Tunable itinerant spin dynamics with polar molecules.

Strongly interacting spins underlie many intriguing phenomena and applications1-4 ranging from magnetism to quantum information processing. Interacting spins combined with motion show exotic spin transport phenomena, such as superfluidity arising from pairing of spins induced by spin attraction5,6. To understand these complex phenomena, an interacting spin system with high controllability is desired. Quantum spin dynamics have been studied on different platforms with varying capabilities7-13. Here we demonstrate tunable itinerant spin dynamics enabled by dipolar interactions using a gas of potassium-rubidium molecules confined to two-dimensional planes, where a spin-1/2 system is encoded into the molecular rotational levels. The dipolar interaction gives rise to a shift of the rotational transition frequency and a collision-limited Ramsey contrast decay that emerges from the coupled spin and motion. Both the Ising and spin-exchange interactions are precisely tuned by varying the strength and orientation of an electric field, as well as the internal molecular state. This full tunability enables both static and dynamical control of the spin Hamiltonian, allowing reversal of the coherent spin dynamics. Our work establishes an interacting spin platform that allows for exploration of many-body spin dynamics and spin-motion physics using the strong, tunable dipolar interaction.

Dipolar evaporation of reactive molecules to below the Fermi temperature.

The control of molecules is key to the investigation of quantum phases, in which rich degrees of freedom can be used to encode information and strong interactions can be precisely tuned1. Inelastic losses in molecular collisions2-5, however, have greatly hampered the engineering of low-entropy molecular systems6. So far, the only quantum degenerate gas of molecules has been created via association of two highly degenerate atomic gases7,8. Here we use an external electric field along with optical lattice confinement to create a two-dimensional Fermi gas of spin-polarized potassium-rubidium (KRb) polar molecules, in which elastic, tunable dipolar interactions dominate over all inelastic processes. Direct thermalization among the molecules in the trap leads to efficient dipolar evaporative cooling, yielding a rapid increase in phase-space density. At the onset of quantum degeneracy, we observe the effects of Fermi statistics on the thermodynamics of the molecular gas. These results demonstrate a general strategy for achieving quantum degeneracy in dipolar molecular gases in which strong, long-range and anisotropic dipolar interactions can drive the emergence of exotic many-body phases, such as interlayer pairing and p-wave superfluidity.

Novel Social Stimulation Ameliorates Memory Deficit in Alzheimer's Disease Model through Activating α-Secretase.

As the most common form of dementia in the world, Alzheimer's disease (AD) is a progressive neurological disorder marked by cognitive and behavioral impairment. According to previous researches, abundant social connections shield against dementia. However, it is still unclear how exactly social interactions benefit cognitive abilities in people with AD and how this process is used to increase their general cognitive performance. In this study, we found that single novel social (SNS) stimulation promoted c-Fos expression and increased the protein levels of mature ADAM10/17 and sAPPα in the ventral hippocampus (vHPC) of wild-type (WT) mice, which are hippocampal dorsal CA2 (dCA2) neuron activity and vHPC NMDAR dependent. Additionally, we discovered that SNS caused similar changes in an AD model, FAD4T mice, and these alterations could be reversed by α-secretase inhibitor. Furthermore, we also found that multiple novel social (MNS) stimulation improved synaptic plasticity and memory impairments in both male and female FAD4T mice, accompanied by α-secretase activation and Aß reduction. These findings provide insight into the process underpinning how social interaction helps AD patients who are experiencing cognitive decline, and we also imply that novel social interaction and activation of the α-secretase may be preventative and therapeutic in the early stages of AD.

Potential molecular mechanism of photosynthesis regulation by PeMPK7 in poplar under para-hydroxybenzoic acid stress.

