Ghadei Surya Kanta, Ficek Mateusz, Sethy Salila Kumar, Ryl Jacek, Gupta Mukul, Sakthivel Ramasamy, Sankaran Kamatchi Jothiramalingam, Bogdanowicz Robert
CSIR-Institute of Minerals and Materials Technology, Bhubaneswar 751013, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
ACS Appl Mater Interfaces. 2024 Oct 2;16(39):52220-52232. doi: 10.1021/acsami.4c08707. Epub 2024 Sep 18.
Self-formation of boron-doped diamond (BDD)-multilayer graphene (MLG) core-shell nanowalls (BDGNWs) via microwave plasma-enhanced chemical vapor deposition is systematically investigated. Here, the incorporation of nitrogen brings out the origin of MLG shells encapsulating the diamond core, resulting in unique sp/sp hybridized frameworks. The evolution mechanism of the nanowall-like morphology with the BDD-MLG core-shell composition is elucidated through a variety of spectroscopic studies. The photocatalytic performance of these core-shell nanowalls is examined by the deterioration of methylene blue (MB) and rhodamine B (RhB) dyes beneath low-power ultraviolet (UV) light irradiation. Starting with 5 ppm dye solutions and employing BDGNWs as the photocatalyst, remarkable degradation efficiencies of 95% for MB within 100 min and 91% for RhB within 220 min are achieved. The effect of varying dye concentrations was also examined. The enhanced photocatalytic activity is driven by carrier photogeneration and mediated by the Schottky junction formed between BDD and MLG, promoting efficient photoinduced charge separation. The stability of the BDGNW photocatalyst is examined, and after five test runs, the photocatalytic behavior for MB and RhB degradation decreases to 87 and 85%, respectively, from initial values of 96 and 91%, demonstrating excellent photostability. These findings underscore the significance of diamond-graphene nanoarchitectures as promising green carbonaceous photocatalysts.
通过微波等离子体增强化学气相沉积法系统地研究了硼掺杂金刚石(BDD)-多层石墨烯(MLG)核壳纳米壁(BDGNWs)的自形成过程。在此,氮的掺入揭示了包裹金刚石核的MLG壳层的起源,从而形成了独特的sp/sp杂化骨架。通过各种光谱研究阐明了具有BDD-MLG核壳结构的纳米壁状形态的演化机制。在低功率紫外(UV)光照射下,通过亚甲基蓝(MB)和罗丹明B(RhB)染料的降解来考察这些核壳纳米壁的光催化性能。以5 ppm的染料溶液为起始,采用BDGNWs作为光催化剂,在100分钟内对MB的降解效率达到95%,在220分钟内对RhB的降解效率达到91%。还考察了不同染料浓度的影响。增强光催化活性由载流子光生驱动,并由BDD和MLG之间形成的肖特基结介导,促进了有效的光生电荷分离。对BDGNW光催化剂的稳定性进行了考察,经过五次测试运行后,MB和RhB降解的光催化行为分别从初始值96%和91%降至87%和85%,表明其具有优异的光稳定性。这些发现强调了金刚石-石墨烯纳米结构作为有前景的绿色碳质光催化剂的重要性。