyl)-2,2′-bitien-5-yl]benzoic acid (ZE-2F) were synthesized to use an interlayer between an ITO electrode and a MoO3 thin film layer in an organic solar cell (OSC) having poly-3 hexylthiophene (P3HT): [6,6]-phenyl C61 butyric acid methyl ester (PC61BM) blend. The work function and surface wetting properties of the ITO were tuned by SAM molecules. The power conversion efficiency of fabricated OSC devices was improved compared to that of the control device from 1.93 to 2.20% and 2.22% with ZE-Ph and ZE-1F-modified ITO electrodes, respectively. The short-circuit current density (J sc) was increased from 6.16 to 7.10 mA/cm2 and 6.94 mA/cm2 with control, ZE-Ph, and ZE-1F-modified solar cells, respectively. The increase in short-circuit current density (J sc) shows that the hole-transporting properties between ITO and MoO3 were improved by the use of ZE-Ph and ZE-1F compared with that of the ITO/MoO3 electrode configuration. The open-circuit voltage (V oc) of the SAM-modified ITO-based devices was also improved compared with the V oc of unmodified ITO-based devices. These results show that using a monolayer as an interlayer in OSCs is an important strategy to improve the performance of OSCs. All the device parameters were characterized by Kelvin probe force microscopy, cyclic voltammetry, contact angle, and I–V measurements. |
Author | Mutlu, Adem Can, Mustafa Arkan, M. Zeliha Tozlu, Cem |
AuthorAffiliation | Institute of Chemistry Graphene Application and Research Center Izmir Katip Celebi University University of Silesia in Katowice Solar Energy Institute |
AuthorAffiliation_xml | – name: University of Silesia in Katowice – name: Izmir Katip Celebi University – name: Institute of Chemistry – name: Solar Energy Institute – name: Graphene Application and Research Center |
Author_xml | – sequence: 1 givenname: Adem orcidid: 0000-0002-1696-4379 surname: Mutlu fullname: Mutlu, Adem email: adem.mutlu@ege.edu.tr organization: Solar Energy Institute – sequence: 2 givenname: M. Zeliha surname: Arkan fullname: Arkan, M. Zeliha organization: University of Silesia in Katowice – sequence: 3 givenname: Mustafa surname: Can fullname: Can, Mustafa organization: Izmir Katip Celebi University – sequence: 4 givenname: Cem surname: Tozlu fullname: Tozlu, Cem email: cem.tozlu@ikcu.edu.tr organization: Izmir Katip Celebi University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38405451$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1063/1.3028094 10.1039/C4TA05492J 10.1039/C3RA44926B 10.1063/1.3600665 10.1016/j.orgel.2009.08.017 10.1063/1.2174093 10.1002/1616-3028(200110)11:5<374::AID-ADFM374>3.0.CO;2-W 10.1021/la803729p 10.1039/c2jm33838f 10.1002/adfm.200500207 10.1021/cr050149z 10.1002/adfm.200500211 10.1016/j.solmat.2006.10.013 10.1039/b921624c 10.1016/j.orgel.2018.01.038 10.1016/s0379-6779(98)00069-1 10.1002/adfm.200902236 10.1063/1.2823579 10.1039/c2ee02806a 10.1016/j.solmat.2010.08.031 10.1016/j.surfrep.2010.10.001 10.1063/1.1620683 10.1063/1.2778548 10.1002/admi.201901469 10.1063/1.1345834 10.1063/1.2730746 10.1002/1616-3028(200102)11:1<15::AID-ADFM15>3.0.CO;2-A 10.1063/1.371859 10.1002/aenm.201200659 10.1016/j.orgel.2011.12.008 10.1016/j.jssc.2014.02.026 10.1007/s10854-020-04642-7 10.1002/adma.200501717 10.1186/s11671-018-2760-6 10.1039/B9PY00201D 10.1007/s12200-015-0531-x 10.1002/adma.200802854 10.1016/j.jphotochem.2021.113554 10.1002/adma.200703050 10.1039/C4TA00937A 10.1007/s10854-018-00606-0 10.1002/adfm.200902247 10.1016/j.solmat.2008.01.005 10.1016/j.solmat.2009.10.005 10.1021/acsami.7b04184 10.1016/j.orgel.2013.04.017 |
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Snippet | A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5′-phenyl-2,2′-bitien-5-yl] benzoic acid (ZE-Ph),... A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5'-phenyl-2,2'-bitien-5-yl] benzoic acid (ZE-Ph),... A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5′-phenyl-2,2′-bitien-5-yl] benzoic acid (ZE-Ph),... |
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Title | Effect of Anode Interfacial Modification by Self-Assembled Monolayers on the Organic Solar Cell Performance |
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