Intrinsic Activity Research Articles

Pioneering Built-In Interfacial Electric Field for Enhanced Anion Exchange Membrane Water Electrolysis.

As a half-reaction in anion exchange membrane water electrolysis (AEMWE) technology, the hydrogen evolution reaction (HER) at the cathode is severely hindered by the sluggish reaction kinetics involved in additional water dissociation step, which results in large overpotentials and low energy conversion efficiency. Here, we develop a nano-heterostructure composed of ultra-thin W5N4 shells over Ni3N nanoparticles (Ni3N@W5N4) as efficient catalysts, in which built-in interfacial electric field (BIEF) is created owing to the distinct lattice arrangements and work functions of biphasic metal nitrides. The BIEF facilitates the electron localization around the interface and enables high valence W and more exposed binding sites in the surface W5N4 shell for accelerating the water dissociation step, ultimately leading to a remarkable reduction in the energy barriers of RDS from 1.40 eV to 0.26 eV. Theoretical calculations and operando X-ray absorption spectroscopy analysis results demonstrated that surface W5N4 serves as the active species for HER. Moreover, the ultra-thin shell characteristics enable the optimized W5N4 with enhanced intrinsic catalytic activity to be fully exposed as active sites. Consequently, the Ni3N@W5N4 exhibits exceptional performance in alkaline HER (60 mV@10 mA cm-2) and remarkable long-term stability (500 mA cm-2 for 100 hours). When employed as the cathode in the AEMWE device, the synthesized Ni3N@W5N4 demonstrates stable performance for 90 hours at a current density of 1 A cm-2.

IrPdCuFeNiCoMo BasedCore-Shell Icosahedron Nanocrystals and Nanocages for Efficient and RobustAcidic Oxygen Evolution.

Facets engineering of high entropy alloy (HEA) nanocrystals might be achieved via shape-controlled synthesis, which is promising but remains challenging in designing Ir-based catalysts towards efficient and robust oxygen evolution reaction (OER) in acidic medium. Herein, icosahedra nanocrystals featured with PdCu core and IrPdCuFeNiCoMo shell were prepared by wet-chemical reduction in one-pot, ascribing to the initial formation PdCu core and subsequent deposition and diffusion of IrPdCuFeNiCoMo HEA shell. Sequential selective chemical etching of PdCu core results in IrPdCuFeNiCoMo HEA nanocages, delivering an overpotential of 235 mV at 10 mA cm-2, 51.0 mV dec-1, and 1624 A gIr-1 at 1.50 V in a conventional three electrode cell. In a proton exchange membrane water electrolyzer, it delivers a low cell voltage of 1.65 and 1.77 V at a current density of 1.0 and 2.0 A cm-2, respectively, and maintains stable over 900 h at 500 mA cm-2. Theoretical calculations attribute the enhanced intrinsic activity to the broad distribution of the binding energy for OER intermediates on IrPdCuFeNiCoMo HEA, which breaks the linear scaling relationship and accelerates the OER process.

Advanced systems for enhanced CO2 electroreduction.

Carbon dioxide (CO2) electroreduction has extraordinary significance in curbing CO2 emissions while simultaneously producing value-added chemicals with economic and environmental benefits. In recent years, breakthroughs in designing catalysts, optimizing intrinsic activity, developing reactors, and elucidating reaction mechanisms have continuously driven the advancement of CO2 electroreduction. However, the industrialization of CO2 electroreduction remains a challenging task, with high energy consumption, high costs, limited reaction products, and restricted application scenarios being the issues that urgently need to be addressed. To accelerate the progress of CO2 electroreduction towards practical application, this review shifts the research focus from catalysts to aspects such as reactions and systems, aiming to improve reaction efficiency, reduce technical costs, expand the range of products, and enhance selectivity, offering readers a new perspective. In particular, innovative and specific design strategies such as CO2 reduction coupled with alternative oxidation, co-reduction reaction of CO2 and C/N/O/S-containing species, cascade systems, and integrated CO2 capture and reduction systems are discussed in detail. Additionally, personal views on the opportunities and future challenges of the aforementioned innovative strategies are provided, offering new insights for the future research and development of CO2 electroreduction.

