TY - JOUR
T1 - Direct Patterning of Colloidal Nanocrystals via Thermally Activated Ligand Chemistry
AU - Li, Fu
AU - Chen, Changhao
AU - Lu, Shaoyong
AU - Chen, Xueguang
AU - Liu, Wangyu
AU - Weng, Kangkang
AU - Fu, Zhong
AU - Liu, Dan
AU - Zhang, Lipeng
AU - Abudukeremu, Hannikezi
AU - Lin, Linhan
AU - Wang, Yuanyuan
AU - Zhong, Minlin
AU - Zhang, Hao
AU - Li, Jinghong
N1 - Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/9/27
Y1 - 2022/9/27
N2 - Precise patterning with microscale lateral resolution and widely tunable heights is critical for integrating colloidal nanocrystals into advanced optoelectronic and photonic platforms. However, patterning nanocrystal layers with thickness above 100 nm remains challenging for both conventional and emerging direct photopatterning methods, due to limited light penetration depths, complex mechanical and chemical incompatibilities, and others. Here, we introduce a direct patterning method based on a thermal mechanism, namely, the thermally activated ligand chemistry (or TALC) of nanocrystals. The ligand cross-linking or decomposition reactions readily occur under local thermal stimuli triggered by near-infrared lasers, affording high-resolution and nondestructive patterning of various nanocrystals under mild conditions. Patterned quantum dots fully preserve their structural and photoluminescent quantum yields. The thermal nature allows for TALC to pattern over 10 μm thick nanocrystal layers in a single step, far beyond those achievable in other direct patterning techniques, and also supports the concept of 2.5D patterning. The thermal chemistry-mediated TALC creates more possibilities in integrating nanocrystal layers in uniform arrays or complex hierarchical formats for advanced capabilities in light emission, conversion, and modulation.
AB - Precise patterning with microscale lateral resolution and widely tunable heights is critical for integrating colloidal nanocrystals into advanced optoelectronic and photonic platforms. However, patterning nanocrystal layers with thickness above 100 nm remains challenging for both conventional and emerging direct photopatterning methods, due to limited light penetration depths, complex mechanical and chemical incompatibilities, and others. Here, we introduce a direct patterning method based on a thermal mechanism, namely, the thermally activated ligand chemistry (or TALC) of nanocrystals. The ligand cross-linking or decomposition reactions readily occur under local thermal stimuli triggered by near-infrared lasers, affording high-resolution and nondestructive patterning of various nanocrystals under mild conditions. Patterned quantum dots fully preserve their structural and photoluminescent quantum yields. The thermal nature allows for TALC to pattern over 10 μm thick nanocrystal layers in a single step, far beyond those achievable in other direct patterning techniques, and also supports the concept of 2.5D patterning. The thermal chemistry-mediated TALC creates more possibilities in integrating nanocrystal layers in uniform arrays or complex hierarchical formats for advanced capabilities in light emission, conversion, and modulation.
KW - colloidal nanocrystals
KW - ligand thermal chemistry
KW - optoelectronics
KW - surface ligands
KW - thermal patterning
UR - http://www.scopus.com/inward/record.url?scp=85135938349&partnerID=8YFLogxK
U2 - 10.1021/acsnano.2c04033
DO - 10.1021/acsnano.2c04033
M3 - Article
C2 - 35867875
AN - SCOPUS:85135938349
SN - 1936-0851
VL - 16
SP - 13674
EP - 13683
JO - ACS Nano
JF - ACS Nano
IS - 9
ER -