过氧化氢
光催化
氮化碳
量子产额
锑
人工光合作用
氧气
化学
石墨氮化碳
氮化物
材料科学
制氢
碳纤维
催化作用
无机化学
光化学
氢
纳米技术
有机化学
量子力学
复合材料
物理
复合数
荧光
图层(电子)
作者
Zhenyuan Teng,Qitao Zhang,Hongbin Yang,Kosaku Kato,Wenjuan Yang,Ying‐Rui Lu,Sixiao Liu,Chengyin Wang,Akira Yamakata,Chenliang Su,Bin Liu,Teruhisa Ohno
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2021-05-21
卷期号:4 (5): 374-384
被引量:646
标识
DOI:10.1038/s41929-021-00605-1
摘要
Artificial photosynthesis offers a promising strategy to produce hydrogen peroxide (H2O2)—an environmentally friendly oxidant and a clean fuel. However, the low activity and selectivity of the two-electron oxygen reduction reaction (ORR) in the photocatalytic process greatly restricts the H2O2 production efficiency. Here we show a robust antimony single-atom photocatalyst (Sb-SAPC, single Sb atoms dispersed on carbon nitride) for the synthesis of H2O2 in a simple water and oxygen mixture under visible light irradiation. An apparent quantum yield of 17.6% at 420 nm together with a solar-to-chemical conversion efficiency of 0.61% for H2O2 synthesis was achieved. On the basis of time-dependent density function theory calculations, isotopic experiments and advanced spectroscopic characterizations, the photocatalytic performance is ascribed to the notably promoted two-electron ORR by forming μ-peroxide at the Sb sites and highly concentrated holes at the neighbouring N atoms. The in situ generated O2 via water oxidation is rapidly consumed by ORR, leading to boosted overall reaction kinetics.
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