TY - JOUR
T1 - Unsupervised learning for local structure detection in colloidal systems
AU - Boattini, Emanuele
AU - Dijkstra, Marjolein
AU - Filion, Laura
PY - 2019/10/21
Y1 - 2019/10/21
N2 - We introduce a simple, fast, and easy to implement unsupervised learning algorithm for detecting different local environments on a single-particle level in colloidal systems. In this algorithm, we use a vector of standard bond-orientational order parameters to describe the local environment of each particle. We then use a neural-network-based autoencoder combined with Gaussian mixture models in order to autonomously group together similar environments. We test the performance of the method on snapshots of a wide variety of colloidal systems obtained via computer simulations, ranging from simple isotropically interacting systems to binary mixtures, and even anisotropic hard cubes. Additionally, we look at a variety of common self-assembled situations such as fluid-crystal and crystal-crystal coexistences, grain boundaries, and nucleation. In all cases, we are able to identify the relevant local environments to a similar precision as "standard," manually tuned, and system-specific, order parameters. In addition to classifying such environments, we also use the trained autoencoder in order to determine the most relevant bond orientational order parameters in the systems analyzed.
AB - We introduce a simple, fast, and easy to implement unsupervised learning algorithm for detecting different local environments on a single-particle level in colloidal systems. In this algorithm, we use a vector of standard bond-orientational order parameters to describe the local environment of each particle. We then use a neural-network-based autoencoder combined with Gaussian mixture models in order to autonomously group together similar environments. We test the performance of the method on snapshots of a wide variety of colloidal systems obtained via computer simulations, ranging from simple isotropically interacting systems to binary mixtures, and even anisotropic hard cubes. Additionally, we look at a variety of common self-assembled situations such as fluid-crystal and crystal-crystal coexistences, grain boundaries, and nucleation. In all cases, we are able to identify the relevant local environments to a similar precision as "standard," manually tuned, and system-specific, order parameters. In addition to classifying such environments, we also use the trained autoencoder in order to determine the most relevant bond orientational order parameters in the systems analyzed.
UR - http://www.scopus.com/inward/record.url?scp=85073757218&partnerID=8YFLogxK
U2 - 10.1063/1.5118867
DO - 10.1063/1.5118867
M3 - Article
C2 - 31640379
AN - SCOPUS:85073757218
SN - 0021-9606
VL - 151
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 15
M1 - 154901
ER -