Impacts of Bond Type and Grafting Density on the Thermal, Structural, and Transport Behaviors of Nanoparticle Organic Hybrid Materials‐Based Electrolytes

Abstract

AbstractNanoscale Organic Hybrid Materials (NOHMs) consist of polymers tethered to a nanoparticle surface, and NOHMs formed with an ionic bond between the polymer and nanoparticle have been proposed for electrochemical applications. NOHMs exhibit negligible vapor pressure, chemical tunability, oxidative thermal stability, and high ionic conductivity making them attractive in reactive and separation systems. In this study, NOHMs are synthesized by tethering Jeffamine M2070 (HPE) to SiO2 nanocores via ionic (NOHM‐I‐HPE) and covalent (NOHM‐C‐HPE) bonding to investigate the effect of the bond type on the thermal, structural and transport properties of the tethered HPE. In the neat state, NOHM‐C‐HPE displays the highest thermal stability in a nitrogen atmosphere, while NOHM‐I‐HPE is the most stable under oxidative conditions. Small‐angle neutron scattering (SANS) reveals the presence of multiple types of HPE polymers in aqueous solutions of NOHM‐I‐HPE (i.e., tethered, interacting, and free), whereas only tethered HPE is observed in NOHM‐C‐HPE systems. Moreover, the SANS profiles identify clustering of NOHM‐C‐HPE in aqueous solutions, but not in the corresponding NOHM‐I‐HPE solutions, suggesting that the free HPE chains stabilize the dispersion of NOHM‐I‐HPE. The results of this study elucidate how the bond type and grafting density can be used to tune the properties of NOHMs.