The adhesion of as-formed gas bubbles on the electrode surface usually impedes mass-transfer kinetics and subsequently decreases electrolysis efficiency. Here it is demonstrated that nanostructured MoS₂ films on conductive substrates show a faster hydrogen evolution reaction (HER), current increase, and a more-stable working state than their flat counterpart by significantly alleviating the adhesion of as-formed gas bubbles on the electrode. This study clearly reveals the importance of a nano-porous structure for HER, which should be general and beneficial for constructing other gas-evolution electrodes.

Multidrug resistance (MDR) occurs frequently after long-term chemotherapy, resulting in refractory cancer and tumor recurrence. Therefore, combatting MDR is an important issue. Autophagy, a self-degradative system, universally arises during the treatment of sensitive and MDR cancer. Autophagy can be a double-edged sword for MDR tumors: it participates in the development of MDR and protects cancer cells from chemotherapeutics but can also kill MDR cancer cells in which apoptosis pathways are inactive. Autophagy induced by anticancer drugs could also activate apoptosis signaling pathways in MDR cells, facilitating MDR reversal. Therefore, research on the regulation of autophagy to combat MDR is expanding and is becoming increasingly important. We summarize advanced studies of autophagy in MDR tumors, including the variable role of autophagy in MDR cancer cells.

Tungsten carbide is one of the most promising electrocatalysts for the hydrogen evolution reaction, although it exhibits sluggish kinetics due to a strong tungsten-hydrogen bond. In addition, tungsten carbide’s catalytic activity toward the oxygen evolution reaction has yet to be reported. Here, we introduce a superaerophobic nitrogen-doped tungsten carbide nanoarray electrode exhibiting high stability and activity toward hydrogen evolution reaction as well as driving oxygen evolution efficiently in acid. Nitrogen-doping and nanoarray structure accelerate hydrogen gas release from the electrode, realizing a current density of −200 mA cm−2 at the potential of −190 mV vs. reversible hydrogen electrode, which manifest one of the best non-noble metal catalysts for hydrogen evolution reaction. Under acidic conditions (0.5 M sulfuric acid), water splitting catalyzed by nitrogen-doped tungsten carbide nanoarray starts from about 1.4 V, and outperforms most other water splitting catalysts.

Graphene, as a class of 2D carbon nanomaterial, has attracted tremendous interest in different areas in recent years including biomedicine. The toxicity and behavior of graphene in biological systems are thus important fundamental issues that require significant attention. In this article, the toxicity of graphene is reviewed by describing the behavior of graphene and its derivatives in microorganisms, cells, and animals. Despite certain inconsistencies in several detailed experimental results and hypotheses of toxicity mechanisms, results from numerous reports all agree that the physicochemical properties such as surface functional groups, charges, coatings, sizes, and structural defects of graphene may affect its in vitro/in vivo behavior as well as its toxicity in biological systems. It is hoped that this review article will provide an overview understanding of the impacts, behavior, and toxicology of graphene and its derivatives in various biological systems.

Selectively exposing active surfaces and judiciously tuning the near-surface composition of electrode materials represent two prominent means of promoting electrocatalytic performance. Here, a new class of Pt Fe zigzag-like nanowires (Pt-skin Pt Fe z-NWs) with stable high-index facets (HIFs) and nanosegregated Pt-skin structure is reported, which are capable of substantially boosting electrocatalysis in fuel cells. These unique structural features endow the Pt-skin Pt Fe z-NWs with a mass activity of 2.11 A mg and a specifc activity of 4.34 mA cm for the oxygen reduction reaction (ORR) at 0.9 V versus reversible hydrogen electrode, which are the highest in all reported PtFe-based ORR catalysts. Density function theory calculations reveal a combination of exposed HIFs and formation of Pt-skin structure, leading to an optimal oxygen adsorption energy due to the ligand and strain effects, which is responsible for the much enhanced ORR activities. In contrast to previously reported HIFs-based catalysts, the Pt-skin Pt Fe z-NWs maintain ultrahigh durability with little activity decay and negligible structure transformation after 50 000 potential cycles. Overcoming a key technical barrier in electrocatalysis, this work successfully extends the nanosegregated Pt-skin structure to nanocatalysts with HIFs, heralding the exciting prospects of high-effcient Pt-based catalysts in fuel cells.

Despite high-energy density and low cost of the lithium-sulfur (Li-S) batteries, their commercial success is greatly impeded by their severe capacity decay during long-term cycling caused by polysulfide shuttling. Herein, a new phase engineering strategy is demonstrated for making MXene/1T-2H MoS 2 -C nanohybrids for boosting the performance of Li-S batteries in terms of capacity, rate ability, and stability. It is found that the plentiful positively charged S-vacancy defects created on MXene/1T-2H MoS 2 -C, proved by high-resolution transmission electron microscopy and electron paramagnetic resonance, can serve as strong adsorption and activation sites for polar polysulfide intermediates, accelerate redox reactions, and prevent the dissolution of polysulfides. As a consequence, the novel MXene/1T-2H MoS 2 -C-S cathode delivers a high initial capacity of 1194.7 mAh g −1 at 0.1 C, a high level of capacity retention of 799.3 mAh g −1 after 300 cycles at 0.5 C, and reliable operation in soft-package batteries. The present MXene/1T-2H MoS 2 -C becomes among the best cathode materials for Li-S batteries.

A micro-/nanostructured "superaerophilic" electrode constructed by direct growth of cobalt-incorporated and nitrogen-doped carbon-nanotube arrays with subsequent hydrophobic modification is demonstrated for a high-performance oxygen-reduction-reaction electrode, superior to the Pt/C-air electrode. This high performance is attributed to the simultaneously accelerated gas-diffusion and electron-transport processes induced by the unique structural advantages.

Metabolic reprogramming in tumors represents a potential therapeutic target. Herein we used shRNA depletion and a novel lactate dehydrogenase (LDHA) inhibitor, GNE-140, to probe the role of LDHA in tumor growth in vitro and in vivo. In MIA PaCa-2 human pancreatic cells, LDHA inhibition rapidly affected global metabolism, although cell death only occurred after 2 d of continuous LDHA inhibition. Pancreatic cell lines that utilize oxidative phosphorylation (OXPHOS) rather than glycolysis were inherently resistant to GNE-140, but could be resensitized to GNE-140 with the OXPHOS inhibitor phenformin. Acquired resistance to GNE-140 was driven by activation of the AMPK-mTOR-S6K signaling pathway, which led to increased OXPHOS, and inhibitors targeting this pathway could prevent resistance. Thus, combining an LDHA inhibitor with compounds targeting the mitochondrial or AMPK-S6K signaling axis may not only broaden the clinical utility of LDHA inhibitors beyond glycolytically dependent tumors but also reduce the emergence of resistance to LDHA inhibition.