Facile Method Research Articles

Insights into the ternary substitution Na2.96+xK0.04 V2-xNix(PO4)2.98F0.06 with superior rate capability and near-zero strain property

Na3V2(PO4)3 (NVP) is considered the most favorable cathode for sodium-ion batteries due to its solid NASICON skeleton. Nevertheless, poor intrinsic conductivity is insufficient for its further commercialization. In this paper, we present a promising K/Ni/F co-doped and carbon nanotubes (CNTs) encapsulated Na2.96+xK0.04 V2-xNix(PO4)2.98F0.06 (KNF@CNTsx) cathode materials. The synthesis of KNF@CNTsx is achieved using a facile sol-gel method. The replacement of Na+ with K+ broadens the migratory pathway and supports the crystal skeleton, while F− substitution reduces the average grain dimension, thereby increasing the diffusion rate of Na+. Furthermore, the reduction of resistance by Ni2+ doping enables optimization of the transport of electrical charge, while also facilitating the optimization of chemically-defined properties. Concurrently, the optimal quantity of carbon capping and wrapping of CNTs facilitate the formation of efficacious conductive network, which diminishes the size of grains and shortens the pathway for the diffusion of Na+. This network could also serve as a buffer against crystal deformation. In conclusion, the modified KNF@CNTsx samples exhibit notable enhancements in their conductivity, ion diffusion capacity, and structural stability. Among them, the KNF@CNTs0.04 sample exhibits a capacity for reversibility of 93.3 mAh g−1 at 50C, with a remaining capacity of 68.5 mAh g−1 after 4000 successive long charge-discharge cycles. Ex-situ electrochemical XRD demonstrates the V3+/V4+ redox reaction occurs accompanied by the phase transfer reaction, during which Na+ prefers to diffuse along c-axial in the crustal structure. Moreover, volume alteration of this KNF@CNTs0.04 cellular entity is miniscule and reversible during the charge-discharge process, further confirming the stabilized construction and near-zero strain property. The after-cycled XRD/SEM/XPS certify the improved chemical and structural stability of KNF@CNTs0.04, indicating the constructive effects of K/Ni/F ternary substitution.

Enhanced catalytic performance of ethyl-levulinate to γ-valerolactone: Effect of copper loading on Ni/KIT-5 catalyst

A facile wet impregnation method was employed to prepare a bimetallic Ni–Cu catalyst on a mesoporous KIT-5 support, keeping the nickel loading constant (5 wt%) while varying the copper wt.% (xCu, where x = 8, 10, 12, 14). Several physico-chemical techniques, including X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) analysis, scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HR-TEM), temperature-programmed desorption of ammonia (NH3-TPD), temperature-programmed reduction of hydrogen (H2-TPR), and X-ray photoelectron spectroscopy (XPS), were utilized for catalyst characterization. An environmentally friendly NiCu bimetallic-supported catalyst system was developed in response to many problems, including metal leaching, sintering, and cost. A mesoporous KIT-5 silica support with a large surface area was used. The hydrogenation of ethyl levulinate to gamma-valerolactone was studied utilizing a high-pressure stirred reactor and a range of reaction temperatures (120–160 °C), hydrogen pressures (10–30 bar), and reaction periods. Various catalysts were used in the investigation. Among all tested catalysts, the 12Cu–5Ni/KIT-5 one shows excellent activity. The best GVL yield is 84% at a conversion of 100% after 8 h of treatment at 150 °C and 25 bar H2 pressure; the promotion is also 76.1%. Optimization of reaction conditions was shown to correlate the physicochemical parameters of the catalyst with its activity.

Modulating the chemical environment of Ni2+ for the oxidative dehydrogenation of ethane: The formation of LAS(Al3+/Ga3+)-Ni-OH site

The oxidative dehydrogenation of ethane to ethylene (ODHE) usually suffers from the issues of ethane conversion-ethylene selectivity seesaw. Herein, a series of alumina-supported Ni and Ga catalysts with different molar ratios of Ni to Ga were synthesized by facile impregnation method constructing the Lewis acid site (LAS) strategy to obtain great ethylene selectivity (97 %). The variation of Ni:Ga ratio adjusted the ionic substitution ability, redox ability and acidity, thus regulate the chemical environment of Ni2+ to the formation of LAS(Al3+/Ga3+)-Ni-OH structure, which was proposed to be the active site for selective oxidation of ethane to ethylene, as proved by H2-TPR, ToF-SIMS, quasi in-situ XPS and in-situ FTIR. Moreover, the probable mechanism of ODHE reaction was proposed that C2H6 molecules were mainly adsorbed on LAS sites and activated on Ni-OH site of the catalyst. The pulse test further suggested that O- was mainly associated with the generation of CO2 and Ni(2-n)+ was connected with the production of CH4. It is highlighted that adjusting the Ni-related species and oxygen species on the catalyst surface are crucial to further improve the ethylene selectivity.

