Hieu Hoang Nhat, Nguyen Van Nghia, Nguyen Vuong Minh, Phan Thanh Hai
Department of Physics and Materials Science, Faculty of Natural Sciences, Quy Nhon University, 170 An Duong Vuong, Quy Nhon, Vietnam.
Nanotechnology. 2023 Aug 29;34(46). doi: 10.1088/1361-6528/acedb3.
3D-ordered porous CdS/AgI/ZnO nanostructures were designed to perform as high-performance photoelectrodes for photoelectrochemical (PEC) water-splitting applications. They rely on the advantages of an extremely large active surface area, high absorption capacity in the visible-light region, fast carrier separation and transportation caused by the intrinsic ladder-like band arrangement. These nanostructures were fabricated by employing a three-stage experiment in a sequence of hard mold-assisted electrochemical deposition, wet chemical method and deposition-precipitation. First, 3D-ordered ZnO nanostructures were electrochemically deposited using a polystyrene film as the sacrificed template. AgI nanoparticles were then decorated on the interfacial ZnO nanostructures by deposition-precipitation. Finally, these binary AgI/ZnO nanoporous networks were thoroughly wet-chemically coated with a CdS film to form a so-called 'ternary interfacial CdS/AgI/ZnO nanostructures'. The PEC water-splitting properties of the fabricated 3D nanostructures were systematically studied and compared. As a result, the highest efficiency of the fabricated 3D-ordered porous CdS/AgI/ZnO measured under the irradiation of solar simulation is about 5.2%, which is relatively 1.5, 3.5 and 11.3 times greater than that of the corresponding CdS/ZnO (3,4%), AgI/ZnO (1.5%) and pristine porous ZnO (0.46%) photoelectrodes, respectively. The significant improvement in the PEC activity is attributed to the enhanced charge separation and transport of ternary photoelectrodes caused by an unconventional ladder-like band arrangement formed between interfacial CdS-AgI-ZnO. Our study provides a promising strategy for developing such ternary photoelectrode generation that possesses higher stability and efficiency towards water-splitting processes.
三维有序多孔硫化镉/碘化银/氧化锌纳米结构被设计用作光催化分解水(PEC)应用的高性能光电极。它们依赖于极大的活性表面积、在可见光区域的高吸收能力、由固有的阶梯状能带排列导致的快速载流子分离和传输等优点。这些纳米结构是通过硬模辅助电化学沉积、湿化学方法和沉积沉淀的三步实验依次制备的。首先,以聚苯乙烯薄膜为牺牲模板电化学沉积三维有序氧化锌纳米结构。然后通过沉积沉淀法在界面氧化锌纳米结构上修饰碘化银纳米颗粒。最后,用硫化镉薄膜对这些二元碘化银/氧化锌纳米多孔网络进行充分的湿化学包覆,形成所谓的“三元界面硫化镉/碘化银/氧化锌纳米结构”。对制备的三维纳米结构的光催化分解水性能进行了系统研究和比较。结果,在太阳模拟照射下测量的制备的三维有序多孔硫化镉/碘化银/氧化锌的最高效率约为5.2%,分别比相应的硫化镉/氧化锌(3.4%)、碘化银/氧化锌(1.5%)和原始多孔氧化锌(0.46%)光电极高1.5倍、3.5倍和11.3倍。光催化活性的显著提高归因于界面硫化镉 - 碘化银 - 氧化锌之间形成的非常规阶梯状能带排列导致的三元光电极电荷分离和传输增强。我们的研究为开发这种对水分解过程具有更高稳定性和效率的三元光电极提供了一种有前景的策略。