| dc.contributor.author | Paritmongkol, Watcharaphol | |
| dc.contributor.author | Feng, Zhifu | |
| dc.contributor.author | Refaely-Abramson, Sivan | |
| dc.contributor.author | Tisdale, William A | |
| dc.contributor.author | Kastl, Christoph | |
| dc.contributor.author | Maserati, Lorenzo | |
| dc.date.accessioned | 2026-02-04T18:39:53Z | |
| dc.date.available | 2026-02-04T18:39:53Z | |
| dc.date.issued | 2025-03-26 | |
| dc.identifier.uri | https://hdl.handle.net/1721.1/164732 | |
| dc.description.abstract | Molecular self-assembly offers an effective and scalable way to design nanostructured materials with tunable optoelectronic properties. In the past 30 years, organic chemistry has delivered a plethora of metal-organic structures based on the combination of organic groups, chalcogens, and a broad range of metals. Among these, several layered metal-organic chalcogenides (MOCs)─including "mithrene" (AgSePh)─recently emerged as interesting platforms to host 2D physics embedded in 3D crystals. Their combination of broad tunability, easy processability, and promising optoelectronic performance is driving a renewed interest in the more general material group of "low-dimensional" hybrids. In addition, the covalent MOC lattice provides higher stability compared with polar materials in operating devices. Here, we provide a perspective on the rise of 2D MOCs in terms of their synthesis approaches, 2D quantum confined exciton physics, and potential future applications in UV and X-ray photodetection, chemical sensors, and electrocatalysis. | en_US |
| dc.language.iso | en | |
| dc.publisher | American Chemical Society | en_US |
| dc.relation.isversionof | 10.1021/acsnano.4c18493 | en_US |
| dc.rights | Creative Commons Attribution | en_US |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_US |
| dc.source | American Chemical Society | en_US |
| dc.title | Layered Metal–Organic Chalcogenides: 2D Optoelectronics in 3D Self-Assembled Semiconductors | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Watcharaphol Paritmongkol, Zhifu Feng, Sivan Refaely-Abramson, William A. Tisdale, Christoph Kastl, and Lorenzo Maserati. ACS Nano 2025 19 (13), 12467-12477. | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Chemical Engineering | en_US |
| dc.relation.journal | ACS Nano | en_US |
| dc.eprint.version | Final published version | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dc.date.updated | 2026-02-04T18:34:08Z | |
| dspace.orderedauthors | Paritmongkol, W; Feng, Z; Refaely-Abramson, S; Tisdale, WA; Kastl, C; Maserati, L | en_US |
| dspace.date.submission | 2026-02-04T18:34:11Z | |
| mit.journal.volume | 19 | en_US |
| mit.journal.issue | 13 | en_US |
| mit.license | PUBLISHER_CC | |
| mit.metadata.status | Authority Work and Publication Information Needed | en_US |