State Key Laboratory of Metal Matrix Composites, School of Materials Science and Engineering and ‡University of Michigan-Shanghai Jiao Tong University Joint Institute, Shanghai Jiao Tong University , 800 Dongchuan Road, Shanghai 200240, P. R. China.
ACS Appl Mater Interfaces. 2017 Apr 12;9(14):12494-12500. doi: 10.1021/acsami.7b01428. Epub 2017 Apr 3.
Construction of a metal-semiconductor heterojunction is a promising method to improve heterogeneous photocatalysis for various reactions. Although the structure and photocatalytic performance of such a catalyst system have been extensively studied, few reports have demonstrated the effect of interface orientation at the metal-semiconductor junction on junction-barrier bending and the electronic transport properties. Here, we construct a Pt/PbS heterojunction, in which Pt nanoparticles are used as highly active catalysts and PbS nanocrystals (NCs) with well-controlled shapes are used as light-harvesting supports. Experimental results show that the photoelectrocatalytic activities of the Pt/PbS catalyst are strongly dependent on the contacting facets of PbS at the junction. Pt/octahedral PbS NCs with exposed PbS(111) facets show the highest photoinduced enhancement of hydrogen evolution reaction activity, which is ∼14.38 times higher than that of the ones with only PbS(100) facets (Pt/cubic PbS NCs). This enhancement can further be rationalized by the different energy barriers of the Pt/PbS Schottky junction due to the specific band structure and electron affinity, which is also confirmed by the calculations based on density functional theory. Therefore, controlling the contacting interfaces of a metal/semiconductor material may offer an effective approach to form the desired heterojunction for optimization of the catalytic performance.
构建金属-半导体异质结是提高各种反应的多相光催化的一种很有前途的方法。尽管这种催化剂体系的结构和光催化性能已经得到了广泛的研究,但很少有报道表明金属-半导体结处的界面取向对结势垒弯曲和电子输运性质的影响。在这里,我们构建了一个 Pt/PbS 异质结,其中 Pt 纳米颗粒用作高活性催化剂,而具有良好控制形状的 PbS 纳米晶体(NCs)用作光捕获载体。实验结果表明,Pt/PbS 催化剂的光电催化活性强烈依赖于结处 PbS 的接触晶面。具有暴露的 PbS(111)晶面的 Pt/八面体 PbS NCs 表现出最高的光诱导增强氢析出反应活性,比仅具有 PbS(100)晶面的 Pt/立方 PbS NCs 高约 14.38 倍。这种增强可以通过 Pt/PbS 肖特基结由于特定的能带结构和电子亲和力而导致的不同能垒来合理地解释,这也通过基于密度泛函理论的计算得到了证实。因此,控制金属/半导体材料的接触界面可能为形成所需的异质结提供一种有效的方法,以优化催化性能。