氮化碳
离子
材料科学
氮化物
载流子
电场
催化作用
表面光电压
光化学
分析化学(期刊)
激子
离解(化学)
化学
光催化
化学物理
光电子学
纳米技术
凝聚态物理
物理化学
物理
有机化学
图层(电子)
量子力学
光谱学
作者
Guoqiang Zhang,Yangsen Xu,Dafeng Yan,Chuanxin He,Yongliang Li,Xiangzhong Ren,Peixin Zhang,Hongwei Mi
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2021-06-01
卷期号:11 (12): 6995-7005
被引量:164
标识
DOI:10.1021/acscatal.1c00739
摘要
The sluggish exciton dissociation and charge transfer and separation due to weak driving force still restrict the further improvement of photocatalytic performance in crystalline carbon nitride (CCN). Here, a series of heptazine-based K+-implanted CCNs (KCCNs) were successfully prepared, while the K+ ion concentration was gradiently inserted by controlling its diffusion from the surface to the bulk in carbon nitride (CN). The built-in electric field (BIEF) induced by the K+ ion concentration gradient and cyano groups has powerful driving force to promote the dissociation of excitons into electrons and holes and accelerate the separation of photogenerated carriers and their transport from the bulk to the surface. Consequently, the KCCN with an optimized BIEF has increased 34 times compared with the original CN for visible light H2 evolution. Our proposed strategy to induce BIEF by constructing concentration gradients through a thermodynamically feasible diffusion-controlled solid-state reaction can be adopted to design other photocatalytic systems.
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