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The inherent dipole moment and higher polarizability of azulene lead to ambipolar characteristics and good gate controllability of azulene-based single-molecule transistors.

A mechano-sliding strategy for controllable assembly of nanowires was demonstrated by directly transferring chemical vapor deposition grown silicon nanowires to obtain nanoscale electronic devices.

A single-molecule field-effect transistor (FET) is the key building block of future electronic circuits. At the same time, a single-molecule FET is also a unique platform for studying physical mechanisms at the single-molecule level. How to construct single-molecule FETs and how to efficiently control the charge transfer characteristics of the devices are two core issues in the development of single-molecule FETs. In this review, we introduce the research progresses of single-molecule FETs with solid or liquid gates. Strategies to design single-molecule FETs are emphasized, including the design of functional molecules, the construction of gate electrodes and the control of molecule-electrode interface coupling. These single-molecule FETs provide a basis for practical applications and the exploration of physical laws. Specifically, the physical mechanisms of single-molecule FETs, especially those related to interfacial coupling, are explained, such as energy level shift, Coulomb blockade effect, Kondo effect and electron-phonon coupling. The applications of single-molecule FETs are summarized, including the regulation of quantum interference, spin, thermoelectric effect and superconductivity. Finally, the current opportunities and challenges in the field of single-molecule FETs are proposed, aiming to promote the future development of single-molecule electronics.

The degradation process of RNA is decisive in guaranteeing high-fidelity translation of genetic information in living organisms. However, visualizing the single-base degradation process in real time and deciphering the degradation mechanism at the single-enzyme level remain formidable challenges. Here, we present a reliable in-situ single-PNPase-molecule dynamic electrical detector based on silicon nanowire field-effect transistors with ultra-high temporal resolution. These devices are capable of realizing real-time and label-free monitoring of RNA analog degradation with single-base resolution, including RNA analog binding, single-nucleotide hydrolysis, and single-base movement. We discover a binding event of the enzyme (near the active site) with the nucleoside, offering a further understanding of the RNA degradation mechanism. Relying on systematic analyses of independent reads, approximately 80% accuracy in RNA nucleoside sequencing is achieved in a single testing process. This proof-of-concept sets up a Complementary Metal Oxide Semiconductor (CMOS)-compatible playground for the development of high-throughput detection technologies toward mechanistic exploration and single-molecule sequencing.

The hydrogenation of CO2 or CO to single organic product has received widespread attentions. Here we show a highly efficient and selective catalyst, Mo3S4@ions-ZSM-5, with molybdenum sulfide clusters ([Mo3S4]n+) confined in zeolitic cages of ZSM-5 molecular sieve for the reactions. Using continuous fixed bed reactor, for CO2 hydrogenation to methanol, the catalyst Mo3S4@NaZSM-5 shows methanol selectivity larger than 98% at 10.2% of carbon dioxide conversion at 180 °C and maintains the catalytic performance without any degeneration during continuous reaction of 1000 h. For CO hydrogenation, the catalyst Mo3S4@HZSM-5 exhibits a selectivity to C2 and C3 hydrocarbons stably larger than 98% in organics at 260 °C. The structure of the catalysts and the mechanism of COx hydrogenation over the catalysts are fully characterized experimentally and theorectically. Based on the results, we envision that the Mo3S4@ions-ZSM-5 catalysts display the importance of active clusters surrounded by permeable materials as mesocatalysts for discovery of new reactions.

Intermolecular charge transport plays a vital role in the fields of electronics, as well as biochemical systems. Here, we design supramolecular dimer junctions and investigate the effects of charge state and energy level alignment on charge transport under nanoconfinement. Incoherent tunneling caused by thermally-induced vibrations is enhanced in positively charged systems. The transition between coherent and incoherent tunneling is associated with specific molecular vibration modes. Positively charged systems with smaller torsional barriers and vibrational frequencies result in lower transition temperatures. Multiple thermal effects have a great impact on the conductance in the off-resonant tunneling, while thermally-induced vibron-assisted tunneling contributes more to the transport in the resonant tunneling. These investigations offer a deep mechanism understanding of intermolecular charge transport and facilitate the development of practical functional molecular devices.

