Harvesting high-performance electro-water oxidation and selective MB degradation through dual functional Gd2O3–La2O3 photo-electrocatalysts

IF 7.1 3区 材料科学 Q1 GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY
Sakthivel Chandrasekar, Nivetha Ambikapathi, Prabha Inbaraj, Qiang Jing, Bo Liu
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Abstract

Interestingly, catalytic oxygen evolution reaction (OER) in an alkaline medium with minimizing the overpotential is the most trustworthy electrocatalyst for the output of hydrogen energy from copious water electrochemical activity. Currently, amalgamated trivalent cations metal oxides have gained desirability as a low-cost anode electrocatalyst to replace noble metal-supported electrocatalysts for water oxidation and are also used for photo-degradation applications. In the present work, we have successfully synthesized GdO supported LaO composites via hydrothermal pathways for efficient and selective methylene blue (MB) degradation applications. XRD, UV–Vis DRS, FT-IR, XPS, SEM-EDX, HR-TEM, DLS, and BET analyzers confirmed the successful synthesis of photo-electrocatalysts. GdO–LaO composites achieved 5.66 and 3.37-fold larger surface areas than LaO and GdO, respectively. The results of the GdO supported LaO composite electrode demonstrated better performance under 1 M , and it exhibited a lower Tafel slope and overpotential of 72 mV dec and 310 mV at 10 mA cm. A chronoamperometry examination confirms that the fabricated GdO–LaO electrode has good stability at a fixed potential of 1.540 V vs. RHE for water oxidation. Although the, Gd inspired LaO electrode actively takes part in OER activity owing to its high C value of 40.222 μF cm. The selective degradation of MB dye using the GdO–LaO composite achieved an acceptable degradation efficiency of 84.80 % compared to other pollutants under UV-light irradiation for 120 min, and the specified pH condition is 9 for the degradation of MB dye, and it follows the first-order kinetics model. Notably, post-OER and photocatalytic results exhibited good stability and reusability characteristics. Therefore, the GdO–LaO catalyst can be used for real-time water oxidation and MB dye removal from polluted water.
通过双功能 Gd2O3-La2O3 光电催化剂获得高性能电氧化水和选择性降解甲基溴的能力
有趣的是,碱性介质中的催化氧进化反应(OER)具有最小的过电位,是从大量水的电化学活动中产生氢能的最可靠的电催化剂。目前,汞齐化的三价阳离子金属氧化物作为一种低成本的阳极电催化剂,取代了贵金属支撑的水氧化电催化剂,在光降解领域也得到了广泛的应用。在本研究中,我们通过水热法成功合成了以氧化钆为支撑的氧化钴复合材料,用于高效、选择性地降解亚甲基蓝(MB)。XRD、UV-Vis DRS、FT-IR、XPS、SEM-EDX、HR-TEM、DLS 和 BET 分析仪证实了光电催化剂的成功合成。GdO-LaO 复合材料的比表面积分别比 LaO 和 GdO 大 5.66 倍和 3.37 倍。GdO 支持的 LaO 复合电极在 1 M 下表现出更好的性能,其 Tafel 斜率和过电位较低,在 10 mA cm 时分别为 72 mV dec 和 310 mV。计时器检验证实,在 1.540 V 的固定电位下,所制造的氧化钆-氧化铝电极对水氧化具有良好的稳定性。尽管钆激发的 LaO 电极因其 40.222 μF cm 的高 C 值而积极参与了 OER 活动,但其在水氧化过程中的选择性降解能力仍然很强。使用 GdO-LaO 复合材料对甲基溴染料进行选择性降解,在紫外光照射 120 分钟后,与其他污染物相比,降解效率达到了 84.80%,降解甲基溴染料的指定 pH 值为 9,并遵循一阶动力学模型。值得注意的是,OER 后和光催化结果显示出良好的稳定性和可重复使用性。因此,GdO-LaO 催化剂可用于实时水氧化和去除污染水中的甲基溴染料。
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来源期刊
CiteScore
5.80
自引率
6.40%
发文量
174
审稿时长
32 days
期刊介绍: Materials Today Sustainability is a multi-disciplinary journal covering all aspects of sustainability through materials science. With a rapidly increasing population with growing demands, materials science has emerged as a critical discipline toward protecting of the environment and ensuring the long term survival of future generations.
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