163 results match your criteria: "Institute of Atomic and Molecular Science[Affiliation]"

Hot electrons (HEs) represent out-of-equilibrium carriers that are capable of facilitating reactions which are inaccessible under conventional conditions. Despite the similarity of the HE process to catalysis, optimization strategies such as orbital alignment and adsorption kinetics have not received significant attention in enhancing the HE-driven reaction yield. Here, we investigate catalytic effects in HE-driven reactions using a compositional catalyst modification (CCM) approach.

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Article Synopsis
  • Lithium-sulfur (Li-S) batteries are gaining interest for their high energy density and eco-friendliness, but issues like the shuttle effect of lithium polysulfides (LiPSs) and inefficient sulfur use hinder their practical use.
  • A new catalyst, created from a metal-organic framework (MOF), has been developed to improve LiPSs management, enhancing both their immobilization and conversion in Li-S batteries.
  • Tests show that the new catalyst significantly boosts battery performance, achieving an initial discharge capacity of 1752.1 mAh/g and maintaining a high efficiency with minimal capacity decay over 1000 cycles.
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  • - A new type of nanowire array made of CoNiP combines both amorphous and crystalline structures, with about 14.5% of it being amorphous, creating unique interfaces that may enhance performance.
  • - The (a-c)CoNiP catalyst shows impressively low overpotentials (38 mV in acid and 64 mV in alkaline) for hydrogen evolution, comparable to the commercial Pt/C catalyst, which requires 35 mV and 55 mV respectively.
  • - The catalyst's amorphous interface provides better corrosion resistance and performance at high current densities than the Pt/C catalyst in both acidic and alkaline environments, indicating its potential for use in commercial hydrogen production.
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Platinum group metals (PGM) have yet to be the most active catalysts in various sustainable energy reactions. Their high cost, however, has made maximizing the activity and minimizing the dosage become an urgent priority for the practical applications of emerging technologies. Herein, a novel 2D Pd nanomesh structure possessing hole inner reconstructed edges (HIER) with exposed high energy facets and overstretched lattice parameters is fabricated through a facile room-temperature reduction method at gram-scale yields.

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Solid-state electrolytes have received widespread attention for solving the problem of the leakage of liquid electrolytes and effectively improving the overall performance of supercapacitors. However, the electrochemical performance and environmental friendliness of solid-state electrolytes still need to be further improved. Here, a binary biomass-based solid electrolyte film (LSE) was successfully synthesized through the incorporation of lignin nanoparticles (LNPs) with sodium alginate (SA).

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Facilely Achieving Near-Infrared-II J-Aggregates through Molecular Bending on a Donor-Acceptor Fluorophore for High-Performance Tumor Phototheranostics.

ACS Nano

October 2024

Center of Super-Diamond and Advanced Films (COSDAF), Department of Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon 999077, Hong Kong SAR, P. R. China.

Constructing J-aggregated organic dyes represents a promising strategy for obtaining biomedical second near-infrared (NIR-II) emissive materials, as they exhibit red-shifted spectroscopic properties upon assembly into nanoparticles (NPs) in aqueous environments. However, currently available NIR-II J-aggregates primarily rely on specific molecular backbones with intricate design strategies and are susceptible to fluorescence quenching during assembly. A facile approach for constructing bright NIR-II J-aggregates using prevalent donor-acceptor (D-A) molecules is still lacking.

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Surface reconstruction plays an essential role in electrochemical catalysis. The structures, compositions, and functionalities of the real catalytic species and sites generated by reconstruction, however, are yet to be clearly understood, for the metastable or transit state of most reconstructed structures. Herein, a series of NiFe oxalates (NiFe CO, x = 1, 0.

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Recent advances in developing nanoscale electro-/photocatalysts for hydrogen production: modification strategies, charge-carrier characterizations, and applications.

Nanoscale

October 2024

School of Energy and Environment, Department of Materials Science and Engineering, Centre for Functional Photonics (CFP), City University of Hong Kong, Kowloon Tong, Hong Kong, China.

Article Synopsis
  • Clean hydrogen production through electrocatalysis and photocatalysis is seen as a key solution to the energy crisis, but finding effective catalysts remains a challenge.
  • The review highlights advanced nanoscale electrocatalysts and photocatalysts designed for various reaction settings, like acidic and alkaline electrolytes and seawater, and discusses modification techniques to enhance performance.
  • It also explores the properties and mechanisms of these catalysts in improving hydrogen production, concluding with insights into future advancements in this field.
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  • This study investigates how ferroelectric catalysts can change their catalytic activities by switching electric polarizations, using layered bismuth oxyselenide (L-BiOSe) microreactors.
  • It introduces a new method called selective-area ionic liquid gating to control the direction of dipole orientation in L-BiOSe, leading to variations in catalytic reactions, with upward polarization favoring oxygen evolution and downward polarization favoring hydrogen evolution.
  • The research demonstrates that by integrating L-BiOSe microreactors with different polarizations, it is possible to achieve overall water splitting, highlighting the potential for designing catalysts that can switch surface polarizations.
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The design and construction of highly efficient electrocatalysts for overall water splitting and urea electrolysis are significantly important for promoting energy conversion and realizing green hydrogen production. In this work, we constructed a multi-phase heterojunction through a simple hydrothermal and phosphorization process. The P-doped NiFeO (P-NiFeO) nanoparticles were uniformly anchored on the bamboo-like N-doped carbon nanotubes (NCNTs) grown via a NiFe-alloy autocatalysis.

