Boundaries can steer active Janus spheres.

Nature communications 6 (2015) 8999-8999

Authors:

Sambeeta Das, Astha Garg, Andrew I Campbell, Jonathan Howse, Ayusman Sen, Darrell Velegol, Ramin Golestanian, Stephen J Ebbens

Abstract:

The advent of autonomous self-propulsion has instigated research towards making colloidal machines that can deliver mechanical work in the form of transport, and other functions such as sensing and cleaning. While much progress has been made in the last 10 years on various mechanisms to generate self-propulsion, the ability to steer self-propelled colloidal devices has so far been much more limited. A critical barrier in increasing the impact of such motors is in directing their motion against the Brownian rotation, which randomizes particle orientations. In this context, here we report directed motion of a specific class of catalytic motors when moving in close proximity to solid surfaces. This is achieved through active quenching of their Brownian rotation by constraining it in a rotational well, caused not by equilibrium, but by hydrodynamic effects. We demonstrate how combining these geometric constraints can be utilized to steer these active colloids along arbitrary trajectories.

Fibonacci optical lattices for tunable quantum quasicrystals

Physical Review A American Physical Society (APS) 92:6 (2015) 063426

Authors:

K Singh, K Saha, SA Parameswaran, DM Weld

Frustration and correlations in stacked triangular-lattice Ising antiferromagnets

Physical Review B American Physical Society (APS) 92:22 (2015) 220417

Authors:

FJ Burnell, JT Chalker

Long-range magnetic order in models for rare-earth quasicrystals

Physical Review B American Physical Society (APS) 92:22 (2015) 224409

Authors:

Stefanie Thiem, JT Chalker

Force-induced rupture of a DNA duplex: from fundamentals to force sensors

ACS Nano American Chemical Society 9:12 (2015) 11993-12003

Authors:

Majid Mosayebi, Ard A Louis, Jonathan Doye, Thomas E Ouldridge

Abstract:

The rupture of double-stranded DNA under stress is a key process in biophysics and nanotechnology. In this article, we consider the shear-induced rupture of short DNA duplexes, a system that has been given new importance by recently designed force sensors and nanotechnological devices. We argue that rupture must be understood as an activated process, where the duplex state is metastable and the strands will separate in a finite time that depends on the duplex length and the force applied. Thus, the critical shearing force required to rupture a duplex depends strongly on the time scale of observation. We use simple models of DNA to show that this approach naturally captures the observed dependence of the force required to rupture a duplex within a given time on duplex length. In particular, this critical force is zero for the shortest duplexes, before rising sharply and then plateauing in the long length limit. The prevailing approach, based on identifying when the presence of each additional base pair within the duplex is thermodynamically unfavorable rather than allowing for metastability, does not predict a time-scale-dependent critical force and does not naturally incorporate a critical force of zero for the shortest duplexes. We demonstrate that our findings have important consequences for the behavior of a new force-sensing nanodevice, which operates in a mixed mode that interpolates between shearing and unzipping. At a fixed time scale and duplex length, the critical force exhibits a sigmoidal dependence on the fraction of the duplex that is subject to shearing.