In heavy-ion collisions at relativistic energies, the incident nuclei travel at nearly the speed of light. These collisions deposit kinetic energy into the overlap region and create a high-temperature environment where hadrons “melt” into deconfined quarks and gluons. The spectator nucleons, which do not undergo scatterings, generate an ultraintense electromagnetic field—on the order of 10¹⁸ G at the Relativistic Heavy Ion Collider and 10¹⁹ G at the Large Hadron Collider. These powerful electromagnetic fields have a substantial impact on the produced particles, not only complicating the study of particle interactions but also inducing novel physical phenomena. To explore the nature of these fields and their interactions with deconfined quarks, we provide a detailed overview, encompassing theoretical estimations of their generation and evolution, as well as experimental efforts to detect them. We also provide physical interpretations of the discovered results and discuss potential directions for future investigations.

Thermoelectric (TE) materials have garnered widespread research interest owing to their capability for direct heat-to-electricity conversion. Binary indium-based chalcogenides (In–X, X = Te, Se, S) stand out in inorganic materials by virtue of their relatively low thermal conductivity. For example, In₄Se_2.35 shows a low thermal conductivity of 0.74 W m⁻¹ K⁻¹ and an impressive zT value of 1.48 along the b–c plane at 705 K, as a result of structural anisotropy. Here, we review the structural features and recent research progress in the TE field for In–X materials. It begins by presenting the characteristics of crystal structure, electronic band structure, and phonon dispersion, aiming to microscopically understand the similarity/dissimilarity among these In–X compounds, notably the role of unconventional bonds (such as In–In) in modulating the band structures and lattice vibrations. Furthermore, TE optimization strategies of such materials were classified and discussed, including defect engineering, crystal orientation engineering, nanostructuring, and grain size engineering. The final section provides an overview of recent progress in optimizing TE properties of indium tellurides, indium selenides, and indium sulfides. An outlook is also presented on the major challenges and opportunities associated with these material systems for future TE applications. This Review is expected to provide critical insights into the development of new strategies to design binary indium-based chalcogenides as promising TE materials in the future.

Tryptophan (Trp), an essential amino acid, performs as a precursor for synthesizing various bioactive molecules primarily metabolized through the kynurenine (Kyn), serotonin, and indole pathways. The diverse metabolites were deeply implicated in multiple physiological processes. Emerging research has revealed the multifaceted contribution of Trp in skeletal health and pathophysiology of bone-related disease with the involvement of specific receptors including aryl hydrocarbon receptor (AhR), which modulated the downstream signaling pathways to manage the expression of pivotal genes and thereby altered cellular biological processes, such as proliferation and differentiation. Accompanied by distinct alterations in immune function, inflammatory responses, endocrine balance, and other physiological aspects, their impact and efficacy in osteochondrogenic disorders have also been well documented. Nevertheless, a thorough understanding of Trp metabolism within bone biology is currently lacking. In this review, we elucidate the complexities of Trp metabolic pathway and several metabolites, delineating their versatile modulatory roles in the physiology and pathology of osteoblasts (OBs), osteoclasts (OCs), chondrocytes, and intercellular coupling effects, as well as in the progression of osteochondral disorder. Moreover, we comprehensively delineate the regulatory mechanisms by which gut microbiota-generated indole derivatives mediate bidirectional crosstalk along the gut–bone axis. The establishment of an elaborate governing network about bone homeostasis provides a novel insight on therapeutic interventions.

The first challenge in building a living robotic system inspired by life evolution is how to replicate the original form of life—the cell. However, current microrobots mimic cell motion control but fail to replicate the functional biological activities of cellular systems. Here, we propose a strategy that programs microparticle swarms encapsulated in droplets at an air/liquid interface to create cell-mimetic droplet microrobots with vitality by employing alternating magnetic fields. Through the design of algorithms and spontaneous interface waves, our collective system embodies reversible transitions between gas, chain, array, and disk-like collective modes, and emulates various complex activities of living cells in nature, including division and exocytosis. Based on these 2 capabilities learned from living cells, the cell-mimetic microrobots navigate the bile duct to the gallbladder under the guidance and control of magnetic fields, completing the drug release task. This cell-mimetic microrobots may provide a fundamental understanding of cellular life and pave the way for the construction of artificial living systems. Furthermore, they hold substantial potential for medical and environmental applications.

Developing low-cost plastic recycling technologies is crucial for ecological sustainability and the circular economy. The recent publication in Science by Conk et al. introduces an innovative method employing base-metal catalysts, specifically WO₃/SiO₂ and Na/γ-Al₂O₃, to efficiently convert polyethylene, polypropylene, or their mixtures into valuable products, representing a marked advancement in the field of base-metal catalysis and plastic recycling.

Enzyme–photosensitizer (PS) conjugates hold great promise for clinical treatment of cancer and infectious diseases via catalysis-augmented photodynamic therapy (PDT). Compared to covalent coupling, physical binding utilizing noncovalent interactions provides a simple and nondestructive strategy to combine PS with enzymes. However, the mechanism of enzyme–PS physical combination remains largely unknown, and physically bonded enzyme–PS conjugates are rarely reported. Here, we systematically investigate the interacting behaviors of representative enzymes with one of the most popular PS of chlorin e6 (Ce6) and elucidate their binding dynamics and crucial determinants. Our results reveal that the positively charged and hydrophobic residues on the surface of enzymes are crucial determinants of Ce6 binding. In addition, we demonstrate that the positively charged surface area of enzymes can be employed as a reliable criterion for assessing and predicting the enzyme–Ce6 binding affinity. Guided by this criterion, we further construct catalase–Ce6 nanoconjugates (CAT–Ce6 NCs) with superior stability and robust photodynamic antimicrobial capability via physical binding. In a showcase treatment of methicillin-resistant Staphylococcus aureus (MRSA)-infected mouse model of subcutaneous abscess, CAT–Ce6 NCs enable hypoxia pathological microenvironment remodeling and bacteria elimination, realizing effective catalysis-augmented PDT. This study deciphers the physical binding mechanism of enzyme–PS and establishes a theoretical framework to facilitate the design and construction of outstanding enzyme–PS NCs for catalysis-augmented PDT.