Due to continuous plantation of poplar, its growth and biomass accumulation may be negatively affected by the accumulation of allelochemicals such as para-hydroxybenzoic acid (pHBA) in soil. As photosynthesis is the most fundamental process in plants, it can be negatively impacted by pHBA stress. Therefore, it is crucial to improve photosynthetic capacity under pHBA stress to facilitate poplar plant growth. The mitogen-activated protein kinase (MAPK) cascade pathway is widely involved in environmental stress responses in plants. However, the regulation mechanisms of photosynthesis-related pathways by MAPK pathway genes under pHBA stress are still unclear. In this study, through transcriptome analysis and weighted gene co-expression network analysis, we observed that PeMPK7 overexpression in poplar can regulate the expression of photosynthesis-related genes and transcription factor genes, namely, WRKY1, WRKY33, and ERF3, during the early stage of pHBA stress. In addition, PeMPK7 can improve photosynthesis in poplar under long-term pHBA stress. Moreover, yeast two-hybrid and pull-down assays confirmed the interaction between PeMPK7 and PeMKK7/10. Based on these results, a schematic diagram of the pathways involved in the regulation of photosynthesis by PeMPK7 was constructed. This study provided novel insights into the molecular mechanisms of regulation of pHBA stress via MAPK cascade pathway.

Working Memory for Spatial Sequences: Developmental and Evolutionary Factors in Encoding Ordinal and Relational Structures.

Sequence learning is a ubiquitous facet of human and animal cognition. Here, using a common sequence reproduction task, we investigated whether and how the ordinal and relational structures linking consecutive elements are acquired by human adults, children, and macaque monkeys. While children and monkeys exhibited significantly lower precision than adults for spatial location and temporal order information, only monkeys appeared to exceedingly focus on the first item. Most importantly, only humans, regardless of age, spontaneously extracted the spatial relations between consecutive items and used a chunking strategy to compress sequences in working memory. Monkeys did not detect such relational structures, even after extensive training. Monkey behavior was captured by a conjunctive coding model, whereas a chunk-based conjunctive model explained more variance in humans. These age- and species-related differences are indicative of developmental and evolutionary mechanisms of sequence encoding and may provide novel insights into the uniquely human cognitive capacities.SIGNIFICANCE STATEMENT Sequence learning, the ability to encode the order of discrete elements and their relationships presented within a sequence, is a ubiquitous facet of cognition among humans and animals. By exploring sequence-processing abilities at different human developmental stages and in nonhuman primates, we found that only humans, regardless of age, spontaneously extracted the spatial relations between consecutive items and used an internal language to compress sequences in working memory. The findings provided insights into understanding the origins of sequence capabilities in humans and how they evolve through development to identify the unique aspects of human cognitive capacity, which includes the comprehension, learning, and production of sequences, and perhaps, above all, language processing.

Bi-MOF Modulating MnO2 Deposition Enables Ultra-Stable Cathode-Free Aqueous Zinc-Ion Batteries.

The Mn-based materials are considered as the most promising cathodes for zinc-ion batteries (ZIBs) due to their inherent advantages of safety, sustainability and high energy density, however suffer from poor cyclability caused by gradual Mn2+ dissolution and irreversible structural transformation. The mainstream solution is pre-adding Mn2+ into the electrolyte, nevertheless faces the challenge of irreversible Mn2+ consumption results from the MnO2 electrodeposition reaction (Mn2+  â†’ MnO2 ). This work proposes a "MOFs as the electrodeposition surface" strategy, rather than blocking it. The bismuth (III) pyridine-3,5-dicarboxylate (Bi-PYDC) is selected as the typical electrodeposition surface to regulate the deposition reaction from Mn2+ to MnO2 . Because of the unique less hydrophilic and manganophilic nature of Bi-PYDC for Mn2+ , a moderate MnO2 deposition rate is achieved, preventing the electrolyte from rapidly exhausting Mn2+ . Simultaneously, the intrinsic stability of deposited R-MnO2 is enhanced by the slowly released Bi3+ from Bi-PYDC reservoir. Furthermore, Bi-PYDC shows the ability to accommodate H+ insertion/extraction. Benefiting from these merits, the cathode-free ZIB using Bi-PYDC as the electrodeposition surface for MnO2 shows an outstanding cycle lifespan of more than 10 000 cycles at 1 mA cm-2 . This electrode design may stimulate a new pathway for developing cathode free long-life rechargeable ZIBs.

Intensifying Hydrogen Spillover for Boosting Electrocatalytic Hydrogen Evolution Reaction.

Hydrogen spillover has attracted increasing interests in the field of electrocatalytic hydrogen evolution reaction (HER) in recent years because of their distinct reaction mechanism and beneficial terms for simultaneously weakening the strong hydrogen adsorption on metal and strengthening the weak hydrogen adsorption on support. By taking advantageous merits of efficient hydrogen transfer, hydrogen spillover-based binary catalysts have been widely investigated, which paves a new way for boosting the development of hydrogen production by water electrolysis. In this paper, we summarize the recent progress of this interesting field by focusing on the advanced strategies for intensifying the hydrogen spillover towards HER. In addition, the challenging issues and some perspective insights in the future development of hydrogen spillover-based electrocatalysts are also systematically discussed.

