光电阴极
法拉第效率
电催化剂
亚硝酸盐
光电化学
氨
材料科学
合理设计
产量(工程)
纳米技术
氧化物
无机化学
纳米线
密度泛函理论
合金
电化学
化学
选择性
化学工程
纳米材料
纳米晶
作者
Kejian Li,Tianyin Qiu,Bingxing Zhang,Zhengwei Ye,Jan Paul Menzel,Wan Jae Dong,Yuyang Pan,Songtao Tang,Zhuoran Long,Víctor S. Batista,Zetian Mi
标识
DOI:10.1021/acs.est.5c04038
摘要
Solar-driven photoelectrochemical conversion of nitrite to ammonia represents a sustainable yet unexplored approach for environmental remediation and resource recovery. Here, we demonstrate that Cu5Pd1 alloy nanoparticles, integrated with vertically grown GaN nanowires on an n+-p Si photocathode (Cu5Pd1/GaN/Si), enable highly efficient and selective nitrite reduction to ammonia. This photoelectrode achieves a Faradaic efficiency of 99.7% for NH3, with a yield rate of 162.2 μmol h-1 cm-2 and a nearly 100% selectivity. Additionally, the Cu5Pd1/GaN/Si photoelectrode maintains robust performance in the presence of various anions and can effectively remove ∼98% of nitrite even at low concentrations. Density functional theory calculations, supported by in situ spectroscopic techniques, reveal that Cu-Pd alloying fundamentally alters the nitrite reduction mechanisms. Unlike the *NOH-mediated pathway on Cu and Pd, which can lead to competing N2 formation, the CuPd alloy preferentially stabilizes the *NHO intermediate, making NH3 production thermodynamically preferred and highly selective. These findings highlight that a rational electrocatalyst design can effectively tune reaction pathways to enhance both the efficiency and selectivity of photoelectrocatalytic nitrite upcycling.
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