Small machines are highly promising for future medicine and new materials. Recent advances in functional nanomaterials have driven the development of synthetic inorganic micromachines that are capable of efficient propulsion and complex operation. Miniaturization and large‐scale manufacturing of these tiny machines with true nanometer dimension are crucial for compatibility with subcellular components and molecular machines in operation. Here, block copolymer lithography is combined with atomic layer deposition for wafer‐scale fabrication of ultrasmall coaxial TiO2/Pt nanotubes as catalytic rocket engines with length below 150 nm and a tubular reactor size of only 20 nm, leading to the smallest man‐made rocket engine reported to date. The movement of the nanorockets is examined using dark‐field microscopy particle tracking and dynamic light scattering. The high catalytic activity of the Pt inner layer and the reaction confined within the extremely small nanoreactor enable highly efficient propulsion, achieving speeds over 35 µm s−1at a low Reynolds number of <10−5. The collective movements of these nanorockets are able to efficiently power the directional transport of significantly larger passive cargo.
Advances in dynamically controlled catalytic reaction engineering
Transient reaction modulation has found its place in many branches of chemical reaction engineering over the past hundred years. Historically, catalytic reactions have been dominated by the impulse to reduce spatial and temporal perturbations in favor of steady, static systems due to their ease of operation and scalability. Transient reactor operation, however, has seen remarkable growth in the past few decades, where new operating regimes are being revealed to enhance catalytic reaction rates beyond the statically achievable limits classically described by thermodynamics and the Sabatier principle. These theoretical and experimental studies suggest that there exists a resonant frequency which coincides with its catalytic turnover that can be exploited and amplified for a given reaction to overcome classical barriers. This review discusses the evolution of thought from thermostatic (equilibrium), to thermodynamic (dynamic equilibrium), and finally dynamic (non-equilibrium) catalysis. Natural and forced dynamic oscillations are explored with periodic reactor operation of catalytic systems that modulate energetics and local concentrations through a multitude of approaches, and the challenges to unlock this new class of catalytic reaction engineering is discussed.
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- NSF-PAR ID:
- 10275598
- Date Published:
- Journal Name:
- Reaction Chemistry & Engineering
- Volume:
- 5
- Issue:
- 12
- ISSN:
- 2058-9883
- Page Range / eLocation ID:
- 2185 to 2203
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/d0re00330a
