Search NASA⌕ Search
Home/Archive/DOE OSTI

DOE OSTI · 2217515

On-Demand Aligned DNA Hydrogel Via Light Scanning

Kim, Juri·Choi, Yun-Seok·Park, Geonhyeong·Kim, Mingeun·Myung, Jin Suk·Choi, Woo Jin·Park, Soon Mo·Yoon, Dong Ki
View original source ↗Read source document ↗Export metadata ↓

Abstract

DNA is an anisotropic, water-attracting, and biocompatible material, an ideal building block for hydrogel. The alignment of the anisotropic DNA chains is essential to maximize hydrogel properties, which has been little explored. Here, we present a method to fabricate the anisotropic DNA hydrogel that allows precise control for the polymerization process of photoreactive cationic monomers. Scanning ultraviolet light enables the uniaxial alignment of DNA chains through the polymerization-induced diffusive mass flow using a concentration gradient. In conclusion, while studying anisotropic mechanical properties and orientation recovery according to the DNA chain alignment direction, we demonstrate the potential of directionally controlled DNA hydrogels as smart materials.

Explore related subjects

36 MATERIALS SCIENCEDNA, hydrogel, liquid crystal, alignment, light scanning, mechanical propertyMaterial Science

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Kim, Juri, Choi, Yun-Seok, Park, Geonhyeong, Kim, Mingeun, Myung, Jin Suk, Choi, Woo Jin, Park, Soon Mo, Yoon, Dong Ki. 2023-11-10. On-Demand Aligned DNA Hydrogel Via Light Scanning. https://doi.org/10.1021/acsnano.3c07493

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related reports

DOE OSTI2026

Cyclic moisture reactivation of calcium sorbents for long duration thermochemical energy storage

The transition to a flexible and reliable energy infrastructure, using electro-thermal energy generation technologies such as geothermal, concentrated solar power, and nuclear, usually demands simultaneous advancement of thermal energy storage (TES) to support on-demand electricity generation and industrial applications while mitigating the inherent intermittency of renewable energy sources and power outages from direct energy generation. Among TES technologies, thermochemical energy storage (TCES) based on calcium looping emerges as a compelling high-power energy storage candidate due to its high reaction enthalpy, compatibility with elevated operating temperatures, and abundance of low-cost materials. However, the long-term durability of calcium-based sorbents for TCES is hindered by surface sintering and particle aggregation, leading to performance degradation over repeated thermal cycles. This study explores a moisture hydration-based strategy to regenerate a degraded calcium sorbent and mitigate performance degradation for long duration TCES. The addition of moisture transforms calcium oxide into calcium hydroxide and produces intercalation water layers, associated with a regenerated surface area and reduced calcium oxide crystallite size. Both these effects are beneficial in restoring the sorbents' reactivity for carbonization. Additionally, an optimized hydration-assisted reactivation protocol balances the recovered energy storage capacity with heating penalty required for moisture removal from hydrated samples, resulting in an enhanced energy storage capacity up to 176% compared to benchmark sorbents that undergo cycling without reactivation after 60 cycles. In conclusion, these results highlight the potential of hydration-assisted reactivation to enhance the long-term performance of TCES, providing an effective pathway to advancing electro-thermal storage technologies.

36 MATERIALS SCIENCE↗