Strategies for Promoting Catalytic Performance of Ru-Based Electrocatalysts towards Oxygen/Hydrogen Evolution Reaction.

Ru-based materials hold great promise for substituting Pt as potential electrocatalysts toward water electrolysis. Significant progress is made in the fabrication of advanced Ru-based electrocatalysts, but an in-depth understanding of the engineering methods and induced effects is still in their early stage. Herein, we organize a review that focusing on the engineering strategies toward the substantial improvement in electrocatalytic OER and HER performance of Ru-based catalysts, including geometric structure, interface, phase, electronic structure, size, and multicomponent engineering. Subsequently, the induced enhancement in catalytic performance by these engineering strategies are also elucidated. Furthermore, some representative Ru-based electrocatalysts for the electrocatalytic HER and OER applications are also well presented. Finally, the challenges and prospects are also elaborated for the future synthesis of more effective Ru-based catalysts and boost their future application.

Pd-Based Metallenes for Fuel Cell Reactions.

Pd-based metallenes, atomically thin layers composed primarily of under-coordinated Pd atoms, have emerged as the newest members in the family of two-dimensional (2D) nanomaterials. Moreover, the unique physiochemical properties, high intrinsic activity associated with metallenes coupled with the ease of applying chemical modifications result in great potential in catalyst engineering for fuel cell reactions. Especially in recent years, interest in Pd-based metallenes is growing, as evidenced by surge in available literatures. Herein, we have reviewed the recent findings achieved in Pd-based metallenes in fuel cells by highlighting the technologies available for deriving metallenes and manifesting the modification strategies for designing them to better suit the application demand. Moreover, we also discuss the perspective insights of Pd-based metallenes for fuel cells regarding the surfactant-free synthesis method, strain engineering, constructing high-entropy alloy, and so on.

A stripe phase with supersolid properties in spin-orbit-coupled Bose-Einstein condensates.

Supersolidity combines superfluid flow with long-range spatial periodicity of solids, two properties that are often mutually exclusive. The original discussion of quantum crystals and supersolidity focused on solid 4He and triggered extensive experimental efforts that, instead of supersolidity, revealed exotic phenomena including quantum plasticity and mass supertransport. The concept of supersolidity was then generalized from quantum crystals to other superfluid systems that break continuous translational symmetry. Bose-Einstein condensates with spin-orbit coupling are predicted to possess a stripe phase with supersolid properties. Despite several recent studies of the miscibility of the spin components of such a condensate, the presence of stripes has not been detected. Here we observe the predicted density modulation of this stripe phase using Bragg reflection (which provides evidence for spontaneous long-range order in one direction) while maintaining a sharp momentum distribution (the hallmark of superfluid Bose-Einstein condensates). Our work thus establishes a system with continuous symmetry-breaking properties, associated collective excitations and superfluid behaviour.

PeMPK17 interacts with PeMKK7 and participates in para-hydroxybenzoic acid stress resistance by removing reactive oxygen species.

Mitogen-activated protein kinase (MAPK) plays a crucial role in plant stress response. Poplar is one of the most important afforestation and timber species and inevitably encounters allelopathy effects during continuous cropping. para-hydroxybenzoic acid (pHBA) is a primary soil allelochemical, which can restrict the growth and biomass of poplar. However, the involvement of MAPKs in the underlying physiological and molecular regulatory mechanisms in response to pHBA stress remains unclear. In this study, PeMPK17, a gene encoding a group D MAPK, was cloned from Populus × euramericana. PeMPK17 protein was localized in both nucleus and plasma membrane. Quantitative real-time polymerase chain reaction analysis demonstrated that PeMPK17 expression in poplar increased when treated with pHBA, PEG, and H2O2. Exogenous pHBA and H2O2 induced PeMPK17 expression mediated by reactive oxygen species (ROS). The transgenic poplar plants overexpressing PeMPK17 demonstrated attenuated phenotypic injury, higher relative water content in leaves, and lower ion leakage under pHBA stress. In transgenic poplar, the activity and expression of antioxidant enzymes including superoxide dismutase, peroxidase, and catalase increased, while the content of H2O2, O2·-, and malondialdehyde decreased. These results suggested that PeMPK17 protects cell membranes from oxidative damage by removing excess ROS. In addition, overexpression of PeMPK17 promoted osmoprotectant accumulation including soluble sugar and free proline, which may aid in the regulation of ROS balance under pHBA treatment. Furthermore, the interaction between PeMPK17 and PeMKK7 was confirmed. Collectively, these data identify the molecular mechanisms and signal pathways associated with PeMPK17 that regulate pHBA response in poplar.

