Haibin Yang

ORCID: 0000-0003-4539-0471
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About
Contact & Profiles
Research Areas
  • Electrocatalysts for Energy Conversion
  • Fuel Cells and Related Materials
  • Oxidative Organic Chemistry Reactions
  • Synthesis and Catalytic Reactions
  • Advanced battery technologies research
  • Organic Chemistry Cycloaddition Reactions
  • Ammonia Synthesis and Nitrogen Reduction
  • Advanced Photocatalysis Techniques
  • CO2 Reduction Techniques and Catalysts
  • Catalytic Processes in Materials Science
  • Asymmetric Synthesis and Catalysis
  • Electrochemical Analysis and Applications
  • Click Chemistry and Applications
  • Spectroscopy Techniques in Biomedical and Chemical Research
  • Chemical Synthesis and Analysis

Peking University
2022-2024

Peking University Shenzhen Hospital
2023

Jilin University
2009-2010

Changchun Institute of Applied Chemistry
2009

Chinese Academy of Sciences
2009

State Key Laboratory of Superhard Materials
2009

Abstract Despite the recent achievements in urea electrosynthesis from co-reduction of nitrogen wastes (such as NO 3 − ) and CO 2 , product selectivity remains fairly mediocre due to competing nature two parallel reduction reactions. Here we report a catalyst design that affords high by sequentially reducing at dynamic catalytic centre, which not only alleviates competition issue but also facilitates C−N coupling. We exemplify this strategy on nitrogen-doped carbon catalyst, where...

10.1038/s41467-023-44131-z article EN cc-by Nature Communications 2024-01-02

In this paper, a hollow Au/Pd core/shell nanostructure with raspberry surface was developed for methanol, ethanol, and formic acid oxidation in alkaline media. The results showed that it possessed better electrocatalyst performance than Au nanospheres or Pd nanoparticles. fabricated via two-step method. Hollow were first synthesized by galvanic replacement reaction, then they coated layer of grains. Several characterizations such as transmission electron microscopy (TEM), scanning (SEM),...

10.1021/jp905007r article EN The Journal of Physical Chemistry C 2009-08-31

Zinc-air batteries (ZABs) have the advantages of high energy density and safety but their large-scale application is hindered by sluggish kinetics four-electron aqueous O2 redox reactions. Widely used Ruthenium (Ru)-based catalysts possess intrinsic oxygen evolution catalytic activity suffer from insufficient reduction reaction (ORR) performance. Herein, to optimize ORR Ru-based catalyst, an iron (Fe)-coordinated, bimetallic RuFe cluster constructed homogeneously dispersed within nitrogen...

10.1016/j.pnsc.2022.11.002 article EN cc-by-nc-nd Progress in Natural Science Materials International 2022-11-25

A new method for the direct functionalization of diamondoids has been developed using photoredox and H-atom transfer catalysis. This C–H alkylation reaction excellent chemoselectivity strong 3º bonds adamantanes in polyfunctional molecules. In substrate competition reactions, a reversal selectivity is observed catalyst reported here when compared to six known photochemical systems. Derivatization broad scope adamantane-containing drugs highlights versatility functional group tolerance this strategy.

10.26434/chemrxiv.7409651.v1 preprint EN cc-by-nc-nd 2018-12-04

A new method for the direct functionalization of diamondoids has been developed using photoredox and H-atom transfer catalysis. This C–H alkylation reaction excellent chemoselectivity strong 3º bonds adamantanes in polyfunctional molecules. In substrate competition reactions, a reversal selectivity is observed catalyst reported here when compared to six known photochemical systems. Derivatization broad scope adamantane-containing drugs highlights versatility functional group tolerance this strategy.

10.26434/chemrxiv.7409651.v2 preprint EN 2019-03-07

ADVERTISEMENT RETURN TO ISSUEPREVAddition/CorrectionORIGINAL ARTICLEThis notice is a correctionCorrection to (DHQ)2AQN-Catalyzed Asymmetric Substitution of Isatin-Derived Hydrazones with O-Boc-Protected Morita–Baylis–Hillman Adducts: A Strategy for Synthesizing Enantioenriched Azo Compounds Incorporating an Oxindole ScaffoldHai-Bin Yang, Yun-Zhou Zhao, Rui Sang, and Min Shi*Cite this: J. Org. Chem. 2014, 79, 11, 5390Publication Date (Web):May 16, 2014Publication History Published online16...

10.1021/jo5009977 article EN The Journal of Organic Chemistry 2014-05-16

<p>A new method for the direct functionalization of diamondoids has been developed using photoredox and H-atom transfer catalysis. This C–H alkylation reaction excellent chemoselectivity strong 3º bonds adamantanes in polyfunctional molecules. In substrate competition reactions, a reversal selectivity is observed catalyst reported here when compared to six known photochemical systems. Derivatization broad scope adamantane-containing drugs highlights versatility functional group...

10.26434/chemrxiv.7409651 preprint EN 2018-12-04
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