光催化
质子化
硝酸盐
化学
催化作用
无机化学
硼
电子空穴
六方氮化硼
选择性
光化学
材料科学
纳米技术
电子
有机化学
离子
石墨烯
物理
量子力学
作者
Cuishuang Jiang,Hongze An,Guojun Dong,Jing Feng,Mingyi Zhang,Yueming Ren,Jun Ma
标识
DOI:10.1016/j.cej.2021.131054
摘要
Hole scavengers must be added into the photocatalytic nitrate reduction system to achieve the efficient NO3− conversion in water. Herein, for the first time, high NO3− conversion of 97.94% and N2 selectivity of 97.31% are obtained without additional hole scavengers, using a catalyst of treated hexagonal boron nitride (h-BN) with modified −OH and −NH2 groups on its edges. The functionalized h-BN presents excellent reuse stability. Moreover, the functions of various groups are explored during photocatalytic nitrate reduction. −NH2 groups and OH− (accompanied product of −NH2 protonation) behave as hole stabilizers and hole scavengers, respectively. They considerably improve the separation of electron-hole pairs, ensuring a remarkable capability to generate electrons for direct nitrate reduction without hole scavengers incorporation. New active sites of −OH groups and NH3+ (product of −NH2 protonation) are much more conducive to the reduction of nitrate than boron-terminated edges. More importantly, −OH groups play a major role in producing N2. This study provides a reference for efficient photocatalytic reduction of NO3− in water without additional hole scavengers by the functionalized catalysts.
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