IodoTMT-labeled redox proteomics reveals the involvement of oxidative post-translational modification in response to para-hydroxybenzoic acid and hydrogen peroxide stresses in poplar.

Poplar is widely planted as an economic and ecological tree species. However, accumulation of the phenolic acid allelochemical para-hydroxybenzoic acid (pHBA) in soil is a severe threat to the growth and productivity of poplar. pHBA stress leads to excessive production of reactive oxygen species (ROS). However, it is unclear which redox-sensitive proteins are involved in the pHBA-induced cellular homeostasis regulatory mechanism. We here identified reversible redox-modified proteins and modified cysteine (Cys) sites in exogenous pHBA- and hydrogen peroxide (H2O2)-treated poplar seedling leaves by using the iodoacetyl tandem mass tag-labeled redox proteomics method. In total, 4786 redox modification sites were identified in 3176 proteins, with 104 and 91 proteins being differentially modified at 118 and 101 Cys sites in response to pHBA and H2O2 stresses, respectively. The differentially modified proteins (DMPs) were predicted to be mainly localized in the chloroplast and cytoplasm, with most proteins being enzymes with catalytic activities. The KEGG enrichment analysis of these DMPs revealed that proteins related to the MAPK signaling pathway, soluble sugar metabolism, amino acid metabolism, photosynthesis, and phagosome pathways were extensively regulated by redox modifications. Moreover, combined with our previous quantitative proteomics data, 8 proteins were upregulated and oxidized under both pHBA and H2O2 stresses. Reversible oxidation of Cys sites in these proteins might be actively responsible for the regulation of tolerance to pHBA-induced oxidative stress. Based on the aforementioned results, a redox regulatory model activated by pHBA- and H2O2-induced oxidative stress was proposed. This study conducts the first redox proteomics analysis of poplar in response to pHBA stress and provides a new insight into the mechanistic framework of reversible oxidative post-translational modifications to gain a better understanding of pHBA-induced chemosensory effects on poplar.

The relationship between adolescent impulsivity, mental health, and internet addiction: a latent profile analysis.

This study aimed to identify group variations in adolescent impulsivity and explore the connections between latent categories of impulsivity and psychological symptoms, social anxiety, and internet addiction. The research involved 2,378 participants from three middle schools in Guangdong Province, China. We assessed the impact of impulsivity levels (measured by BBIS) on depression (measured by KADS-11), anxiety (measured by SCARED), social anxiety (measured by SASC), and internet addiction (measured by YDQ). Latent profile analysis was employed to examine the diversity in adolescent impulsivity, establish latent classifications, and investigate the variances in psychological symptoms, social anxiety, and internet addiction. The middle school students were categorized into five latent groups based on their BBIS scores. Statistical analysis revealed five impulsivity categories, strongly linked to psychological symptoms and social anxiety but less strongly associated with internet addiction. The high impulsivity group (C5) exhibited higher scores in psychological symptoms and social anxiety compared to other groups, whereas the poor self-regulation group (C3) displayed greater psychological symptoms, social anxiety scores, and internet addiction than the impulsive behavior group (C4). Future investigations should investigate the underlying factors contributing to the observed differences among these groups.

ACE-Inhibitory Peptides Identified from Quinoa Bran Glutelin-2 Hydrolysates: In Silico Screening and Characterization, Inhibition Mechanisms of ACE, Coordination with Zinc Ions, and Stability.