Wurtzite CuIn(SxSe1-x)2 Nanocrystals: Colloidal Synthesis and Band-Gap Engineering.

CuIn(SxSe1-x)2 nanocrystals as an emerging class of functional materials present huge potential for industrial applications; however, the synthesis of CuIn(SxSe1-x)2 nanocrystals remains a formidable challenge in achieving both tunable band gap and phase. Here, we reported a facile hot-injection method for synthesizing a family of wurtzite CuIn(SxSe1-x)2 nanocrystals, enabling manipulation of the S and Se contents across the entire compositional range (0 ≤ x ≤ 1). The obtained nanocrystals exhibit band gaps ranging from 1.21 to 1.58 eV, which vary depending on the S/Se ratios in the products. This approach can be readily extended to other scenarios involving chalcogenide nanomaterials, thereby facilitating the advancement of next-generation functional materials and applications.

Anchoring atomic Pd on molybdenum disulfide with state-of-the-art specific activity in the electrochemical dehalogenation of florfenicol

The widespread discharge of halogenated organic pollutants (HOPs) in wastewater brings significant risks to the environment and human health due to potent high toxicity, antibacterial activity, and strong biodegradation resistance. Adsorbed atomic hydrogen (H*ads)-mediated electrocatalytic hydrodehalogenation (EHDH) has been recognized as an efficient strategy for HOPs removal through selectively breaking carbon-halogen bonds. In this work atomic Pd uniformly anchored on molybdenum disulfide (denoted as Pd-MoS2) was synthesized through a facile hydrothermal method and found with state-of-the-art specific activity in florfenicol (FLO) removal via the H*ads-mediated EHDH process. Pd-MoS2 completely dehalogenated (∼100 %) FLO within 30 min at a rate constant of 0.15 min−1, which was 6.0, 6.5 and 33.1 times the value of MoS2, Pd/C and carbon paper samples, respectively. Notably, the toxicity of the wastewater was reduced to 1/6 of its original value after the treatment. Moreover, Pd-MoS2 presented superior catalytic stability in five successive cycles. Furthermore, Pd-MoS2 was also robust in complex water environment with practical applicability for industrial wastewater treatment. A dual-active-center mechanism with enhanced H*ads production capacity and the improved H*ads utilization efficiency was contributed to the increased EHDH activity on Pd-MoS2.

4,4'-Sulfonyldianiline Derived Aggregation-Induced Emission Luminogen for the Detection of Ofloxacin.

The excessive use of antibiotic ofloxacin (Oflx) can cause serious detrimental effects to human health. Therefore, the utmost research priority is required to develop facile methods to detect Oflx. Herein, a V-shaped aggregation-induced emission (AIE) active Schiff base SDANA was introduced for the fluorescent turn-on detection of Oflx. The Schiff base SDANA was synthesized by condensing 4,4'-sulfonyldianiline with two equivalents of 2-hydroxy-1-naphthaldehyde. The nearly non-fluorescent SDANA in DMSO showed strong orange emission with the increase in HEPES buffer (H2O, 10 mM, pH 7.4) fractions in DMSO from 70 %-95 % due to the combined effects of AIE and ESIPT. The DLS and SEM analyses were performed to complement the formation of self-aggregates of SDANA. With the addition of Oflx, the fluorescence emission of AIE luminogen (AIEgen) SDANA (λem=575 nm, λex=400 nm) was blue-shifted and enhanced at 530 nm. The interactions of Oflx over the surface of SDANA aggregates disrupted the intramolecular charge transfer and aggregation morphology of SDANA, which gave a distinct fluorescence response to detect Oflx. The detection limit for Oflx was estimated as 0.81 μM, and the developed probe AIEgen SDANA was applied for the quantification of Oflx in human blood serum.

