Kulkarni Aniruddha K, Praveen C S, Sethi Yogesh A, Panmand Rajendra P, Arbuj Sudhir S, Naik Sonali D, Ghule Anil V, Kale Bharat B
Nanocrystalline Laboratory, Centre for Material for Electronic Technology (CMET), Ministry of Electronics and Information Technology (MeitY), Govt. of India, Panchawati, Off Pashan Road, Pune 411007, India.
Dalton Trans. 2017 Nov 7;46(43):14859-14868. doi: 10.1039/c7dt02611k.
The synthesis of orthorhombic nitrogen-doped niobium oxide (NbON) nanostructures was performed and a photocatalytic study carried out in their use in the conversion of toxic HS and water into hydrogen under UV-Visible light. Nanostructured orthorhombic NbON was synthesized by a simple solid-state combustion reaction (SSCR). The nanostructural features of NbON were examined by FESEM and HRTEM, which showed they had a porous chain-like structure, with chains interlocked with each other and with nanoparticles sized less than 10 nm. Diffuse reflectance spectra depicted their extended absorbance in the visible region with a band gap of 2.4 eV. The substitution of nitrogen in place of oxygen atoms as well as Nb-N bond formation were confirmed by X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. A computational study (DFT) of NbON was also performed for investigation and conformation of the crystal and electronic structure. N-Substitution clearly showed a narrowing of the band gap due to N 2p bands cascading above the O 2p band. Considering the band gap in the visible region, NbON exhibited enhanced photocatalytic activity toward hydrogen evolution (3010 μmol h g) for water splitting and (9358 μmol h g) for HS splitting under visible light. The enhanced photocatalytic activity of NbON was attributed to its extended absorbance in the visible region due to its electronic structure being modified upon doping, which in turn generates more electron-hole pairs, which are responsible for higher H generation. More significantly, the mesoporous nanostructure accelerated the supression of electron and hole recombination, which also contributed to the enhancement of its activity.
合成了正交晶系氮掺杂氧化铌(NbON)纳米结构,并对其在紫外-可见光下将有毒的HS和水转化为氢气的光催化性能进行了研究。通过简单的固态燃烧反应(SSCR)合成了纳米结构的正交晶系NbON。利用场发射扫描电子显微镜(FESEM)和高分辨率透射电子显微镜(HRTEM)对NbON的纳米结构特征进行了研究,结果表明其具有多孔链状结构,链与链相互联锁,且纳米颗粒尺寸小于10nm。漫反射光谱显示其在可见光区域具有扩展的吸光度,带隙为2.4eV。通过X射线光电子能谱(XPS)和拉曼光谱证实了氮取代氧原子以及Nb-N键的形成。还对NbON进行了理论计算研究(DFT),以研究和确定其晶体结构和电子结构。氮取代明显显示出带隙变窄,这是由于N 2p能带在O 2p能带之上层叠。考虑到其在可见光区域的带隙,NbON在可见光下对水分解制氢表现出增强的光催化活性(3010 μmol h g),对HS分解制氢表现出增强的光催化活性(9358 μmol h g)。NbON光催化活性增强的原因是其掺杂后电子结构发生改变,在可见光区域具有扩展的吸光度,进而产生更多的电子-空穴对,这些电子-空穴对负责更高的氢气生成。更重要的是,介孔纳米结构加速了电子和空穴复合的抑制,这也有助于其活性的增强。