To obtain Angiotensin-I-Converting Enzyme (ACE) inhibition peptides with Zn-chelating capacity, quinoa bran glutelin-2 hydrolysates (QBGH) by Flavourzyme and Papain were subjected to Sephadex G-15 gel chromatography, reverse phase-high liquid performance chromatography and UPLC-ESI-MS/MS analysis. Four oligopeptides including GGGSGH, EAGAE, AGGGAGGG and AVPKPS were identified. Of these, only the hexapeptide AVPKPS had both ACE-inhibitory activity (IC50: 123.13 µmol/L) and Zn-chelating ability (17.36 mg/g). Molecular docking showed AVPKPS could bind with active residues Glu384 and Ala354 (both belong to the central S1 pocket of ACE including) through short hydrogen bond and hydrophobic interactions, respectively. Inhibition kinetics verified that AVPKPS was a competitive inhibitor of ACE. Moreover, AVPKPS can affect the zinc tetrahedral coordination in ACE through binding with residues His387 and His383. Fourier-transform infrared spectroscopy analysis demonstrated that the amino and carboxyl groups of AVPKPS were the main chelating sites for zinc ions. Under the gastrointestinal digestion, the ACE inhibition capacity of AVPKPS was relatively stable, and the zinc solubility of AVPKPS-zinc complexes was more stable than zinc sulfate (p < 0.05). These results suggest that quinoa peptides have potential applications as ingredients for antihypertension or zinc fortification.

Framework-Hotspot Enhanced Trans Cleavage of CRISPR-Cas12a for Clinical Samples Detection.

The trans-cleavage property of CRISPR-Cas12a system makes it an excellent tool for disease diagnosis. Nevertheless, most methods based on CRISPR-Cas system still require pre-amplification of the target to achieve the desired detection sensitivity. Here we generate Framework-Hotspot reporters (FHRs) with different local densities to investigate their effect on trans-cleavage activity of Cas12a. We find that the cleavage efficiency increases and the cleavage rate accelerates with increasing reporter density. We further construct a modular sensing platform with CRISPR-Cas12a-based target recognition and FHR-based signal transduction. Encouragingly, this modular platform enables sensitive (100 fM) and rapid (<15 min) detection of pathogen nucleic acids without pre-amplification, as well as detection of tumor protein markers in clinical samples. The design provides a facile strategy for enhanced trans cleavage of Cas12a, which accelerates and broadens its applications in biosensing.

A highly efficient In2S3/Ag2S/TiO2NTAs photoelectrodes for photocathodic protection of Q235 carbon steel under visible light.

A novel In2S3/Ag2S/TiO2nanotube arrays (NTAs) was successfully fabricated by successive ionic layer adsorption and reaction method and electrochemical anodic oxidation method, and served as photoanode for photocathodic protection application. The micromorphologies, optical absorption properties, crystalline structure and elemental valence states of the composites were performed by field emission scanning electron microscopy, high resolution transmission electron microscope, UV-vis diffuse reflectance absorption spectra, x-ray diffractometer and x-ray photoelectron spectroscopy, respectively. The photocathodic protection performances of In2S3/Ag2S/TiO2NTAs on the Q235 carbon steel (CS) were also studied. The In2S3/Ag2S/TiO2nanocomposites show better photoelectrocatalytic and photocathodic protection performance than pure TiO2NTAs. The photocurrent density of In2S3(9)/Ag2S(8)/TiO2photoelectrode coupled with Q235 CS reach 211µA cm-2, which is about 4.5 times higher than that of TiO2NTAs. The photogenerated potential of Q235 CS coupled to In2S3(9)/Ag2S(8)/TiO2under illumination shows a negative shift to -0.92 V versus SCE. Results indicate that the co-sensitization of In2S3and Ag2S could extend the light absorption of TiO2to the visible light range and enhance its photoelectric conversion efficiency.

Direct Z-scheme MgIn2S4/TiO2heterojunction for enhanced photocathodic protection of metals under visible light.

