TY - JOUR
T1 - Patchy nanoparticles by atomic stencilling
AU - Kim, Ahyoung
AU - Kim, Chansong
AU - Waltmann, Tommy
AU - Vo, Thi
AU - Kim, Eun Mi
AU - Kim, Junseok
AU - Shao, Yu Tsun
AU - Michelson, Aaron
AU - Crockett, John R.
AU - Kalutantirige, Falon C.
AU - Yang, Eric
AU - Yao, Lehan
AU - Hwang, Chu Yun
AU - Zhang, Yugang
AU - Liu, Yu Shen
AU - An, Hyosung
AU - Gao, Zirui
AU - Kim, Jiyeon
AU - Mandal, Sohini
AU - Muller, David A.
AU - Fichthorn, Kristen A.
AU - Glotzer, Sharon C.
AU - Chen, Qian
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/10/16
Y1 - 2025/10/16
N2 - Stencilling, in which patterns are created by painting over masks, has ubiquitous applications in art, architecture and manufacturing. Modern, top-down microfabrication methods have succeeded in reducing mask sizes to under 10 nm (refs. 1,2), enabling ever smaller microdevices as today’s fastest computer chips. Meanwhile, bottom-up masking using chemical bonds or physical interactions has remained largely unexplored, despite its advantages of low cost, solution-processability, scalability and high compatibility with complex, curved and three-dimensional (3D) surfaces3,4. Here we report atomic stencilling to make patchy nanoparticles (NPs), using surface-adsorbed iodide submonolayers to create the mask and ligand-mediated grafted polymers onto unmasked regions as ‘paint’. We use this approach to synthesize more than 20 different types of NP coated with polymer patches in high yield. Polymer scaling theory and molecular dynamics (MD) simulation show that stencilling, along with the interplay of enthalpic and entropic effects of polymers, generates patchy particle morphologies not reported previously. These polymer-patched NPs self-assemble into extended crystals owing to highly uniform patches, including different non-closely packed superlattices. We propose that atomic stencilling opens new avenues in patterning NPs and other substrates at the nanometre length scale, leading to precise control of their chemistry, reactivity and interactions for a wide range of applications, such as targeted delivery, catalysis, microelectronics, integrated metamaterials and tissue engineering5, 6, 7, 8, 9, 10–11.
AB - Stencilling, in which patterns are created by painting over masks, has ubiquitous applications in art, architecture and manufacturing. Modern, top-down microfabrication methods have succeeded in reducing mask sizes to under 10 nm (refs. 1,2), enabling ever smaller microdevices as today’s fastest computer chips. Meanwhile, bottom-up masking using chemical bonds or physical interactions has remained largely unexplored, despite its advantages of low cost, solution-processability, scalability and high compatibility with complex, curved and three-dimensional (3D) surfaces3,4. Here we report atomic stencilling to make patchy nanoparticles (NPs), using surface-adsorbed iodide submonolayers to create the mask and ligand-mediated grafted polymers onto unmasked regions as ‘paint’. We use this approach to synthesize more than 20 different types of NP coated with polymer patches in high yield. Polymer scaling theory and molecular dynamics (MD) simulation show that stencilling, along with the interplay of enthalpic and entropic effects of polymers, generates patchy particle morphologies not reported previously. These polymer-patched NPs self-assemble into extended crystals owing to highly uniform patches, including different non-closely packed superlattices. We propose that atomic stencilling opens new avenues in patterning NPs and other substrates at the nanometre length scale, leading to precise control of their chemistry, reactivity and interactions for a wide range of applications, such as targeted delivery, catalysis, microelectronics, integrated metamaterials and tissue engineering5, 6, 7, 8, 9, 10–11.
UR - https://www.scopus.com/pages/publications/105018878335
UR - https://www.scopus.com/pages/publications/105018878335#tab=citedBy
U2 - 10.1038/s41586-025-09605-8
DO - 10.1038/s41586-025-09605-8
M3 - Article
C2 - 41094247
AN - SCOPUS:105018878335
SN - 0028-0836
VL - 646
SP - 592
EP - 600
JO - Nature
JF - Nature
IS - 8085
ER -