石墨烯
光催化
材料科学
吸附
化学工程
纳米技术
光化学
催化作用
化学
有机化学
工程类
作者
Ping Wang,Pinsi Deng,Yulian Cao
标识
DOI:10.1016/j.ijhydene.2021.10.095
摘要
Graphene as a prospective cocatalyst can obviously promote the photocatalytic H2-evolution performance of photocatalysts by rapidly transferring photogenerated electrons. For an efficient graphene-modified photocatalytic system for H2 evolution, the fast H2-evolution reaction is as important as the rapid photoelectron transfer via graphene. In this paper, edge-sulfonated graphene (rGO-SO3H) with high H+-adsorbed activity was successfully synthesized by the formation of covalent bonds between graphene and benzenesulfonic acid through a diazotization reaction, which couples with TiO2 nanoparticles to prepare rGO-SO3H/TiO2 photocatalyst for accelerating H2-evolution reaction. The results showed that the rGO-SO3H/TiO2 displayed the highest H2-production rate of 197.1 μmol h−1 g−1 as high as 5.38, 2.81, and 3.40 times of TiO2, rGO/TiO2, and SO3H/TiO2, respectively. The improved efficiency of rGO-SO3H/TiO2 can be attributable to the synergetic action of graphene as a photoelectron cocatalyst and sulfonate ions as H+-adsorbed active sites. This study provides a new insight for the efficient hydrogen-evolution graphene-based photocatalysts.
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