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Metal–organic frameworks (MOFs) are increasingly being investigated as electrocatalysts for the oxygen evolution reaction (OER). Despite their promising catalytic activity, many fundamental questions concerning their structure−performance relationships—especially those regarding the roles of active species—remain to be answered. Here we show the structural transformation of a Ni 0.5 Co 0.5 -MOF-74 during the OER by operando X-ray absorption spectroscopy analysis and high-resolution transmission electron microscopy imaging. We suggest that Ni 0.5 Co 0.5 OOH 0.75 , with abundant oxygen vacancies and high oxidation states, forms in situ and is responsible for the high OER activity observed. The ratio of Ni to Co in the bimetallic centres alters the geometric and electronic structure of as-formed active species and in turn the catalytic activity. Based on our understanding of this system, we fabricate a Ni 0.9 Fe 0.1 -MOF that delivers low overpotentials of 198 mV and 231 mV at 10 mA cm −2 and 20 mA cm −2 , respectively. Metal–organic frameworks (MOFs) are increasingly being explored for electrocatalytic oxygen evolution, which is half of the water splitting reaction. Here the authors show that, under reaction conditions, mixed metal oxyhydroxides form at the nodes of bimetallic MOFs, which are highly catalytically active.

Cancer cells typically display redox imbalance compared with normal cells due to increased metabolic rate, accumulated mitochondrial dysfunction, elevated cell signaling, and accelerated peroxisomal activities. This redox imbalance may regulate gene expression, alter protein stability, and modulate existing cellular programs, resulting in inefficient treatment modalities. Therapeutic strategies targeting intra‐ or extracellular redox states of cancer cells at varying state of progression may trigger programmed cell death if exceeded a certain threshold, enabling therapeutic selectivity and overcoming cancer resistance to radiotherapy and chemotherapy. Nanotechnology provides new opportunities for modulating redox state in cancer cells due to their excellent designability and high reactivity. Various nanomaterials are widely researched to enhance highly reactive substances (free radicals) production, disrupt the endogenous antioxidant defense systems, or both. Here, the physiological features of redox imbalance in cancer cells are described and the challenges in modulating redox state in cancer cells are illustrated. Then, nanomaterials that regulate redox imbalance are classified and elaborated upon based on their ability to target redox regulations. Finally, the future perspectives in this field are proposed. It is hoped this review provides guidance for the design of nanomaterials‐based approaches involving modulating intra‐ or extracellular redox states for cancer therapy, especially for cancers resistant to radiotherapy or chemotherapy, etc. Cancer cells display redox imbalance compared to normal cells, thus targeting these distinctive biochemical attributes provides new opportunities for cancer treatment. This work focuses on recent advancements in the design of stimuli‐responsive nanomaterials that selectively regulate redox balance in cancer cells over the threshold for activating cancer cell death.

Preventing aggregation of amyloid beta (Aβ) peptides is a promising strategy for the treatment of Alzheimer’s disease (AD), and gold nanoparticles have previously been explored as a potential anti-Aβ therapeutics. Here we design and prepare 3.3 nm L- and D-glutathione stabilized gold nanoparticles (denoted as L3.3 and D3.3, respectively). Both chiral nanoparticles are able to inhibit aggregation of Aβ42 and cross the blood-brain barrier (BBB) following intravenous administration without noticeable toxicity. D3.3 possesses a larger binding affinity to Aβ42 and higher brain biodistribution compared with its enantiomer L3.3, giving rise to stronger inhibition of Aβ42 fibrillation and better rescue of behavioral impairments in AD model mice. This conjugation of a small nanoparticle with chiral recognition moiety provides a potential therapeutic approach for AD. Nanoparticles are being explored as a potential method to target Aβ aggregation in Alzheimer’s disease. Here, the authors develop gold nanoparticles that were capped with chiral L or D-glutathione which has been shown to improve BBB permeability and demonstrate their ability to improve cognitive function in a mouse model of AD.