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Organic nano carbon source inducing 3D silica nanoparticles-graphene nanosheet layer on Cu current collector for high-performance anode-free lithium metal batteries.

J Colloid Interface Sci

October 2024

Materials Institute of Atomic and Molecular Science, School of Physics & Information Science, Shaanxi University of Science and Technology, Xi'an 710021, China; Key Laboratory of Interface Science and Engineering in Advanced Materials, Ministry of Education, Taiyuan University of Technology, Taiyuan, Shanxi 030024, China; Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering, Taiyuan, Shanxi 030024, China. Electronic address:

Anode-free lithium metal batteries (AFLBs) have attracted considerable attention due to their high theoretical specific capacity and absence of Li. However, the heterogeneous Li deposition and stripping on the lithiophobic Cu collector hamper AFLBs in practice. To achieve a uniform and reversible Li deposition, a carbon-based layer on the Cu collector has attracted intense interest due to its high conductivity.

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Ultranarrow Deep-Blue Luminescence of Perovskite Nanocrystals by A-Site Cation Control.

ACS Appl Mater Interfaces

June 2024

State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Northwestern Polytechnical University and Shaanxi Joint Laboratory of Graphene, Xi'an 710072, China.

Metal-halide perovskite nanocrystals (NCs) are one of the most promising emitters for the application of display and nanolight sources. The full width at half-maximum (FWHM) of photoluminescence (PL) emission is essential for color purity, which however remains a difficulty to further reduce the FWHM of the perovskite NCs at room temperature. Here, we show the quasi-sphere perovskite NCs with narrow PL emission at a deep-blue wavelength of ∼430 nm; its PL FWHM reaches ∼11 nm at room temperature, owing to the monodispersion in size distribution as well as the symmetric quasi-sphere morphology of NCs releasing the fine structure splitting-induced inhomogeneous broadening.

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Molecular Probing of the Microscopic Pressure at Contact Interfaces.

J Am Chem Soc

May 2024

van 't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, The Netherlands.

Obtaining insights into friction at the nanoscopic level and being able to translate these into macroscopic friction behavior in real-world systems is of paramount importance in many contexts, ranging from transportation to high-precision technology and seismology. Since friction is controlled by the local pressure at the contact it is important to be able to detect both the real contact area and the nanoscopic local pressure distribution simultaneously. In this paper, we present a method that uses planarizable molecular probes in combination with fluorescence microscopy to achieve this goal.

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Over the past few decades, the critical role played by cellular contractility associated mechanotransduction in the regulation of cell functions has been revealed. In this case, numerous biomaterials have been chemically or structurally designed to manipulate cell behaviors through the regulation of cellular contractility. In particular, adhesive proteins including fibronectin, poly-L-lysine and collagen type I have been widely applied in various biomaterials to improve cell adhesion.

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Two 2,7-dicyaonfluorene-based molecules 27-DCN and 27-tDCN are utilized as acceptors (A) to combine with hexaphenylbenzene-centered donors (D) TATT and DDT-HPB for probing the exciplex formation. The photophysical characteristics reveal that the steric hindered 27-tDCN not only can increase the distance of D and A, resulting in a hypsochromic emission, but also dilute the concentration of triplet excitons to suppress non-radiative process. The 27-tDCN-based exciplex-forming blends exhibit better photoluminescence quantum yield (PLQY) as compared to those of 27-DCN-based pairs.

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The design and synthesis of efficient, inexpensive, and long-term stable heterostructured electrocatalysts with high-density dislocations for hydrogen evolution reaction in alkaline media and seawater are still a great challenge. An amorphous/crystalline/amorphous sandwiched structure with abundant dislocations were synthesized through thermal phosphidation strategies. The dislocations play an important role in the hydrogen evolution reactions.

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TiO nanotube arrays-based photoelectrocatalyst: Tri-Doping engineering and carbon coating engineering boosting visible activity, and stable hydrogen evolution.

J Colloid Interface Sci

March 2024

Materials Institute of Atomic and Molecular Science, Shaanxi University of Science and Technology, Xi'an 710021, PR China; Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering, Taiyuan 030024, PR China. Electronic address:

The integration of non-metallic doping and carbon coating for TiO-based photoelectrocatalysts can be recognized as a promising strategy to enhance their hydrogen production performance. To this end, this study explored the carbon coating engineering to induce stable multi-element doping with an aim to develop high-performance TiO nanotube array-based photoelectrocatalysts. The resulting structures consisted of carbon-nitrogen-sulfur-tri-doped TiO nanotube arrays with a nitrogen-sulfur-codoped carbon coating (CNS-TNTA/NSC).

