TY - JOUR
T1 - Kinetic Reconstruction of DNA-Programed Plasmonic Metal Nanostructures with Predictable Shapes and Optical Properties
AU - Wang, Yiming
AU - Satyavolu, Nitya Sai Reddy
AU - Yang, Hong
AU - Lu, Yi
N1 - Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/3/16
Y1 - 2022/3/16
N2 - It is desirable to rationally engineer plasmonic metal nanostructures with sets of structural parameters that lead to specific functions. However, it is still challenging to predict the nanostructured outcome of a synthesis reaction by design because not only the exact kinetic path for the structural evolution is very complicated but also the relationships among various functional and structural parameters are often tangled. It is necessary to deconvolute the structure-function relationships and understand the co-evolution of structural and functional parameters as the nanostructures grow. DNA is a programable biomolecular capping ligand that was shown to be capable of precisely controlling the evolution of metal nanostructures. In this study, we systematically analyzed the evolution of two structural parameters and several functional parameters in the growth of Au-Ag nanostructures controlled by two DNA sequences. We deconvoluted the contributions from the two structural parameters in affecting the plasmonic properties in different kinetic and geometric domains. We further designed new nanostructures by exchanging DNA sequences in the growth environment, which also changed their evolution pathways. The resulting structural and functional parameters could be predictively tuned by the timing of the exchange. This study demonstrates the powerful toolbox provided by programable biomolecules in producing novel nanostructures in a predictable manner. It also shows that by understanding the kinetic evolution of the structural parameters and their relationships with the function parameters, it is possible to design the precise combinations of structural and functional parameters in the nanostructured products.
AB - It is desirable to rationally engineer plasmonic metal nanostructures with sets of structural parameters that lead to specific functions. However, it is still challenging to predict the nanostructured outcome of a synthesis reaction by design because not only the exact kinetic path for the structural evolution is very complicated but also the relationships among various functional and structural parameters are often tangled. It is necessary to deconvolute the structure-function relationships and understand the co-evolution of structural and functional parameters as the nanostructures grow. DNA is a programable biomolecular capping ligand that was shown to be capable of precisely controlling the evolution of metal nanostructures. In this study, we systematically analyzed the evolution of two structural parameters and several functional parameters in the growth of Au-Ag nanostructures controlled by two DNA sequences. We deconvoluted the contributions from the two structural parameters in affecting the plasmonic properties in different kinetic and geometric domains. We further designed new nanostructures by exchanging DNA sequences in the growth environment, which also changed their evolution pathways. The resulting structural and functional parameters could be predictively tuned by the timing of the exchange. This study demonstrates the powerful toolbox provided by programable biomolecules in producing novel nanostructures in a predictable manner. It also shows that by understanding the kinetic evolution of the structural parameters and their relationships with the function parameters, it is possible to design the precise combinations of structural and functional parameters in the nanostructured products.
UR - http://www.scopus.com/inward/record.url?scp=85126270988&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85126270988&partnerID=8YFLogxK
U2 - 10.1021/jacs.1c11333
DO - 10.1021/jacs.1c11333
M3 - Article
C2 - 35234474
AN - SCOPUS:85126270988
SN - 0002-7863
VL - 144
SP - 4410
EP - 4421
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 10
ER -