No abstract

Recent advances in heterogeneous catalysts indicate that single atoms (SAs), anchored/stabilized on metal oxide nanostructures, exhibit not only high catalyst atom efficiency but also intriguing reactivity and selectivity. Herein, isolated Pt SA-anchored CuCrO2 (CCO) has been designed by a glycine–nitrate solution combustion synthesis (SCS) route. The density of isolated Pt SAs achieves the highest value of ∼100 μm–2 for the 1.39 wt % Pt-anchored CCO sample, which results in the drastically boosted H2S response characteristics, including a high response of 1250 (35 times higher than that of pure CCO) at 10 ppm H2S and a low operating temperature of 100 °C. Except for CH4S, the responses of a 1.39 wt % Pt-anchored CCO chemiresistor to diverse vapors with concentrations of 50–100 ppm are less than 2, exhibiting excellent selectivity. Various ex situ characterizations indicate that the spillover catalytic effect of Pt SA sites, other than the conventional sulfuration–desulfuration mechanism, plays a dominant role in the outstanding H2S response characteristics.

The dimension of TiO2 nanotubes (TNTs) ranges from several nanometers to hundreds of nanometers. This variety raises the difficulty of screening suitable nanotube dimension for biomedical applications. Herein, we report the use of a simple one-step bipolar anodization method for fabrication of TNT gradients with diameter range from 30 to 100 nm. The gradient TNTs were successfully applied for high-throughput screening of TNT size effect on cell responses, including cell adhesion, proliferation, and differentiation. Results reveal that no significant difference in adherent cell number could be found within the range of 30–87 nm in both the presence and absence of serum proteins. On the contrary, large nanotubes (with outer diameter >87 nm) profoundly reduce cell adhesion in both the presence and absence of serum proteins, indicating TNT size could affect cell adhesion directly without the adsorbed proteins. The size effect on cell behavior becomes prominent with time that cell proliferation and differentiation decrease with increasing nanotube size. This size effect can be comprehended by protein adsorption and the formation of focal adhesion. Another two sample applications of gradient TNTs demonstrate gradient TNTs are promising for high-throughput screening.