Stacking interactions are of significant importance in the fields of chemistry, biology, and material optoelectronics because they determine the efficiency of charge transfer between molecules and their quantum states. Previous studies have proven that when two monomers are π-stacked in series to form a dimer, the electrical conductance of the dimer is significantly lower than that of the monomer. Here, we present a strong opposite case that when two anthanthrene monomers are π-stacked to form a dimer in a scanning tunneling microscopic break junction, the conductance increases by as much as 25 in comparison with a monomer, which originates from a room-temperature quantum interference. Remarkably, both theory and experiment consistently reveal that this effect can be reversed by changing the connectivity of external electrodes to the monomer core. These results demonstrate that synthetic control of connectivity to molecular cores can be combined with stacking interactions between their π systems to modify and optimize charge transfer between molecules, opening up a wide variety of potential applications ranging from organic optoelectronics and photovoltaics to nanoelectronics and single-molecule electronics.

Precise tuning of chemical reactions with predictable and controllable manners, an ultimate goal chemists desire to achieve, is valuable in the scientific community. This tunability is necessary to understand and regulate chemical transformations at both macroscopic and single-molecule levels to meet demands in potential application scenarios. Herein, we realise accurate tuning of a single-molecule Mizoroki-Heck reaction via applying gate voltages as well as complete deciphering of its detailed intrinsic mechanism by employing an in-situ electrical single-molecule detection, which possesses the capability of single-event tracking. The Mizoroki-Heck reaction can be regulated in different dimensions with a constant catalyst molecule, including the molecular orbital gating of Pd(0) catalyst, the on/off switching of the Mizoroki-Heck reaction, the promotion of its turnover frequency, and the regulation of each elementary reaction within the Mizoroki-Heck catalytic cycle. These results extend the tuning scope of chemical reactions from the macroscopic view to the single-molecule approach, inspiring new insights into designing different strategies or devices to unveil reaction mechanisms and discover novel phenomena.

Charge transport in a single-molecule junction is extraordinarily sensitive to both the internal electronic structure of a molecule and its microscopic environment. Two distinct conductance states of a prototype terphenyl molecule are observed, which correspond to the bistability of outer phenyl rings at each end. An azobenzene unit is intentionally introduced through atomically precise side-functionalization at the central ring of the terphenyl, which is reversibly isomerized between trans and cis forms by either electric or optical stimuli. Both experiment and theory demonstrate that the azobenzene side-group delicately modulates charge transport in the backbone via a single-molecule stereoelectronic effect. We reveal that the dihedral angle between the central and outer phenyl ring, as well as the corresponding rotation barrier, is subtly controlled by isomerization, while the behaviors of the phenyl ring away from the azobenzene are hardly affected. This tunability offers a new route to precisely engineer multiconfigurational single-molecule memories, switches, and sensors.

The production of functionalized anilines by chemoselective hydrogenation of nitroarenes occupies an important position in the chemical industries. Recently, cobalt and nitrogen codoped carbon (Co–...

This paper reports a quasilinear hydrazone-based mononuclear dysprosium(III) compound, namely, {Dy(Hppyh)2(SCN)3}·2MeOH (I), where Hppyh is pyrazine-2-carboxylic acid pyridin-2-ylmethylene-hydrazide. Compound I behaves as a single-ion magnet (SIM) based on the optimal dc field application of 0.7 kOe, showing a complex magnetic relaxation phenomenon with a tunneling relaxation time of 6.1 ± 0.3 × 10−3 s and an effective spin reversal barrier of 22.6 ± 1.1 K for the low- and high-frequency regions, respectively. More importantly, detailed comparative experimental and theoretical investigations reveal that the complex magnetic relaxation was most likely associated with the single DyIII ion behavior as well as the short-range intermolecular magnetic dipolar interactions.

Neoadjuvant therapy has become a standard treatment for patients with locally advanced rectal cancer to achieve better prognostic outcomes. The response to treatment has been shown to correlate closely with the prognosis. However, current evaluation systems only provide coarse assessment on limited information, due to the lack of accurate and reproducible approach for quantitation of different types of responses. In this study, a novel stain-free, slide-free multimodal multiphoton microscopy imaging technique was applied to image rectal cancer tissues after neoadjuvant therapies with high resolution and contrast. Qualitative and quantitative evaluation of tumor, stromal, and inflammatory responses were demonstrated which are consistent with current tumor regression grading system using American Joint Committee on Cancer criteria, showing the great potential of such approach to build a more informative grading system for accurate and standardizable assessment of neoadjuvant therapy in rectal cancer.

