Dual-mode crystal-bound and X-type passivation of quantum dots
- Vanderbilt Univ., Nashville, TN (United States). Dept. of Chemistry and Vanderbilt Inst. of Nanoscale Science and Engineering
- Vanderbilt Univ., Nashville, TN (United States). Dept. of Physics and Astronomy; Univ. of Memphis, Memphis, TN (United States). Dept. of Physics and Materials Science
- Vanderbilt Univ., Nashville, TN (United States). Dept. of Chemistry and Vanderbilt Inst. of Nanoscale Science and Engineering; Univ. of Central Florida, Orlando, FL (United States). Dept. of Chemistry
- Vanderbilt Univ., Nashville, TN (United States). Vanderbilt Inst. of Nanoscale Science and Engineering; Tennessee State Univ., Nashville, TN (United States). Dept. of Chemistry
- Vanderbilt Univ., Nashville, TN (United States). Vanderbilt Inst. of Nanoscale Science and Engineering, Dept. of Physics and Astronomy and Dept. of Electrical Engineering and Computer Science
- Vanderbilt Univ., Nashville, TN (United States). Dept. of Chemistry and Dept. of Physics and Astronomy
In this work, we present a new path to the control of quantum dot surface chemistry that can lead to a better understanding of nanoscale interfaces and the development of improved photocatalysts. Control of the synthetic methodology leads to QDs that are concomitantly ligated by crystal-bound organics at the surface anion sites and small X-type ligands on the surface cation sites.
- Research Organization:
- Vanderbilt Univ., Nashville, TN (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC), Basic Energy Sciences (BES). Scientific User Facilities Division; National Science Foundation (NSF); National Insttutes of Health (NIH)
- Grant/Contract Number:
- FG02-09ER46554; AC02-05CH11231; NSF-1253105; NSF EPS-1004083; 2T34GM007663
- OSTI ID:
- 1466989
- Journal Information:
- ChemComm, Vol. 52, Issue 82; ISSN 1359-7345
- Publisher:
- Royal Society of ChemistryCopyright Statement
- Country of Publication:
- United States
- Language:
- English
Cited by: 18 works
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