Chiral Photomelting of DNA-Nanocrystal Assemblies Utilizing Plasmonic Photoheating

被引:25
作者
Avalos-Ovando, Oscar [2 ]
Besteiro, Lucas, V [1 ]
Movsesyan, Artur [2 ,3 ]
Markovich, Gil [4 ]
Liedl, Tim [5 ,6 ]
Martens, Kevin [5 ,6 ]
Wang, Zhiming [3 ]
Correa-Duarte, Miguel A. [1 ]
Govorov, Alexander O. [2 ]
机构
[1] Univ Vigo, CINBIO, Vigo 36310, Spain
[2] Ohio Univ, Dept Phys & Astron, Athens, OH 45701 USA
[3] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610054, Peoples R China
[4] Tel Aviv Univ, Raymond & Beverly Sackler Fac Exact Sci, Sch Chem, IL-6997801 Tel Aviv, Israel
[5] Ludwig Maximilians Univ Munchen, Fac Phys, D-80539 Munich, Germany
[6] Ludwig Maximilians Univ Munchen, Ctr NanoSci CeNS, D-80539 Munich, Germany
基金
欧洲研究理事会; 中国国家自然科学基金;
关键词
Chiral plasmonics; chiral nanocrystals; bioassembly; photochemistry; circular dichroism; photothermal effect; heat generation; DNA melting; CIRCULAR-DICHROISM; NANOPARTICLES; NANOSTRUCTURES; TEMPERATURE;
D O I
10.1021/acs.nanolett.1c02479
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral plasmonic nanostructures exhibit anomalously strong chiroptical signals and offer the possibility to realize asymmetric photophysical and photochemical processes controlled by circularly polarized light. Here, we use a chiral DNA-assembled nanorod pair as a model system for chiral plasmonic photomelting. We show that both the enantiomeric excess and consequent circular dichroism can be controlled with chiral light. The nonlinear chiroptical response of our plasmonic system results from the chiral photothermal effect leading to selective melting of the DNA linker strands. Our study describes both the singlecomplex and collective heating regimes, which should be treated with different models. The chiral asymmetry factors of the calculated photothermal and photomelting effects exceed the values typical for the chiral molecular photochemistry at least 10-fold. Our proposed mechanism can be used to develop chiral photoresponsive systems controllable with circularly polarized light.
引用
收藏
页码:7298 / 7308
页数:11
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