Enhanced hydrogen generation via overall water splitting using novel MoS2-BN nanoflowers assembled TiO2 ternary heterostructures

三元运算 异质结 分解水 过电位 电化学 材料科学 制氢 化学工程 纳米技术 化学 光电子学 电极 催化作用 光催化 计算机科学 物理化学 生物化学 工程类 程序设计语言
作者
Syed Asim Ali,Tokeer Ahmad
出处
期刊:International Journal of Hydrogen Energy [Elsevier BV]
卷期号:48 (58): 22044-22059 被引量:94
标识
DOI:10.1016/j.ijhydene.2023.03.118
摘要

Envisaging headway in the applicability of sustainable H2 energy, the novel report of the fabrication of MoS2-BN/TiO2 (MBT) heterogeneous nanostructures has been proposed via facile in-situ hydrothermal route with an aim to propound the superior substitute of noble metal based conventionally employed catalytic system to surmount their exorbitant cost. We inferred the ascendancy of MoS2-BN nanoflowers over pristine MoS2 counterpart in an establishment of TiO2 based heterostructured catalysis. MBT heterostrucutres were extensively scrutinized with respect to their structural, optoelectronic and computational characteristics. En route to enhanced H2 evolution, we have investigated the significance of interfacial junctions and exposed sites in the MBT heterostructures. In order to achieve broader pertinence in green H2 fuel, the performance of MBT heterostrucutres was ascertained with subject to photochemical, electrochemical and photo-electrochemical (PEC) water splitting. Loaded concentration of MoS2-BN was varied in MBT catalysts and 2.5 wt% MoS2-BN/TiO2 exhibited optimum photocatalytic response with an H2 production rate of 2.6 mmol/g/h with 6.94% AQY and improved photo-current response of 0.99 mA/cm2 towards PEC. Electrochemical investigations further intensified the caliber of MBT as HER catalyst ascribed to the higher cathodic current density of 49.23 mA/cm2 at 1.22 V potential. The advancement in the catalytic efficiency of MBT heterostructures was evidenced by the synergetic relationship between MoS2-BN and TiO2 which stimulated the separation and transfer of photo-charged carriers, and lowered the overpotential values consequently surging the kinetics of H2 evolution.
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