One-Pot Fast Electrochemical Synthesis of Ternary Ni-Cu-Fe Particles for Improved Urea Oxidation

The climate crisis has become the most serious concern of human beings and environments worldwide in the 21st century. Global concerns about cancer epidemiology mainly originate from anthropogenic activities, particularly fossil-based operations. A key solution to this problem is the use of fuel cells—devices—capable of the direct conversion of fuel chemical energies like urea into electricity. To make their commercialization reasonable, one of the problems that needs to be solved is the development of anodic materials. The majority of investigations on urea oxidation are based on nickel, but its inadequate activity limits the efficiency of these devices. In this work, we propose and synthesize a Ni-Cu-Fe ternary electrocatalyst for urea oxidation through a fast and facile electrodeposition method. The properties of the synthesized material are examined by Scanning Electron Microscopy (SEM) conjugated with Energy Dispersive X-ray Spectroscopy (EDS), Transmission Electron Microscopy (TEM), and X-ray Diffraction (XRD). Its electrochemical properties were also examined in a 1 M KOH solution with and without 0.15 M urea. We found that the prepared powder is active in the electro-oxidation of urea, with 1.65 Vvs RHE required for a current density of 10 mA cm−2 and a stable potential of 2.38 Vvs RHE required for 3 h of polarization at 10 mA cm−2.

Ag‐Catalyzed Asymmetric 1,3‐Dipolar Cycloaddition of N‐2,2,2‐Trifluoroethylisatin Ketimines with Conjugated Exocyclic Double Bonds: Access to Pyrrolidines with Four Consecutive Stereocenters Including Two Adjacent Spiro‐Quaternary Centers

AbstractAg‐catalyzed enantioselective 1,3‐dipolar cycloaddition of N‐2,2,2‐trifluoroethylisatin ketimines with conjugated exocyclic double bonds including α‐alkylidene succinimides and aurone derivatives was developed for the first time. Using a catalyst system consisting of a ferrocenyl P,N‐ligand and AgNO2, the reaction provides a facile method for the construction of chiral pyrrolidines bearing four consecutive stereocenters and two adjacent spiro‐quaternary chiral centers, as well as offers a direct route to structurally diverse enantioenriched CF3‐containing 3,2′‐pyrrolidinyl spirooxindole derivatives.

Synthesis and characterization of new organometallic lanthanides metal complexes for photodynamic therapy

New Schiff base ligand: 4-methoxy salicaldhyde-2-2-phenyl-hydrazono acetaldehíyde prepared by facile method. The molecular structures characterized by elemental analysis and proton magnetic resonance spectra (1H-NMR spectra). This spectra at the chemical shifts (3.5–10.39 ppm) confirmed the types and the numbers of protons. The sharp melting point at the range 110–112 °C confirmed purity. New optically active metal (samarium, terbium and gadolinium) complexes of the Schiff base synthesized in a one pot reaction. Vibrational IR spectra confirmed functional groups. Scanning electron microscopy micrographs confirmed that the modified microstructure of the metal complexes differed in morphology than the ligand. Powder X-ray diffraction patterns confirmed good crystalline structure. The optically activity of the solid metal complexes confirmed from electronic absorption spectra. The UV absorbance band at the wavelength range 280–390 nm and the intense phosphorescence bands up to 830 nm enabled application in photo dynamic therapy for apoptosis cancer cells by conversion triplet oxygen in the tissues into reactive singlet oxygen. Low charge transfer energy: 2.59–2.61 eV, high molar extinction coefficients (ε) at the order of magnitude \\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\:{10}^{6}$$\\end{document} M− 1 cm− 1 and the intense phosphorescence bands reflected good photodynamic activity. The metal complexes are thermally stable.

Exosomes: A Fluid Biopsy Source for Clinical Interventions of Noncommunicable Diseases Treatment: A Review

Introduction: The beginning of exosome biosynthesis is marked by the emergence of the initial endosomes through the inward splitting of the plasma cell membrane. This process is facilitated through the endosomal categorization complex essential for transport, which is also involved in the production of different extracellular vesicles. Exosomes are naturally occurring nanosized vesicles found in all bodily fluids and can be successfully extracted from preserved biological materials, while maintaining their structural integrity. Methods: The articles published recently in high-quality journals (Science Direct, Springer, Institute of Electrical and Electronics Engineers (IEEE), and Taylor & Francis) indexed in various indexing sources such as Scopus, Web of Science, PubMed, Google Scholar, and so on were collected using keywords such as fluid biopsy (FB) exosomes, endosomes, and noncommunicable diseases (NCDs) treatment, new biomarkers, and treatment. Discussion: In recent years, exosomes have emerged as an exciting option for “FB” that has demonstrated significant potential in the areas of noninvasive medical testing, predictions, as well as tracking responses to therapy for noncommunicable diseases. Nevertheless, specific constraints need to be addressed to expand the application of exosome-based FB as a widely accepted and reliable testing method in typical medical facilities. Conclusion: This review provides a comprehensive overview of our present understanding of exosomes to be an FB method for diagnosing, predicting outcomes, and tracking treatment responses in NCDs. It also discusses the main constraints, innovations in technology, as well as future possibilities of using this application in medical treatment.