The majority of the protein structures have been elucidated under equilibrium conditions. The aim herein is to provide a better understanding of the dynamic behavior inherent to proteins by fabricating a label-free nanodevice comprising a single-peptide junction to measure real-time conductance, from which their structural dynamic behavior can be inferred. This device contains an azobenzene photoswitch for interconversion between a well-defined cis, and disordered trans isomer. Real-time conductance measurements revealed three distinct states for each isomer, with molecular dynamics simulations showing each state corresponds to a specific range of hydrogen bond lengths within the cis isomer, and specific dihedral angles in the trans isomer. These insights into the structural dynamic behavior of peptides may rationally extend to proteins. Also demonstrated is the capacity to modulate conductance which advances the design and development of bioinspired electronic nanodevices.

Summary Here, we report a high-performance catalyst Cu@Na-Beta, prepared via a unique method to embed 2∼5 nm Cu nanoparticles in crystalline particles of Na-Beta zeolite, for CO2 hydrogenation to ethanol as the only organic product in a traditional fixed-bed reactor. The ethanol yield in a single pass can reach ∼14% at 300°C, ∼12,000 mL·gcat−1·h−1, and 2.1 MPa, corresponding to a space-time yield of ∼398 mg·gcat−1·h−1. The key step of the reaction is considered as the rapid bonding of CO2∗ with surface methyl species at step sites of Cu nanoparticles to CH3COO∗ that converts to ethanol in following hydrogenation steps. The points of the catalyst seemed to be that the irregular copper nanoparticles stuck in zeolitic frameworks offer high density of step sites and the intimate surrounding of zeolitic frameworks strongly constrain the CO2 reactions at the copper surface and block by-products, such as methanol, formic acid, and acetyl acid.

Heterogeneous interfaces that are ubiquitous in optoelectronic devices play a key role in the device performance and have led to the prosperity of today's microelectronics. Interface engineering provides an effective and promising approach to enhancing the device performance of organic field-effect transistors (OFETs) and even developing new functions. In fact, researchers from different disciplines have devoted considerable attention to this concept, which has started to evolve from simple improvement of the device performance to sophisticated construction of novel functionalities, indicating great potential for further applications in broad areas ranging from integrated circuits and energy conversion to catalysis and chemical/biological sensors. In this review article, we provide a timely and comprehensive overview of current efficient approaches developed for building various delicate functional interfaces in OFETs, including interfaces within the semiconductor layers, semiconductor/electrode interfaces, semiconductor/dielectric interfaces, and semiconductor/environment interfaces. We also highlight the major contributions and new concepts of integrating molecular functionalities into electrical circuits, which have been neglected in most previous reviews. This review will provide a fundamental understanding of the interplay between the molecular structure, assembly, and emergent functions at the molecular level and consequently offer novel insights into designing a new generation of multifunctional integrated circuits and sensors toward practical applications.

Discrete nanosheets of silicon-doped AlPO4 molecular sieves (SAPO-34) with a thickness of ≈7 nm have been prepared through morphology-reserved synthesis with a lamellar aluminum phosphate as precursor. Cages of the nanosheets are in situ incorporated with copper oxide clusters. The CuO@SAPO-34 nanosheets exhibit a large external surface area with a high number of (010) channel pores on the surface. Due to the thin morphology, copper oxide clusters occupy the outmost cages with a probability >50 %. The distinctive configuration facilitates a new concept of pore mouth catalysis, i.e., reactant molecules larger than the pores cannot enter the interior of the molecular sieves but can interact with the CuO clusters at "the mouth" of the pore. In heterogeneous catalysis, CuO@SAPO-34 nanosheets have shown top performance in one-pot oxidation of cyclohexane to adipic acid by O2 , a key compound for the manufacture of nylon-66, which is so far produced using non-green nitric acid oxidation.

Device fabrication with organic single crystals is an important method for high device performance. High-quality organic semiconductor crystals are usually grown by a lab solution method, by which it is difficult to fabricate crystal arrays on the substrate, let alone achieve industrial production. Therefore, in this work, oriented single crystal arrays have been prepared by epitaxial growth. As an example, 2,7-dioctyl[1]benzothieno[3,2-b]benzothiophene (C8-BTBT) was spin-coated on the surface of a highly oriented melt-drawn isotactic polypropylene (iPP) film on 300 nm SiO2 substrates as an auxiliary dielectric layer, and highly oriented arrays of C8-BTBT single crystals are obtained by epitaxial growth in the solvent vapor annealing (SVA) approach. The devices based on the thus prepared C8-BTBT array have a yield of up to 81%, an average mobility of 2.5 cm2 V−1 s−1, a maximum mobility of 9.3 cm2 V−1 s−1 and an on/off ratio of 107. Hence, our method facilitates the large-scale fabrication of highly oriented single crystal arrays with high quality, which will promote further industrial application.

