Significance When two sheets of graphene are twisted to the magic angle of 1.1 ∘ , the resulting flat moiré bands can host exotic correlated electronic states such as superconductivity and ferromagnetism. Here, we show transport properties of a twisted bilayer graphene device at 1.38 ∘ , far enough above the magic angle that we do not expect exotic correlated states. Instead, we see several unusual behaviors in the device’s resistivity upon tuning both charge carrier density and perpendicular magnetic field. We can reproduce these behaviors with a surprisingly simple model based on Hofstadter’s butterfly. These results shed light on the underlying properties of twisted bilayer graphene.

The physical properties of a material tuned to the cusp between two distinct ground states can be quite exotic, and unlike those in either of the neighboring phases [1,2]. The prospect of capturing such behavior in a simple model is tantalizing; for example, the interplay between heavy fermion physics and magnetic ordering in certain materials is often rationalized in terms of the quantum phase transition in the two-impurity Kondo model [3,4]. However, this model is oversimplified for the purpose: its quantum critical point does not reflect the distinctive properties of a magnetic lattice surrounded by mobile electrons [5,6]. In this work, we study a tunable nanoelectronic circuit comprising two coupled charge-Kondo quantum islands, realizing a new model which captures the essence of competition between local and collective screening of magnetic moments. This may have relevance for materials in which collective many-body effects drive lattice coherence [7]- [9]. We tune our device to a novel quantum critical point, and show experimentally that deviations as we tune away from this point match non-trivial predictions from the model. This work on the crucial role of inter-island interactions is a necessary first step in scaling up such circuits from individual sites to networks or lattices.

We report on a method to improve in vitro diagnostic assays that detect immune response, with specific application to HIV-1. The inherent polyclonal diversity of the humoral immune response was addressed by using sequential in situ click chemistry to develop a cocktail of peptide-based capture agents, the components of which were raised against different, representative anti-HIV antibodies that bind to a conserved epitope of the HIV-1 envelope protein gp41. The cocktail was used to detect anti-HIV-1 antibodies from a panel of sera collected from HIV-positive patients, with improved signal-to-noise ratio relative to the gold standard commercial recombinant protein antigen. The capture agents were stable when stored as a powder for two months at temperatures close to 60oC.

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