In situ noble metal-ion modified TiO2 rutile nanobars with highly exposed {110} facets: Synthesis, structure, and catalytic properties

IF 4.7 3区 材料科学 Q2 CHEMISTRY, PHYSICAL
Shihui Jiao , Mingyu Shang , Yan Chen , Guangsheng Pang
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引用次数: 0

Abstract

The in situ anchoring of metal elements on the surface of nanomaterials is a state-of-the-art technology that can significantly enhance the performance of materials. We have successfully fabricated noble metal-ion modified rutile TiO2 nanobars, which exhibit exceptional catalytic activity in both H2 generation and CO oxidation. Firstly, we synthesized Ti3+ self-doped rutile TiO2-x nanobars by a simple solvothermal method using Zn as a reductant, resulting in highly crystalline structures with a significant proportion of (110) surfaces. The reduced nanobars chemically absorb the noble metal cations with the addition of a solution of a noble metal salt in the absence of light to form in situ noble metal-ion modified catalysts. TiO2 nanobars with 1 wt% Pt2+ and Pd2+ exhibited excellent performance in photocatalytic H2 generation from water and low temperature CO oxidation. Moreover, the samples modified with low noble metal ions (0.1 wt%) also show effective activity in H2 generation.

Abstract Image

具有高暴露{110}面的原位贵金属离子修饰 TiO2 金红石纳米棒:合成、结构和催化特性
在纳米材料表面原位锚定金属元素是一种最先进的技术,可显著提高材料的性能。我们成功地制备了贵金属离子修饰的金红石 TiO2 纳米棒,它在 H2 生成和 CO 氧化方面都表现出卓越的催化活性。首先,我们以 Zn 为还原剂,通过简单的溶解热法合成了 Ti3+ 自掺杂的金红石 TiO2-x 纳米棒,得到了具有大量 (110) 表面的高结晶结构。在无光条件下,加入贵金属盐溶液,还原后的纳米棒会化学吸收贵金属阳离子,形成原位贵金属离子修饰催化剂。含有 1 wt% Pt2+ 和 Pd2+ 的 TiO2 纳米棒在光催化水生成 H2 和低温 CO 氧化中表现出优异的性能。此外,用低贵金属离子(0.1 wt%)修饰的样品也能有效地产生 H2。
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来源期刊
Colloid and Interface Science Communications
Colloid and Interface Science Communications Materials Science-Materials Chemistry
CiteScore
9.40
自引率
6.70%
发文量
125
审稿时长
43 days
期刊介绍: Colloid and Interface Science Communications provides a forum for the highest visibility and rapid publication of short initial reports on new fundamental concepts, research findings, and topical applications at the forefront of the increasingly interdisciplinary area of colloid and interface science.
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