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      Electrospray deposition of structurally complex molecules revealed by atomic force microscopy

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          Abstract

          Unravelling structures of organic molecules after their deposition on Au(111) with electrospray.

          Abstract

          Advances in organic chemistry allow the synthesis of large, complex and highly functionalized organic molecules having potential applications in optoelectronics, molecular electronics and organic solar cells. Their integration into devices as individual components or highly ordered thin-films is of paramount importance to address these future prospects. However, conventional sublimation techniques in vacuum are usually not applicable since large organic compounds are often non-volatile and decompose upon heating. Here, we prove by atomic force microscopy and scanning tunneling microscopy, the structural integrity of complex organic molecules deposited onto an Au(111) surface using electrospray ionisation deposition. High resolution AFM measurements with CO-terminated tips unambiguously reveal their successful transfer from solution to the gold surface in ultra-high vacuum without degradation of their chemical structures. Furthermore, the formation of molecular structures from small islands to large and highly-ordered self-assemblies of those fragile molecules is demonstrated, confirming the use of electrospray ionisation to promote also on-surface polymerization reactions of highly functionalized organic compounds, biological molecules or molecular magnets.

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          Most cited references56

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          Electrospray ionization for mass spectrometry of large biomolecules

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            Small molecule semiconductors for high-efficiency organic photovoltaics.

            Organic photovoltaic cells (OPVs) are a promising cost-effective alternative to silicon-based solar cells, and possess light-weight, low-cost, and flexibility advantages. Significant progress has been achieved in the development of novel photovoltaic materials and device structures in the last decade. Nowadays small molecular semiconductors for OPVs have attracted considerable attention, due to their advantages over their polymer counterparts, including well-defined molecular structure, definite molecular weight, and high purity without batch to batch variations. The highest power conversion efficiencies of OPVs based on small molecular donor/fullerene acceptors or polymeric donor/fullerene acceptors are up to 6.7% and 8.3%, respectively, and meanwhile nonfullerene acceptors have also exhibited some promising results. In this review we summarize the developments in small molecular donors, acceptors (fullerene derivatives and nonfullerene molecules), and donor-acceptor dyad systems for high-performance multilayer, bulk heterojunction, and single-component OPVs. We focus on correlations of molecular chemical structures with properties, such as absorption, energy levels, charge mobilities, and photovoltaic performances. This structure-property relationship analysis may guide rational structural design and evaluation of photovoltaic materials (253 references).
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              Engineering atomic and molecular nanostructures at surfaces.

              The fabrication methods of the microelectronics industry have been refined to produce ever smaller devices, but will soon reach their fundamental limits. A promising alternative route to even smaller functional systems with nanometre dimensions is the autonomous ordering and assembly of atoms and molecules on atomically well-defined surfaces. This approach combines ease of fabrication with exquisite control over the shape, composition and mesoscale organization of the surface structures formed. Once the mechanisms controlling the self-ordering phenomena are fully understood, the self-assembly and growth processes can be steered to create a wide range of surface nanostructures from metallic, semiconducting and molecular materials.
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                Author and article information

                Journal
                NANOHL
                Nanoscale
                Nanoscale
                Royal Society of Chemistry (RSC)
                2040-3364
                2040-3372
                2018
                2018
                : 10
                : 3
                : 1337-1344
                Affiliations
                [1 ]Department of Physics
                [2 ]University of Basel
                [3 ]CH 4056 Basel
                [4 ]Switzerland
                [5 ]International Center for Materials Nanoarchitectonics
                [6 ]National Institute for Materials Science
                [7 ]Tsukuba
                [8 ]Japan
                [9 ]Department of Chemistry and Biochemistry
                [10 ]University of Bernn Freiestrasse 3
                [11 ]CH 3012 Bern
                [12 ]Max Planck Institute for Polymer Research
                [13 ]55128 Mainz
                [14 ]Germany
                Article
                10.1039/C7NR06261C
                29296988
                c59dd3bb-756d-4321-a331-acf2908ede1a
                © 2018

                http://rsc.li/journals-terms-of-use

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