Bio‐MOF‐11 Derived Amorphous Cobalt Hollow Nanospheres to Access Bioactive Quinazolinone Scaffolds and Aromatic Amines

AbstractA facile synthetic strategy is reported to afford bioactive quinazolinones and aromatic amines by employing amorphous cobalt hollow nanospheres (Co HNS) derived from a Bio‐MOF, cobalt adeninate, as a catalyst. Modulated electron states of the amorphous cobalt with a high concentration of surficial active sites and Co–N sites enhance the intrinsic catalytic activity while the support, activated carbon, facilitates the formation of hollow structure.

Electrostatic Aspect of the Proton Reactivity in Concentrated Electrolyte Solutions.

Water-in-salt electrolytes with a surprisingly large electrochemical stability window of ≤3 V have revived interest in aqueous electrolytes for rechargeable lithium-ion batteries. However, recent reports of acidic pH measured in concentrated electrolyte solutions appear to be in contradiction with the suppressed activity of the hydrogen evolution reaction (HER). Therefore, the fundamental thermodynamics of proton reactivity in concentrated electrolyte solutions remains elusive. In this work, we have used density functional theory-based molecular dynamics (MD) simulations and the proton insertion method to investigate how the HER potential shifts in concentrated LiCl solutions under both acidic and alkaline conditions. Our results show that the intrinsic HER activity increases significantly with the salt concentration under acidic conditions but remains relatively constant under alkaline conditions. Moreover, by leverage over finite-field MD simulations, it is found that a determining factor for the HER activity is the Poisson potential of the liquid phase, which increases in concentrated electrolyte solutions with comparable values from both density functional theory and point-charge models.

Expediting the Volmer Step of Alkaline Hydrogen Oxidation with High-Efficiency and CO-Tolerance by Ru-O-Eu Bridge.

The quest for economical and highly efficient nanomaterials for the alkaline hydrogen oxidation reaction (HOR) is imperative in advancing the technology of anion exchange membrane fuel cells (AEMFCs). Efforts using Pt-based electrocatalysts for alkaline HOR are greatly plagued by their finitely intrinsic activities and significant CO poisoning, stemming from the difficulty of simultaneously optimizing surface adsorption toward different hydrogen-related adsorbates. Herein, Ru clusters coupled with Eu2O3 immobilized within N-doped carbon nanofibers (Ru/Eu2O3@N-CNFs) are developed toward drastically boosted electrocatalysis for HOR via a d-p-f gradient orbital coupling strategy. Theoretical calculations and in situ operando spectroscopy discover that the induction of Eu2O3 optimizes the Ru site electronic structure via constructing the gradient orbital coupling of Ru(3d)-O(2p)-Eu(4f), leading to optimal H intermediates, improved adsorption ability of OH and reduced energy barrier of water formation, and promoted CO oxidation, endowing the Ru/Eu2O3 as the promising catalyst alternative for fast alkaline hydrogen electrooxidation. As a result, the Ru/Eu2O3@N-CNFs reach an impressive kinetic current densities (jk) value of 156.3 mA cm-2 at 50 mV (38.4 times higher than Pt/C), and decent stability over 35000 s continuous operation. This comprehensive investigation featuring d-p-f gradient orbital coupling provides valuable insights for the strategic development of high-performance Ru-based materials for HOR and beyond.

