Researcher profile

Greg van Anders

Greg van Anders contributes to research discovery and scholarly infrastructure.

ResearcherAffiliation not importedOpen to collaborate

Trust snapshot

Quick read

Trust 21 - EmergingVerification L1Unclaimed author
10works
0followers
12topics
4close collaborators

Actions

Decide how to stay connected

Follow researcher0

Identity and collaboration

How to connect with this researcher

Claiming links this public author record to a researcher profile and unlocks direct collaboration workflows.

Log in to claim

Direct collaboration

Open a focused conversation when the fit is right

Claim this author entity first to unlock direct invitations.

Research graph

See the researcher in context

Open full explorer

Inspect adjacent work, topics, institutions and collaborators without jumping out to a separate graph page.

Building this graph slice

BZPEER is loading the nearby papers, people, topics and institutions for this page.

Published work

10 published item(s)

preprint2026arXiv

Entropic Auto-Encoding via Implicit Free-Energy Minimization

Despite their ubiquity, variational autoencoders (VAEs) inherently suffer from posterior collapse, a failure mode in which latent variables are effectively ignored. This failure arises because explicit prior imposition drives optimization toward loss landscape regions corresponding to uninformative latent representations. Here, we introduce Entropic Autoencoders (EAEs), a framework in which reconstruction loss is the only explicit objective, and entropy generates the latent variables' prior implicitly through a free energy-minimizing ensemble of encoders. This ensemble biases learning toward high-volume regions of near-optimal solutions, while decoder updates direct the search trajectories toward informative latent representations. We demonstrate that EAEs mitigate posterior collapse by learning non-Gaussian, multimodal latent distributions that yield diverse, data-consistent generations and preserve different forms of underlying structure in the data. As a proof-of-concept, we show that an EAE captures a superposition of the known low-dimensional dynamics of a reaction-diffusion process. Then, we show that an EAE identifies implicit categorical distinctions in MNIST latent representations, and displays a hierarchical understanding of facial structure on the CelebA dataset, from an "all-human" face to individual-dependent features.

preprint2021arXiv

Avoidance, Adjacency, and Association in Distributed Systems Design

Patterns of avoidance, adjacency, and association in complex systems design emerge from the system's underlying logical architecture (functional relationships among components) and physical architecture (component physical properties and spatial location). Understanding the physical--logical architecture interplay that gives rise to patterns of arrangement requires a quantitative approach that bridges both descriptions. Here, we show that statistical physics reveals patterns of avoidance, adjacency, and association across sets of complex, distributed system design solutions. Using an example arrangement problem and tensor network methods, we identify several phenomena in complex systems design, including placement symmetry breaking, propagating correlation, and emergent localization. Our approach generalizes straightforwardly to a broad range of complex systems design settings where it can provide a platform for investigating basic design phenomena.

preprint2021arXiv

Shape and Interaction Decoupling for Colloidal Pre-Assembly

Creating materials with structure that is independently controllable at a range of scales requires breaking naturally occurring hierarchies. Breaking these hierarchies can be achieved via the decoupling of building block attributes from structure during assembly. Here, we demonstrate both geometric and interaction decoupling in pre-assembled colloidal structures of cube-like particles with rounded edges. Through computer simulations and experiments, we show that compressing a small number of such cubes in spherical confinement results in clusters with highly reproducible structures that can be used as mesoscale building blocks to form the next level of structural hierarchy. These clusters demonstrate geometric decoupling between particle shape and cluster structure; namely, for clusters of up to nine particles, the colloidal superballs pack consistently like spheres, despite the presence of shape anisotropy and facets in the cubic-like particles. We confirm that cluster structure is also decoupled from inter-particle interaction, showing that the same structures arise from the spherical confinement of both non-magnetic and magnetic colloidal cubes with strong dipolar interactions. To highlight the potential of these superball clusters for hierarchical assembly, we demonstrate, using computer simulations, that clusters of six to nine particles can self-assemble into high-order structures that differ from those of similarly shaped particles without pre-assembly. These results demonstrate decoupling for anisotropic building blocks that can be further exploited for hierarchical materials development.

preprint2016arXiv

Crossover Behavior in the Packing and Assembly of Multivalent Lock-and-Key Colloids

Emergent behaviors occur in a vast array of systems across many scales, and are of fundamental physical importance because of the intrinsic difficulty in linking microscopic system properties to macroscopic behaviors. Here we study the emergent self-assembly behavior of model systems of recently synthesized families of concave dimpled hard spheres, or lock-and-key colloids. We find that as dimple size increases each family exhibits a crossover from a structure that does not reflect the particle symmetry to one that does and, surprisingly, the point at which this crossover occurs is approximately independent of the particle symmetry. Using a combination of numerical and analytic techniques we study systems at infinite and finite pressure, and find different common control parameters in each limit. Our results suggest there exists a set of experimentally realizable colloidal systems that exhibit complex emergent behaviors that can be traced to a common underlying microscopic control parameter.