Green and Fast Synthesis of NiCo-MOF for Simultaneous Purification-Immobilization of Bienzyme to Catalyze the Synthesis of Ginsenoside Rh2.

Traditional metal-organic frameworks (MOFs) preparation is generally time-consuming, polluting, and lacking specificity for enzyme immobilization. This paper introduced a facile, rapid, and green method to produce three MOFs subsequently employed to purify and coimmobilize recombinant glycosyltransferase (UGT) and recombinant sucrose synthetase (SUSy) using histidine tag (His-tag) for the specific adsorption of Ni2+ and Co2+ from MOFs. This method simplified enzyme purification from crude extracts and enabled enzymes to be reused. The results demonstrated that NiCo-MOF exhibited a higher enzyme load (115.9 mg/g) than monometallic MOFs. Additionally, the NiCo-MOF@UGT&SUSy demonstrated excellent stability and efficiently produced the rare ginsenoside Rh2 by catalyzing a coupling reaction (95.6 μg/mL), solving the problem of the substrate cost of uridine diphosphate glucose (UDPG). The NiCo-MOF@UGT&SUSy retained 68.97% of the initial activity after 10 cycles. Finally, molecular docking studies elucidated the conversion mechanism of the target product Rh2. This technique is important in the industrialization of ginsenoside production and enzyme purification.

Cu(I)‐Induced ‘Click Reaction’ Involving Coordination and Covalent Assembly of Hybrid Borates for the Electrocatalytic CO2 Reduction

AbstractThe design and synthesis of hybrid borates by the organic ligand modification method are urgent and undeveloped areas of research. It is difficult to directly integrate organoboronic acids within inorganic borate chemistry by adopting the traditional preparation approaches. This work reports a facile synthetic method to synthesize a large family of pyrazole molecule‐protected borates in a rapid and precise manner under mild conditions. A unique cyclic eight‐membered B4O4‐ring has been identified as the cluster core for all these hybrid borates with two different conformations (boat and crown). This strategy can be applied to a system of pyrazolyl molecules to generate such hybrid borates in two independent routes from organoboronic or inorganic boric acids. Furtherly, the mechanism of ‘click reaction’ between boric acid and pyrazole induced by copper ions has been proposed based on the synthetic conditions and the structure of intermediate. Due to the bimetallic Cu sites and the functional surfaces, these materials can be used as electrocatalysts for CO2 reduction reaction and efficiently enhance the selectivity of HCOOH and C2H4. Our strategy can be regarded as a typical template technique for organic molecule‐protected borates.

Facile Electrodeposition Method for Constructing Li2S as Artificial Solid Electrolyte Interphase for High-Performance Li Metal Anode.

Designing current collectors and constructing efficient artificial solid electrolyte interphase (SEI) layers are promising strategies for achieving dendrite-free Li deposition and practical applications in Li metal batteries (LMBs). Electrodeposition is advantageous for large-scale production and allows the direct formation of current collectors without binders, making them immediately usable as electrodes. In this study, an adherent Cu2S thin-layer on Cu foil is synthesized through anodic electrodeposition from a Na2S solution in a one-step process, followed by the generation of Li2S layers as artificial SEI layers via a conversion reaction (3DLi2S-Cu foil). The Li2S layers move from the 3D Cu surface to the deposited Li surface, facilitating uniform and dense Li deposition. The 3DLi2S-Cu foil structure demonstrates stable cycling performance over 350 cycles in an asymmetric cell, with a capacity of 1 mAh cm-2 at 1 mA cm-2. Moreover, symmetric cells with 5 mAh cm-2 of deposited Li exhibit a stable cycle life for over 1200 h. When paired with commercial LiFePO4 (LFP), the full cells show substantially enhanced cyclability, regardless of the amount of deposited Li. This study provides new insights into the construction of artificial SEIs for facilitating commercial applications.