Alloying Strategy Regulating Size and Electronic Structure of Mo0.25Nb0.75Se2 to Achieve High‐Performance Lithium–Sulfur Batteries

The utilization of catalysts in lithium−sulfur batteries has proven to be an efficacious avenue for enhancing the kinetics of polysulfide conversion. Specially, the size and electronic structure of catalysts play a pivotal role in harnessing the active sites and intrinsic catalysis activity. Outstanding MoSe2 and NbSe2 are selected from 16 universal transition metal selenides based on the proposed binary descriptor. Then, an alloying strategy is devised to prepare Mo0.25Nb0.75Se2 flakelets for further improvement of the intrinsic catalysis. The integration of density functional theory calculations and electrochemical analysis demonstrates that alloying Mo with Nb can regulate the surface energy and indexes of band match and lattice mismatch, thereby enabling Mo0.25Nb0.75Se2 to possess a small size, suitable adsorption energy and low reaction energy barrier. This optimization enhances the catalysis of sulfur reduction/evolution reaction and the reversible deposition/stripping of lithium. Consequently, an assembled Ah‐level pouch cell is realized with dramatic cycle stability. With the electrolyte/sulfur ratio of 2.36 μL mg S–1, the cell can deliver a high energy density of up to 505.4 Wh kgtotal−1. This work pioneers a universal strategy for sculpting the geometric configurations and electronic structures of catalysts, to achieve enhanced catalytic activity and precise interpretation of structure−activity relationships.

A simulated sunlight-activated plastic mimic enzyme for dual-mode detection of D-penicillamine and serum iron

No reports disclosed that whether the plastic centrifuge tube with intrinsic photoenzyme activity can be used for the specific sensing of pharmaceuticals and biomarkers in biofluids so far. We herein report the plastic eppendorf (EP) tube as both reaction vessel and sunlight-activated plastic mimic enzyme for colorimetric/smartphone dual-mode detection of D-penicillamine (D-PA) and iron (Ⅲ) ions in goat and rabbit serums accordingly. The photooxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) combined with simulated sunlight-activated EP tube was selectively inhibited by adding D-PA, and the absorbance at 652 nm of oxidized TMB decreased. Good linearity between the absorbance variation (or R/(R + G + B)) and D-PA level ranging from 10 to 300 µM was obtained, and the limits of detection (LOD) were determined as 8.50 μM (colorimetric) and 6.92μM (smartphone). Furthermore, the polyvinyl alcohol hydrogel encapsulated TMB in EP tube as a smartphone biosensor had been triumphantly used to monitor D-PA level in goat serum. Interestingly, the adsorption band of photo-oxidized EP tube-TMB system inhibited by D-PA gradually increased as the enhancement of iron (Ⅲ) ions concentration. Based on the “on–off-on” effect, a sensitive and selective method was further used for selectively sensing iron (Ⅲ) in rabbit serum. Notably, the dual-mode sensing platforms exhibited outstanding detection performance, with LOD values as low as 0.50 µM and 0.65 µM respectively. In short, this work not only excavated a photoactivated-plastic mimics, but also developed a robust, low-cost, simple and sensitive biosensor for simultaneous detection of D-PA and Fe (Ⅲ) ions in biofluids. The current photoactivated sensor does not requires the introduction of exogenous catalyst except for simulated sunlight, plastic tube and chromogenic substrate.

Cyclic Peptide MV6, an Aminoglycoside Efficacy Enhancer Against Acinetobacter baumannii

