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Investigating catalytic behavior of heterogeneous catalysts, especially at the crystal facets level, is crucial for rational catalyst design in the energy and environmental fields. Here we demonstrate an efficient approach to in situ visualize and analyze the heterogeneity of electrocatalytic activity on different facets at the subparticle level via electrochemiluminescence (ECL) microscopy. ZnO crystals with various exposed facet proportions were synthesized, and the correlation between their electrocatalytic performance toward luminol analogue degradation and the exposed facets is established. It is clearly imaged that the ZnO (002) facet has superior catalytic performance compared to the ZnO (100) facet, which is supported by theoretical computation and electrochemical experiments as the facet-induced heterogeneity of the catalytic effect on oxygen reduction into the key reactant for ECL. Accordingly, the spatial heterogeneity of electrocatalytic activity at different facets on one particle is visualized for the first time. The realization of subparticle ECL imaging and kinetic analysis could provide a special approach to visualize facet-induced spatial heterogeneity of catalytic behavior and valuable information for the catalysis study and analysis.

Developing an electrochemiluminescence (ECL) coreactant to minimize the biotoxicity and to maximize the enhancement factor is critical to single-cell ECL microscopy. Here, we reported a guanine-rich single-stranded DNA (G-ssDNA)-loaded high-index faceted gold nanoflower (Hi-AuNF) as a synergistic coreactant of Ru­(bpy)3 2+ for single-cell ECL imaging. Because of the excellent catalytic performance and huge specific surface area, Hi-AuNF serves as not only an ECL enhancer but also a carrier for G-ssDNA. Guanine in G-ssDNA specifically reacts with Ru­(bpy)3 2+ through a so-called “catalytic route” and thus significantly enhances the ECL signal of Ru­(bpy)3 2+. To endow targeting ability to the synergistic coreactant, an aptamer of carcinoembryonic antigen (CEA) is incorporated into the G-ssDNA to form G-ssDNA-Apt for the recognition of human breast adenocarcinoma cells, which overexpress CEA on the cytomembrane. Accordingly, the ECL imaging of CEA on the cytomembrane was realized by using the highly selective Hi-AuNF@G-ssDNA-Apt as the probe as well as the luminophore of Ru­(bpy)3 2+. Compared with the common coreactant tripropylamine with high toxicity and volatility, the Hi-AuNF@G-ssDNA-Apt is considered as a high-performance and biocompatible coreactant, providing exciting opportunities in single-cell imaging and detection.

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Bioinspired smart superwetting surfaces with special wettability have aroused great attention from fundamental research to technological applications including self‐cleaning, oil–water separation, anti‐icing/corrosion/fogging, drag reduction, cell engineering, liquid manipulation, and so on. However, most of the reported smart superwetting surfaces switch their wettability by reversibly changing surface chemistry rather than surface microstructure. Compared with surface chemistry, the regulation of surface microstructure is more difficult and can bring novel functions to the surfaces. As a kind of stimulus‐responsive material, shape‐memory polymer (SMP) has become an excellent candidate for preparing smart superwetting surfaces owing to its unique shape transformation property. This review systematically summarizes the recent progress of smart superwetting SMP surfaces including fabrication methods, smart superwetting phenomena, and related application fields. The smart superwettabilities, such as superhydrophobicity/superomniphobicity with tunable adhesion, reversible switching between superhydrophobicity and superhydrophilicity, switchable isotropic/anisotropic wetting, slippery surface with tunable wettability, and underwater superaerophobicity/superoleophobicity with tunable adhesion, can be obtained on SMP micro/nanostructures by regulating the surface morphology. Finally, the challenges and future prospects of smart superwetting SMP surfaces are discussed.

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