Single Vesicle Surface Protein Profiling and Machine Learning-Based Dual Image Analysis for Breast Cancer Detection

Single-vesicle molecular profiling of cancer-associated extracellular vesicles (EVs) is increasingly being recognized as a powerful tool for cancer detection and monitoring. Mask and target dual imaging is a facile method to quantify the fraction of the molecularly targeted population of EVs in biofluids at the single-vesicle level. However, accurate and efficient dual imaging vesicle analysis has been challenging due to the interference of false signals on the mask images and the need to analyze a large number of images in clinical samples. In this work, we report a fully automatic dual imaging analysis method based on machine learning and use it with dual imaging single-vesicle technology (DISVT) to detect breast cancer at different stages. The convolutional neural network Resnet34 was used along with transfer learning to produce a suitable machine learning model that could accurately identify areas of interest in experimental data. A combination of experimental and synthetic data were used to train the model. Using DISVT and our machine learning-assisted image analysis platform, we determined the fractions of EpCAM-positive EVs and CD24-positive EVs over captured plasma EVs with CD81 marker in the blood plasma of pilot HER2-positive breast cancer patients and compared to those from healthy donors. The amount of both EpCAM-positive and CD24-positive EVs was found negligible for both healthy donors and Stage I patients. The amount of EpCAM-positive EVs (also CD81-positive) increased from 18% to 29% as the cancer progressed from Stage II to III. No significant increase was found with further progression to Stage IV. A similar trend was found for the CD24-positive EVs. Statistical analysis showed that both EpCAM and CD24 markers can detect HER2-positive breast cancer at Stages II, III, or IV. They can also differentiate individual cancer stages except those between Stage III and Stage IV. Due to the simplicity, high sensitivity, and high efficiency, the DISVT with the AI-assisted dual imaging analysis can be widely used for both basic research and clinical applications to quantitatively characterize molecularly targeted EV subtypes in biofluids.

C60 Fullerene‐Induced Reduction of Metal Ions: Synthesis of C60‐Metal Cluster Heterostructures with High Electrocatalytic Hydrogen‐Evolution Performance

AbstractMetal clusters, due to their small dimensions, contain a high proportion of surface atoms, thus possessing a significantly improved catalytic activity compared with their bulk counterparts and nanoparticles. Defective and modified carbon supports are effective in stabilizing metal clusters, however, the synthesis of isolated metal clusters still requires multiple steps and harsh conditions. Herein, we develop a C60 fullerene‐driven spontaneous metal deposition process, where C60 serves as both a reductant and an anchor, to achieve uniform metal (Rh, Ir, Pt, Pd, Au and Ru) clusters without the need for any defects or functional groups on C60. Density functional theory calculations reveal that C60 possesses multiple strong metal adsorption sites, which favors stable and uniform deposition of metal atoms. In addition, owing to the electron‐withdrawing properties of C60, the electronic structures of metal clusters are effectively regulated, not only optimizing the adsorption behavior of reaction intermediates but also accelerating the kinetics of hydrogen evolution reaction. The synthesized Ru/C60‐300 exhibits remarkable performance for hydrogen evolution in an alkaline condition. This study demonstrates a facile and efficient method for synthesizing effective fullerene‐supported metal cluster catalysts without any pretreatment and additional reducing agent.

Spectrofluorometric Turn-Off Sensing Probe for Tolmetin Determination Using Cerium and Nitrogen Codoped Carbon Dots.

A facile, low-cost, and rapid method was developed for spectrofluorometric determination of tolmetin (TOL) using highly fluorescent (QY = 35%) cerium and nitrogen codoped carbon dots (Ce-NCDs) sensing platform prepared by one-step hydrothermal method. Owing to the severe overlap between TOL absorption and Ce-NCDs excitation spectra around 320 nm, TOL could attenuate the emission of Ce-NCDs at 407 nm through primary inner filter effect (IFE). This concentration dependent attenuation was linear between 2 and 10 μg/mL (r = 0.9993) with a limit of detection of 0.5 μg/mL. The sensor showed very good accuracy (% recovery = 98%-100%) and precision (%RSD < 2). The developed sensing strategy was successfully applied for TOL detection as an active pharmaceutical ingredient in pharmaceutical formulation and as a potential pollutant in environmental water samples, such as tap and river water, with acceptable recovery and considerable selectivity. Thus, the direct single-step spectrofluorometric determination of TOL was enabled without extensive processing or chemical derivatization.

