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Highly efficient S2−-adsorbed MoSx-modified TiO2 photocatalysts: A general grafting strategy and boosted interfacial charge transfer
Journal of Materials Science & Technology ( IF 11.2 ) Pub Date : 2020-03-05 , DOI: 10.1016/j.jmst.2020.02.031
Duoduo Gao , Ranran Yuan , Jiajie Fan , Xuekun Hong , Huogen Yu

Exploiting efficient and low-cost cocatalyst with a facile grafting strategy is of critical importance for significantly boosting the photocatalytic H2-evolution activity. In this study, S2−-adsorbed MoSx nanoparticle as a superior H2-evolutoin cocatalyst was successfully grafted on the TiO2 surface to greatly boost its photocatalytic activity via one-step lactic acid-induced synthesis strategy. Herein, the lactic acid can induce the homogeneous production of amorphous MoSx (a-MoSx) nanoparticles from MoS42− precursor, while the symbiotic S2- ions can be easily and availably self-adsorbed on the a-MoSx surface, resulting in the formation of S2--adsorbed a-MoSx nanoparticles with a small size of 0.5−3 nm. Photocatalytic results manifested that the S2−-adsorbed MoSx nanoparticles could dramatically facilitate the H2-generation rate of TiO2 photocatalysts (3452 μmol h-1 g-1, AQE = 16.5 %). In situ irradiated XPS in conjunction with transient-state PL and photoelectrochemical tests reveal that the improved H2-generation activity can be ascribed to the synergistic effect of boosted interfacial charge transfer from TiO2 to S2−-adsorbed MoSx and the superior H2-evolution reaction on self-adsorbed S2− ions. In addition, the S2−-adsorbed MoSx nanoparticles can also act as the general H2-generation cocatalyst to obviously promote the activity of other typical host photocatalysts such as g-C3N4 and CdS. This work provides an innovative approach to develop high-efficiency MoSx-based cocatalyst with boosted interfacial charge transfer toward highly efficient photocatalytic materials.



中文翻译:

高效S 2−吸附的MoS x改性的TiO 2光催化剂:通用的接枝策略和增强的界面电荷转移

利用有效的接枝策略开发高效,低成本的助催化剂对于显着提高光催化H 2的进化活性至关重要。在这项研究中,将S 2-吸附的MoS x纳米粒子作为一种优良的H 2-外泌尿素助催化剂成功地接枝到TiO 2表面上,通过一步法乳酸诱导的合成策略极大地提高了其光催化活性。本文中,乳酸可以诱导从MoS 4 2-前体均匀生成非晶态MoS x(a-MoS x)纳米颗粒,而共生S 2-离子可以轻松,有效地自我吸附在a-MoS x表面,导致形成S 2-吸附的a-MoS x纳米颗粒,尺寸为0.5-3 nm。光催化结果表明,S 2−吸附的MoS x纳米颗粒可以显着促进TiO 2光催化剂的H 2生成速率(3452μmolh -1  g -1,AQE = 16.5%)。原位辐照XPS结合瞬态PL和光电化学测试表明,改善的H 2生成活性可归因于TiO促进界面电荷转移的协同效应。2到S 2-吸附的MoS x和对自吸附S 2-离子的优良H 2演化反应。此外,吸附有S 2−的MoS x纳米颗粒还可以充当一般的H 2生成助催化剂,从而明显提高其他典型主体光催化剂(如gC 3 N 4和CdS)的活性。这项工作提供了一种创新的方法来开发基于MoS x的高效助催化剂,同时将界面电荷转移到高效的光催化材料上。

更新日期:2020-03-05
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