Chien Liang Cheng, Chiang Chen Wei, Lao Chou Chio, Lin Yung-I, Lin Hao-Wu, Keng Pei Yuin
Department of Materials Science and Engineering, National Tsing Hua University, Hsinchu City, 30013, Taiwan.
Nanoscale Res Lett. 2021 Dec 11;16(1):176. doi: 10.1186/s11671-021-03629-5.
Boron-based nanomaterials are emerging as non-toxic, earth-abundant (photo)electrocatalyst materials in solar energy conversion for the production of solar hydrogen fuel and environmental remediation. Boron carbon oxynitride (BCNO) is a quaternary semiconductor with electronic, optical, and physicochemical properties that can be tuned by varying the composition of boron, nitrogen, carbon, and oxygen. However, the relationship between BCNO's structure and -photocatalytic activity relationship has yet to be explored. We performed an in-depth spectroscopic analysis to elucidate the effect of using two different nitrogen precursors and the effect of annealing temperatures in the preparation of BCNO. BCNO nanodisks (D = 6.7 ± 1.1 nm) with turbostratic boron nitride diffraction patterns were prepared using guanidine hydrochloride as the nitrogen source precursor upon thermal annealing at 800°C. The X-ray photoelectron spectroscopy (XPS) surface elemental analysis of the BCNO nanodisks revealed the B, C, N, and O compositions to be 40.6%, 7.95%, 37.7%, and 13.8%, respectively. According to the solid-state B NMR analyses, the guanidine hydrochloride-derived BCNO nanodisks showed the formation of various tricoordinate BN(OH) species, which also served as one of the photocatalytic active sites. The XRD and in-depth spectroscopic analyses corroborated the preparation of BCNO-doped hexagonal boron nitride nanodisks. In contrast, the BCNO annealed at 600 °C using melamine as the nitrogen precursor consisted of layered nanosheets composed of B, C, N, and O atoms covalently bonded in a honeycomb lattice as evidence by the XRD, XPS, and solid-state NMR analysis (B and C) analyses. The XPS surface elemental composition of the melamine-derived BCNO layered structures consisted of a high carbon composition (75.1%) with a relatively low boron (5.24%) and nitrogen (7.27%) composition, which indicated the formation of BCNO-doped graphene oxides layered sheet structures. This series of melamine-derived BCNO-doped graphene oxide layered structures were found to exhibit the highest photocatalytic activity, exceeding the photocatalytic activity of graphitic carbon nitride. In this layered structure, the formation of the tetracoordinate BN(OH)(CO) species and the rich graphitic domains were proposed to play an important role in the photocatalytic activity of the BCNO-doped graphene oxides layered structures. The optical band gap energies were measured to be 5.7 eV and 4.2 eV for BCNO-doped hexagonal boron nitride nanodisks and BCNO-doped graphene oxides layered structures, respectively. Finally, BCNO exhibited an ultralong photoluminescence with an average decay lifetime of 1.58, 2.10, 5.18, and 8.14 µs for BGH01, BGH03, BMH01, BMH03, respectively. This study provides a novel metal-free photocatalytic system and provides the first structural analysis regarding the origin of BCNO-based photocatalyst.
硼基纳米材料正作为无毒、储量丰富的(光)电催化剂材料崭露头角,可用于太阳能转换以生产太阳能氢燃料及进行环境修复。硼碳氮氧化物(BCNO)是一种四元半导体,其电子、光学和物理化学性质可通过改变硼、氮、碳和氧的组成来调节。然而,BCNO的结构与光催化活性之间的关系尚未得到探索。我们进行了深入的光谱分析,以阐明使用两种不同氮前驱体的效果以及退火温度对BCNO制备的影响。在800°C热退火时,以盐酸胍作为氮源前驱体制备了具有六方氮化硼衍射花样的BCNO纳米盘(直径D = 6.7±1.1 nm)。对BCNO纳米盘进行的X射线光电子能谱(XPS)表面元素分析表明,B、C、N和O的组成分别为40.6%、7.95%、37.7%和13.8%。根据固态硼核磁共振分析,由盐酸胍衍生的BCNO纳米盘显示形成了各种三配位的BN(OH)物种,这些物种也作为光催化活性位点之一。XRD和深入的光谱分析证实了BCNO掺杂的六方氮化硼纳米盘的制备。相比之下,以三聚氰胺作为氮前驱体在600°C退火的BCNO由层状纳米片组成,XRD、XPS和固态核磁共振分析(B和C)分析表明,这些纳米片由在蜂窝晶格中通过共价键结合的B、C、N和O原子组成。由三聚氰胺衍生的BCNO层状结构的XPS表面元素组成包含高碳组成(75.1%),硼(5.24%)和氮(7.27%)的组成相对较低,这表明形成了BCNO掺杂的氧化石墨烯层状结构。发现这一系列由三聚氰胺衍生的BCNO掺杂的氧化石墨烯层状结构表现出最高的光催化活性,超过了石墨相氮化碳的光催化活性。在这种层状结构中,四配位的BN(OH)(CO)物种的形成和丰富的石墨域被认为在BCNO掺杂的氧化石墨烯层状结构的光催化活性中起重要作用。测得BCNO掺杂的六方氮化硼纳米盘和BCNO掺杂的氧化石墨烯层状结构的光学带隙能量分别为5.7 eV和4.2 eV。最后,BCNO表现出超长的光致发光,BGH01、BGH03、BMH01、BMH03的平均衰减寿命分别为1.58、2.10、5.18和8.14 μs。本研究提供了一种新型的无金属光催化体系,并首次对基于BCNO的光催化剂的起源进行了结构分析。