Magnetic liquid metal (LM) soft robots attract considerable attentions because of distinctive immiscibility, deformability and maneuverability. However, conventional LM composites relying on alloying between LM and metallic magnetic powders suffer from diminished magnetism over time and potential safety risk upon leakage of metallic components. Herein, we report a strategy to composite inert and biocompatible iron oxide (Fe 3 O 4 ) magnetic nanoparticles into eutectic gallium indium LM via reactive wetting mechanism. To address the intrinsic interfacial non-wettability between Fe 3 O 4 and LM, a silver intermediate layer was introduced to fuse with indium component into Ag x In y intermetallic compounds, facilitating the anchoring of Fe 3 O 4 nanoparticles inside LM with improved magnetic stability. Subsequently, a miniature soft robot was constructed to perform various controllable deformation and locomotion behaviors under actuation of external magnetic field. Finally, practical feasibility of applying LM soft robot in an ex vivo porcine stomach was validated under in-situ monitoring by endoscope and X-ray imaging. Interfacial non-wettability between biocompatible iron oxide and liquid metal caused by the substantial mismatch in surface energy remains an issue. Here, the authors introduce a silver intermediate layer to reduce compositional mismatch and improve the wetting ability between iron oxide and liquid metal.

Di(2-ethylhexyl) phthalate (DEHP) with continuous high concentration was used as the sole carbon and energy source to isolate a new bacterial consortium (K1) from agricultural soil covered with plastic film for a long time. Unclassified Comamonadaceae, Achromobacter, and Pseudomonas in K1 were identified as major genera of the consortium by high-throughput sequencing, and unclassified Commanadaceae was first reported to be related to DEHP degradation. Response surface method (RSM) showed that the optimum conditions for K1 to degrade DEHP were 31.4 °C, pH 7.3, and a concentration of 420 mg L−1. K1 maintains normal cell viability and stable DEHP degradation efficiency in the range of 10–3000 mg L−1 DEHP concentration, which is superior to existing research. The biodegradation of DEHP followed first-order kinetics when the initial concentration of DEHP was between 100 and 3,000 mg L−1. GC-MS analysis of different treatment groups showed that DEHP was degraded by the consortium group through the de-esterification pathway, and treatment effect was significantly better than that of the single bacteria treatment group. The subsequent substrate utilization experiment further confirmed that K1 could quickly mineralize DEHP. In addition, K1 has high degradation capacity for the most common phthalate acid esters in the environment.

Food spoilage caused by microbial contamination remains a global challenge, driving demand for sustainable antibacterial packaging. Conventional photocatalytic materials suffer from limited spectral response, rapid charge recombination, and insufficient reactive oxygen species (ROS) generation under visible light. Here, a Z-scheme heterojunction was constructed by coupling zeolitic imidazolate framework-8 (ZIF-8) with Ag3PO4, achieving dual-spectral absorption and spatial charge separation. The directional electron transfer from Ag3PO4’s conduction band to ZIF-8 effectively suppresses electron-hole recombination, prolonging carrier lifetimes and amplifying ROS production (·O2−/·OH). Synergy with Ag+ release further enhances bactericidal efficacy. Incorporated into a cellulose acetate matrix (CAM), the ZIF-8/Ag3PO4/CAM film demonstrates 99.06% antibacterial efficiency against meat surface microbiota under simulated sunlight, alongside high transparency. This study proposes a Z-scheme heterojunction strategy to maximize ROS generation efficiency and demonstrates a scalable fabrication approach for active food packaging materials, effectively targeting microbial contamination control and shelf-life prolongation.

The design and synthesis of efficient electrocatalysts are important for electrochemical conversion technologies. The oxygen evolution reaction (OER) is a key process in such conversions, having applications in water splitting and metal–air batteries. Here, we report ultrathin metal–organic frameworks (MOFs) as promising electrocatalysts for the OER in alkaline conditions. Our as-prepared ultrathin NiCo bimetal–organic framework nanosheets on glassy-carbon electrodes require an overpotential of 250 mV to achieve a current density of 10 mA cm −2 . When the MOF nanosheets are loaded on copper foam, this decreases to 189 mV. We propose that the surface atoms in the ultrathin MOF sheets are coordinatively unsaturated—that is, they have open sites for adsorption—as evidenced by a suite of measurements, including X-ray spectroscopy and density-functional theory calculations. The findings suggest that the coordinatively unsaturated metal atoms are the dominating active centres and the coupling effect between Ni and Co metals is crucial for tuning the electrocatalytic activity. Efficient electrocatalysts for the oxygen–evolution reaction are desired due to their importance in applications such as water splitting and metal–air batteries. Here, the authors engineer ultrathin metal–organic frameworks that require low overpotential to generate oxygen from alkaline media.

