Ultrafast dense DNA functionalization of quantum dots and rods for scalable 2D array fabrication with nanoscale precision

被引:17
作者
Chen, Chi [1 ]
Luo, Xin [1 ,2 ]
Kaplan, Alexander E. K. [3 ]
Bawendi, Moungi G. [3 ]
Macfarlane, Robert J. [2 ]
Bathe, Mark [1 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Chem, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
RESONANCE ENERGY-TRANSFER; POLARIZED EMISSION; SEMICONDUCTOR NANOROD; THIN-FILMS; FLUORESCENCE; CDSE; HETEROSTRUCTURES; ALIGNMENT; CDTE; HYBRIDIZATION;
D O I
10.1126/sciadv.adh8508
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Scalable fabrication of two-dimensional (2D) arrays of quantum dots (QDs) and quantum rods (QRs) with nanoscale precision is required for numerous device applications. However, self-assembly-based fabrication of such arrays using DNA origami typically suffers from low yield due to inefficient QD and QR DNA functionalization. In addition, it is challenging to organize solution-assembled DNA origami arrays on 2D device substrates while maintaining their structural fidelity. Here, we reduced manufacturing time from a few days to a few minutes by preparing high-density DNA-conjugated QDs/QRs from organic solution using a dehydration and rehydration process. We used a surface-assisted large-scale assembly (SALSA) method to construct 2D origami lattices directly on solid substrates to template QD and QR 2D arrays with orientational control, with overall loading yields exceeding 90%. Our fabrication approach enables the scalable, high fidelity manufacturing of 2D addressable QDs and QRs with nanoscale orientational and spacing control for functional 2D photonic devices.
引用
收藏
页数:16
相关论文
共 82 条
[81]   DNA-Based Assembly of Quantum Dots into Dimers and Helices [J].
Zhang, Tao ;
Liedl, Tim .
NANOMATERIALS, 2019, 9 (03)
[82]   Fluorescence resonance energy transfer between a quantum dot donor and a dye acceptor attached to DNA [J].
Zhou, DJ ;
Piper, JD ;
Abell, C ;
Klenerman, D ;
Kang, DJ ;
Ying, LM .
CHEMICAL COMMUNICATIONS, 2005, (38) :4807-4809