TY - JOUR
T1 - Building large-scale unimolecular scaffolding for electronic devices
AU - Escorihuela, E.
AU - Concellón, A.
AU - Marín, I.
AU - Kumar, V. J.
AU - Herrer, L.
AU - Moggach, S. A.
AU - Vezzoli, A.
AU - Nichols, R. J.
AU - Low, P. J.
AU - Cea, P.
AU - Serrano, J. L.
AU - Martín, S.
N1 - Funding Information:
E.E. gratefully acknowledges the award of a DGA fellowship from the Government of Aragon and Campus Iberus – Erasmus+Programme, Universidad de Zaragoza, Fundación Bancaria Ibercaja, and Fundación CAI (CB 7/21) for extranational research stays co-funding. P.C. J.L.S. and S.M. are grateful for financial assistance in the framework of the projects PID2019-105881RB-I00 funded by MCIN/AEI/10.13039/501100011033 and PGC-2018-097583-I00 and Gobierno de Aragón through the grants E31_20R and E47_20R with European Social Fund (Construyendo Europa desde Aragón). P.J.L. thanks the Australian Research Council for generous funding through DP190100073 and DP190100074. V.J.K. gratefully acknowledges scholarship and support from the Schlumberger Foundation through the Faculty for the Future Program and the Scholarship for International Research Fees from the University of Western Australia. S.A.M. holds an ARC Future Fellowship (FT200100243). AV thanks the Royal Society for generous funding (Fellowship URFøR1ø191241). RJN thanks EPSRC for funding (EP/M029522/1 and EP/M014169/1) and funding from the Leverhulme Foundation (RPG-2019-308).
Funding Information:
E.E. gratefully acknowledges the award of a DGA fellowship from the Government of Aragon and Campus Iberus – Erasmus+Programme, Universidad de Zaragoza, Fundación Bancaria Ibercaja, and Fundación CAI (CB 7/21) for extranational research stays co-funding. P.C., J.L.S. and S.M. are grateful for financial assistance in the framework of the projects PID2019-105881RB-I00 funded by MCIN/AEI/10.13039/501100011033 and PGC-2018-097583-I00 and Gobierno de Aragón through the grants E31_20R and E47_20R with European Social Fund (Construyendo Europa desde Aragón). P.J.L. thanks the Australian Research Council for generous funding through DP190100073 and DP190100074 . V.J.K. gratefully acknowledges scholarship and support from the Schlumberger Foundation through the Faculty for the Future Program and the Scholarship for International Research Fees from the University of Western Australia. S.A.M. holds an ARC Future Fellowship (FT200100243). AV thanks the Royal Society for generous funding (Fellowship URFøR1ø191241). RJN thanks EPSRC for funding (EP/M029522/1 and EP/M014169/1) and funding from the Leverhulme Foundation ( RPG-2019-308 ).
Publisher Copyright:
© 2022 The Author(s)
PY - 2022/12
Y1 - 2022/12
N2 - The fabrication of a future generation of (opto)electronic devices based on molecular components and materials will require careful chemical design, coupled with assembly methods that permit precise spatial orientation and arrangement of the functional molecules within device structures. Although unimolecular electronics are already a laboratory reality, the variation in the arrangement of the molecule within a molecular junction from measurement to measurement is considerable. Consequently, controlling the precise geometry at the molecule–metal contacts is a long-standing and largely unresolved challenge. Here, a strategy to fabricate uniform unimolecular junctions distributed in a regular pattern is reported. A monolayer of zinc metalloporphyrins, peripherally functionalised by bulky dendrons, is used to provide a well-defined array of molecular binding sites with precise spatial distribution. The dendrons are then photochemically cross-linked to form a robust base-layer. Parallel, uniformly-spaced unimolecular structures are subsequently assembled on these binding sites through a layer-by-layer (LbL) strategy. This LbL strategy proceeds through coordination of an α,ω-amino functionalised oligo(phenylene)ethynylene (OPE) molecule to the zinc ions of the metalloporphyrin template base-layer. The structure is then extended through alternating self-assembled layers of (cross-linked) zinc porphyrin and OPE. The coordination interaction between the zinc(II) sites and the bifunctional OPE wire ensures a high degree of registry between the layers and good electrical contact through the extended arrays and offer fine control over the chemical composition.
AB - The fabrication of a future generation of (opto)electronic devices based on molecular components and materials will require careful chemical design, coupled with assembly methods that permit precise spatial orientation and arrangement of the functional molecules within device structures. Although unimolecular electronics are already a laboratory reality, the variation in the arrangement of the molecule within a molecular junction from measurement to measurement is considerable. Consequently, controlling the precise geometry at the molecule–metal contacts is a long-standing and largely unresolved challenge. Here, a strategy to fabricate uniform unimolecular junctions distributed in a regular pattern is reported. A monolayer of zinc metalloporphyrins, peripherally functionalised by bulky dendrons, is used to provide a well-defined array of molecular binding sites with precise spatial distribution. The dendrons are then photochemically cross-linked to form a robust base-layer. Parallel, uniformly-spaced unimolecular structures are subsequently assembled on these binding sites through a layer-by-layer (LbL) strategy. This LbL strategy proceeds through coordination of an α,ω-amino functionalised oligo(phenylene)ethynylene (OPE) molecule to the zinc ions of the metalloporphyrin template base-layer. The structure is then extended through alternating self-assembled layers of (cross-linked) zinc porphyrin and OPE. The coordination interaction between the zinc(II) sites and the bifunctional OPE wire ensures a high degree of registry between the layers and good electrical contact through the extended arrays and offer fine control over the chemical composition.
KW - Large area unimolecular devices
KW - Layer-by-layer self-assembly
KW - Metalloporphiryn
KW - Wire-like oligophenylene
UR - http://www.scopus.com/inward/record.url?scp=85135344136&partnerID=8YFLogxK
U2 - 10.1016/j.mtchem.2022.101067
DO - 10.1016/j.mtchem.2022.101067
M3 - Article
AN - SCOPUS:85135344136
SN - 2468-5194
VL - 26
JO - Materials Today Chemistry
JF - Materials Today Chemistry
M1 - 101067
ER -