preprint2016arXiv

Digital Alchemy for Materials Design: Colloids and Beyond

Starting with the early alchemists, a holy grail of science has been to make desired materials by modifying the attributes of basic building blocks. Building blocks that show promise for assembling new complex materials can be synthesized at the nanoscale with attributes that would astonish the ancient alchemists in their versatility. However, this versatility means that making direct connection between building block attributes and bulk behavior is both necessary for rationally engineering materials, and difficult because building block attributes can be altered in many ways. Here we show how to exploit the malleability of the valence of colloidal nanoparticle "elements" to directly and quantitatively link building block attributes to bulk behavior through a statistical thermodynamic framework we term "digital alchemy". We use this framework to optimize building blocks for a given target structure, and to determine which building block attributes are most important to control for self assembly, through a set of novel thermodynamic response functions, moduli and susceptibilities. We thereby establish direct links between the attributes of colloidal building blocks and the bulk structures they form. Moreover, our results give concrete solutions to the more general conceptual challenge of optimizing emergent behaviors in nature, and can be applied to other types of matter. As examples, we apply digital alchemy to systems of truncated tetrahedra, rhombic dodecahedra, and isotropically interacting spheres that self assemble diamond, FCC, and icosahedral quasicrystal structures, respectively.

preprint2014arXiv

Entropically Patchy Particles: Engineering Valence through Shape Entropy

Patchy particles are a popular paradigm for the design and synthesis of nanoparticles and colloids for self-assembly. In "traditional" patchy particles, anisotropic interactions arising from patterned coatings, functionalized molecules, DNA, and other enthalpic means create the possibility for directional binding of particles into higher-ordered structures. Although the anisotropic geometry of non-spherical particles contributes to the interaction patchiness through van der Waals, electrostatic, and other interactions, how particle shape contributes entropically to self-assembly is only now beginning to be understood. It has been recently demonstrated that, for hard shapes, entropic forces are directional. A newly proposed theoretical framework that defines and quantifies directional entropic forces demonstrates the anisotropic--that is, patchy--nature of these emergent, attractive forces. Here we introduce the notion of entropically patchy particles as the entropic counterpart to enthalpically patchy particles. Using three example "families" of shapes, we judiciously modify entropic patchiness by introducing geometric features to the particles so as to target specific crystal structures, which then assembled with Monte Carlo simulations. We quantify the emergent entropic valence via a potential of mean force and torque. We generalize these shape operations to shape anisotropy dimensions, in analogy with the anisotropy dimensions introduced for enthalpically patchy particles. Our findings demonstrate that entropic patchiness and emergent valence provide a way of engineering directional bonding into nanoparticle systems, whether in the presence or absence of additional, non-entropic forces.

preprint2014arXiv

Understanding shape entropy through local dense packing

Entropy drives the phase behavior of colloids ranging from dense suspensions of hard spheres or rods to dilute suspensions of hard spheres and depletants. Entropic ordering of anisotropic shapes into complex crystals, liquid crystals, and even quasicrystals has been demonstrated recently in computer simulations and experiments. The ordering of shapes appears to arise from the emergence of directional entropic forces (DEFs) that align neighboring particles, but these forces have been neither rigorously defined nor quantified in generic systems. Here, we show quantitatively that shape drives the phase behavior of systems of anisotropic particles upon crowding through DEFs. We define DEFs in generic systems, and compute them for several hard particle systems. We show that they are on the order of a few kT at the onset of ordering, placing DEFs on par with traditional depletion, van der Waals, and other intrinsic interactions. In experimental systems with these other interactions, we provide direct quantitative evidence that entropic effects of shape also contribute to self-assembly. We use DEFs to draw a distinction between self-assembly and packing behavior. We show that the mechanism that generates directional entropic forces is the maximization of entropy by optimizing local particle packing. We show that this mechanism occurs in a wide class of systems, and we treat, in a unified way, the entropy-driven phase behavior of arbitrary shapes incorporating the well-known works of Kirkwood, Onsager, and Asakura and Oosawa.

preprint2010arXiv

Holographic Non-Fermi Liquids and the Luttinger Theorem

We show that the Luttinger theorem, a robust feature of Fermi liquids, can be violated in non-Fermi liquids. We compute non-Fermi liquid Green functions using duality to black holes and find that the volume of the Fermi surface depends exponentially on the scaling dimension, which is a measure of the coupling. This demonstrates that Luttinger's theorem does not extend to non-Fermi liquids. We comment on possible experimental signatures.

preprint2006arXiv

Little String Theory from Double-Scaling Limits of Field Theories

We show that little string theory on S^5 can be obtained as double-scaling limits of the maximally supersymmetric Yang-Mills theories on RxS^2 and RxS^3/Z_k. By matching the gauge theory parameters with those in the gravity duals found by Lin and Maldacena, we determine the limits in the gauge theories that correspond to decoupling of NS5-brane degrees of freedom. We find that for the theory on RxS^2, the 't Hooft coupling must be scaled like ln^3(N), and on RxS^3/Z_k, like ln^2(N). Accordingly, taking these limits in these field theories gives Lagrangian definitions of little string theory on S^5.