Tian‐Jian Zhao

ORCID: 0000-0002-9870-1491
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About
Contact & Profiles
Research Areas
  • Electrocatalysts for Energy Conversion
  • Nanomaterials for catalytic reactions
  • Advanced battery technologies research
  • Advanced Photocatalysis Techniques
  • Asymmetric Hydrogenation and Catalysis
  • Carbon dioxide utilization in catalysis
  • CO2 Reduction Techniques and Catalysts
  • Gas Sensing Nanomaterials and Sensors
  • Ammonia Synthesis and Nitrogen Reduction
  • Catalytic Processes in Materials Science
  • Catalysis for Biomass Conversion
  • Surface Chemistry and Catalysis
  • Chemical Synthesis and Reactions
  • Electrochemical Analysis and Applications
  • Fuel Cells and Related Materials
  • Supercapacitor Materials and Fabrication
  • Chromium effects and bioremediation
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Power Transformer Diagnostics and Insulation
  • Catalysis and Hydrodesulfurization Studies
  • Metal-Organic Frameworks: Synthesis and Applications
  • Electronic and Structural Properties of Oxides
  • E-commerce and Technology Innovations
  • Catalysts for Methane Reforming
  • Hydrogen Storage and Materials

Midea Group (China)
2023

Shanghai Jiao Tong University
2015-2020

Beijing University of Agriculture
2018

Institute of Coal Chemistry
2015-2016

Shanxi University
2014-2016

State Key Laboratory of Coal Conversion
2016

Shanxi University of Traditional Chinese Medicine
2014-2016

Abstract Production of ammonia is currently realized by the Haber–Bosch process, while electrochemical N 2 fixation under ambient conditions recognized as a promising green substitution in near future. A lack efficient electrocatalysts remains primary hurdle for initiation potential electrocatalytic synthesis ammonia. For cheaper metals, such copper, limited progress has been made to date. In this work, we boost reduction reaction catalytic activity Cu nanoparticles, which originally...

10.1038/s41467-019-12312-4 article EN cc-by Nature Communications 2019-09-26

Highly efficient fixation of CO2 for the synthesis useful organic carbonates has drawn much attention. The design sustainable Lewis acid-base pairs, which mainly relied on expensive ligands, is key challenge in activation substrate and molecule. Here, we report application Mott-Schottky type nanohybrids composed electron-deficient Cu electron-rich N-doped carbon fixation. A ligand-free additive-free method was used to boost basicity supports acidity by increasing Schottky barrier at their...

10.1021/jacs.8b08267 article EN Journal of the American Chemical Society 2018-12-10

Abstract Oxygen vacancies can help to capture oxygen‐containing species and act as active centers for oxygen evolution reaction (OER). Unfortunately, effective methods generating a high amount of on the surface various nanocatalysts are rather limited. Here, we described an way generate oxygen‐vacancy‐rich transition metal oxides, exemplified with Co 3 O 4 , simply by constructing highly coupled interface ultrafine nanocrystals metallic Ti. Impressively, amounts vacancy /Ti surpassed...

10.1002/cssc.201700779 article EN ChemSusChem 2017-06-14

Primary alkyl alcohols can be directly converted into acetals and H<sub>2</sub><italic>via</italic> TiO<sub>2</sub>-photocatalytic dehydrogenation coupling at room temperature, with no need for any hydrogen acceptors.

10.1039/c4gc00413b article EN Green Chemistry 2014-01-01

Abstract As a new type of heterogeneous catalyst with “homogeneous‐like” activity, single‐site transition‐metal materials are usually treated as integrated but separate active centers. A novel grouping effect is reported for single Ni−N 4 sites in nitrogen‐doped carbon (Ni/NC), where an effective ligand‐stabilized polycondensation method endows Ni/NC nanocatalysts high content Ni up to 9.5 wt %. The enhanced electron density at each site promotes highly efficient hydrogen transfer, which...

10.1002/anie.201809858 article EN Angewandte Chemie International Edition 2018-09-25

Cobalt nanoparticles containing both Co<sup>2+</sup> and Co<sup>0</sup> species supported on carbon nitride can function as heterogeneous nanocatalysts for a general transfer hydrogenation reaction in aqueous ammonia-borane solution at room temperature.

10.1039/c5ra19869k article EN RSC Advances 2015-01-01

The exploitation of metal-free organic polymers as electrodes for water splitting reactions is limited by their presumably low activity and poor stability, especially the oxygen evolution reaction (OER) under more critical conditions. Now, thickness a cheap robust polymer, poly(p-phenylene pyromellitimide) (PPPI) was rationally engineered an in situ polymerization method to make polymer available first time flexible, tailorable, efficient, ultra-stable oxidation over wide pH range. PPPI...