Background/Objectives: Acinetobacter baumannii is a globally emerging pathogen with widespread antimicrobial resistance driven by multiple mechanisms, such as altered expression of efflux pumps like AdeABC, placing it as a priority for research. Driven by the lack of new treatments, alternative approaches are being explored to combat its infections, among which efficacy-enhancing adjuvants can be found. This study presents and characterizes MV6, a synthetic cyclic peptide that boosts aminoglycoside efficacy. Methods: MV6’s activity was assessed through antimicrobial susceptibility testing in combination with different antibiotic classes against A. baumannii strains characterized by PCR and RT-qPCR. PAβN served as a reference efflux pump inhibitor. Synergy was evaluated using checkerboard assays, and spontaneous mutants were generated with netilmicin with/without MV6 (100 mg/L). Whole-genome sequencing and variant calling analysis were then performed. Results: MV6 presented low antimicrobial activity in A. baumannii with MICs higher than 2048 mg/L. MV6 showed a better boosting effect for aminoglycosides, especially netilmicin, exceeding that of PAβN. Checkerboard assays confirmed a strong synergy between netilmicin and MV6, and a significant correlation was found between netilmicin MIC and adeB overexpression, which was mitigated by the presence of MV6. MV6 reduced, by 16-fold, the mutant prevention concentration of netilmicin. Mutations in a TetR-family regulator and ABC-binding proteins were found in both groups, suggesting a direct or indirect implication of these proteins in the resistance acquisition process. Conclusions: MV6 lacks intrinsic antimicrobial activity, minimizing selective pressure, yet enhances netilmicin’s effectiveness except for strain 210, which lacks the AdeABC efflux pump. Resistant mutants indicate specific aminoglycoside resistance mechanisms involving efflux pump mutations, suggesting synergistic interactions. Further research, including transcriptomic analysis, is essential to elucidate MV6’s role in enhancing netilmicin efficacy and its resistance mechanisms.

Facilitating the electrooxidation of 5-hydroxymethylfurfural on nickel hydroxide through deintercalation

The electrocatalytic of 5-hydroxymethylfurfural oxidation reaction (HMFOR) is an alternative route for the green production of valuable oxygenated chemicals. Nickel hydroxides, which consist of hydroxide layers and interlayer charge-balancing anions, are a type of promising catalysts for HMFOR. Progresses have been made on elucidating the correlation between the hydroxide layer and HMFOR performance, while the effect of intercalated anions on the activity remains unclear. Herein, two self-supported nickel hydroxide catalysts (i.e., pristine Ni(OH)2/CP-F and deintercalated Ni(OH)2/CP-A) are employed for revealing the relationship between anion-deintercalation and HMFOR activity. Physical characterizations demonstrate that the deintercalation phenomenon can alter the d-band center and increase the electron density of the Ni site. This endows the deintercalated Ni(OH)2/CP-A with improved electrochemical properties (conversion = 99.99 %; FDCA yield > 99 %; FE > 99 %), enhanced adsorption strength for HMF, and increased intrinsic activity, compared to the pristine Ni(OH)2/CP-F. This work not only reports an excellent HMFOR electrocatalyst, but also manifests the crucial effect of deintercalation on the electrochemical oxidation performance of Ni(OH)2.

Effect of composition of multicomponent supports on properties of supported Nickel catalysts

Ni catalysts supported on combinations of alumina, magnesia, zirconia with rare earth supports are studied for the steam reforming of ethanol (ESR). The composition of the supports is systematically varied to identify the role of individual components and their contribution when they are combined. Supports containing magnesia or zirconia show contrasting behavior of acidity, XRD crystallite size of NiO, reducibility, dispersion of Ni(0), OSC, coking and metals sintering characteristics. Catalyst activity and deactivation are strongly influenced due to these differences. HRTEM indicates the redispersion of Ni(0) during reduction of NiO on catalysts containing magnesia. Magnesia and alumina-magnesia based catalysts show hindered reduction of nickel and highest intrinsic activity (H2 yields). But sintering of Ni is their nemesis. Moderate interaction of Ni with zirconia-based supports (H2-TPR) lends sintering stability in ESR. Quaternary Alumina-Magnesia-Zirconia catalysts imbibe advantages of individual components and are overall best with fair H2 yield, good stability and regenerability. Long duration (80 hours) performance tests give holistic results because they encompass multiple factors influencing deactivation. Intrinsic chemical reactivity (as opposed to) active metal dispersion is important while comparing the activity of catalysts with different compositions. Degree of reducibility of nickel is an important consideration while measuring metal dispersion by chemisorption. Metal reducibility by H2-TPR, dispersion measurement by chemisorption and particle size determination by HRTEM are used as complementary techniques for rationalizing results of metal dispersion measurement.

