Novel A-π-D-π-A-type BODIPY dyads as small-molecule donors for solution-processed organic solar cells. Issue 8 (3rd February 2022)
- Record Type:
- Journal Article
- Title:
- Novel A-π-D-π-A-type BODIPY dyads as small-molecule donors for solution-processed organic solar cells. Issue 8 (3rd February 2022)
- Main Title:
- Novel A-π-D-π-A-type BODIPY dyads as small-molecule donors for solution-processed organic solar cells
- Authors:
- Xie, Bao
Yin, Lunxiang
Fan, Junmei
Liu, Chang
Li, Yanqin - Abstract:
- Abstract : Two novel narrow-bandgap A-π-D-π-A-type BODIPY dyes were synthesized via a one-step Stille reaction with "D-π" segment at the β-site of BODIPY unit, where CTBDP -based device gave an impressive PCE of 5.85% with an excellent J sc of 17.70 mA cm −2 . Abstract : The boron dipyrromethane (BODIPY) unit has attracted interest due to its strong molar extinction coefficient and tunable electrochemical properties, and thus, currently, BODIPY-based organic photovoltaic materials featuring near-infrared absorption and deep HOMO levels are widely constructed and investigated. Herein, two novel A-π-D-π-A-type BODIPY small-molecule donors (SMDs), namely, CTBDP and DCTBDP, in which carbazole and indolo-[3, 2- b ]carbazole as the electron-donating core (D) connect the electron-withdrawing BODIPY moiety (A) with thiophene as a π-bridge, respectively, were designed and synthesized via Stille coupling reaction with a "D-π" segment at the β-site of BODIPY. CTBDP and DCTBDP exhibited a deep-lying HOMO level of −5.46 eV and −5.34 eV and narrow optical bandgap of 1.51 eV and 1.56 eV, respectively, together with a broad absorption in the range of 300–900 nm in films. Interestingly, the CTBDP -device exhibited an impressive PCE of 5.85% with an outstanding J sc of 17.70 mA cm −2 and V oc of 0.81 V, which are the highest PCE and J sc values reported to date for A–D–A-type BODIPY-SMDs for solution-processed OSCs. Our work demonstrates that carbazole/indolo[3, 2- b ]carbazole-BODIPYAbstract : Two novel narrow-bandgap A-π-D-π-A-type BODIPY dyes were synthesized via a one-step Stille reaction with "D-π" segment at the β-site of BODIPY unit, where CTBDP -based device gave an impressive PCE of 5.85% with an excellent J sc of 17.70 mA cm −2 . Abstract : The boron dipyrromethane (BODIPY) unit has attracted interest due to its strong molar extinction coefficient and tunable electrochemical properties, and thus, currently, BODIPY-based organic photovoltaic materials featuring near-infrared absorption and deep HOMO levels are widely constructed and investigated. Herein, two novel A-π-D-π-A-type BODIPY small-molecule donors (SMDs), namely, CTBDP and DCTBDP, in which carbazole and indolo-[3, 2- b ]carbazole as the electron-donating core (D) connect the electron-withdrawing BODIPY moiety (A) with thiophene as a π-bridge, respectively, were designed and synthesized via Stille coupling reaction with a "D-π" segment at the β-site of BODIPY. CTBDP and DCTBDP exhibited a deep-lying HOMO level of −5.46 eV and −5.34 eV and narrow optical bandgap of 1.51 eV and 1.56 eV, respectively, together with a broad absorption in the range of 300–900 nm in films. Interestingly, the CTBDP -device exhibited an impressive PCE of 5.85% with an outstanding J sc of 17.70 mA cm −2 and V oc of 0.81 V, which are the highest PCE and J sc values reported to date for A–D–A-type BODIPY-SMDs for solution-processed OSCs. Our work demonstrates that carbazole/indolo[3, 2- b ]carbazole-BODIPY conjugated small molecules can simultaneously achieve a narrow bandgap and low HOMO level via their rational molecular design, which provides crucial guidance for the development of high-efficiency BODIPY-based photovoltaic materials in the future. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 10:Issue 8(2022)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 10:Issue 8(2022)
- Issue Display:
- Volume 10, Issue 8 (2022)
- Year:
- 2022
- Volume:
- 10
- Issue:
- 8
- Issue Sort Value:
- 2022-0010-0008-0000
- Page Start:
- 3248
- Page End:
- 3258
- Publication Date:
- 2022-02-03
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1tc04981j ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21067.xml