材料科学
异质结
量子点
石墨烯
载流子
光催化
分解水
制氢
离域电子
工作职能
表面光电压
光电子学
量子产额
密度泛函理论
半导体
纳米技术
电子迁移率
化学物理
光化学
电子受体
开尔文探针力显微镜
电子
电荷密度
X射线光电子能谱
量子效率
光催化分解水
太阳能燃料
氢
聚合物太阳能电池
碳纤维
结合能
可逆氢电极
人工光合作用
太阳能
氧化还原
作者
Mengyuan Ren,Fengzhang Ye,Jiu Luo,Wei Xie,Junqing Ye,Mingyang He,Junfeng Qian,Qun Chen
标识
DOI:10.1021/acsami.6c00264
摘要
Hydrogen (H2) energy is a clean, renewable energy carrier with a high energy density and zero carbon emissions. Photocatalytic water splitting offers a promising route to H2 production by utilizing abundant solar energy; yet, it is often limited by sluggish charge carrier kinetics and low quantum efficiency. Herein, we incorporate graphene quantum dots (GQDs) as cocatalysts into the S-scheme heterojunction inorganic semiconductor Bi2MoO6@Cu2O (BMO@Cu2O) to boost photocatalytic H2 evolution. Under simulated sunlight, the GQDs/BMO@Cu2O composite achieves an exceptional H2 production rate of 16.1 mmol·g–1·h–1 and an apparent quantum yield of 33.6% at 420 nm. The built-in electric field (IEF) between BMO and Cu2O promotes S-scheme charge transfer, enhancing carrier separation. GQDs function as electron acceptors and active sites, where their delocalized π-electron cloud in the sp2-hybridized carbon skeleton shortens charge migration paths and lowers the energy barrier for surface H2 evolution. In situ X-ray photoelectron spectroscopy, Kelvin probe force microscopy, and density functional theory calculations collectively confirm the IEF and S-scheme electron transfer. This work presents a strategic design of GQDs-mediated heterojunctions with efficient charge separation and strong redox capacity, advancing solar-driven H2 production technology.
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