
Chongqing University
UniversityChongqing, China
Research output, citation impact, and the most-cited recent papers from Chongqing University (China). Aggregated across the NobleBlocks index of 300M+ scholarly works.
Top-cited papers from Chongqing University
LiDAR-based or RGB-D-based object detection is used in numerous applications, ranging from autonomous driving to robot vision. Voxel-based 3D convolutional networks have been used for some time to enhance the retention of information when processing point cloud LiDAR data. However, problems remain, including a slow inference speed and low orientation estimation performance. We therefore investigate an improved sparse convolution method for such networks, which significantly increases the speed of both training and inference. We also introduce a new form of angle loss regression to improve the orientation estimation performance and a new data augmentation approach that can enhance the convergence speed and performance. The proposed network produces state-of-the-art results on the KITTI 3D object detection benchmarks while maintaining a fast inference speed.
A fast parallel thinning algorithm is proposed in this paper. It consists of two subiterations: one aimed at deleting the south-east boundary points and the north-west corner points while the other one is aimed at deleting the north-west boundary points and the south-east corner points. End points and pixel connectivity are preserved. Each pattern is thinned down to a "skeleton" of unitary thickness. Experimental results show that this method is very effective.
Cancer development and its response to therapy are regulated by inflammation, which either promotes or suppresses tumor progression, potentially displaying opposing effects on therapeutic outcomes. Chronic inflammation facilitates tumor progression and treatment resistance, whereas induction of acute inflammatory reactions often stimulates the maturation of dendritic cells (DCs) and antigen presentation, leading to anti-tumor immune responses. In addition, multiple signaling pathways, such as nuclear factor kappa B (NF-kB), Janus kinase/signal transducers and activators of transcription (JAK-STAT), toll-like receptor (TLR) pathways, cGAS/STING, and mitogen-activated protein kinase (MAPK); inflammatory factors, including cytokines (e.g., interleukin (IL), interferon (IFN), and tumor necrosis factor (TNF)-α), chemokines (e.g., C-C motif chemokine ligands (CCLs) and C-X-C motif chemokine ligands (CXCLs)), growth factors (e.g., vascular endothelial growth factor (VEGF), transforming growth factor (TGF)-β), and inflammasome; as well as inflammatory metabolites including prostaglandins, leukotrienes, thromboxane, and specialized proresolving mediators (SPM), have been identified as pivotal regulators of the initiation and resolution of inflammation. Nowadays, local irradiation, recombinant cytokines, neutralizing antibodies, small-molecule inhibitors, DC vaccines, oncolytic viruses, TLR agonists, and SPM have been developed to specifically modulate inflammation in cancer therapy, with some of these factors already undergoing clinical trials. Herein, we discuss the initiation and resolution of inflammation, the crosstalk between tumor development and inflammatory processes. We also highlight potential targets for harnessing inflammation in the treatment of cancer.
autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field.
Developing highly efficient catalysts for the oxygen reduction reaction (ORR) is key to the fabrication of commercially viable fuel cell devices and metal-air batteries for future energy applications. Herein, we review the most recent advances in the development of Pt-based and Pt-free materials in the field of fuel cell ORR catalysis. This review covers catalyst material selection, design, synthesis, and characterization, as well as the theoretical understanding of the catalysis process and mechanisms. The integration of these catalysts into fuel cell operations and the resulting performance/durability are also discussed. Finally, we provide insights into the remaining challenges and directions for future perspectives and research.
Grain refinement can make conventional metals several times stronger, but this comes at dramatic loss of ductility. Here we report a heterogeneous lamella structure in Ti produced by asymmetric rolling and partial recrystallization that can produce an unprecedented property combination: as strong as ultrafine-grained metal and at the same time as ductile as conventional coarse-grained metal. It also has higher strain hardening than coarse-grained Ti, which was hitherto believed impossible. The heterogeneous lamella structure is characterized with soft micrograined lamellae embedded in hard ultrafine-grained lamella matrix. The unusual high strength is obtained with the assistance of high back stress developed from heterogeneous yielding, whereas the high ductility is attributed to back-stress hardening and dislocation hardening. The process discovered here is amenable to large-scale industrial production at low cost, and might be applicable to other metal systems.
A facile approach for preparation of photoluminescent (PL) carbon dots (CDs) is reported. The three resulting CDs emit bright and stable red, green and blue (RGB) colors of luminescence, under a single ultraviolet-light excitation. Alterations of PL emission of these CDs are tentatively proposed to result from the difference in their particle size and nitrogen content. Interestingly, up-conversion (UC)PL of these CDs is also observed. Moreover, flexible full-color emissive PVA films can be achieved through mixing two or three CDs in the appropriate ratios. These CDs also show low cytotoxicity and excellent cellular imaging capability. The facile preparation and unique optical features make these CDs potentially useful in numerous applications such as light-emitting diodes, full-color displays, and multiplexed (UC)PL bioimaging.