Microbial fuel cells (MFCs) that can directly convert chemical energy of organic matter into electrical energy are expected to continuously obtain energy from wastewater. However, the practical application of MFCs is still limited by unsatisfactorily low power output due to low bacterial loading capacity and relatively poor extracellular electron transport (EET) efficiency between anode and electrochemically active biofilm. Herein, hierarchical porous carbon foams (HPCFs) prepared by pyrolyzing nanoscale Fe‐MIL‐88B‐NH2 modified seitan composite were developed as 3D free‐standing MFC anodes. Its marcoporous structure and good biocompatibility favor the bacterial adhesion, while the N‐doped carbon skeleton, abundant mesopores and iron ions boost the bacteria‐electrode charge transfer efficiency. As a result, the HPCF anodes equipped MFCs deliver a maximum power density of 11.21 W m−3 and a current density of 23.11 A m−3, outperforming the most previously reported 3D porous anodes. This study provides a new idea for the design of anodes for high‐performance MFCs. The iron‐based MOF nanoparticles/seitan derived hierarchical porous carbon foams (HPCF) provide marcopores for exoelectrogens enrichment and growth, as well as mesopores with N heteroatoms and iron ions for promoting extracellular electron transfer mainly via bound flavin pathway. MFCs equipped by HPCF anode achieve a power density of 11.21 W m−3 and a COD removal speed of 493 mg L−1 d−1.

Single site catalysts provide a unique platform for mimicking natural enzyme due to their tunable interaction between metal center and coordinated ligand. However, most works have focused on preparing structural and functional models of nature enzyme, with less reports also taking the local chemical environment, i.e., functional/catalytic residues around the active site which is an essential feature of enzymes, into consideration. Herein, we report a Co-centered porphyrinic polymer containing the enzyme-mimic micro-environment, where the linker triazole over CoN 4 site enables formation of hydrogen bond with the *COOH intermediate, thus promoting the electrocatalytic reduction of CO 2 . As-prepared catalyst achieves the CO 2 -to-CO conversion of 5, 788 h −1 turnover frequency value and near unit (∼ 96%) faradaic efficiency at −0.61 V versus reversible hydrogen electrode. This strategy will bring new dimension of designing highly active single-site catalysts.

Polyhydroxybutyrate (PHB), as a biodegradable and green polymer, holds significant potential for replacing traditional petroleum-based plastics. However, its production efficiency and cost remain bottlenecks limiting large-scale application. In recent years, hybrid systems constructed from photosensitive nanomaterials and microorganisms have provided a novel pathway for enhancing PHB synthesis efficiency. These systems augment the supply of intracellular reducing power through efficient photo-generated electron injection, thereby driving microbial carbon fixation and PHB anabolic metabolism. This review systematically summarizes the mechanisms and performance of various types of photosensitive materials (including g-C3N4, CdS, polymer dots, etc.) in regulating PHB synthesis in microorganisms, such as Cupriavidus necator H16. It focuses on the influence of material composition, structure, energy band characteristics, and their interfacial interactions with microorganisms on electron transfer efficiency and biocompatibility. Furthermore, the article outlines the current challenges faced by these hybrid systems in key energy and mass transfer processes, including light energy conversion, transmembrane electron transport, and NADPH regeneration. It also prospects the design principles of novel bio-inspired multi-level heterojunction materials and their application potential in constructing efficient “material microbe” collaborative synthesis systems. This review aims to provide a material-level theoretical foundation and design strategies for developing high-performance and sustainable light-driven biomanufacturing technologies for PHB.