In nanobiotechnology, the importance of controlling interactions between biological molecules and surfaces is paramount. In recent years, many devices based on nanostructured silicon materials have been presented, such as nanopores and nanochannels. However, there is still a clear lack of simple, reliable, and efficient protocols for preventing and controlling biomolecule adsorption in such structures. In this work, we show a simple method for passivation or selective biofunctionalization of silica, without the need for polymerization reactions or vapor-phase deposition. The surface is simply exposed stepwise to three different chemicals over the course of ∼1 h. First, the use of aminopropylsilatrane is used to create a monolayer of amines, yielding more uniform layers than conventional silanization protocols. Second, a cross-linker layer and click chemistry are used to make the surface reactive toward thiols. In the third step, thick and dense poly(ethylene glycol) brushes are prepared by a grafting-to approach. The modified surfaces are shown to be superior to existing options for silica modification, exhibiting ultralow fouling (a few ng/cm2) after exposure to crude serum. In addition, by including a fraction of biotinylated polymer end groups, the surface can be functionalized further. We show that avidin can be detected label-free from a serum solution with a selectivity (compared to nonspecific binding) of more than 98% without the need for a reference channel. Furthermore, we show that our method can passivate the interior of 150 nm × 100 nm nanochannels in silica, showing complete elimination of adsorption of a sticky fluorescent protein. Additionally, our method is shown to be compatible with modifications of solid-state nanopores in 20 nm thin silicon nitride membranes and reduces the noise in the ion current. We consider these findings highly important for the broad field of nanobiotechnology, and we believe that our method will be very useful for a great variety of surface-based sensors and analytical devices.

The nuclear pore complex is a nanoscale assembly that achieves “shuttle-cargo” transport of biomolecules: a certain cargo molecule can only pass the barrier if it is attached to a shuttle...

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Mercury is a highly toxic heavy metal, and improved removal processes are required in a range of industrial applications to limit the environmental impacts. At present, no viable removal methods exist commercially for mercury removal of aqueous solutions at high acidic conditions, such as concentrated sulfuric acid. Herein, we show that electrochemical mercury removal based on electrochemical alloy formation on platinum, forming PtHg4, can be used to remove mercury from concentrated sulfuric acid. Thin platinum film electrodes and porous electrodes with supported platinum are used to remove more than 90% of mercury from concentrated acid from a zinc smelter with an initial mercury concentration of 0.3–0.9 mg/kg, achieving high-quality acid (<0.08 mg/kg) within 80 h. The removal process is carried out in 50 mL laboratory-scale experiments and scaled up to a 20 L pilot reactor with retained removal efficiency, highlighting excellent scalability of the method. In addition, the removal efficiency and stability of different electrode substrate materials are studied to ensure high-quality acid and a long lifetime of the electrodes in harsh chemical conditions, offering a potential method for future large-scale mercury decontamination of sulfuric acid.