Publications by authors named "Changdong Qin"

Article Synopsis
  • High-capacity electrodes struggle with cycling stability due to particle fragmentation and electrolyte decomposition leading to failures in the conductive network and solid electrolyte interphase (SEI) formation.
  • The introduction of selenium (Se) as a self-adjusting electrolyte additive helps create a novel triple-layer SEI on high-capacity FeS anodes, enhancing sodium storage stability and efficiency.
  • The unique triple-layer SEI reduces electrolyte consumption and gas evolution, resulting in an impressive lifespan of 6000 cycles at high current rates while also being applicable to other high-capacity anodes like SnS.
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Surface modification is an effective approach for overcoming the interfacial degradations to enable high electrochemical performance of battery materials, yet it is still challenging to realize high-quality surface modification with simple processing, low cost, and mass production. Herein, a thermal-induced surface precipitation phenomenon is reported in a Ti-dopped LiCoO , which can realize an ultrathin (≈5 nm) and uniform surface modification by a simple annealing process. It is revealed that surface Li-deficiency enables bulk Ti to precipitate and segregate on the non-(003) surface facets, forming a Ti-enriched disordered layered structure.

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The structural studies of macromolecules in their physiological context, particularly in tissue, is constrained by the bottleneck of sample preparation. In this study, we present a practical pipeline for preparing multicellular samples for cryo-electron tomography. The pipeline comprises sample isolation, vitrification, and lift-out-based lamella preparation using commercially available instruments.

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Folate (vitamin B) is the coenzyme involved in one-carbon transfer biochemical reactions essential for cell survival and proliferation, with its inadequacy causing developmental defects or severe diseases. Notably, mammalian cells lack the ability to de novo synthesize folate but instead rely on its intake from extracellular sources via specific transporters or receptors, among which SLC19A1 is the ubiquitously expressed one in tissues. However, the mechanism of substrate recognition by SLC19A1 remains unclear.

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Article Synopsis
  • Oxide semiconductors play a crucial role in technologies like displays and solar cells, but developing high mobility p-type versions has been challenging due to their valence band structure.
  • The study modifies the valence band of perovskite Ba BiMO (where M = Bi, Nb, Ta) using Bi 6s states, achieving high hole mobility up to 21 cm²/Vs and varying optical bandgaps from 1.5 to 3.2 eV.
  • Advanced techniques like x-ray photoemission and density functional theory enhance understanding of the electronic structure, revealing that strong interactions between Bi 6s and O 2p help achieve low hole effective masses and enabling promising applications in high-quality electronic devices.
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High initial coulombic efficiency is highly desired because it implies effective interface construction and few electrolyte consumption, indicating enhanced batteries' life and power output. In this work, a high-capacity sodium storage material with FeS nanoclusters (≈1-2 nm) embedded in N, S-doped carbon matrix (FeS /N,S-C) was synthesized, the surface of which displays defects-repaired characteristic and detectable dot-matrix distributed Fe-N-C/Fe-S-C bonds. After the initial discharging process, the uniform ultra-thin NaF-rich (≈6.

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Size and crystallinity of building units in the perovskite layer are of great significance to photovoltaic performance. Thus, to fabricate large-grain-size perovskite materials with the advantage of good crystallinity is quite necessary. The oriented attachment strategy has been proofed as an efficient method to control crystal growth.

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Architecting grain crystallographic orientation can modulate charge distribution and chemomechanical properties for enhancing the performance of polycrystalline battery materials. However, probing the interplay between charge distribution, grain crystallographic orientation, and performance remains a daunting challenge. Herein, we elucidate the spatially resolved charge distribution in lithium layered oxides with different grain crystallographic arrangements and establish a model to quantify their charge distributions.

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