Electrochemical evaluation of the real surface area of copper-zinc alloys

Accurate measurements of real surface area (RSA) are essential in fundamental electrocatalysis for evaluating the intrinsic activity of various materials. However, existing electrochemical methods for determining RSA values in metallic alloys, particularly those containing active metals, remain underexplored. This study critically assesses the efficacy of capacitance measurement techniques for calculating RSA values in copper-zinc alloys, which are commonly employed as electrocatalysts for CO2 reduction. We investigate optimal conditions for estimating RSA through cyclic voltammetry, focusing on electrolyte selection and appropriate potential ranges to ensure reliable RSA assessments. Additionally, we emphasize the necessity of using suitable reference samples for accurate specific capacitance calculations. Our findings reveal that potential uncertainties arising from the use of inappropriate reference samples across different Cu-Zn compositions can reach an order of magnitude, rendering them unsuitable for electrocatalytic studies. This research highlights the need for robust surface area quantification techniques to reduce uncertainties in reporting the activities of alloy-based materials in various electrochemical applications.

Enhancement of the urea oxidation reaction by constructing hierarchical CoFe-PBA@S/NiFe-LDH nanoboxes with strengthened built-in electric fields

The slow kinetics of the oxygen evolution reaction (OER) present a major obstacle for efficient hydrogen production via water electrolysis. In contrast, the urea oxidation reaction (UOR), with its lower thermodynamic barrier, presents a promising alternative to OER. In this study, we designed and synthesized hierarchical CoFe- PBA@S/NiFe-LDH nanoboxes. Sulfur doping in nickel–iron layered double hydroxides (S/NiFe-LDH) introduces a weak built-in electric field (BIEF), which is further strengthened when combined with cobalt-iron Prussian blue analogue (CoFe-PBA) to form a heterojunction. This heterojunction created localized charge polarization at the interface, facilitating efficient electron transfer and reducing the adsorption energy of reaction intermediates, thereby significantly improving intrinsic catalytic activity. Under conditions of 1 M KOH and 0.33 M urea, the CoFe-PBA@S/NiFe-LDH catalyst achieved a current density of 50 mA cm−2 at a relatively low potential of 1.321 V, accompanied by a low Tafel slope (53 mV dec−1). Additionally, it maintained stability at 30 mA cm−2 for 40 h. This work provides vital insights for the strategic design of highly effective heterojunction catalysts for the UOR.

Iron-Induced vacancy and electronic regulation of nickle phosphides for ampere-level alkaline water/seawater splitting

Rational design of non-precious metal catalysts can accelerate the oxygen evolution reaction (OER) kinetics. Herein, inspired by theoretical analysis, in-situ Fe-doped Ni2P/Ni12P5 with rich P vacancies (Fe-NiPx) is designed and constructed, in which the production of P vacancies is induced by Fe doping. Relevant characterizations confirm that the Fe doping and P vacancies can co-adjust the crystal and electronic structures, thereby optimizing the reconstruction behavior and improving the intrinsic activity of reconstructed-derived Ni(Fe)OOH. As a result, it exhibits excellent OER activity with overpotentials of 256 and 276 mV to achieve the current density of 100 mA cm−2 in 1 M KOH solutions and alkaline seawater, respectively. Furthermore, the Fe-NiPx electrode only requires 1.861 and 1.889 V to drive the 1.0 A cm−2 overall water and seawater splitting, respectively, and maintains stable output as high as 1000 h. Also, to demonstrate the great application potential, green energy-to-hydrogen systems are established. Electrochemical tests and theoretical calculations reveal that reconstructed-Fe-NiPx facilitates the OER kinetics under the adsorbate evolution mechanism (AEM) pathway, with optimized adsorption free energies of intermediates and reduced reaction energy barriers. This work provides new insights into efficient water and seawater splitting through in-situ heteroatom doping and vacancy engineering.

