Rekha B. Rajput , Komal S. Wagh , Sagar M. Mane , Jaewoong Lee , Rohidas B. Kale
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A sample with 70 wt% SnO<sub>2</sub> nanospheres and 30 wt% TiO<sub>2</sub> spheres achieved 94 % degradation of anionic MO dye in 20 min under LED irradiation and 90 % degradation in 2 min under sunlight. For cationic Crystal Violet dye, it reached 92 % degradation within 20 min under sunlight irradiation. Electrochemical estimations exploiting linear sweep voltammetry (LSV) in an alkaline media of potassium hydroxide demonstrated that the composite catalysts that have optimum photocatalytic performance flashed heightened electrocatalytic performance compared to individual TiO₂, SnO₂, and other composite ratios. As an electrocatalyst, the 70 %Sn −30 %Ti loaded on the Ni-foam reveals an overpotential of 211 mV with a Tafel slope of 108.6 mV dec<sup>−1</sup> during HER activity. This electrode also exhibits superior performance during OER activity, with a minimal potential of 296.2 mV and a Tafel slope of 104.3 mV dec<sup>−1</sup>. Furthermore, the electrolyzer composed of symmetric 70 %Sn-30 %Ti shows off a potential of 1.69 V. It maintains exceptional consistency with a negligible change of 1.17 % after 22 h, sustaining at a 10 mA cm<sup>−2</sup> current density during electrocatalytic overall water splitting. The focus is placed on showcasing the versatile potential of TiO<sub>2</sub>@SnO<sub>2</sub> composites as highly effective photocatalysts and electrocatalysts.</div></div>","PeriodicalId":22097,"journal":{"name":"Sustainable Materials and Technologies","volume":"43 ","pages":"Article e01246"},"PeriodicalIF":9.2000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic SnO₂-TiO₂ nanostructures: Dual function catalysts as efficient photocatalyst for industrial dye removal and bifunctional electrocatalyst for energy generation through overall water splitting\",\"authors\":\"Rekha B. Rajput , Komal S. Wagh , Sagar M. Mane , Jaewoong Lee , Rohidas B. 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For cationic Crystal Violet dye, it reached 92 % degradation within 20 min under sunlight irradiation. Electrochemical estimations exploiting linear sweep voltammetry (LSV) in an alkaline media of potassium hydroxide demonstrated that the composite catalysts that have optimum photocatalytic performance flashed heightened electrocatalytic performance compared to individual TiO₂, SnO₂, and other composite ratios. As an electrocatalyst, the 70 %Sn −30 %Ti loaded on the Ni-foam reveals an overpotential of 211 mV with a Tafel slope of 108.6 mV dec<sup>−1</sup> during HER activity. This electrode also exhibits superior performance during OER activity, with a minimal potential of 296.2 mV and a Tafel slope of 104.3 mV dec<sup>−1</sup>. Furthermore, the electrolyzer composed of symmetric 70 %Sn-30 %Ti shows off a potential of 1.69 V. 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引用次数: 0
摘要
为了提供更复杂的环境应用,本工作研究了复合材料的双重功能,包括二氧化钛球和二氧化锡纳米球的锚定。具体来说,所制备的复合材料对工业染料污染物的有效破坏(光催化剂)和整体水分解能力(电催化剂)进行了探索。研究了LED和日光照射下对阴离子染料污染物甲基橙(MO)的去除效果,并将优化后的复合材料用于日光照射下对阳离子染料结晶紫(CV)的降解。在LED照射下,含有70 wt% SnO2纳米球和30 wt% TiO2纳米球的样品在20分钟内降解了94%的阴离子MO染料,在2分钟内降解了90%的日光。对于阳离子晶紫染料,在日光照射下,20 min内降解率可达92%。利用线性扫描伏安法(LSV)在碱性氢氧化钾介质中的电化学评价表明,与单独的TiO 2, SnO 2和其他复合材料相比,具有最佳光催化性能的复合催化剂闪现出更高的电催化性能。作为电催化剂,负载在泡沫镍上的70% Sn−30% Ti在HER活性期间的过电位为211 mV, Tafel斜率为108.6 mV dec−1。该电极在OER活动中也表现出优异的性能,其最小电位为296.2 mV, Tafel斜率为104.3 mV dec−1。此外,70% sn - 30% Ti组成的对称电解槽显示出1.69 V的电位。它在22小时后保持异常的一致性,变化可忽略不计,为1.17%,在电催化整体水分解过程中保持在10 mA cm - 2电流密度。重点是展示TiO2@SnO2复合材料作为高效光催化剂和电催化剂的多用途潜力。
Synergistic SnO₂-TiO₂ nanostructures: Dual function catalysts as efficient photocatalyst for industrial dye removal and bifunctional electrocatalyst for energy generation through overall water splitting
To provide more sophisticated environmental applications, this work investigates the dual functioning of composite including titanium dioxide spheres anchored with tin dioxide nanospheres. Specifically, the fabricated composite was explored for the effective destruction of industrial dye pollutants (photocatalysts) and overall water-splitting capabilities (electrocatalysts). The removal of the anionic dye pollutant Methyl Orange (MO) was studied under both LED and sunlight irradiation, while the optimized composite was utilized for the degradation of the cationic dye Crystal Violet (CV) under sunlight exposure. A sample with 70 wt% SnO2 nanospheres and 30 wt% TiO2 spheres achieved 94 % degradation of anionic MO dye in 20 min under LED irradiation and 90 % degradation in 2 min under sunlight. For cationic Crystal Violet dye, it reached 92 % degradation within 20 min under sunlight irradiation. Electrochemical estimations exploiting linear sweep voltammetry (LSV) in an alkaline media of potassium hydroxide demonstrated that the composite catalysts that have optimum photocatalytic performance flashed heightened electrocatalytic performance compared to individual TiO₂, SnO₂, and other composite ratios. As an electrocatalyst, the 70 %Sn −30 %Ti loaded on the Ni-foam reveals an overpotential of 211 mV with a Tafel slope of 108.6 mV dec−1 during HER activity. This electrode also exhibits superior performance during OER activity, with a minimal potential of 296.2 mV and a Tafel slope of 104.3 mV dec−1. Furthermore, the electrolyzer composed of symmetric 70 %Sn-30 %Ti shows off a potential of 1.69 V. It maintains exceptional consistency with a negligible change of 1.17 % after 22 h, sustaining at a 10 mA cm−2 current density during electrocatalytic overall water splitting. The focus is placed on showcasing the versatile potential of TiO2@SnO2 composites as highly effective photocatalysts and electrocatalysts.
期刊介绍:
Sustainable Materials and Technologies (SM&T), an international, cross-disciplinary, fully open access journal published by Elsevier, focuses on original full-length research articles and reviews. It covers applied or fundamental science of nano-, micro-, meso-, and macro-scale aspects of materials and technologies for sustainable development. SM&T gives special attention to contributions that bridge the knowledge gap between materials and system designs.