induced scission measurements, imaging with AFM and TEM, and analysis of data. A.J.L. performed FRET measurements and analysis of the data. X.Z., T.C.-T., and Y.C. performed solution X-ray scattering, and analysis of the data. A.J.L. and Y.C. conceptualized nanoribbon thread processing and Y.C. and M.G. prepared nanoribbon threads. M.G. performed tensile testing of nanoribbon threads and analysis of the data. T.C.-T. and Y.C. performed X-ray scattering of solid-state nanoribbon threads and analysis of the data. J.

The self-assembly of amphiphilic small molecules in water leads to nanostructures with customizable structure-property relationships arising from their tunable chemistries. Characterization of these assemblies is generally limited to their static...

Surface oxygen reduction reaction (ORR) rates at n-type oxide-based mixed ionic–electronic conducting (MIEC) solid oxide fuel cell (SOFC) cathodes can be expected to be enhanced relative to that at p-type MIEC cathodes due to the greater availability of electrons at higher energies in the band structure needed for the charge transfer reaction. However, given the difficulty of achieving coexisting oxygen vacancies and electrons in the conduction band under oxidizing cathode conditions, no stable n-type MIEC cathodes have been reported to date. In this study, a predominantly n-type MIEC conductivity is confirmed in a Ba–In-based oxide (BNIM) co-doped with Nd and Mn at high temperature and high P O2 confirmed by the P O2 dependence of the electrical conductivity and negative Seebeck coefficients, combined with readily measurable oxide ion transference numbers. This coexistence of n-type electronic and oxide ion conductivities is discussed based on the electrical behavior of BNIM with different Mn levels and is attributed to the significant change in the degree of anion Frenkel ordering and the band structure associated with heavy donor doping of Ba2In2O5. This novel n-type MIEC has the potential for enhancing the ORR at SOFC cathodes at reduced temperatures and thereby identifying new potential candidate cathode materials for next-generation SOFCs.

Strongly interacting amphiphilic molecules self-assemble in water. The flexibility of the amphiphiles and their head group repulsion mediate their nanostructure geometry.