As conventional silicon-based transistors are fast approaching the physical limit, it is essential to seek alternative candidates, which should be compatible with or even replace microelectronics in the future. Here, we report a robust solid-state single-molecule field-effect transistor architecture using graphene source/drain electrodes and a metal back-gate electrode. The transistor is constructed by a single dinuclear ruthenium-diarylethene (Ru-DAE) complex, acting as the conducting channel, connecting covalently with nanogapped graphene electrodes, providing field-effect behaviors with a maximum on/off ratio exceeding three orders of magnitude. Use of ultrathin high-k metal oxides as the dielectric layers is key in successfully achieving such a high performance. Additionally, Ru-DAE preserves its intrinsic photoisomerisation property, which enables a reversible photoswitching function. Both experimental and theoretical results demonstrate these distinct dual-gated behaviors consistently at the single-molecule level, which helps to develop the different technology for creation of practical ultraminiaturised functional electrical circuits beyond Moore’s law.

An accurate single-molecule kinetic isotope effect (sm-KIE) was applied to circumvent the inherent limitation of conventional ensemble KIE by using graphene-molecule-graphene single-molecule junctions.

Measurements on single molecules can sometimes reveal features that can be difficult to detect using techniques that probe the averaged properties of many molecules. Here, we report on the use of graphene-molecule-graphene single-molecule junctions (GMG-SMJs) to probe the shuttling dynamics of an individual [2]rotaxane molecule. The experiments show variations in the thermodynamic and kinetic shuttling parameters over a temperature range, and in different solvents, allowing the single-molecule data to be quantitatively related to simulation and ensemble experiments. The structural (∼1 nm) and temporal (∼17 μs) resolution of the GMG-SMJ enables direct observation of a previously unidentified weak-binding intermediate, arising from the formation of weak hydrogen bonds between the ring and triazole units. The results illustrate how GMG-SMJ measurements provide new opportunities for elucidating aspects of the structure, dynamics, and operational mechanisms of synthetic molecular machines that may be hidden to techniques that probe averaged behavior of an ensemble.

International audience; The aim of molecular electronics is to miniaturize active electronic devices and ultimately construct single-molecule nanocircuits using molecules with diverse structures featuring various functions, which is extremely challenging. Here, we realize a gate-controlled rectifying function (the on/off ratio reaches ∼60) and a high-performance field effect (maximum on/off ratio >100) simultaneously in an initially symmetric single-molecule photoswitch comprising a dinuclear ruthenium-diarylethene (Ru-DAE) complex sandwiched covalently between graphene electrodes. Both experimental and theoretical results consistently demonstrate that the initially degenerated frontier molecular orbitals localized at each Ru fragment in the open-ring Ru-DAE molecule can be tuned separately and shift asymmetrically under gate electric fields. This symmetric orbital shifting (AOS) lifts the degeneracy and breaks the molecular symmetry, which is not only essential to achieve a diode-like behavior with tunable rectification ratio and controlled polarity, but also enhances the field-effect on/off ratio at the rectification direction. In addition, this gate-controlled symmetry-breaking effect can be switched on/off by isomerizing the DAE unit between its open-ring and closed-ring forms with light stimulus. This new scheme offers a general and efficient strategy to build high-performance multifunctional molecular nanocircuits.

Single-molecule detection is a rapidly developing area within the analytical chemistry field that requires ultrasensitive technologies to detect a range of molecules. Over the past few decades, various optically-, mechanically-, and electrically-based strategies have been employed for single-molecule detection to uncover information in biological processes. These strategies enable real-time monitoring with single-molecule/single-event sensitivity. In addition, their high temporal resolution enables investigation of the underlying mechanisms of biological functions from static to dynamic, from qualitative to quantitative, and from one to multiple disciplines. In this review, we provide a brief overview of the prominent, real-time single-molecule detection nanotechnologies and their potential applications within the life science fields.

An oxide catalyst plays an important role in environmental catalysis. Metal chlorides are widely used as precursors in the preparation of oxide catalysts. However, residual chlorine usually influen...

