Sulaeman Allyn Pramudya, Pratama Rifky Adhia, Pratomo Uji, Matharu Avtar S, Primadona Indah
Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran Sumedang 45363 Indonesia.
Green Chemistry Centre of Excellence, Department of Chemistry, University of York York YO10 5DD UK.
RSC Adv. 2023 Jun 19;13(27):18396-18403. doi: 10.1039/d3ra02907g. eCollection 2023 Jun 15.
ZnO photoanodes in photoelectrochemical (PEC) water splitting for green-hydrogen production are limited due to the large bandgap that is only confined to UV light. One of the strategies for broadening the photo absorption range and improving light harvesting is to modify a one-dimensional (1D) nanostructure to a three-dimensional (3D) ZnO superstructure coupling with a narrow-bandgap material, in this case, a graphene quantum dot photosensitizer. Herein, we studied the effect of sulfur and nitrogen co-doped graphene quantum dot (S,N-GQD) sensitization on the surface of ZnO nanopencil (ZnO NPc) to give a photoanode in the visible light spectrum. In addition, the photo energy harvesting between the 3D-ZnO and 1D-ZnO, as represented by neat ZnO NPc and ZnO nanorods (ZnO NRs), was also compared. Several instruments, including SEM-EDS, FTIR, and XRD revealed the successful loading of S,N-GQDs on the ZnO NPc surfaces through the layer-by-layer assembly technique. The advantages are S,N-GQDs's band gap energy (2.92 eV) decreasing ZnO NPc's band gap value from 3.169 eV to 3.155 eV after being composited with S,N-GQDs and facilitating the generation of electron-hole pairs for PEC activity under visible light irradiation. Furthermore, the electronic properties of ZnO NPc/S,N-GQDs were improved significantly over those of bare ZnO NPc and ZnO NR. The PEC measurements revealed that the ZnO NPc/S,N-GQDs stood out with a maximum current density of 1.82 mA cm at +1.2 V ( Ag/AgCl), representing a 153% and 357% improvement over the bare ZnO NPc (1.19 mA cm) and the ZnO NR (0.51 mA cm), respectively. These results suggest that ZnO NPc/S,N-GQDs could have potential for water splitting applications.
用于光催化分解水制绿氢的氧化锌光阳极,因其较大的带隙仅局限于紫外光而受到限制。拓宽光吸收范围和提高光捕获效率的策略之一,是将一维(1D)纳米结构改性为三维(3D)氧化锌超结构,并与窄带隙材料(在本文中为石墨烯量子点光敏剂)耦合。在此,我们研究了硫氮共掺杂石墨烯量子点(S,N-GQD)敏化对氧化锌纳米铅笔(ZnO NPc)表面的影响,以制备在可见光谱范围内的光阳极。此外,还比较了由纯氧化锌纳米铅笔(ZnO NPc)和氧化锌纳米棒(ZnO NRs)代表的3D-ZnO和1D-ZnO之间的光能捕获情况。包括扫描电子显微镜-能谱仪(SEM-EDS)、傅里叶变换红外光谱仪(FTIR)和X射线衍射仪(XRD)在内的多种仪器表明,通过逐层组装技术,S,N-GQDs成功负载在ZnO NPc表面。其优势在于,S,N-GQDs的带隙能量(2.92 eV)与ZnO NPc复合后,将ZnO NPc的带隙值从3.169 eV降低至3.155 eV,并促进了在可见光照射下光催化分解水活性的电子-空穴对的产生。此外,ZnO NPc/S,N-GQDs的电子性能相比裸ZnO NPc和ZnO NR有显著改善。光催化分解水测量结果表明,ZnO NPc/S,N-GQDs表现突出,在+1.2 V(Ag/AgCl)时的最大电流密度为1.82 mA cm,分别比裸ZnO NPc(1.19 mA cm)和ZnO NR(0.51 mA cm)提高了153%和357%。这些结果表明,ZnO NPc/S,N-GQDs在光催化分解水应用方面具有潜力。