Understanding the origin of high activity of Fe-N-C electrocatalysts in oxygen reduction reaction (ORR) is critical but still challenging for developing efficient sustainable nonprecious metal catalysts in fuel cells and metal-air batteries. Herein, we developed a new highly active Fe-N-C ORR catalyst containing Fe-N(x) coordination sites and Fe/Fe3C nanocrystals (Fe@C-FeNC), and revealed the origin of its activity by intensively investigating the composition and the structure of the catalyst and their correlations with the electrochemical performance. The detailed analyses unambiguously confirmed the coexistence of Fe/Fe3C nanocrystals and Fe-N(x) in the best catalyst. A series of designed experiments disclosed that (1) N-doped carbon substrate, Fe/Fe3C nanocrystals or Fe-N(x) themselves did not deliver the high activity; (2) the catalysts with both Fe/Fe3C nanocrystals and Fe-N(x) exhibited the high activity; (3) the higher content of Fe-N(x) gave the higher activity; (4) the removal of Fe/Fe3C nanocrystals severely degraded the activity; (5) the blocking of Fe-N(x) downgraded the activity and the recovery of the blocked Fe-N(x) recovered the activity. These facts supported that the high ORR activity of the Fe@C-FeNC electrocatalysts should be ascribed to that Fe/Fe3C nanocrystals boost the activity of Fe-N(x). The coexistence of high content of Fe-N(x) and sufficient metallic iron nanoparticles is essential for the high ORR activity. DFT calculation corroborated this conclusion by indicating that the interaction between metallic iron and Fe-N4 coordination structure favored the adsorption of oxygen molecule. These new findings open an avenue for the rational design and bottom-up synthesis of low-cost highly active ORR electrocatalysts.
Tremendous efforts have been dedicated into the development of high-performance energy storage devices with nanoscale design and hybrid approaches. The boundary between the electrochemical capacitors and batteries becomes less distinctive. The same material may display capacitive or battery-like behavior depending on the electrode design and the charge storage guest ions. Therefore, the underlying mechanisms and the electrochemical processes occurring upon charge storage may be confusing for researchers who are new to the field as well as some of the chemists and material scientists already in the field. This review provides fundamentals of the similarities and differences between electrochemical capacitors and batteries from kinetic and material point of view. Basic techniques and analysis methods to distinguish the capacitive and battery-like behavior are discussed. Furthermore, guidelines for material selection, the state-of-the-art materials, and the electrode design rules to advanced electrode are proposed.
Study of flexible nanodielectric materials (FNDMs) with high permittivity is one of the most active academic research areas in advanced functional materials. FNDMs with excellent dielectric properties are demonstrated to show great promise as energy-storage dielectric layers in high-performance capacitors. These materials, in common, consist of nanoscale particles dispersed into a flexible polymer matrix so that both the physical/chemical characteristics of the nanoparticles and the interaction between the nanoparticles and the polymers have crucial effects on the microstructures and final properties. This review first outlines the crucial issues in the nanodielectric field and then focuses on recent remarkable research developments in the fabrication of FNDMs with special constitutents, molecular structures, and microstructures. Possible reasons for several persistent issues are analyzed and the general strategies to realize FNDMs with excellent integral properties are summarized. The review further highlights some exciting examples of these FNDMs for power-energy-storage applications.
In the past two years, significant progresses have been achieved in high-performance cast and wrought magnesium and magnesium alloys, magnesium-based composites, advanced cast technologies, advanced processing technologies, and functional magnesium materials, such as Mg ion batteries, hydrogen storage Mg materials, bio-magnesium alloys, etc. Great contributions to the development of new magnesium alloys and their processing technologies have been made by Chongqing University, Shanghai Jiaotong University, Chinese Academy of Sciences, Helmholtz Zentrum Geesthacht, Queensland University, Brunel University, etc. This review paper is aimed to summarize the latest important advances in cast magnesium alloys, wrought magnesium alloys and functional magnesium materials worldwide in 2018–2019, including both the development of new materials and the innovation of their processing technologies. Based on the issues and challenges identified here, some future research directions are suggested, including further development of high-performance magnesium alloys having high strength and superior plasticity together with high corrosion resistance and low cost, and fundamental research on the phase diagram, diffusion, precipitation, etc., as well as the development of advanced welding and joining technology.
