Animal‐sourced hydrogels, such as collagen, are widely used as extracellular‐matrix (ECM) mimics in tissue engineering but are plagued with problems of reproducibility, immunogenicity, and contamination. Synthetic, chemically defined hydrogels can avoid such issues. Despite the abundance of collagen in the ECM, synthetic collagen hydrogels are extremely rare due to design challenges brought on by the triple‐helical structure of collagen. Sticky‐ended symmetric self‐assembly (SESSA) overcomes these challenges by maximizing interactions between the strands of the triple helix, allowing the assembly of collagen‐mimetic peptides (CMPs) into robust synthetic collagen nanofibers. This optimization, however, also minimizes interfiber contacts. In this work, symmetric association states for the SESSA of short CMPs to probe their increased propensity for interfiber association are modelled. It is found that 33‐residue CMPs not only self‐assemble through sticky ends, but also form hydrogels. These self‐assemblies behave with remarkable consistency across multiple scales and present a clear link between their triple‐helical architecture and the properties of their hydrogels. The results show that SESSA is an effective and robust design methodology that enables the rational design of synthetic collagen hydrogels.
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Yang, Yang ; Dang, Lianna ; Shearer, Melinda J. ; Sheng, Hongyuan ; Li, Wenjie ; Chen, Jie ; Xiao, Peng ; Zhang, Yunhuai ; Hamers, Robert J. ; Jin, Song ( , Advanced Energy Materials)
Abstract The development of efficient and robust earth‐abundant electrocatalysts for the oxygen evolution reaction (OER) is an ongoing challenge. Here, a novel and stable trimetallic NiFeCr layered double hydroxide (LDH) electrocatalyst for improving OER kinetics is rationally designed and synthesized. Electrochemical testing of a series of trimetallic NiFeCr LDH materials at similar catalyst loading and electrochemical surface area shows that the molar ratio Ni:Fe:Cr = 6:2:1 exhibits the best intrinsic OER catalytic activity compared to other NiFeCr LDH compositions. Furthermore, these nanostructures are directly grown on conductive carbon paper for a high surface area 3D electrode that can achieve a catalytic current density of 25 mA cm−2at an overpotential as low as 225 mV and a small Tafel slope of 69 mV dec−1in alkaline electrolyte. The optimized NiFeCr catalyst is stable under OER conditions and X‐ray photoelectron spectroscopy, electron paramagnetic resonance spectroscopy, and elemental analysis confirm the stability of trimetallic NiFeCr LDH after electrochemical testing. Due to the synergistic interactions among the metal centers, trimetallic NiFeCr LDH is significantly more active than NiFe LDH and among the most active OER catalysts to date. This work also presents general strategies to design more efficient metal oxide/hydroxide OER electrocatalysts.
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Song, Bo ; Li, Kai ; Yin, Ying ; Wu, Tao ; Dang, Lianna ; Cabán-Acevedo, Miguel ; Han, Jiecai ; Gao, Tangling ; Wang, Xianjie ; Zhang, Zhihua ; et al ( , ACS Catalysis)
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Chen, Jie ; Morrow, Darien J. ; Fu, Yongping ; Zheng, Weihao ; Zhao, Yuzhou ; Dang, Lianna ; Stolt, Matthew J. ; Kohler, Daniel D. ; Wang, Xiaoxia ; Czech, Kyle J. ; et al ( , Journal of the American Chemical Society)