Wang Cai-He, Qin Dong-Dong, Shan Duo-Liang, Gu Jing, Yan Yong, Chen Jing, Wang Qiu-Hong, He Cai-Hua, Li Yang, Quan Jing-Jing, Lu Xiao-Quan
Key Lab of Bioelectrochemistry and Environmental Analysis of Gansu, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of China.
Department of Chemistry, San Diego State University, San Diego, CA 92182-1030, USA.
Phys Chem Chem Phys. 2017 Feb 8;19(6):4507-4515. doi: 10.1039/c6cp08066a.
Graphitic carbon nitride (g-CN) has been widely studied as a metal-free photocatalyst, leading to some excellent results; however, the rapid recombination of photogenerated charge carriers substantially limits its performance. Here, we establish two types of g-CN-based heterojunction (type II and nonmediator assisted Z-scheme) photoanodes on a transparent conducting substrate via coupling with rod-like and nanoparticulate WO, respectively. In these composites, g-CN film grown by electrophoretic deposition of exfoliated g-CN serves as the host or guest material. The optimized type II WO/g-CN composite exhibits an enhanced photocurrent of 0.82 mA cm at 1.23 V vs. RHE and an incident photo-to-current conversion efficiency (IPCE) of 33% as compared with pure WO nanorods (0.22 mA cm for photocurrent and 15% for IPCE). Relative to pure g-CN film (with a photocurrent of several microampere and an IPCE of 2%), a largely improved photocurrent of 0.22 mA cm and an IPCE of 20% were acquired for the Z-scheme g-CN/WO composite. The enhancement can be attributed to accelerated charge separation in the heterointerface because of the suitably aligned band gap between WO and g-CN, as confirmed by optical spectroscopy and ultraviolet photoelectron spectroscopy (UPS) analysis. The photocatalytic process and mechanism of the g-CN-based heterojunctions are proposed herein, which potentially explain the origin of the enhanced photoelectrochemical performance. This achievement and the fundamental information supplied here indicate the importance of rationally designing heterojunction photoelectrodes to improve the performance of semiconductors. This is particularly important for materials such as pure g-CN and WO, as their photoactivities are strongly restricted by high recombination rates.
石墨相氮化碳(g-CN)作为一种无金属光催化剂已得到广泛研究,并取得了一些优异成果;然而,光生载流子的快速复合严重限制了其性能。在此,我们分别通过与棒状和纳米颗粒状的WO耦合,在透明导电基底上建立了两种基于g-CN的异质结(II型和无介质辅助Z型)光阳极。在这些复合材料中,通过对剥离的g-CN进行电泳沉积生长的g-CN薄膜用作主体或客体材料。优化后的II型WO/g-CN复合材料在相对于可逆氢电极(RHE)为1.23 V时,光电流增强至0.82 mA cm²,与纯WO纳米棒相比,其入射光电流转换效率(IPCE)为33%(纯WO纳米棒的光电流为0.22 mA cm²,IPCE为15%)。相对于纯g-CN薄膜(光电流为几微安,IPCE为2%),Z型g-CN/WO复合材料获得了大幅提高的光电流0.22 mA cm²和20%的IPCE。这种增强可归因于WO和g-CN之间适当对齐的带隙导致异质界面处电荷分离加速,这已通过光谱学和紫外光电子能谱(UPS)分析得到证实。本文提出了基于g-CN的异质结的光催化过程和机理,这可能解释了光电化学性能增强的起源。这一成果以及此处提供的基础信息表明了合理设计异质结光电极以提高半导体性能的重要性。这对于诸如纯g-CN和WO等材料尤为重要,因为它们的光活性受到高复合率的强烈限制。