Rameshbabu R, Ravi P, Pecchi Gina, Delgado Eduardo J, Mangalaraja R V, Sathish M
Departamento Físico Química, Facultad Ciencias Químicas, Universidad de Concepción, Concepción 4030000, Chile; Millenium Nuclei on Catalytic Processes towards Sustainable Chemistry (CSC), Concepcion 4030000, Chile.
Electrochemical Power Source Division, CSIR-Central Electrochemical Research Institute, Karaikudi 630 003, Tamil Nadu, India; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
J Colloid Interface Sci. 2021 May 15;590:82-93. doi: 10.1016/j.jcis.2021.01.023. Epub 2021 Jan 14.
The development of the efficient photocatalysts with improved photoexcited charge separation and transfer is an essential for the effective photocatalytic H generation using light energy. So far, owing to the unique properties and characteristics, the transition metal phosphides (TMPs) have been proven to be high performance co-catalysts to replace some of the classic precious metal materials in the photocatalytic water splitting. In the present work, we report a novel copper phosphide (CuP) as a co-catalyst to form a well-designed fabricated photocatalyst with blacktrumpet mushroom-like ZnS semiconductor for the first time. The synthesis of CuP/ZnS consists of two-step hydrothermal and ball milling methods. The physical properties of the materials so prepared were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), ultraviolet-visible diffuse reflectance spectroscopy (UV-DRS), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) analyses. In order to study the role of CuP, electrochemical impedance spectroscopy (EIS) measurements were used to investigate the photogenerated charge properties of ZnS. The experiments of photocatalytic production of H confirm that the CuP co-catalysts effectively promote the separation of photogenerated charge carriers in ZnS, and consequently enhance the H evolution activity. The 3% CuP/ZnS sample delivers the highest catalyst activity and the consistent H evolution rate is14,937 µmol h g, which is 10-fold boosted compared to the pristine ZnS. The stability of the catalyst was tested by reusing the used 3% CuP/ZnS photocatalyst in five consecutive runs, and their respective activity in the H production activity was evaluated. A possible mechanism is proposed and discussed.
开发具有改善的光激发电荷分离和转移效率的光催化剂,对于利用光能进行有效的光催化产氢至关重要。到目前为止,由于其独特的性质和特征,过渡金属磷化物(TMPs)已被证明是高性能的助催化剂,可在光催化水分解中替代一些传统的贵金属材料。在本工作中,我们首次报道了一种新型磷化铜(CuP)作为助催化剂,与黑喇叭蘑菇状的ZnS半导体形成精心设计的光催化剂。CuP/ZnS的合成包括两步水热法和球磨法。通过X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、紫外可见漫反射光谱(UV-DRS)、X射线光电子能谱(XPS)和布鲁诺尔-埃米特-泰勒(BET)分析对如此制备的材料的物理性质进行了表征。为了研究CuP的作用,采用电化学阻抗谱(EIS)测量来研究ZnS的光生电荷性质。光催化产氢实验证实,CuP助催化剂有效地促进了ZnS中光生电荷载流子的分离,从而提高了析氢活性。3% CuP/ZnS样品表现出最高的催化活性,一致的析氢速率为14937 μmol h g,与原始ZnS相比提高了10倍。通过连续五次重复使用用过的3% CuP/ZnS光催化剂来测试催化剂的稳定性,并评估它们在产氢活性中的各自活性。提出并讨论了一种可能的机理。