Qian Jiang

ORCID: 0009-0003-4107-7151
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About
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Research Areas
  • Catalytic Processes in Materials Science
  • Atmospheric chemistry and aerosols
  • Electrocatalysts for Energy Conversion
  • Supramolecular Self-Assembly in Materials
  • Catalysts for Methane Reforming
  • Atmospheric Ozone and Climate
  • Fuel Cells and Related Materials
  • Air Quality and Health Impacts
  • Synthesis and Catalytic Reactions
  • Plant responses to elevated CO2
  • Asymmetric Hydrogenation and Catalysis
  • Advanced Photocatalysis Techniques
  • Oral microbiology and periodontitis research
  • Ionic liquids properties and applications
  • Surfactants and Colloidal Systems
  • Catalytic C–H Functionalization Methods
  • Luminescence and Fluorescent Materials
  • Advanced Sensor and Energy Harvesting Materials
  • Dental Health and Care Utilization
  • Polydiacetylene-based materials and applications
  • Muscle metabolism and nutrition
  • Asymmetric Synthesis and Catalysis
  • Crystallization and Solubility Studies
  • Biochemical effects in animals
  • Nanomaterials for catalytic reactions

Chinese Academy of Sciences
2016-2025

Yangtze University
2024-2025

Guangzhou Institute of Energy Conversion
2022-2025

Institute of Coal Chemistry
2024

Institute of Soil Science
2009-2024

ShanghaiTech University
2020-2024

Huazhong University of Science and Technology
2020-2024

Zhejiang Wanli University
2024

Shaoxing People's Hospital
2024

Zhejiang Chinese Medical University
2024

Abstract It is widely accepted that single Ni atoms coordinated with N can highly efficiently promote CO 2 electroreduction to CO. Very recently, probably due limited access high‐angle annular dark‐field scanning transmission electron microscopy (HAADF‐STEM) techniques, a misleading conclusion nitrogen‐doped carbon‐encapsulated nanoparticles (NPs) possess activity similar of was reported and quickly followed by several reports. The current contribution aims end this performing well‐designed...

10.1002/aenm.202101477 article EN Advanced Energy Materials 2021-08-08

Carbon-supported bimetallic PtmNin electrocatalysts with different Pt/Ni atomic ratios were synthesized through a modified polyol process. The as-prepared characterized by X-ray diffraction, transmission electron microscopy, voltammetry techniques, and single-cell tests. It was revealed that the nanoparticles uniformly distributed on carbon supports average diameters of about 3 nm. Pt Ni partially alloyed, indicated decreased lattice constants compared pure Pt. results electrochemical...

10.1021/jp1039755 article EN The Journal of Physical Chemistry C 2010-11-04

With the aging of population, dental caries in elderly has received increasing attention. A comprehensive study oral microbiome is required to understand its polymicrobial etiology. The results previous studies are limited and remain controversial. In this study, subjects 60 years older with without were recruited. Unstimulated saliva plaque collected from each subject bacterial 16S rDNA was amplified using PCR sequenced by Illumina MiSeq high-throughput sequencing. total 92 samples 24...

10.3389/fcimb.2018.00442 article EN cc-by Frontiers in Cellular and Infection Microbiology 2019-01-04

Abstract MXenes, a novel family of 2D materials, are energy materials that have gained considerable attention, particularly for their catalytic applications in emerging areas such as CO 2 and N hydrogenation. Herein, the first time, it is shown surface reducibility Ti 3 C T x MXene can be tuned by doping, which induces change properties supported Co nanoparticles. Pristine Co–Ti favors production during hydrogenation, whereas CH 4 favored when subjected to simple doping. X‐ray photoelectron...

10.1002/smll.202007509 article EN Small 2021-06-04

Abstract A versatile kinetic resolution of protecting‐group‐free BINAMs and NOBINs has been realized through chiral phosphoric acid catalyzed triazane formation with azodicarboxylates. series mono‐N‐protected unprotected BINAMs, diphenyl diamines NOBIN derivatives could be kinetically resolved excellent performances (with s factor up to 420). The gram‐scale reactions facile derivatizations the products demonstrate potential these methods in asymmetric synthesis catalysts ligands.

10.1002/anie.202009395 article EN Angewandte Chemie International Edition 2020-09-14

Alkyl thiocyanates are prevalent in natural products, drugs, and biologically active compounds. We report here a novel, mild, efficient Pd-catalyzed site-selective sp3 C-H bond thiocyanation of 2-aminofurans. Using Na2S2O8 as the oxidant readily available NaSCN reagent, kinetically favorable 2-amino-4-thiocyanatomethylfurans selectively synthesized promising yields with broad substrate scope. This reaction represents first example transition-metal-catalyzed thiocyanation, thus offering novel...

10.1021/acs.joc.7b02700 article EN The Journal of Organic Chemistry 2017-12-18

Two carbon-supported molybdenum nitrides, MoN/C and Mo2N/C, were prepared by varying the experimental conditions in NH3 atmosphere. The physical properties of catalysts characterized X-ray diffraction, transmission electron microscopy, energy-dispersive spectroscopy, photoelectron spectroscopy. catalytic activities toward oxygen reduction reaction (ORR) methanol oxidation (MOR) potentiodynamic measurements. results show that exhibits higher activity ORR than Mo2N/C. Both are inert to...

10.1021/jp102284s article EN The Journal of Physical Chemistry C 2010-10-01

Understanding the basis for intraspecific yield variability may be important in elucidating biological mechanisms that are associated with superior performance response to projected increases carbon dioxide concentration, [CO₂]. Using a free-air CO₂ enrichment (FACE) facility, two rice lines, S63 and W14, which differed consistently their enhancement of seed when grown at elevated [CO₂] multiple field trials, were examined. To determine if different cultivar responses linked changes...

10.1093/jxb/eru344 article EN Journal of Experimental Botany 2014-09-01

Au active sites (Au<sup>0</sup>–CO and Au<sup>step</sup>–CO) surrounded by Cu species activate CO molecules at lower temperature. Strong interactions between suppress the adsorption/activation, resulting in dynamic adsorption equilibria higher temperatures.

10.1039/c7nr06018a article EN Nanoscale 2017-01-01
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