As a non‐toxic species, Zn fulfills a multitude of biological roles, but its promoting effect on electrocatalysis has been rarely explored. Herein, the theoretic predications and experimental investigations that nonelectroactive Zn behaves as an effective promoter for CoP‐catalyzed hydrogen evolution reaction (HER) in both acidic and alkaline media is reported. Density function theory calculations reveal that Zn doing leads to more thermal‐neutral hydrogen adsorption free energy and thus enhanced HER activity for CoP catalyst. Electrochemical tests show that a Zn0.08Co0.92P nanowall array on titanium mesh (Zn0.08Co0.92P/TM) needs overpotentials of only 39 and 67 mV to drive a geometrical catalytic current of 10 mA cm‐2 in 0.5 m H2SO4 and 1.0 m KOH, respectively. This Zn0.08Co0.92P/TM is also superior in activity over CoP/TM for urea oxidation reaction (UOR), driving 115 mA cm‐2 at 0.6 V in 1.0 m KOH with 0.5 m urea. The high HER and UOR activity of this bifunctional electrode enables a Zn0.08Co0.92P/TM‐based two‐electrode electrolyzer for energy‐saving hydrogen production, offering 10 mA cm‐2 at a low voltage of 1.38 V with strong long‐term electrochemical stability.

In this paper, the hierarchical SnO2 nanostructures (HTNs) were prepared by a facile hydrothermal process. The prepared HTNs were characterized in detail by various analytical techniques that reveal the well-crystallinity with tetragonal rutile structure of SnO2 for the as-prepared material. By detailed experiments, interestingly, it was observed that the shapes and sizes of as-prepared HTNs could be tailored by varying the precursor concentration and reaction time. The synthesized HTNs were used as the efficient photocatalysts for the photocatalytic degradation of methylene blue (MB) under light illumination which showed almost complete degradation (∼99%) of MB dye in 20 min. The observed degradation for MB dye was higher than other commonly used dyes, i.e. methyl orange (MO; 96% in 50 min) and Rhodamine B (RhB; 97% in 40 min.). Further, the prepared HTNs were used as the effective gas sensing material to examine a series of volatile gases, such as ethanol, ammonia, benzene, acetone, toluene, methanol, diethyl ether, and methanol. By the detailed experiments, it was observed that the prepared HTNs exhibited tremendous gas sensing performance toward ethanol. Finally, because of the unique morphology and the fast ion and electron transfer characteristics, the prepared HTNs show excellent supercapacitor performances.

An amphiphilic dendrimer bearing a hydrophobic alkyl chain and hydrophilic poly(amidoamine) dendrons is able to combine the advantageous features of lipid and dendrimer vectors to deliver a heat shock protein 27 siRNA and produce potent gene silencing and anticancer activity in vitro and in vivo in a prostate cancer model. This dendrimer can be used alternatively for treating various diseases.

We present the synthesis and multifunctional utilization of core-shell Fe3O4 polydopamine nanoparticles (Fe3O4@PDA NPs) to serve as the enabling platform for a range of applications including responsive drug delivery, recyclable catalyst support, and adsorbent. Magnetite Fe3O4 NPs formed in a one-pot process by the hydrothermal approach were coated with a polydopamine shell layer of ~20 nm in thickness. The as prepared Fe3O4@PDA NPs were used for the controlled drug release in a pH-sensitive manner via reversible bonding between catechol and boronic acid groups of PDA and the anticancer drug bortezomib (BTZ), respectively. The facile deposition of Au NPs atop Fe3O4@PDA NPs was achieved by utilizing PDA as both the reducing agent and the coupling agent. The nanocatalysts exhibited high catalytic performance for the reduction of o-nitrophenol. Furthermore, the recovery and reuse of the catalyst was demonstrated 10 times without any detectible loss in activity. Finally, the PDA layers were converted into carbon to obtain Fe3O4@C and used as an adsorbent for the removal of Rhodamine B from an aqueous solution. The synergistic combination of unique features of PDA and magnetic nanoparticles establishes these core-shell NPs as a versatile platform for multiple applications.

siRNA delivery remains a major challenge in RNAi- based therapy. Here, we report for the first time that an amphiphilic dendrimer is able to self-assemble into adaptive supramolecular assemblies upon interaction with siRNA, and effectively delivers siRNAs to various cell lines, including human primary and stem cells, thereby outperforming the currently available nonviral vectors. In addition, this amphi- philic dendrimer is able to harness the advantageous features of both polymer and lipid vectors and hence promotes effective siRNA delivery. Our study demonstrates for the first time that dendrimer-based adaptive supramolecular assemblies repre- sent novel and versatile means for functional siRNA delivery, heralding a new age of dendrimer-based self-assembled drug delivery in biomedical applications

Ni2P nanoflake arrays on carbon cloth act as an efficient and durable catalyst electrode for the urea oxidation reaction (UOR) and hydrogen evolution reaction (HER). Its two-electrode alkaline electrolyzer needs 1.35 V for 50 mA cm−2, which is 0.58 V less than that required for pure water splitting.

Ammonia (NH3) is an activated nitrogen building block for the manufacture of modern fertilizers, plastics, fibers, explosives, etc.; however, its production is limited to the traditional Haber–Bosch process.

The latest advances and perspectives in the development of TMP-based catalysts with enhanced electrocatalysis for hydrogen evolution.