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Atomically thin two-dimensional (2D) materials have emerged as promising candidates for efficient energy harvesting from ionic gradients. However, the exploration of robust 2D atomically thin nanopore membranes, which hold sufficient ionic selectivity and high ion permeability, remains challenging. Here, the single-layer hexagonal boron nitride (hBN) nanopores are demonstrated as various high-performance ion-gradient nanopower harvesters.

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Lithium-sulfur (Li-S) batteries have ultrahigh theoretical specific capacity and energy density, which are considered to be very promising energy storage devices. However, the slow redox kinetics of polysulfides are the main reason for the rapid capacity decay of Li-S batteries. A reasonable electrocatalyst for the Li-S battery should reduce the reaction barrier and accelerate the reaction kinetics of the bidirectional catalytic conversion of lithium polysulfides (LiPSs), thereby reducing the cumulative concentration of LiPSs in the electrolyte.

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Artificial Optoelectronic Synapse Based on Violet Phosphorus Microfiber Arrays.

Small

March 2024

CAS Center for Excellence in Nanoscience, Beijing Key Laboratory of Micro-nano Energy and Sensor, Beijing Institute of Nanoenergy and Nanosystems, Chinese Academy of Sciences, Beijing, 101400, P. R. China.

Memristor-based artificial synapses are regarded as the most promising candidate to develop brain-like neuromorphic network computers and overcome the bottleneck of Von-Neumann architecture. Violet phosphorus (VP) as a new allotrope of available phosphorus with outstanding electro-optical properties and stability has attracted more and more attention in the past several years. In this study, large-scale, high-yield VP microfiber vertical arrays have been successfully developed on a Sn-coated graphite paper and are used as the memristor functional layers to build reliable, low-power artificial synaptic devices.

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Single-atomic transition metal-nitrogen-carbon (M-N-C) structures are promising alternatives toward noble-metal-based catalysts for oxygen reduction reaction (ORR) catalysis involved in sustainable energy devices. The symmetrical electronic density distribution of the M─N moieties, however, leads to unfavorable intermediate adsorption and sluggish kinetics. Herein, a Fe-N-C catalyst with electronic asymmetry induced by one nearest carbon vacancy adjacent to Fe─N is conceptually produced, which induces an optimized d-band center, lowered free energy barrier, and thus superior ORR activity with a half-wave potential (E ) of 0.

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In situ lithiation modulation of LiNiCoMnO as bifunctional electrocatalysts for highly efficient overall water splitting.

J Colloid Interface Sci

January 2024

Materials Institute of Atomic and Molecular Science, Shaanxi University of Science and Technology, Xi'an 710021, China; Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering, Taiyuan 030000, China; Key Laboratory of Interface Science and Engineering in Advanced Materials, Taiyuan University of Technology, Taiyuan 030024, China. Electronic address:

LiNiCoMnO (NCM811) is a common cathode material in lithium-ion batteries (LIBs), and the ever-increasing consumption of large quantities of LIBs raises critical concerns about their recycling. Herein, we propose an in-situ lithiation route to tune the structure and electrocatalytic properties of NCM811 by Li intercalation and exfoliation in LIBs. In this strategy, the morphology and microstructure of the lithiated NCM811 can be controlled by a specified discharge voltage.

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Three organic conjugated small molecules, , , and comprising an antiaromatic 5,10-ditolylphenazine (DTPZ) core and electron-donating peripheral substituents with high HOMOs (-4.2 to -4.7 eV) and multiple reversible oxidative potentials are reported.

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Quantum-well intermixing (QWI) technology is commonly considered as an effective methodology to tune the post-growth bandgap energy of semiconductor composites for electronic applications in diode lasers and photonic integrated devices. However, the specific influencing mechanism of the interfacial strain introduced by the dielectric-layer-modulated multiple quantum well (MQW) structures on the photoluminescence (PL) property and interfacial quality still remains unclear. Therefore, in the present study, different thicknesses of SiO-layer samples were coated and then annealed under high temperature to introduce interfacial strain and enhance atomic interdiffusion at the barrier-well interfaces.

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Dye-sensitized solar cells (DSSCs) have emerged as a potential candidate for third-generation thin film solar energy conversion systems because of their outstanding optoelectronic properties, cost-effectiveness, environmental friendliness, and easy manufacturing process. The electron transport layer is one of the most essential components in DSSCs since it plays a crucial role in the device's greatest performance. Silver ions as a dopant have drawn attention in DSSC device applications because of their stability under ambient conditions, decreased charge recombination, increased efficient charge transfer, and optical, structural, and electrochemical properties.

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