<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>55</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>12(1)</volume><submitter>Seo DB</submitter><pubmed_abstract>A controllable approach that combines surface plasmon resonance and two-dimensional (2D) graphene/MoS&lt;sub>2&lt;/sub> heterojunction has not been implemented despite its potential for efficient photoelectrochemical (PEC) water splitting. In this study, plasmonic Ag-decorated 2D MoS&lt;sub>2&lt;/sub> nanosheets were vertically grown on graphene substrates in a practical large-scale manner through metalorganic chemical vapor deposition of MoS&lt;sub>2&lt;/sub> and thermal evaporation of Ag. The plasmonic Ag-decorated MoS&lt;sub&gt;2&lt;/sub> nanosheets on graphene yielded up to 10 times higher photo-to-dark current ratio than MoS&lt;sub>2&lt;/sub> nanosheets on indium tin oxide. The significantly enhanced PEC activity could be attributed to the synergetic effects of SPR and favorable graphene/2D MoS&lt;sub>2&lt;/sub> heterojunction. Plasmonic Ag nanoparticles not only increased visible-light and near-infrared absorption of 2D MoS&lt;sub>2&lt;/sub>, but also induced highly amplified local electric field intensity in 2D MoS&lt;sub>2&lt;/sub>. In addition, the vertically aligned 2D MoS&lt;sub>2&lt;/sub> on graphene acted as a desirable heterostructure for efficient separation and transportation of photo-generated carriers. This study provides a promising path for exploiting the full potential of 2D MoS&lt;sub>2&lt;/sub> for practical large-scale and efficient PEC water-splitting applications.</pubmed_abstract><journal>Nano-micro letters</journal><pagination>172</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7770824</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Plasmonic Ag-Decorated Few-Layer MoS&lt;sub>2&lt;/sub> Nanosheets Vertically Grown on Graphene for Efficient Photoelectrochemical Water Splitting.</pubmed_title><pmcid>PMC7770824</pmcid><pubmed_authors>Sohn Y</pubmed_authors><pubmed_authors>Seo DB</pubmed_authors><pubmed_authors>Kim ET</pubmed_authors><pubmed_authors>Trung TN</pubmed_authors><pubmed_authors>Duc DV</pubmed_authors><pubmed_authors>Jeong JR</pubmed_authors><pubmed_authors>Kim DO</pubmed_authors><pubmed_authors>Hong S</pubmed_authors><view_count>55</view_count></additional><is_claimable>false</is_claimable><name>Plasmonic Ag-Decorated Few-Layer MoS&lt;sub>2&lt;/sub> Nanosheets Vertically Grown on Graphene for Efficient Photoelectrochemical Water Splitting.</name><description>A controllable approach that combines surface plasmon resonance and two-dimensional (2D) graphene/MoS&lt;sub>2&lt;/sub> heterojunction has not been implemented despite its potential for efficient photoelectrochemical (PEC) water splitting. In this study, plasmonic Ag-decorated 2D MoS&lt;sub>2&lt;/sub> nanosheets were vertically grown on graphene substrates in a practical large-scale manner through metalorganic chemical vapor deposition of MoS&lt;sub>2&lt;/sub> and thermal evaporation of Ag. The plasmonic Ag-decorated MoS&lt;sub&gt;2&lt;/sub> nanosheets on graphene yielded up to 10 times higher photo-to-dark current ratio than MoS&lt;sub>2&lt;/sub> nanosheets on indium tin oxide. The significantly enhanced PEC activity could be attributed to the synergetic effects of SPR and favorable graphene/2D MoS&lt;sub>2&lt;/sub> heterojunction. Plasmonic Ag nanoparticles not only increased visible-light and near-infrared absorption of 2D MoS&lt;sub>2&lt;/sub>, but also induced highly amplified local electric field intensity in 2D MoS&lt;sub>2&lt;/sub>. In addition, the vertically aligned 2D MoS&lt;sub>2&lt;/sub> on graphene acted as a desirable heterostructure for efficient separation and transportation of photo-generated carriers. This study provides a promising path for exploiting the full potential of 2D MoS&lt;sub>2&lt;/sub> for practical large-scale and efficient PEC water-splitting applications.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Aug</publication><modification>2024-11-15T10:59:08.168Z</modification><creation>2022-02-10T15:48:14.832Z</creation></dates><accession>S-EPMC7770824</accession><cross_references><pubmed>34138153</pubmed><doi>10.1007/s40820-020-00512-3</doi></cross_references></HashMap>