Macrophages participate in the immune system by recognizing and engulfing foreign bodies inside phagosomes, which fuse with lysosomes in their cytoplasm to form mature phagolysosomes. Lysosomes have an acidic interior and generate and release reactive oxygen and nitrogen species (ROS/RNS) to destroy the endocytosed entities. It has been previously reported that intra-lysosomal pH plays an essential role in the regulation of ROS/RNS. However, the exact regulatory mechanism remains to be elucidated. Taking advantage of the large number of active lysosomes distributed along the phagocytic lumen during frustrated phagocytosis of glass fibers by macrophages, the intensity of 4 primary ROS/RNS released fluxes (ONOO⁻, H₂O₂, NO, and NO₂⁻) was monitored with platinum nanoelectrochemical sensors, thereby revealing the important role of intra-lysosomal pH on ROS/RNS fluxes after pharmacological modulations. Acidification (pH <5.0) does not alter the rate of production of ROS/RNS precursors (superoxide ions, O₂^•−, and parent NO) but promotes O₂^•− protonation, leading to an increase of H₂O₂ release. In contrast, the initial production of NO, which subsequently increased the release of ONOO⁻ and NO₂⁻, was enhanced by alkalinization (pH >6.0). The resulting increased oxidative stress was associated with massive proinflammatory cytokine release. Taken together, these results provide important information about the impact of lysosomal pH on ROS/RNS regulation.

Ferroptosis has promising potential for augmenting antitumor effects, but monotherapy with ferroptosis inducers in vivo has been reported to have limited efficacy in tumor management. The development of synergistic strategies with targeted capabilities is crucial for enhancing the antitumor efficacy of ferroptosis inducers. In this study, we designed and characterized a novel self-assembled nanomedicine by mixing ferrous ions (Fe²⁺) and epigallocatechin gallate (EGCG) in a controllable manner and encapsulating the ferroptosis inducer RSL3, named Fe-EGCG@RSL3. This multifunctional nanomedicine effectively induces ferroptosis and growth inhibition in bladder cancer cells and patient-derived organoids. In vivo, Fe-EGCG@RSL3 was enriched in the subcutaneous tumors of allogenic and xenograft mouse models, thereby substantially overcoming RSL3 resistance. Intravesical instillation of Fe-EGCG@RSL3 controls orthotopic bladder tumor progression. Furthermore, nanomedicine potentiates the therapeutic effect of anti-programmed cell death protein 1 (PD1) immunotherapy by increasing the cytotoxicity of CD8⁺ T cells to cancer cells and modulating the proportions of both T-cell and myeloid cell subpopulations within the tumor immune microenvironment. Overall, Fe-EGCG@RSL3 has dual functions as a multifaceted nanomedicine that integrates ferroptosis induction with immunomodulation, offering a novel and clinically translatable strategy for bladder cancer therapy.

Ocean acidification is becoming more prevalent and may contribute to coral reef degradation, yet our understanding of its role in global reef decline remains limited. Therefore, there is an urgent need to study the impact of reduced pH levels on the growth patterns of major reef-building corals. Here, we studied the skeleton-forming strategies of 4 widely distributed coral species in a simulated acidified habitat with a pH of 7.6 to 7.8. We reconstructed and visualized the skeleton-forming process, quantified elemental calcium loss, and determined gene expression changes. The results suggest that different reef-building corals have diverse growing strategies in lower pH conditions. A unique “cavity-like” forming process starts from the inside of the skeletons of Acropora muricata, which sacrifices skeletal density to protect its polyp–canal system. The forming patterns in Pocillopora damicornis, Montipora capricornis, and Montipora foliosa were characterized by “osteoporosis”, exhibiting disordered skeletal structures, insufficient synthesis of adhesion proteins, and low bone mass, correspondingly. In addition, we found that damage from acidification particularly affects pre-existing skeletal structures in the colony. These results enhance our understanding of skeleton-forming strategies in major coral species under lower pH conditions, providing a foundation for coral reef protection and restoration amidst increasing ocean acidification.

Bistable structures, which leverage mechanical instability, have emerged as a promising paradigm in the development of robotic grippers, providing advantages including rapid response and low energy consumption. A critical limitation of existing bistable grippers, however, lies in their invariable energy barriers, which hinder the balance between compliant triggering and powerful grasping. In this study, we propose a bistable robotic gripper capable of in situ energy barrier modulation, inspired by the adaptive seed dispersal behavior of Impatiens pods. This robotic gripper features an elastic curved beam-based architecture integrated with a motor-driven mechanism, enabling dynamic regulation of its energy landscape. This approach allows the energy barrier to be tuned over an order of magnitude during manipulation. In the low-barrier state, the robotic gripper initiates object interaction with a triggering force as low as 0.66 N, allowing for delicate manipulation. Upon state transition, instant energy barrier modulation ~(300 ms) enhances grasping stability, achieving failure forces up to 12.08 N. This adaptive modulation strategy enables our robotic gripper to implement rapid, compliant, and powerful interaction. When incorporated into an unmanned aerial vehicle, the robotic gripper showcases reliable perching across diverse scenarios, highlighting the potential of energy barrier modulation to advance the adaptability and functionality of robotic systems.