<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Meng L</submitter><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>1410</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8931007</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>As conventional silicon-based transistors are fast approaching the physical limit, it is essential to seek alternative candidates, which should be compatible with or even replace microelectronics in the future. Here, we report a robust solid-state single-molecule field-effect transistor architecture using graphene source/drain electrodes and a metal back-gate electrode. The transistor is constructed by a single dinuclear ruthenium-diarylethene (Ru-DAE) complex, acting as the conducting channel, connecting covalently with nanogapped graphene electrodes, providing field-effect behaviors with a maximum on/off ratio exceeding three orders of magnitude. Use of ultrathin high-k metal oxides as the dielectric layers is key in successfully achieving such a high performance. Additionally, Ru-DAE preserves its intrinsic photoisomerisation property, which enables a reversible photoswitching function. Both experimental and theoretical results demonstrate these distinct dual-gated behaviors consistently at the single-molecule level, which helps to develop the different technology for creation of practical ultraminiaturised functional electrical circuits beyond Moore's law.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Dual-gated single-molecule field-effect transistors beyond Moore's law.</pubmed_title><pmcid>PMC8931007</pmcid><funding_grant_id>21727806 and 21933001</funding_grant_id><pubmed_authors>Norel L</pubmed_authors><pubmed_authors>Xin N</pubmed_authors><pubmed_authors>Meng S</pubmed_authors><pubmed_authors>Selvanathan P</pubmed_authors><pubmed_authors>Jia C</pubmed_authors><pubmed_authors>Guo X</pubmed_authors><pubmed_authors>Jiang H</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Hu C</pubmed_authors><pubmed_authors>Yan Z</pubmed_authors><pubmed_authors>Guo H</pubmed_authors><pubmed_authors>He X</pubmed_authors><pubmed_authors>Gu L</pubmed_authors><pubmed_authors>Meng L</pubmed_authors><pubmed_authors>Ji Y</pubmed_authors><pubmed_authors>Rigaut S</pubmed_authors><pubmed_authors>Sabea HA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dual-gated single-molecule field-effect transistors beyond Moore's law.</name><description>As conventional silicon-based transistors are fast approaching the physical limit, it is essential to seek alternative candidates, which should be compatible with or even replace microelectronics in the future. Here, we report a robust solid-state single-molecule field-effect transistor architecture using graphene source/drain electrodes and a metal back-gate electrode. The transistor is constructed by a single dinuclear ruthenium-diarylethene (Ru-DAE) complex, acting as the conducting channel, connecting covalently with nanogapped graphene electrodes, providing field-effect behaviors with a maximum on/off ratio exceeding three orders of magnitude. Use of ultrathin high-k metal oxides as the dielectric layers is key in successfully achieving such a high performance. Additionally, Ru-DAE preserves its intrinsic photoisomerisation property, which enables a reversible photoswitching function. Both experimental and theoretical results demonstrate these distinct dual-gated behaviors consistently at the single-molecule level, which helps to develop the different technology for creation of practical ultraminiaturised functional electrical circuits beyond Moore's law.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T03:20:06.346Z</modification><creation>2025-04-04T03:20:06.346Z</creation></dates><accession>S-EPMC8931007</accession><cross_references><pubmed>35301285</pubmed><doi>10.1038/s41467-022-28999-x</doi></cross_references></HashMap>