Understanding the Cu-catalyzed electrochemical CO2 reduction reaction (CO2RR) under ambient conditions is both fundamentally interesting and technologically important for selective CO2RR to hydroca...

The increasing need for clean and sustainable energy inspires researchers to explore low-cost nonprecious metal electrocatalysts for advanced energy storage and conversion. Herein, we develop a rea...

Molecular self-assembly into crystallised films or wires on surfaces produces a big family of motifs exhibiting unique optoelectronic properties. However, little attention has been paid to the fundamental mechanism of molecular crystallisation. Here we report a biomimetic design of phosphonate engineered, amphiphilic organic semiconductors capable of self–assembly, which enables us to use real-time in-situ scanning probe microscopy to monitor the growth trajectories of such organic semiconducting films as they nucleate and crystallise from amorphous solid states. The single-crystal film grows through an evolutionary selection approach in a two-dimensional geometry, with five distinct steps: droplet flattening, film coalescence, spinodal decomposition, Ostwald ripening, and self-reorganised layer growth. These sophisticated processes afford ultralong high-density microwire arrays with high mobilities, thus promoting deep understanding of the mechanism as well as offering important insights into the design and development of functional high-performance organic optoelectronic materials and devices through molecular and crystal engineering., Little attention has been paid to the fundamental mechanism of molecular self-assembly into crystallised films or wires on surfaces. Here the authors use real time in-situ scanning probe microscopy to monitor the growth trajectories of organic semiconducting films as they crystallize from an amorphous solid state under ambient conditions.

A noncrystalline Ni–B alloy in the shape of nanotubes has demonstrated its superior catalytic performance for some hydrogenation reactions. Remarkable synergistic effects have been observed in many reactions when bimetallic catalysts were used; however, bimetallic noncrystalline alloy nanotubes are far less investigated. Here, we report a simple acetone-assisted lamellar liquid crystal approach for synthesizing a series of bimetallic Ni–Co–B nanotubes and investigate their catalytic performances. The dilution effect of acetone on liquid crystals was characterized by small-angle X-ray diffraction (SAXRD) and scanning electron microscopy (SEM). The Ni/Co molar ratio of the catalyst was varied to study the composition, porous structure, electronic interaction, and catalytic efficiency. In the liquid-phase hydrogenation of p-chloronitrobenzene, the as-prepared noncrystalline alloy Ni–Co–B nanotubes exhibited higher catalytic activity and increased stability as compared to Ni–B and Co–B alloy nanotubes due to electronic interactions between the nickel and cobalt. The excellent hydrogenation performance of the Ni–Co–B nanotubes was attributed to their high specific surface area and the characteristic confinement effects, compared with Ni–Co–B nanoparticles.

Molecule-based field-effect transistors (FETs) are of great significance as they have a wide range of application prospects, such as logic operations, information storage and sensor monitoring. This account mainly introduces and reviews our recent work in molecular FETs. Specifically, through molecular and device design, we have systematically investigated the construction and performance of FETs from macroscale to nanoscale and even single molecule. In particular, we have proposed the broad concept of molecular FETs, whose functions can be achieved through various external controls, such as light stimulation, and other physical, chemical or biological interactions. In the end, we tend to focus the discussion on the development challenges of single-molecule FETs, and propose prospects for further breakthroughs in this field.

An efficient CuPd nanoparticle (NP) catalyst (3 nm CuPd NPs deposited on carbon support) is designed for catalyzing electrochemical allylic alkylation in water/isopropanol (1:1 v/v) and 0.2 m KHCO3 solution at room temperature. The Pd catalysis was Pd/Cu composition-dependent, and CuPd NPs with a Pd/Cu ratio close to one are the most efficient catalyst for the selective cross-coupling of alkyl halides and allylic halides to form C-C hydrocarbons with product yields reaching up to 99 %. This NP-catalyzed electrochemical allylic alkylation expands the synthetic scope of cross-coupling reactions and can be further extended to other organic reaction systems for developing green chemistry electrosynthesis methods.

