Search

While nanoporous graphene oxide (GO) is recognized as one of the most promising reverse osmosis desalination membranes, limited attention has been paid to controlling desalination performance through the large GO pores, primarily due to significant ion leakage resulting in the suboptimal performance of these pores. In this study, we employed a molecular dynamics simulation approach to demonstrate that Mg2+ ions, adhered to carboxylated GO nanopores, can function as gates, regulating the transport of ions (Na+ and Cl−) through the porous GO membrane. Specifically, the presence of divalent cations near a nanopore reduces the concentration of salt ions in the vicinity of the pore and prolongs their permeation time across the pore. This subsequently leads to a notable enhancement in salt rejection rates. Additionally, the ion rejection rate increases with more adsorbed Mg2+ ions. However, the presence of the adsorbed Mg2+ ions compromises water transport. Here, we also elucidate the impact of graphene oxidation degree on desalination. Furthermore, we design an optimal combination of adsorbed Mg2+ ion quantity and oxidation degree to achieve high water flux and salt rejection rates. This work provides valuable insights for developing new nanoporous graphene oxide membranes for controlled water desalination. [ABSTRACT FROM AUTHOR]

Ion desorption is extremely challenging for adsorbents with superior performance, and widely used conventional desorption methods involve high acid or base concentrations and large consumption of reagents. Here, we experimentally demonstrate the rapid and efficient desorption of ions on magnetite-graphene oxide (M-GO) by adding low amounts of Al3+. The corresponding concentration of Al3+ used is reduced by at least a factor 250 compared to conventional desorption method. The desorption rate reaches ~97.0% for the typical radioactive and bivalent ions Co2+, Mn2+, and Sr2+ within ~1 min. We achieve effective enrichment of radioactive 60Co and reduce the volume of concentrated 60Co solution by approximately 10 times compared to the initial solution. The M-GO can be recycled and reused easily without compromising its adsorption efficiency and magnetic performance, based on the unique hydration anionic species of Al3+ under alkaline conditions. Density functional theory calculations show that the interaction of graphene with Al3+ is stronger than with divalent ions, and that the adsorption probability of Al3+ is superior than that of Co2+, Mn2+, and Sr2+ ions. This suggests that the proposed method could be used to enrich a wider range of ions in the fields of energy, biology, environmental technology, and materials science. Desorption of ions from sorbents generally involves high acid or base concentrations and long desorption times, especially for multivalent ions. Here the authors report a rapid and efficient desorption of Co2+, Mn2+, and Sr2+ adsorbed on magnetite-graphene oxide that occurs by adding low amounts of Al3+, which is shown to interact with graphene more strongly than divalent ions. [ABSTRACT FROM AUTHOR]

[Display omitted] Water dissociation is of fundamental importance in scientific fields and has drawn considerable interest in diverse technological applications. However, the high activation barrier of breaking the O H bond within the water molecule has been identified as the bottleneck, even for the water adsorbed on the graphene oxide (GO). Herein, using the density functional theory calculations, we demonstrate that the water molecule can be spontaneously dissociated on GO supported by the (1 1 1) surface of the copper substrate (Copper-GO). This process involves a proton transferring from water to the interfacial oxygen group, and a hydroxide covalently bonding to GO. Compared to that on GO, the water dissociation barrier on Copper-GO is significantly decreased to be less than or comparable to thermal fluctuations. This is ascribed to the orbital-hybridizing interaction between copper substrate and GO, which enhances the reaction activity of interfacial oxygen groups along the basal plane of GO for water dissociation. Our work provides a novel strategy to access water dissociation via the substrate-enhanced reaction activity of interfacial oxygen groups on GO and indicates that the substrate can serve as an essential key to tuning the catalytic performance of various two-dimensional material devices. [ABSTRACT FROM AUTHOR]

[Display omitted] • The GO humidity sensor fabricated by a simple way. • The GO humidity sensor with ultrafast response and recovery time less than 0.3s. • Protons generated from oxygen-containing groups and water molecules revealed. • An array of sensors was successfully fabricated to demonstrate its application. • LEDs lighted up by power-generating device made from humidity sensors. Next-generation humidity sensor, as one of the smart devices in artificial skin or flexible electronics, will need to be self-powered, flexible, fast and accurately detecting in the microenvironment. Although various flexible humidity sensors have already been demonstrated, most of them rely on large external power sources to operate, and still suffer from slow response, poor selectivity in environmental stimuli, and expensive and complicated procedures. Here, we realize a self-powered humidity sensor with ultrafast response and recovery time of less than 0.3 s by flexible GO film. Importantly, of all state-of-the-art humidity sensors, this is the fastest response for humidity sensor. Moreover, the sensor has a high sensitivity within a wide range of RH from 33% to 98%, and an excellent selective response to humidity under multiple environmental stimuli, due to its moist-induced generator. Theoretical computations reveal that protons generated spontaneously from oxygen-containing groups and water molecules, have a fast diffusion behavior as Grotthuss hopping. In particular, we build four real-time measurement systems capable of respiration monitoring of human, smart leaf surface humidity sensor, and energy harvesting. Our work provides a simple way to fabricate next-generation self-powered sensor using GO film with outstanding humidity sensor performance. [ABSTRACT FROM AUTHOR]