Evidence for two electronic components in high-temperature superconductivity from NMR

A new analysis of 63Cu and 17O NMR shift data on La1.85Sr0.15CuO4 is reported that supports earlier work arguing for a two-component description of this material, but conflicts with the widely held view that the cuprates are a one-component system. The data are analyzed in terms of two components A and B with susceptibilities Chi(A), Chi(B), and Chi(AB)=Chi(BA) . We find that above Tc, Chi(AB) and Chi(BB) are independent of temperature and obtain for the first time the temperature dependence of all three susceptibilities above Tc as well as the complete temperature dependence of Chi(AA)+Chi(AB) and of Chi(AB)+Chi(BB) below Tc. The form of the results agrees with that recently proposed by Barzykin and Pines.Comment: 14 pages, 4 figure

Synthetic routes toward MOF nanomorphologies.

As metal–organic frameworks (MOFs) are coming of age, their structural diversity, exceptional porosity and inherent functionality need to be transferred into useful applications. Fashioning MOFs into various shapes and at the same time controlling their size constitute an essential step toward MOF-based devices. Moreover, downsizing MOFs to the nanoscale triggers a whole new set of properties distinguishing nanoMOFs from their bulk counterparts. Therefore, dimensionality-controlled miniaturization of MOFs enables the customised use of nanoMOFs for specific applications where suitable size and shape are key prerequisites. In this feature article we survey the burgeoning field of nanoscale MOF synthesis, ranging from classical protocols such as microemulsion synthesis all the way to microfluidic-based techniques and template-directed epitaxial growth schemes. Along these lines, we will fathom the feasibility of rationally designing specific MOF nanomorphologies—zero-, one- and two-dimensional nanostructures—and we will explore more complex “second-generation” nanostructures typically evolving from a high level of interfacial control. As a recurring theme, we will review recent advances made toward the understanding of nucleation and growth processes at the nanoscale, as such insights are expected to further push the borders of nanoMOF science

Solving the COF trilemma: towards crystalline,stable and functional covalentorganic frameworks

Covalent organic frameworks (COFs) have entered the stage as a new generation of porous polymers which stand out by virtue of their crystallinity, diverse framework topologies and accessible pore systems. An important – but still underdeveloped – feature of COFs is their potentially superior stability in comparison to other porous materials. Achieving COFs which are simultaneously crystalline, stable, and functional is still challenging as reversible bond formation is one of the prime prerequisites for the crystallization of COFs. However, as the COF field matures new strategies have surfaced that bypass this crystallinity – stability dichotomy. Three major approaches for obtaining both stable and crystalline COFs have taken form in recent years: Tweaking the reaction conditions for reversible linkages, separating the order inducing step and the stability inducing step, and controlling the structural degrees of freedom during assembly and in the final COF. This review discusses rational approaches to stability and crystallinity engineering in COFs, which are apt at overcoming current challenges in COF design and open up new avenues to new real-world applications of COFs