Grain size control in quasi-two-dimensional perovskite thin film via intermediate phase engineering for efficient bound exciton generation

AbstractQuasi-two dimensional (2D) perovskites have emerged as a promising class of materials due to their remarkable photoluminescence efficiency, which stems from their exceptionally high exciton binding energies. The spatial confinement of excitons within smaller grain sizes could enhance the formation of biexcitons leading to higher radiative recombination efficiency. However, the synthesis of high-quality quasi-2D perovskite thin films with controllable grain sizes remains a challenging task. In this study, we present a facile method for achieving quasi-2D perovskite thin films with controllable grain sizes ranging from 500 to 900 nm. This is accomplished by intermediate phase engineering during the film fabrication process. Our results demonstrate that quasi-2D perovskite films with smaller grain sizes exhibit more efficient bound exciton generation and a reduced stimulated emission threshold down to 15.89 µJ cm−2. Furthermore, femtosecond transient absorption measurements reveal that the decay time of bound excitons is shorter in quasi-2D perovskites with smaller grain sizes compared to that of those with larger grains at the same pump density, which is 230.5 ps. This observation suggests a more efficient exciton recombination process in the smaller grain size regime. Our findings would offer a promising approach for the development of efficient bound exciton lasers.

Construction of magnetic FeP/CdS composites as photo‐Fenton‐like catalysts to realize high‐efficiency degradation of tetracycline hydrochloride

Photocatalysis is an efficient technology for the degradation of pollutants. However, it still needs to be improved. In this study, magnetic Z‐scheme FeP/CdS composites heterojunction photocatalysts were prepared by a facile hydrothermal method, and the structure, morphology, optical and photocatalytic properties of the prepared composites were investigated in detail. The efficiency of tetracycline hydrochloride (TCH) removal by FeP/CdS composites was investigated under different reaction conditions (including different FeP and CdS ratios, catalyst dosage, hydrogen peroxide consumption, temperature, and initial pH). FeP/CdS composites exhibited better catalytic performance compared with pure components. The F1Cd1 composite (mass ratio of FeP to CdS is 1:1) achieved 92.7% removal efficiency of TCH, moreover, the F1Cd1 composite still exhibits a high stability after five consecutive cycles. The capture experiments on the active material showed that the removal of TCH by the F1Cd1 composite was mainly dominated by •OH; however, •O2−, e‐, and h+ played a minor role, and the degradation mechanism was revealed by combining various characterization techniques. The introduction of cadmium sulfide formed an effective photogenerated carrier transport channel at the interface with the iron phosphide surface, which could accelerate the transfer and separation of photo‐excited e‐/h+ pairs, thus improving the degradation performance of TCH.

Facile method to improve toughness and biodegradability of polylactide by modified CaCO3

Facile method to improve toughness and biodegradability of polylactide by modified CaCO3

Boosting Enzyme Activity in an Anhydrous Gas Flux with Amphiphilic Polymers

AbstractGas‐phase enzymatic catalysis offers great potential for both green synthesis and the efficient degradation of volatile chemicals. However, solid enzymes often exhibit extremely low activity compared to their counterparts in native aqueous phase. Although a few immobilization methods have succeeded in increasing activity by preserving enzyme structure, approaches for boosting enzyme activity remain underdeveloped. In this study, we propose a general and facile method to boost enzyme activity in the gas phase, which utilizes amphiphilic polymers to energize enzyme conformational dynamics and thus enhance enzyme catalysis kinetics. The triblock copolymer Pluronics with low melting points were co‐lyophilized with Candida antarctica lipase B (CalB), yielding Pluronic/CalB powders that appeared a 70‐fold increase in activity compared to free CalB powder. Low‐field nuclear magnetic resonance (LF‐NMR), solid‐state nuclear magnetic resonance (ssNMR) and dielectric relaxation spectroscopy identified the enhancement of enzyme dynamics on the µs–ms timescale, whereas Fourier transform infrared spectroscopy (FTIR) detected structural perturbations of the native enzyme in Pluronic/CalB. The apparent activity of the enzyme/polymer powders correlated positively with both enzyme dynamics and polymer flexibility. These findings provide new molecular physical insights into gas‐phase enzyme catalysis, which are essential for advancing enzyme applications in nonnatural scenario.