Publications by authors named "Jingcong Hu"

The charge density wave (CDW), a charge ordering phase, offers a valuable framework for exploring electron-electron interactions, electron-phonon coupling, and quantum phase transitions. In CDW materials, carrier density substantially influences the ground state, typically altered through foreign ion doping and investigated at macro- or mesoscopic scales via photoemission or transport techniques. However, atomic-scale visualization, particularly in doped CDW systems without foreign ions, remains rare.

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The broad bandgap tunability of both perovskites and organic semiconductors enables the development of perovskite-organic tandem solar cells with promising theoretical efficiency. However, the certified efficiencies of reported perovskite-organic tandem solar cells remain lower than those of single-junction perovskite solar cells, primarily because of insufficient near-infrared photocurrent in narrow-bandgap organic subcells. Here we design and synthesize an asymmetric non-fullerene acceptor (NFA), P2EH-1V, featuring a unilateral conjugated π-bridge to reduce the optical bandgap to 1.

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Superlattices (SLs) based on colloidal nanocrystals (NCs) represent a fascinating structure with long-range and ordered NCs inside the assembled superstructures, displaying great potential application in electronic devices because of the customizable arrangement of building blocks. It is a great challenge to achieve macroscopical SL films by a solution process due to the inherent sensitivity and difficulty in controlling colloidal NCs. In this study, we propose a controllable strategy to create perovskite CsPbBr NC SL films through a surface in situ cross-linking reaction incorporating conjugated linoleic acid (CLA), a naturally polymerizable small molecule.

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Rapid bulk charge recombination and mediocre surface catalytic sites harshly restrict the photocatalytic activities. Herein, the aforementioned concerns are well addressed by coupling macroscopic spontaneous polarization and atomic-site engineering of CdS single-crystal nanorods for superb H photo-production. The oriented growth of CdS nanorods along the polar axis, vectorially superimposing substantial polar units with orderly arrangement, renders a strong polarization electric field (20.

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Cu-based catalysts are promising candidates for CO reduction owing to the favorable energetics of Cu sites for CO adsorption and transformation. However, CO reduction involving insurmountable activation barriers and various byproducts remains a significant challenge to achieve high activity and selectivity. Herein, a photocatalyst constructed with single-Ru-site-on-Cu-nanoparticle on BiTiO exhibits exceptional activity and selectivity for CO conversion to CO.

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High carrier separation efficiency and rapid surface catalytic reaction are crucial for enhancing catalytic CO photoreduction reaction. Herein, integrated surface decoration strategy with oxygen vacancies (Ov) and anchoring CuO (1 < x < 2) nanodots below 10 nm is realized on BiMoO for promoting CO photoreduction performance. The charge interaction between Ov and anchored CuO enables the formation of enhanced internal electric field, which provides a strong driving force for accelerating the separation of photocharge carriers on the surface of BiMoO (η ≈71%).

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The development of pure-blue perovskite light-emitting diodes (PeLEDs) faces challenges of spectral stability and low external quantum efficiency (EQE) due to phase separation in mixed halide compositions. Perovskite quantum dots (QDs) with strong confinement effects are promising alternatives to achieve high-quality pure-blue PeLEDs, yet their performance is often hindered by the poor size distribution and high trap density. A strategy combining thermodynamic control with a polishing-driven ligand exchange process to produce high-quality QDs is developed.

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Article Synopsis
  • Efficient pure-red emission LEDs are crucial for high-definition displays, but challenges like phase segregation and spectral instability complicate their development.
  • A novel method using a benzene-series solvent instead of traditional ones prevents contamination and enhances the dissolution of halides, leading to the creation of precisely sized CsPbI quantum dots (QDs).
  • These optimized QDs result in PeLEDs that achieve pure-red electroluminescence nearing Rec. 2020 standards, with impressive efficiency metrics.
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Single-atom catalysts show excellent catalytic performance because of their coordination environments and electronic configurations. However, controllable regulation of single-atom permutations still faces challenges. Herein, we demonstrate that a polarization electric field regulates single atom permutations and forms periodic one-dimensional Au single-atom arrays on ferroelectric BiTiO nanosheets.

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Article Synopsis
  • Developing new methods for creating durable single-atom catalysts (SACs) from precious metals is tough for industrial use.
  • The strategy involves using bimetallic nanocrystals to convert noble metals into single atoms that bind to aluminum oxide, enhancing stability and creating many anchoring sites.
  • The resulting Pd/AlCoO-AlO catalyst demonstrates improved performance at lower temperatures and excellent stability during tough conditions, making it promising for pollution control.
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The slow charge dynamics and large activation energy of CO severely hinder the efficiency of CO photoreduction. Defect engineering is a well-established strategy, while the function of common zero-dimensional defects is always restricted to promoting surface adsorption. In this work, a gradient layer of tungsten vacancies with a thickness of 3-4 nm is created across Bi WO nanosheets.

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Atomic-scale ferroelectrics are of great interest for high-density electronics, particularly field-effect transistors, low-power logic, and nonvolatile memories. We devised a film with a layered structure of bismuth oxide that can stabilize the ferroelectric state down to 1 nanometer through samarium bondage. This film can be grown on a variety of substrates with a cost-effective chemical solution deposition.

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Developing efficient piezocatalytic systems for two-electron water splitting (TEWS) with producing H and H O shows great promise to meet the industrial demand. Herein, Ag single atoms (SAs) and clusters are co-anchored on carbon nitride (Ag -CN) to serve as the multifunctional sites for efficient TEWS. The Ag SAs enhance the in-plane piezoelectric polarization of CN that is intimately modulated by the atomic coordination induced charge redistribution, and Ag clusters afford strong interfacial electric field to remarkably promote the out-of-plane migration of piezoelectrons from CN.

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Preparation of highly efficient and stable perovskite light-emitting diodes (PeLEDs) with reproducible device performance is challenging. This protocol describes steps for fabrication of high-performance and self-healing PeLEDs. These include instructions for synthesis of charge-transporting zinc oxide (ZnO) nanocrystals, step-by-step device fabrication, and control over self-healing of the degraded devices.

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Titanium dioxide (TiO ) nanocrystals have attracted great attention in heterogeneous photocatalysis and photoelectricity fields for decades. However, contradicting conclusions on the crystallographic orientation and exposed facets of TiO nanocrystals frequently appear in the literature. Herein, using anatase TiO nanocrystals with highly exposed {001} facets as a model, the misleading conclusions that exist on anatase nanocrystals are clarified.

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Article Synopsis
  • To achieve a zero-carbon economy, advanced catalysts are needed for hydrogen production and biomass upgrading using renewable energy.
  • Nickel-based non-precious electrocatalysts are promising candidates, but understanding their site coordination is still a challenge.
  • The study focuses on creating different oxyanion-coordinated nickel oxyhydroxides through electrochemical oxidation, revealing that the specific coordination environment of NiOOH-PO enhances its catalytic activity for converting methanol to formate.
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Theoretical studies have shown that surface terminations, such as MAI or PbI layers, greatly affect the environmental stability of organic-inorganic perovskite. However, until now, there has been little effort to experimentally detect the existence of MAI or PbI terminations on MAPbI grains, let alone disclose their effects on the humidity degradation pathway of perovskite solar cell. Here, we successfully modified and detected the surface terminations of MAI and PbI species on polycrystalline MAPbI films.

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