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Pierre Wiltzius

Publications and source records attributed to Pierre Wiltzius.

2 recordsLinked to original sources

Humidity-sensing inverse opal hydrogels.

Soft material hydrogel sensors have seen increased interest recently. Most of these sensors are used in an aqueous environment. In this study, we depart from this trend and analyze the ability of a periodic hydrogel structure to respond to variations in ambient humidity through an optical change. First, a polyacrylamide inverse opal hydrogel structure was created from a colloidal crystal template. Next, this material was tested under various humidity conditions and responded to these changes by shifting its optical reflection peak noticeably within the visible wavelength range. This effect opens the doors for these materials as humidity sensors. The kinetics of the peak shifts was also observed, showing a rapid response to ambient humidity changes. Finally, the structural dimension change is compared through peak shifts, Fabry-Perot fringes of the optical cavity, and scanning electron microscopy observations.

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Structural evolution of colloidal crystals with increasing ionic strength.

We have directly observed the structural evolution of colloidal crystals as a function of increasing ionic strength using confocal scanning laser microscopy. Silica colloids were sedimented onto a glass substrate in deionized water to create large, single domain crystals. The solution ionic strength was then increased by one of three methods of controlled electrolyte addition: (1) direct injection of electrolyte solutions, (2) single step diffusion of electrolyte solutions through a dialysis membrane, and (3) multiple step diffusion of electrolyte solutions of increasing ionic strength through a dialysis membrane. During direct injection of electrolyte solutions, initially large, single domain colloidal crystals were shear melted and then evolved into polycrystalline structures at low ionic strengths and gels at higher ionic strengths. Diffusion of electrolyte solutions though dialysis membranes in a single step produced gradient-driven transport that also melted initial single domain crystals to yield polycrystalline and gel structures similar to the injection approach. Interestingly, the multistep diffusion of several electrolyte solutions through dialysis membranes facilitated retention of large, single domain crystals even as particles came into adhesive contact. This was achieved by reducing the contraction rate of the crystalline lattice to allow sufficient time for diffusion-limited configurational rearrangements to occur within the evolving structure. These mechanically robust, single domain colloidal crystals may find important applications as templates for photonic materials and sensors.

Journal Article↗