This article develops new deep learning methods, namely, deep residual shrinkage networks, to improve the feature learning ability from highly noised vibration signals and achieve a high fault diagnosing accuracy. Soft thresholding is inserted as nonlinear transformation layers into the deep architectures to eliminate unimportant features. Moreover, considering that it is generally challenging to set proper values for the thresholds, the developed deep residual shrinkage networks integrate a few specialized neural networks as trainable modules to automatically determine the thresholds, so that professional expertise on signal processing is not required. The efficacy of the developed methods is validated through experiments with various types of noise.
The photocatalytic performance of the star photocatalyst g-C3N4 was restricted by the low efficiency because of the fast charge recombination. The present work developed a facile in situ method to construct g-C3N4/g-C3N4 metal-free isotype heterojunction with molecular composite precursors with the aim to greatly promote the charge separation. Considering the fact that g-C3N4 samples prepared from urea and thiourea separately have different band structure, the molecular composite precursors of urea and thiourea were treated simultaneously under the same thermal conditions, in situ creating a novel layered g-C3N4/g-C3N4 metal-free heterojunction (g-g CN heterojunction). This synthesis method is facile, economic, and environmentally benign using easily available earth-abundant green precursors. The confirmation of isotype g-g CN heterojunction was based on XRD, HRTEM, valence band XPS, ns-level PL, photocurrent, and EIS measurement. Upon visible-light irradiation, the photogenerated electrons transfer from g-C3N4 (thiourea) to g-C3N4 (urea) driven by the conduction band offset of 0.10 eV, whereas the photogenerated holes transfer from g-C3N4 (urea) to g-C3N4 (thiourea) driven by the valence band offset of 0.40 eV. The potential difference between the two g-C3N4 components in the heterojunction is the main driving force for efficient charge separation and transfer. For the removal of NO in air, the g-g CN heterojunction exhibited significantly enhanced visible light photocatalytic activity over g-C3N4 alone and physical mixture of g-C3N4 samples. The enhanced photocatalytic performance of g-g CN isotype heterojunction can be directly ascribed to efficient charge separation and transfer across the heterojunction interface as well as prolonged lifetime of charge carriers. This work demonstrated that rational design and construction of isotype heterojunction could open up a new avenue for the development of new efficient visible-light photocatalysts.
Underwater wireless communications refer to data transmission in unguided water environment through wireless carriers, i.e., radio-frequency (RF) wave, acoustic wave, and optical wave. In comparison to RF and acoustic counterparts, underwater optical wireless communication (UOWC) can provide a much higher transmission bandwidth and much higher data rate. Therefore, we focus, in this paper, on the UOWC that employs optical wave as the transmission carrier. In recent years, many potential applications of UOWC systems have been proposed for environmental monitoring, offshore exploration, disaster precaution, and military operations. However, UOWC systems also suffer from severe absorption and scattering introduced by underwater channels. In order to overcome these technical barriers, several new system design approaches, which are different from the conventional terrestrial free-space optical communication, have been explored in recent years. We provide a comprehensive and exhaustive survey of the state-of-the-art UOWC research in three aspects: 1) channel characterization; 2) modulation; and 3) coding techniques, together with the practical implementations of UOWC.
We systematically summarize the recent progress in the green synthesis and formation mechanism of CDs with the hope to provide guidance for developing CDs with the concept of green chemistry. In addition, we discuss and organize the current opinions on the fluorescence origin of CDs and the latest progress of CDs in fluorescence sensing applications.
The Jiangmen Underground Neutrino Observatory (JUNO), a 20 kton multi-purpose\nunderground liquid scintillator detector, was proposed with the determination\nof the neutrino mass hierarchy as a primary physics goal. It is also capable of\nobserving neutrinos from terrestrial and extra-terrestrial sources, including\nsupernova burst neutrinos, diffuse supernova neutrino background, geoneutrinos,\natmospheric neutrinos, solar neutrinos, as well as exotic searches such as\nnucleon decays, dark matter, sterile neutrinos, etc. We present the physics\nmotivations and the anticipated performance of the JUNO detector for various\nproposed measurements. By detecting reactor antineutrinos from two power plants\nat 53-km distance, JUNO will determine the neutrino mass hierarchy at a 3-4\nsigma significance with six years of running. The measurement of antineutrino\nspectrum will also lead to the precise determination of three out of the six\noscillation parameters to an accuracy of better than 1\\%. Neutrino burst from a\ntypical core-collapse supernova at 10 kpc would lead to ~5000\ninverse-beta-decay events and ~2000 all-flavor neutrino-proton elastic\nscattering events in JUNO. Detection of DSNB would provide valuable information\non the cosmic star-formation rate and the average core-collapsed neutrino\nenergy spectrum. Geo-neutrinos can be detected in JUNO with a rate of ~400\nevents per year, significantly improving the statistics of existing geoneutrino\nsamples. The JUNO detector is sensitive to several exotic searches, e.g. proton\ndecay via the $p\\to K^++\\bar\\nu$ decay channel. The JUNO detector will provide\na unique facility to address many outstanding crucial questions in particle and\nastrophysics. It holds the great potential for further advancing our quest to\nunderstanding the fundamental properties of neutrinos, one of the building\nblocks of our Universe.