10.1002/anie.201808036 article EN Angewandte Chemie International Edition 2018-08-07

Self-supported aerogel composed of carbon nitride nanolayers can act as a bifunctional photocatalyst and show enhanced photoreduction photooxidation performance due to the large surface areas nitrogen vacancies. The catalyze hydrogen evolution at rate nearly 4.2 mmol h-1 g-1 oxidize benzyl alcohols with high conversion efficiency selectivity under milder conditions. Note that activity for photochemical alcohol oxidation shows outstanding compared based photocatalysts. Both density functional...

10.1021/acsami.9b10123 article EN ACS Applied Materials & Interfaces 2019-09-03

A hydrogenation–dehydrogenation coupling process efficiently realized an intermolecular hydrogen transfer from isopropanol to LA under photocatalytic conditions over gold-loaded TiO<sub>2</sub> catalysts.

10.1039/c5gc02971f article EN Green Chemistry 2016-01-01

Abstract Electrochemical gas evolution and activation reactions are complicated processes, involving not only active electrocatalysts but also the interaction among solid electrodes, electrolyte, gas‐phase products reactants. In this study, multiphase interfaces of superadsorbing graphene‐based electrodes were controlled without changing centers to significantly facilitate mass diffusion kinetics for superior performance. The achieved in‐depth understanding how regulate interfacial...

10.1002/cssc.201800826 article EN ChemSusChem 2018-05-31

We described an effective way to generate a Co3O4 mesocrystal array with well-developed porosity, simply by uniting coupled interface hydrazine treatment. Due the fast electron transfer and sufficient active sites, Ti mesh-supported nanoneedles electrode could provide current density of 49.9 mA cm-2 at 570 mV OER overpotential has exceptionally high stability.

10.1039/c9cc00791a article EN Chemical Communications 2019-01-01

The inactive g-C<sub>3</sub>N<sub>4</sub> nanolayers could act as a voltage-driven “pump” to extract electrons from BiVO<sub>4</sub> and promote the hole–electron separation efficiency.

10.1039/c7cc05444k article EN Chemical Communications 2017-01-01

Enzyme catalysts always show an excellent catalytic selectivity, which is important in biochemistry, especially synthesis and biopharming. This selectivity achieved by combining the binding effect induced electrostatic of enzyme to attract a specific substrate then prearrangement substrates inside pocket. Herein, we report proof-of-concept application interfacial field constructing Schottky heterojunctions mimic catalysis enzyme. In combination with 3 D structure, transition metal/carbon...

10.1002/cssc.201902937 article EN ChemSusChem 2020-01-16

Abstract As a new type of heterogeneous catalyst with “homogeneous‐like” activity, single‐site transition‐metal materials are usually treated as integrated but separate active centers. A novel grouping effect is reported for single Ni−N 4 sites in nitrogen‐doped carbon (Ni/NC), where an effective ligand‐stabilized polycondensation method endows Ni/NC nanocatalysts high content Ni up to 9.5 wt %. The enhanced electron density at each site promotes highly efficient hydrogen transfer, which...

10.1002/ange.201809858 article EN Angewandte Chemie 2018-09-25

Abstract The exploitation of metal‐free organic polymers as electrodes for water splitting reactions is limited by their presumably low activity and poor stability, especially the oxygen evolution reaction (OER) under more critical conditions. Now, thickness a cheap robust polymer, poly( p ‐phenylene pyromellitimide) (PPPI) was rationally engineered an in situ polymerization method to make polymer available first time flexible, tailorable, efficient, ultra‐stable oxidation over wide pH...

10.1002/ange.201808036 article EN Angewandte Chemie 2018-08-07

Direct activation of oxygen gas is achieved over dendritic carbons, resulting in an ultra-high current density without a diffusion plateau.

10.1039/c8qi00356d article EN Inorganic Chemistry Frontiers 2018-01-01

Transformer fault diagnosis is a necessary operation to ensure the stable of power system.

10.1039/d2ay01745h article EN Analytical Methods 2022-12-22

Abstract Carbon dioxide has been important in green chemistry, especially catalytic and chemical engineering applications. While exploring CO 2 to produce cyclohexanone for nylon or 66 that is currently produced with low yields using harsh methods, we made the exciting discovery carbonic acid, generated from dissolved water, was utilized as molecular ligand via hydrogenation of nitrobenzene aqueous solution uses Pd catalysts a total yield higher than 90 %. Importantly, gaseous nature H 3...

10.1002/cctc.201900389 article EN ChemCatChem 2019-04-24
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