Nature-inspired self-cleaning surfaces have attracted considerable attention from both fundamental research and practical applications. This review adopts a chemical-engineering point of view and focuses on mechanisms, modelling, and manufacturing (M3) of nature-inspired self-cleaning surfaces. We will introduce six nature-inspired self-cleaning mechanisms: The Lotus-effect, superhydrophobic-induced droplet jumping, superhydrophobic-induced unidirectional movement of water droplet, underwater-superoleophobic-based self-cleaning, slippery-based self-cleaning, and dry self-cleaning. These mechanisms of nature self-cleaning examples are popular and well-known as well as have been widely applied or exhibited potential applications in our daily life and industrial productions. The mathematical and numerical modelling of the identified self-cleaning mechanisms will be carefully introduced, which will contribute to the rational design and reproducible construction of these functional self-cleaning surfaces. Finally, we will discuss how these materials can be produced, with a focus on scalable manufacturing. We hope this review will strengthen the understanding on nature-inspired self-cleaning surfaces and stimulate interdisciplinary collaboration of material science, biology and engineering.

The photolysis dynamics of m-fluorophenol (m-FPhOH) and o-fluorophenol (o-FPhOH) have been investigated with time-resolved velocity map imaging (TR-VMI) and time-resolved ion-yield (TR-IY) techniques. Following excitation to the origin of S-1 (pi pi*) state of m- and o-FPhOH, H atoms elimination mediated by tunneling through the potential barrier under the S-1 (pi pi*)/S-2 (pi sigma*) conical intersection (CI) has been observed as a Gaussian feature signal centered at a total kinetic energy release (TKER) of similar to 6000 cm(-1) for both molecules. The quantum tunneling mechanism has been identified as the main decay pathway of Si state for m-FPhOH, and the tunneling lifetime of 2.1 ns has been obtained from the TR-VMI measurements of H fragments. This tunneling mechanism is further confirmed by the studies on the selective O-H deuterated species, m-FPhOD, and consolidated by our theoretical calculations. However, the photolysis dynamics is quite different for the photoexcited o-FPhOH. The much lower yield of the H atoms originating from tunneling hinders the extraction of a reliable tunneling lifetime for o-FPhOH. Our theoretical calculations exhibit a broader and higher potential barrier exists beneath the S-1/S-2 CI of o-FPhOH, which increase the difficulty for tunneling. Furthermore, the special existence of intramolecular hydrogen bond in o-FPhOH is probably also the key factor that affects the tunneling rate, which would restrict the O-H stretch motion. (C) 2020 Elsevier Ltd. All rights reserved.

The ability to switch the hydrophilicity/hydrophobicity of nanoparticles promises great potential for applications. Here we report a generic approach that allows hydrophobization of cationic surfaces by light-induced photoacid switching from the unbound zwitterionic form to the electrostatically bound anionic form. Importantly, this allows reversible assembly and disassembly of cationic AuNPs, with disassembly kinetics controlled by temperature. The AuNPs can be repeatedly transferred between aqueous and non-polar solvents using light, showing potential in purification processes. In the macroscopic scale, nontrivially, light triggers the in situ hydrophobization of a flat cationized gold surface. The current approach is generic and opens up a new way to control the surface properties and self-assembly of nanoparticles.

Awareness of instrument inaccuracies will boost the development of liquid-repellent coatings

Time-resolved photoelectron imaging is employed to investigate the relaxation dynamics of the lowest two excited electronic states S1(ππ*) and S2(π3s/πσ*) in 2,4-difluoroaniline (24DFA). As the S1(ππ*) state is populated directly following 289 nm excitation, the population undergoes ultrafast intramolecular vibrational redistribution on a 540 fs time scale, followed by efficient intersystem crossing from S1(ππ*) to the triplet state within 379 ps, and the subsequent slower deactivation process of the triplet state. For excitation to the S2(π3s/πσ*) state at 238 nm, the population probably bifurcates into two decay channels. The dominant channel with 84 fs involves ultrafast internal conversion to the S1(ππ*) state, from which it relaxes to the electronic ground state on a 116 ps time scale. The other appears to involve motion along the S2(π3s/πσ*) potential energy surface. Our data also determine experimentally the electronic energies of S2(π3s/πσ*), S3(ππ*), and several Rydberg states in 24DFA.

A simple, green, robust and efficient method has been developed for the preparation of an anti-biofouling coating by directly mixing antifouling enzymes with a castor oil-based waterborne polyurethane (WPU) dispersion.