Application of Nanocomposites in Covalent Organic Framework-Based Electrocatalysts

In recent years, the development of high-performance electrocatalysts for energy conversion and environmental remediation has become a topic of great interest. Covalent organic frameworks (COFs), linked by covalent bonds, have emerged as promising materials in the field of electrocatalysis due to their well-defined structures, high specific surface areas, tunable pore structures, and excellent acid–base stability. However, the low conductivity of COF materials often limits their intrinsic electrocatalytic activity. To enhance the catalytic performance of COF-based catalysts, various nanomaterials are integrated into COFs to form composite catalysts. The stable and tunable porous structure of COFs provides an ideal platform for these nanomaterials, leading to improved electrocatalytic activity. Through rational design, COF-based composite electrocatalysts can achieve synergistic effects between nanomaterials and the COF carrier, enabling efficient targeted electrocatalysis. This review summarizes the applications of nanomaterial-incorporated COF-based catalysts in hydrogen evolution, oxygen evolution, oxygen reduction, carbon dioxide reduction, and nitrogen reduction. Additionally, it outlines design principles for COF-based composite electrocatalysis, focusing on structure–activity relationships and synergistic effects in COF composite nanomaterial electrocatalysts, as well as challenges and future perspectives for next-generation composite electrocatalysts.

Enhancing the photo-induced oxidase-like activity of fluorescein with methyl viologen for colorimetric detection of organophosphorus pesticide

Overcoming the intrinsic low activity of most photoinduced oxidase mimics has been extremely challenging. In this work, we developed a methyl viologen (MV2+) mediated strategy to enhance the oxidase-like activity of fluorescein. The presence of MV2+ gives it a high affinity for TMB with a low Michaelis-Menten constant (Km) of 0.053 mM, which is about 2.8 times lower than that of fluorescein and with a remarkable catalytic constant (Kcat) as 0.2490 s−1, which is 3 times as high as that of fluorescein. Fluorescein diacetate (FDA) without oxidase-like activity can be hydrolyzed in situ to produce fluorescein in the presence of carboxylesterases (CaE). Based on the inhibition of CaE activity by organophosphorus pesticides (OP), a novel colorimetric signal biosensor was established with a wide linear range from 1.0 to 200 ng/mL. This work not only provides a convenient and feasible strategy for enhancing the activity of photoinduced oxidase mimics but also blazes a new pathway for the sensitive detection of OP.

Solvent-assisted thermogalvanic cell for enhanced low-grade heat harvesting over an extended temperature range

In the pursuit of sustainable energy harvesting from low-grade heat, thermogalvanic cells (TGCs) have received considerable attention, but still confront profound challenges in efficiency and cost-effectiveness, limiting their real-world applications. To expedite the deployment of TGCs, this study delves into the mechanistic interplay of three crucial determinants: intrinsic temperature coefficient, concentration gradient, and activity coefficient of redox couples, elucidating their impact on TGCs' thermoelectric performance. We report a solvent-assisted liquid-state thermogalvanic cell (SA-LTC) by incorporating organic solvents into the sodium ferrocyanide-based TGCs system. With ethanol as a regulator to the concentration gradient and solvation structure, the temperature coefficient of [Fe(CN)6]3-/4- can be enhanced from − 1.39 to − 4.32 mV K−1, leading to a five-fold increase in thermoelectric power and efficiency. Meanwhile, ethanol imparts a lower freezing point and wider working temperature range to the system, showing its better environmental adaptability. In particular, SA-LTC performs better at lower temperatures, at which it achieved a record-high temperature coefficient of − 5.26 mV K−1 and a power density of 2.17 mW m−2 K−2 at 10–20 °C. This study not only provides useful guidance to the optimization of electrolyte design, but also highlights the potential of TGCs for sustainable energy conversion in varied thermal conditions for practical applications.

