Journal
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 6, Issue 3, Pages 4026-4036Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.7b04403
Keywords
Photocatalytic hydrogen evolution; Charge carrier separation; g-C3N4 nanosheets; Noble-metal-free copper phosphide (Cu3P); p-n heterojunctions
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Funding
- National Natural Science Foundation of China [51672089]
- Special Funding on Applied Science and Technology in Guangdong [2017B020238005]
- State Key Laboratory of Advanced Technology for Material Synthesis and Processing (Wuhan University of Technology) [2015-KF-7]
- U.S. National Science Foundation [DMR-1609061]
- College of Arts and Sciences, University of Missouri-Kansas City
- University of Missouri Research Board
- Division Of Materials Research
- Direct For Mathematical & Physical Scien [1609061] Funding Source: National Science Foundation
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The rational design of sustainable noble-metal-free heterojunctions remains a key challenge for highly efficient and durable photocatalytic H-2 production. In this study, it was revealed that the robust copper phosphide (Cu3P) nanoparticles may serve as a cocatalyst and a p type semiconductor at low (1.5 wt %) and high (10 wt %) loading contents, respectively. Both Cu3P cocatalyst and semiconductor could evidently boost visible-light-driven photocatalytic H-2 production over graphitic carbon nitride (g-C3N4) nanosheets. Comparably speaking, the heterojunction effects between p-type Cu3P and n-type g-C3N4 are speculated to play a more prominent role in dramatically boosting photocatalytic H-2 production than the electron-sink roles of surface Cu3P cocatalysts. Impressively, among all the as-fabricated photocatalysts, high quality 10 wt % g-C3N4 Cu3P could achieve the highest photocatalytic H-2-production rate of 159.41 pmol which is approximately 1014 times higher than that of pristine g-C3N4. In cycling experiments, g-C3N4-10 wt % Cu3P exhibited an acceptable photostability. More importantly, it was further demonstrated that earth-abundant dual-functional Cu3P nanoparticles could markedly facilitate the separation of electron hole pairs and H-2-evolution kinetics, thus achieving distinctly boosted photocatalytic H-2 generation. This work will provide new insights into the rational design of environmentally friendly gC(3)N(4)-based hybrid nanoheterojunctions for visible-light-responsive photocatalytic H-2 generation through loading noble-metal free bifunctional cocatalysts on semiconductors.
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