Graphene-oxide (GO) membrane with notable ions sieving properties has attracted significant attention for many applications. However, because of the water swelling of GO membrane, the rejection of monovalent metal cations is generally low. In this work, we developed a fast and facile method to fabricate a kind of reduced GO membranes using the thermal treatment method at 160 °C for only one minute, which denoted as fast reduced GO membrane (FRGO). Surprising, the FRGO membrane represents high ion sieving ability and ultrahigh water/ions selectivity, compared with other reduced GO membranes with similar average interlayer spacings, and even superior to most of GO-based membranes reported in literature. Building on these findings, we provide a new light on fabricating of energy- and environment-related high desalination performance of GO-based membranes as well as a new insight into the transport mechanism within 2D laminar nanochannels.

Self-powered wearable pressure sensors based on flexible electronics have emerged as a new trend due to the increasing demand for intelligent and portable devices. Improvements in pressure-sensing performance, including in the output voltage, sensitivity and response time, can greatly expand their related applications; however, this remains challenging. Here, we report on a highly sensitive piezoelectric sensor with novel light-boosting pressure-sensing performance, based on a composite membrane of copper phthalocyanine (CuPC) and graphene oxide (GO) (CuPC@GO). Under light illumination, the CuPC@GO piezoelectric sensor demonstrates a remarkable increase in output voltage (381.17 mV, 50 kPa) and sensitivity (116.80 mV/kPa, <5 kPa), which are approximately twice and three times of that the sensor without light illumination, respectively. Furthermore, light exposure significantly improves the response speed of the sensor with a response time of 38.04 µs and recovery time of 58.48 µs, while maintaining excellent mechanical stability even after 2000 cycles. Density functional theory calculations reveal that increased electron transfer from graphene to CuPC can occur when the CuPC is in the excited state, which indicates that the light illumination promotes the electron excitation of CuPC, and thus brings about the high polarization of the sensor. Importantly, these sensors exhibit universal spatial non-contact adjustability, highlighting their versatility and applicability in various settings.

The resulting rGO/MXene heterogeneous membranes exhibited a high water permeance of up to 401.2 L m⁻ ² h⁻¹ bar⁻¹ together with 99.7% rejection of dye molecules.

Ripples on graphene play a crucial role in manipulating its physical and chemical properties. However, producing ripples, especially at the nanoscale, remains challenging with current experimental methods. In this study, we report that tiny ripples in graphene can be generated by the adsorption of a single metal cation (Na⁺, K⁺, Mg²⁺, Ca²⁺, Cu²⁺, Fe³⁺) onto a graphene sheet, based on the density functional theory calculations. We attribute this to the cation–π interaction between the metal cation and the aromatic rings on the graphene surface, which makes the carbon atoms closer to metal ions, causing deformation of the graphene sheet, especially in the out-of-plane direction, thereby creating ripples. The equivalent pressures applied to graphene sheets in out-of-plane direction, generated by metal cation–π interactions, reach magnitudes on the order of gigapascals (GPa). More importantly, the electronic and mechanical properties of graphene sheets are modified by the adsorption of various metal cations, resulting in opened bandgaps and enhanced rigidity characterized by a higher elastic modulus. These findings show great potential for applications for producing ripples at the nanoscale in graphene through the regulation of metal cation adsorption.

Novel NaO ₂ - Pa 3 ice with cubic structure and face-centered cubic sublattice exhibits metallic property, owing to the electron orbital coupling of oxygen atoms in close proximity.