4.8 Article

Palladium as a Superior Cocatalyst to Platinum for Hydrogen Evolution Using Covalent Triazine Frameworks as a Support

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 11, Pages 12774-12782

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b21903

Keywords

covalent triazine frameworks; hydrogen evolution; cocatalyst; palladium; photocatalysis; water splitting

Funding

  1. National Natural Science Foundation of China [21975086]
  2. International S&T Cooperation Program of China [2018YFE010498]
  3. HUST Innovation Funding [2018JYCXJJ041]
  4. Science and Technology Department of Hubei Province [2019CFA008, 2018AAA057]
  5. Program for HUST Interdisciplinary Innovation Team [2016JCTD104]

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Abundant pyridinic nitrogen in the triazine units of covalent triazine frameworks (CTFs) is very useful in various heterogeneous catalysis reactions. Herein, a tunable CTF platform with the same porous structure was designed and synthesized to study the interaction between palladium/platinum (Pd/Pt) and pyridinic nitrogen of CTFs. The smaller Pd nanoparticles were formed because of the stronger interaction between Pd and pyridinic nitrogen atoms of CTFs, which is more beneficial for the separation of photogenerated electron- hole pairs. Moreover, the stronger interaction between the Pd nanoparticles and CTFs is also beneficial for photoelectron transfer. Under the same conditions, the hydrogen evolution rate of 1 wt % Pdp CTF-HC6 is up to 11 times more than that of 1 wt % Pt@CTF-HC6. The hydrogen evolution rate of 1 wt % Pd@CTF-N approaches 10 556 mu mol h(-1 )g(-1 )and is about 5 times more than that of of 1 Pt@CTF-N.

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