Monitoring complex interactions of biological systems at the molecular level provides new opportunities to uncover fundamental details of the basic processes of life, of crucial importance to biology, diagnosis and drug discovery. Here, we detailed a reliable single-molecule electrical approach for achieving label-free, ultrasensitive electrical detection of DNA functions, using DNA intercalations by individual EB/SGs as a representative, based on DNA-functionalized molecular junctions. The analysis principle relies on the distortion mechanism of intercalative binding on the structural integrity of DNAs at the single-event level, resulting in significant step-wise changes in DNA charge transport. Such an understanding led to direct, rapid intercalator detection with subfemtomolar sensitivity. This single-molecule electrical approach provides a foundation for future molecular dynamics studies with single-molecule sensitivity, which will lead to direct observation of new effects and fundamental discoveries of the details of the most basic processes of life.

Uniform single-crystalline hydroxyapatite nanotubes with hexagonal facets are synthesized via a distinctive organoamines-assisted biomimetic route. These novel HA nanotubes exhibit exceptional performance in stimulating osteoblast proliferation, which gives them intriguing potential for bone repair.

Two-dimensional (2D) materials have attracted great attention due to their unique physical and chemical properties derived from the dimensionality effect and modulation in their band structure. Herein, an important industrial catalytic material, gamma alumina (γ-Al2O3) with well-defined two-dimensional nanosheet structure was fabricated by a designed crown ether induced assembly approach. The obtained γ-Al2O3 nanosheets with a thickness of ∼4 nm possess high surface area (351 m2/g) and 16% pentacoordinate Al3+ sites which are the main catalytic active sites for ethanol dehydration to ethylene, compared to almost no pentacoordinate Al3+ sites for the commercial γ-Al2O3 nanoparticles. Furtherly, systematical investigation reveals that the crown ether plays the key role in the assembly of nanosheet structure. As a catalyst for ethanol dehydration to ethylene, the obtained alumina nanosheets with easily-accessible surface and more active sites, exhibit a superior catalytic performance to the commercial alumina with a much higher yield at large space velocity.

The construction of earth-abundant and non-noble-metal-based oxygen evolution reaction (OER) electrocatalysts that could work effectively with long-term stability in alkaline electrolyte is of prim...

Benefiting from the development of molecular electronics and molecular plasmonics, the interplay of light and electronic transport in molecular junctions has attracted growing interest among researchers in both fields, leading to a new research direction of “single-molecule optoelectronics”. Here, we review the latest developments of photo-modulated charge transport, electroluminescence and Raman spectroscopy from single-molecule junctions, and suggest future directions for single-molecule optoelectronics.

The present work investigated the effect of reduction-oxidation(R-O) pretreatment on the CO oxidation activity of Co3O4/Al2O3 catalyst. After the reduction-oxidation treatment, the crystalline size of Co3O4 supported on the Al2O3 decreased and it exposed more Co3+, resulting in the improvement of CO oxidation activity. Compared with the as-prepared conventional Co3O4/Al2O3 catalyst, the Co3O4/Al2O3-R-O catalyst is easy to be reduced at lower temperature. The surface reconstruction occurred during the reduction-oxidation pretreatment accounting for the improvement of the catalytic activity. This study reveals the importance of R-O pretreatment as a strategy for the improvement of supported metal oxide catalyst with advanced catalytic performance.

Two kinds of warm-toned (yellow/orange-emitting) long-lasting phosphorescent composites, namely, SiO2/red-emitting color converter@SrAl2O4:Eu2+, Dy3+ (SiO2/RECC@SAOED) and PMMA/red-emitting color converter@SrAl2O4:Eu2+, Dy3+ (PMMA/RECC@SAOED), were prepared in this study. Their morphological and luminescent properties were compared with those of the uncoated SAOED phosphor and analyzed in detail. SiO2/RECC@SAOED and PMMA/RECC@SAOED particles presented a coarse surface with an increased diameter of 12 µm. In addition to the first emission peak at 525 nm similar to that of the uncoated SAOED, an emission peak occurred in the emission spectra of SiO2/RECC@SAOED and PMMA/RECC@SAOED at 610 and 612 nm, respectively. The chromaticity coordinates of SiO2/RECC@SAOED and PMMA/RECC@SAOED moved to the yellow (x = 0.3769, y = 0.5006) and orange (x = 0.4647, y = 0.4671) areas compared with those of the uncoated SAOED in the green area (x = 0.2781, y = 0.5777). The afterglow decay curve revealed that the afterglow property of SiO2/RECC@SAOED was better than that of PMMA/RECC@SAOED.

With the successful preparation of γ-alumina with high-energy external surfaces such as {111} facets, the crystal-facet effect of γ-Al2O3 on surface-loaded CrOx has been explored for semihydrogenat...