Design Principle and Regulation Strategy of Noble Metal‐Based Materials for Practical Proton Exchange Membrane Water Electrolyzer

AbstractGreen hydrogen holds immense promise in combating climate change and building a sustainable future. Owing to its high power‐to‐gas conversion efficiency, compact structure, and fast response, the proton exchange membrane water electrolyzer (PEMWE) stands out as the most viable option for the widespread production of green hydrogen. However, the harsh operating conditions of PEMWE make it heavily dependent on noble metal‐based catalysts (NMCs) and incur high operational and maintenance costs, which hinder its extensive adoption. Hence, it is imperative to improve the performance and lifespan of NMCs and develop advanced components to reduce the overall costs of integrating PEMWE technology into practical applications. In light of this, the fundamental design principles of NMCs employed in acidic water electrolysis are summarized, as well as recent advancements in compositional and structural engineering to enhance intrinsic activity and active site density. Moreover, recent innovations in stack components of practical PEMWE and their impact on cost‐benefit and lifespan are presented. Finally, the current challenges are examined, and potential solutions for optimizing NMCs and PEMWE in electrocatalytic hydrogen production are discussed.

Imparting P vacancy in Ni-doped CoP derived from double-ligand MOF strategy as robust electrocatalyst

Efficient and stable bifunctional electrocatalysts are pivotal for electrocatalytic water splitting applications. Here, a dual-ligand (dithiooxamide and 2-methylimidazole) MOF-derived Ni–CoP has been successfully prepared. The 1D nanowire hydroxide is employed as template precursor to obtain the regular morphology of MOFs. The Co and P in dual-ligand MOF-derived Ni-CoPv exhibits different electronic state compared to single-ligand (2-methylimidazole) MOF-derived Ni–CoP. Importantly, the Ni-CoPv possesses larger number of P vacancy and poor crystal degree. Based on above-mentioned results, Ni-CoPv exhibits superior activity for HER, which requires only 263 mV to reach 500 mA cm−2 without IR correction and shows long-term stability. The HER process for Ni-CoPv follows the V–H mechanism. As a bifunctional electrocatalyst, Ni-CoPv electrode requires 1.57 V to reach 10 mA cm−2 for the water splitting. Compared to Ni–CoP-M derived from single-ligand MOF, Ni-CoPv exhibits higher intrinsic activity HER/OER. We pave a simple way for the construction of a kind of CoP catalyst with rich P vacancies.

Static and temporal dynamic changes of intrinsic brain activity in early-onset and adult-onset schizophrenia: a fMRI study of interaction effects

BackgroundSchizophrenia is characterized by altered static and dynamic spontaneous brain activity. However, the conclusions regarding this are inconsistent. Evidence has revealed that this inconsistency could be due to mixed effects of age of onset.MethodsWe enrolled 66/84 drug-naïve first-episode patients with early-onset/adult-onset schizophrenia (EOS/AOS) and matched normal controls (NCs) (46 adolescents, 73 adults), undergoing resting-state functional magnetic resonance imaging. Two-way ANOVA was used to determine the amplitude of low-frequency fluctuation (ALFF) and dynamic ALFF (dALFF) among the four groups.ResultCompared to NCs, EOS had a higher ALFF in inferior frontal gyrus bilateral triangular part (IFG-tri), left opercular part (IFG-oper), left orbital part (IFG-orb), and left middle frontal gyrus (MFG). The AOS had a lower ALFF in left IFG-tri, IFG-oper, and lower dALFF in left IFG-tri. Compared to AOS, EOS had a higher ALFF in the left IFG-orb, and MFG, and higher dALFF in IFG-tri. Adult NCs had higher ALFF and dALFF in the prefrontal cortex (PFC) than adolescent NCs. The main effects of diagnosis were found in the PFC, medial temporal structures, cerebrum, visual and sensorimotor networks, the main effects of age were found in the visual and motor networks of ALFF and PFC of dALFF.ConclusionOur findings unveil the static and dynamic neural activity mechanisms involved in the interaction between disorder and age in schizophrenia. Our results underscore age-related abnormalities in the neural activity of the PFC, shedding new light on the neurobiological mechanisms underlying the development of schizophrenia. This insight may offer valuable perspectives for the specific treatment of EOS in clinical settings.