Visualizing interfacial collective reaction behaviour of Li-S batteries.

Benefiting from high energy density (2,600 Wh kg-1) and low cost, lithium-sulfur (Li-S) batteries are considered promising candidates for advanced energy-storage systems1-4. Despite tremendous efforts in suppressing the long-standing shuttle effect of lithium polysulfides5-7, understanding of the interfacial reactions of lithium polysulfides at the nanoscale remains elusive. This is mainly because of the limitations of in situ characterization tools in tracing the liquid-solid conversion of unstable lithium polysulfides at high temporal-spatial resolution8-10. There is an urgent need to understand the coupled phenomena inside Li-S batteries, specifically, the dynamic distribution, aggregation, deposition and dissolution of lithium polysulfides. Here, by using in situ liquid-cell electrochemical transmission electron microscopy, we directly visualized the transformation of lithium polysulfides over electrode surfaces at the atomic scale. Notably, an unexpected gathering-induced collective charge transfer of lithium polysulfides was captured on the nanocluster active-centre-immobilized surface. It further induced an instantaneous deposition of nonequilibrium Li2S nanocrystals from the dense liquid phase of lithium polysulfides. Without mediation of active centres, the reactions followed a classical single-molecule pathway, lithium polysulfides transforming into Li2S2 and Li2S step by step. Molecular dynamics simulations indicated that the long-range electrostatic interaction between active centres and lithium polysulfides promoted the formation of a dense phase consisting of Li+ and Sn2- (2 < n ≤ 6), and the collective charge transfer in the dense phase was further verified by ab initio molecular dynamics simulations. The collective interfacial reaction pathway unveils a new transformation mechanism and deepens the fundamental understanding of Li-S batteries.

Nonlinear metasurface engineering with disordered gold nanorods on ITO: a cost-effective approach to broadband response, polarization-independence, and weak nonlinear index dispersion.

The strong coupling of epsilon-near-zero materials with nanoantennas has demonstrated enhanced nonlinear optical responses, yet practical challenges persist. Here, we propose an alternative: an ultrathin metasurface featuring broadband response with a weakly dispersive nonlinear index, achieved through a simple implementation. Our metasurface, comprising a disordered gold nanorod array on indium tin oxide, exhibits polarization-independent behavior and a large average nonlinear refractive index of 5 cm2/GW across a broad wavelength range (1000-1300 nm). Enhanced performance is attributed to the weak coupling between gold nanorods and indium tin oxide, offering a cost-effective method for nonlinear optical metasurfaces and a flexible design in nanophotonic applications.

Atomic Scale Tracking of Single Layer Oxide Formation: Self-Peeling and Phase Transition in Solution.

Liquid phase electron microscopy (TEM) is used to track the formation of In2 O3 ultrathin nanosheet in solution at atomic scale. This observation reveals that the formation of few atomic layer nanosheet goes through a complicated phase transition process from InCl3 . 3H2 O to In(OH)3 and then to In2 O3 . Interestingly, the intermediate InCl3 . 3H2 O nanosheet can grow via either layer by layer or the strain-driven enation growth from precursor solution. Moreover, in situ TEM results and density functional theory (DFT) calculations demonstrate that the oleylamine is responsible for the self-peeling process. These findings can provide atomic-level insight for the understanding of how 2D nanomaterial grows and transforms in solution.