Jian Jin

Abstract Nanofiltration (NF) membranes with ultrahigh permeance and high rejection are highly beneficial for efficient desalination and wastewater treatment. Improving water permeance while maintaining the high rejection of state-of-the-art thin film composite (TFC) NF membranes remains a great challenge. Herein, we report the fabrication of a TFC NF membrane with a crumpled polyamide (PA) layer via interfacial polymerization on a single-walled carbon nanotubes/polyether sulfone composite support loaded with nanoparticles as a sacrificial templating material, using metal-organic framework nanoparticles (ZIF-8) as an example. The nanoparticles, which can be removed by water dissolution after interfacial polymerization, facilitate the formation of a rough PA active layer with crumpled nanostructure. The NF membrane obtained thereby exhibits high permeance up to 53.5 l m −2 h −1 bar −1 with a rejection above 95% for Na 2 SO 4 , yielding an overall desalination performance superior to state-of-the-art NF membranes reported so far. Our work provides a simple avenue to fabricate advanced PA NF membranes with outstanding performance.

An innovative strategy of fabricating electrode material by layered assembling two kinds of one-atom-thick sheets, carboxylated graphene oxide (GO) and Co-Al layered double hydroxide nanosheet (Co-Al LDH-NS) for the application as a pseudocapacitor is reported. The Co-Al LDH-NS/GO composite exhibits good energy storage properties.

Precious metals have broad applications in modern industry and renewable energy technologies. The high cost and limited availability of these materials, however, have caused a grand challenge for sustainability. Here, we report on the plating of a precious metal on nonprecious metal nanoparticles for the development of sustainable electrocatalysts. Cobalt/platinum core/shell (denoted as Co@Pt) nanoparticles were synthesized via seed-mediated growth. The Co seeds were first synthesized by thermal decomposition of cobalt carbonyl, and the Pt shell was overgrown in situ by adding platinum acetylacetonate (Pt(acac)2). The galvanic replacement reaction between Co and the Pt precursor was successfully suppressed by taking advantage of CO (generated from the decomposition of cobalt carbonyl) as the stabilizing ligand and/or reducing agent. The obtained Co@Pt nanoparticles were further found to exhibit enhanced catalytic activity for the oxygen reduction reaction (ORR).

Described herein is the first study of metal oxide deposition on an electrode with a solid/liquid/gas triphase reaction interface. Such an electrode enables the formation of a locally high interface pH value that is independent of the bulk conditions, and allows the deposition of a wide variety of metal oxides in a robust electrolyte. The results reveal that the control of electrode surface wettability is of significant importance for the regulation of the electrode-electrolyte local interface environment, which provides a new set of guidelines and perspective for future electrode preparation and application.

Abstract Tailoring the geometric configuration of anodic TiO 2 nanotubes enables their use in various applications. This paper demonstrates that the methods for pretreating electrolyte solutions significantly influence the growth of anodic nanotubes. Pretreatment is usually ignored by studies, but is a crucial and non‐negligible factor in the control of nanotube growth. The results indicate that magnetic stirring and ultrasonic agitation facilitate the dissolution and mass transport of ionic species in the solution, resulting in a homogeneous solution and a high TiO 2 nanotube growth rate. Isolation of the solution from wide contact with the atmosphere through simple sealing further increases the growth rate. This is attributed to the hindrance of humidity absorption, which biases the original water content of the solution and thus causes the formation of an initial thick compact oxide layer that prevents ion diffusion. The findings can serve as a guide to electrolyte pretreatment routes for studying nanotube growth mechanisms and for tailoring nanotube features toward different applications.