Graphitic carbon nitride (g-C3N4) has been widely investigated and applied in photocatalysis and catalysis, but its performance is still unsatisfactory. Here, we demonstrated that K-doped g-C3N4 with a unique electronic structure possessed highly enhanced visible-light photocatalytic performance for NO removal, which was superior to Na-doped g-C3N4. DFT calculations revealed that K or Na doping can narrow the bandgap of g-C3N4. K atoms, intercalated into the g-C3N4 interlayer via bridging the layers, could decrease the electronic localization and extend the π conjugated system, whereas Na atoms tended to be doped into the CN planes and increased the in-planar electron density. On the basis of theoretical calculation results, we synthesized K-doped g-C3N4 and Na-doped g-C3N4 by a facile thermal polymerization method. Consistent with the theoretical prediction, it was found that K was intercalated into the space between the g-C3N4 layers. The K-intercalated g-C3N4 sample showed increased visible-light absorption, efficient separation of charge carriers, and strong oxidation capability, benefiting from the narrowed band gap, extended π conjugated systems, and positive-shifted valence band position, respectively. Despite that the Na-doped g-C3N4 exhibited narrowed bandgap, the high recombination rate of carriers resulted in the reduced photocatalytic performance. Our discovery provides a promising route to manipulate the photocatalytic activity simply by introducing K atoms in the interlayer and gains a deep understanding of doping chemistry with congeners. The present work could provide new insights into the mechanistic understanding and the design of electronically optimized layered photocatalysts for enhanced solar energy conversion.
Mitochondria are organelles that are able to adjust and respond to different stressors and metabolic needs within a cell, showcasing their plasticity and dynamic nature. These abilities allow them to effectively coordinate various cellular functions. Mitochondrial dynamics refers to the changing process of fission, fusion, mitophagy and transport, which is crucial for optimal function in signal transduction and metabolism. An imbalance in mitochondrial dynamics can disrupt mitochondrial function, leading to abnormal cellular fate, and a range of diseases, including neurodegenerative disorders, metabolic diseases, cardiovascular diseases and cancers. Herein, we review the mechanism of mitochondrial dynamics, and its impacts on cellular function. We also delve into the changes that occur in mitochondrial dynamics during health and disease, and offer novel perspectives on how to target the modulation of mitochondrial dynamics.
Mesenchymal stem cells (MSCs) are multilineage cells with the ability to self-renew and differentiate into a variety of cell types, which play key roles in tissue healing and regenerative medicine. Bone marrow-derived mesenchymal stem cells (BMSCs) are the most frequently used stem cells in cell therapy and tissue engineering. However, it is prerequisite for BMSCs to mobilize from bone marrow and migrate into injured tissues during the healing process, through peripheral circulation. The migration of BMSCs is regulated by mechanical and chemical factors in this trafficking process. In this paper, we review the effects of several main regulatory factors on BMSC migration and its underlying mechanism; discuss two critical roles of BMSCs-namely, directed differentiation and the paracrine function-in tissue repair; and provide insight into the relationship between BMSC migration and tissue repair, which may provide a better guide for clinical applications in tissue repair through the efficient regulation of BMSC migration.
In recent years, gas sensors have been increasingly used in industrial production and daily life. Metal oxide semiconductor gas sensing materials are favoured for their outstanding physical and chemical properties, low cost and simple preparation methods. However, the gas sensing mechanisms of metal oxide semiconductors have not been considered by researchers, resulting in omissions and errors in the interpretation of gas sensing mechanisms in many articles. This review organizes and introduces several common gas sensing mechanisms of metal oxide semiconductors in detail and classifies them into two categories. The scope and relationship of these mechanisms are clarified. In addition, this review selects four strategies for enhancing the gas sensing properties of metal oxide semiconductors and analyses the gas sensing mechanisms to highlight the importance of the gas sensing mechanism. Finally, some perspectives for future investigations on the gas sensing mechanisms of metal oxide semiconductors are discussed as well.