TY - JOUR
T1 - N=8 Armchair Graphene Nanoribbons
T2 - Solution Synthesis and High Charge Carrier Mobility**
AU - Yao, Xuelin
AU - Zhang, Heng
AU - Kong, Fanmiao
AU - Hinaut, Antoine
AU - Pawlak, Rémy
AU - Okuno, Masanari
AU - Graf, Robert
AU - Horton, Peter N.
AU - Coles, Simon J.
AU - Meyer, Ernst
AU - Bogani, Lapo
AU - Bonn, Mischa
AU - Wang, Hai I.
AU - Müllen, Klaus
AU - Narita, Akimitsu
N1 - Publisher Copyright:
© 2023 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.
PY - 2023/11/13
Y1 - 2023/11/13
N2 - Structurally defined graphene nanoribbons (GNRs) have emerged as promising candidates for nanoelectronic devices. Low band gap (<1 eV) GNRs are particularly important when considering the Schottky barrier in device performance. Here, we demonstrate the first solution synthesis of 8-AGNRs through a carefully designed arylated polynaphthalene precursor. The efficiency of the oxidative cyclodehydrogenation of the tailor-made polymer precursor into 8-AGNRs was validated by FT-IR, Raman, and UV/Vis-near-infrared (NIR) absorption spectroscopy, and further supported by the synthesis of naphtho[1,2,3,4-ghi]perylene derivatives (1 and 2) as subunits of 8-AGNR, with a width of 0.86 nm as suggested by the X-ray single crystal analysis. Low-temperature scanning tunneling microscopy (STM) and solid-state NMR analyses provided further structural support for 8-AGNR. The resulting 8-AGNR exhibited a remarkable NIR absorption extending up to ∼2400 nm, corresponding to an optical band gap as low as ∼0.52 eV. Moreover, optical-pump TeraHertz-probe spectroscopy revealed charge-carrier mobility in the dc limit of ∼270 cm2 V−1 s−1 for the 8-AGNR.
AB - Structurally defined graphene nanoribbons (GNRs) have emerged as promising candidates for nanoelectronic devices. Low band gap (<1 eV) GNRs are particularly important when considering the Schottky barrier in device performance. Here, we demonstrate the first solution synthesis of 8-AGNRs through a carefully designed arylated polynaphthalene precursor. The efficiency of the oxidative cyclodehydrogenation of the tailor-made polymer precursor into 8-AGNRs was validated by FT-IR, Raman, and UV/Vis-near-infrared (NIR) absorption spectroscopy, and further supported by the synthesis of naphtho[1,2,3,4-ghi]perylene derivatives (1 and 2) as subunits of 8-AGNR, with a width of 0.86 nm as suggested by the X-ray single crystal analysis. Low-temperature scanning tunneling microscopy (STM) and solid-state NMR analyses provided further structural support for 8-AGNR. The resulting 8-AGNR exhibited a remarkable NIR absorption extending up to ∼2400 nm, corresponding to an optical band gap as low as ∼0.52 eV. Moreover, optical-pump TeraHertz-probe spectroscopy revealed charge-carrier mobility in the dc limit of ∼270 cm2 V−1 s−1 for the 8-AGNR.
KW - Carbon Materials
KW - Graphene Nanoribbons
KW - High Charge Carrier Mobility
KW - Low Bandgap
KW - Time-Resolved Spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=85173761569&partnerID=8YFLogxK
U2 - 10.1002/anie.202312610
DO - 10.1002/anie.202312610
M3 - Article
C2 - 37750665
AN - SCOPUS:85173761569
SN - 1433-7851
VL - 62
SP - 1
EP - 7
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 46
M1 - e202312610
ER -