In Situ Synthesis of CdS/Graphdiyne Heterojunction for Enhanced Photocatalytic Activity of Hydrogen Production.

ACS Appl Mater Interfaces

Institute for New Energy Materials and Low Carbon Technologies, School of Materials Science and Engineering , Tianjin University of Technology, Tianjin 300384 , China.

Published: January 2019

Hydrogen production through artificial photosynthesis has been regarded as a promising strategy for dealing with energy shortage and environmental problems. In this work, graphdiyne (GD) was first introduced to the visible-light catalytic system for hydrogen production, in which a CdS/GD heterojunction was prepared through a simple in situ growth process by adding Cd(AcO) into a dimethyl sulfoxide (DMSO) solution containing GD substrate. The as-prepared CdS/GD heterojunction exhibits much higher performance for photocatalytic hydrogen evolution compared to that of pristine GD and CdS nanoparticles. The photocatalytic performance of CdS/GD heterostructure containing 2.5 wt % of GD (GD2.5) is 2.6 times higher than that of the pristine CdS nanoparticles. The enhanced catalytic performance can be ascribed to the formation of CdS/GD heterojunction, in which the presence of GD can not only stabilize CdS nanoparticles by preventing the agglomeration of CdS nanoparticles but also act as a photogenerated hole transfer material for efficiently separating photogenerated electron-hole pairs in CdS. Accordingly, this work provides the potential of GD-derived materials for solar energy conversion and storage.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.8b03326DOI Listing

Publication Analysis

Top Keywords

cds nanoparticles
16
hydrogen production
12
cds/gd heterojunction
12
pristine cds
8
cds
5
situ synthesis
4
synthesis cds/graphdiyne
4
heterojunction
4
cds/graphdiyne heterojunction
4
heterojunction enhanced
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!