TY - JOUR
T1 - Addressing Multiple Resistive States of Polyoxovanadates
T2 - Conductivity as a Function of Individual Molecular Redox States
AU - Linnenberg, Oliver
AU - Moors, Marco
AU - Notario-Estévez, Almudena
AU - López, Xavier
AU - De Graaf, Coen
AU - Peter, Sophia
AU - Baeumer, Christoph
AU - Waser, Rainer
AU - Monakhov, Kirill Yu
N1 - Funding Information:
This work was supported by the Emmy Noether program of the Deutsche Forschungsgemeinschaft (DFG). We are also grateful to the Spanish government (projects CTQ2014-52774 and CTQ2017-83566-P) and the Generalitat de Catalunya (2017-SGR629) for funding. We thank U. Simon (RWTH Aachen University) for access to the IRRAS equipment and R. Borowski (Forschungszentrum Jülich) and T. Pössinger (RWTH Aachen University) for technical assistance.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/12/5
Y1 - 2018/12/5
N2 - The sustainable development of IT-systems requires a quest for novel concepts to address further miniaturization, performance improvement, and energy efficiency of devices. The realization of these goals cannot be achieved without an appropriate functional material. Herein, we target the technologically important electron modification using single polyoxometalate (POM) molecules envisaged as smart successors of materials that are implemented in today's complementary metal-oxide-semiconductor (CMOS) technology. Lindqvist-type POMs were physisorbed on the Au(111) surface, preserving their structural and electronic characteristics. By applying an external voltage at room temperature, the valence state of the single POM molecule could be changed multiple times through the injection of up to 4 electrons. The molecular electrical conductivity is dependent on the number of vanadium 3d electrons, resulting in several discrete conduction states with increasing conductivity. This fundamentally important finding illustrates the far-reaching opportunities for POM molecules in the area of multiple-state resistive (memristive) switching.
AB - The sustainable development of IT-systems requires a quest for novel concepts to address further miniaturization, performance improvement, and energy efficiency of devices. The realization of these goals cannot be achieved without an appropriate functional material. Herein, we target the technologically important electron modification using single polyoxometalate (POM) molecules envisaged as smart successors of materials that are implemented in today's complementary metal-oxide-semiconductor (CMOS) technology. Lindqvist-type POMs were physisorbed on the Au(111) surface, preserving their structural and electronic characteristics. By applying an external voltage at room temperature, the valence state of the single POM molecule could be changed multiple times through the injection of up to 4 electrons. The molecular electrical conductivity is dependent on the number of vanadium 3d electrons, resulting in several discrete conduction states with increasing conductivity. This fundamentally important finding illustrates the far-reaching opportunities for POM molecules in the area of multiple-state resistive (memristive) switching.
UR - http://www.scopus.com/inward/record.url?scp=85058080470&partnerID=8YFLogxK
U2 - 10.1021/jacs.8b08780
DO - 10.1021/jacs.8b08780
M3 - Article
C2 - 30418764
AN - SCOPUS:85058080470
VL - 140
SP - 16635
EP - 16640
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 48
ER -