To improve the photocathodic protection performance of traditional TiO2photoanodes for metals, constructing a Z-scheme heterojunction is one of the most promising and creative strategies. Herein, we fabricated a novel Z-scheme MgIn2S4nanosheets/TiO2nanotube nanocomposite through anodization and hydrothermal method. The optimized Z-scheme MgIn2S4/TiO2nanocomposites exhibited stronger visible light absorption, higher separation efficiency of photoelectrons and photocathodic protection performances in comparison to pure TiO2. The theoretical analysis and experimental results show that the Z-scheme heterojunction and oxygen vacancies jointly improved the separation efficiency of photogenerated electron-hole pairs and visible light absorption capacity, thereby improving the photoelectric conversion performance of the MgIn2S4/TiO2nanocomposites. Furthermore, the influence of the precursor solution concentration on the photocathodic protection performances of the composites was investigated. As a result, when the concentration of magnesium source in the precursor solution was 0.06 mmol, the prepared MgIn2S4/TiO2-0.06 displayed the best photocathodic protection performance. In addition, the hydroxyl radicals (·OH) generated in the electron spin resonance (ESR) experiment verified the Z-scheme heterojunction mechanism of the MgIn2S4/TiO2composite, and also demonstrated the excellent redox performance of the composite. This work provides valuable reference for the construction of high-performance Z-scheme heterojunctions for photocathode protection of metals.

Statistical inference of body representation in the macaque brain.

The sense of one's own body is a pillar of self-consciousness and could be investigated by inducing human illusions of artificial objects as part of the self. Here, we present a nonhuman primate version of a rubber-hand illusion that allowed us to determine its computational and neuronal mechanisms. We implemented a video-based system in a reaching task in monkeys and combined a casual inference model to establish an objective and quantitative signature for the monkey's body representation. Similar to humans, monkeys were more likely to perceive an external object as part of the self when the dynamics (spatial disparity) and the features (shape and structure) of visual (V) input was closer to proprioceptive (P) signals. Neural signals in the monkey's premotor cortex reflected the strength of illusion and the likelihood of misattributing the illusory hand to oneself, thus, revealing a cortical representation of body ownership.

Dynamical Generation of Spin Squeezing in Ultracold Dipolar Molecules.

We study a bulk fermionic dipolar molecular gas in the quantum degenerate regime confined in a two-dimensional geometry. Using two rotational states of the molecules, we encode a spin 1/2 degree of freedom. To describe the many-body spin dynamics of the molecules, we derive a long-range interacting XXZ model valid in the regime where motional degrees of freedom are frozen. Because of the spatially extended nature of the harmonic oscillator modes, the interactions in the spin model are very long ranged, and the system behaves close to the collective limit, resulting in robust dynamics and generation of entanglement in the form of spin squeezing even at finite temperature and in the presence of dephasing and chemical reactions. We discuss how the internal state structure can be exploited to realize time reversal and enhanced metrological sensing protocols.

A novel CaIn2S4/TiO2NTAs heterojunction photoanode for highly efficient photocathodic protection performance of 316 SS under visible light.

Designing heterojunction photocatalysts with matched band structure and good interface contact is an effective method to improve the photoelectrochemical activity. Herein, novel CaIn2S4/TiO2nanotube arrays (NTAs) heterojunction photoanodes were successfully prepared by electrochemical anodization and hydrothermal method. The microstructures, compositions, crystal structures, chemical valence states and light absorption performances of the composites were evaluated by field emission scanning electron microscopy, energy dispersive x-ray spectroscopy transmission electron microscope, high-resolution transmission electron microscope, x-ray diffractometer, x-ray photoelectron spectroscopy and ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS), respectively. The photocathodic protection performances of CaIn2S4/TiO2composites for 316 stainless steel (SS) and the influences of the CaIn2S4content on the performances were studied. The microstructural examination revealed the uniform doping of CaIn2S4nanofragments on the TiO2NTAs, and the composite was made up cubic CaIn2S4and anatase TiO2. The photogenerated electrons were transferred from the TiO2to CaIn2S4at the interface of the composite. Compared with pure TiO2NTAs, CaIn2S4/TiO2NTAs exhibited better photocathodic protection performance for 316 SS under visible light. Potential drop reached 0.78 V versus saturated calomel electrode for the 316 SS coupled with CaIn2S4/TiO2NTAs. The photocurrent density of the 316 SS coupled with the composite photoanode (235.4µA cm-2) was 17.4 times that of TiO2. The improved photocathodic protection property of CaIn2S4/TiO2NTAs was ascribed to the enhanced separation efficiency of the photogenerated carriers and the strong visible light absorption of the material. The CaIn2S4/TiO2NTAs exhibited continuous protection of the 316 SS for more than 12 h even in the dark. Therefore, the CaIn2S4/TiO2NTAs heterojunction composite is an outstanding and efficient photoanode for the photocathodic protection of metals.