Bi Lingling, Meng Dedong, Bu Qijing, Lin Yanhong, Wang Dejun, Xie Tengfeng
College of Chemistry, Jilin University, Changchun 130012, People's Republic of China.
Phys Chem Chem Phys. 2016 Nov 23;18(46):31534-31541. doi: 10.1039/c6cp05618k.
Nickel, a non-noble metal, is one of the most promising candidates for photocatalysis because it is inexpensive and an earth-abundant metal. Herein, Ni/CM-CN nanocomposites with Ni as a cocatalyst were synthesized by a simple solvothermal method. Field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD) confirmed that Ni nanoparticles were loaded onto the surface of CM-CN. The prepared Ni/CM-CN nanocomposites exhibited an enhanced hydrogen evolution activity. The most active catalyst contained 10% Ni and produced H at a rate of 313.2 μmol h g, which was obviously higher than that of pure CM-CN. The results of photoluminescence (PL) and photoacoustics (PA) studies indicated that the recombination efficiency of photo-induced electron-hole pairs was decreased for CM-Ni10 as compared to that for unmodified CM-CN. The transient photovoltage (TPV) measurements directly demonstrated that the recombination time of electron-hole pairs in CM-Ni10 was prolonged. More importantly, the reversed surface photovoltage (SPV) and the declined surface photocurrent (SPC) response of CM-Ni10 revealed that the photogenerated electrons could be trapped by Ni, leading to a better separation efficiency and a superior hydrogen production. Finally, the possible mechanism is proposed to illuminate the photogenerated charge behavior between CM-CN and Ni, which might provide a theoretical basis to develop efficient cocatalysts for photocatalytic water splitting.
镍作为一种非贵金属,是光催化领域最具潜力的候选材料之一,因为它价格低廉且在地壳中储量丰富。在此,通过简单的溶剂热法合成了以镍为助催化剂的Ni/CM-CN纳米复合材料。场发射扫描电子显微镜(FESEM)、透射电子显微镜(TEM)和X射线衍射(XRD)证实镍纳米颗粒负载在CM-CN表面。制备的Ni/CM-CN纳米复合材料表现出增强的析氢活性。活性最高的催化剂含有10%的镍,产氢速率为313.2 μmol h g,明显高于纯CM-CN。光致发光(PL)和光声(PA)研究结果表明,与未改性的CM-CN相比,CM-Ni10中光生电子-空穴对的复合效率降低。瞬态光电压(TPV)测量直接表明CM-Ni10中电子-空穴对的复合时间延长。更重要的是,CM-Ni10的反向表面光电压(SPV)和表面光电流(SPC)响应下降表明光生电子可以被镍捕获,从而实现更好的分离效率和更高的产氢量。最后,提出了可能的机理来解释CM-CN和镍之间的光生电荷行为,这可能为开发用于光催化水分解的高效助催化剂提供理论基础。