制氢
纤维素
化学工程
溶解
材料科学
纤维二糖
生物量(生态学)
氢
溶解矿浆
牙髓(牙)
三元运算
制浆造纸工业
化学
有机化学
纤维素酶
医学
海洋学
病理
地质学
工程类
程序设计语言
计算机科学
作者
Na Zhong,Xinti Yu,Heng Zhao,Jinguang Hu,Ian D. Gates
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2022-07-26
卷期号:12 (8): 819-819
被引量:4
标识
DOI:10.3390/catal12080819
摘要
Photocatalytic hydrogen production is a promising route to the provision of sustainable and green energy. However, the excess addition of traditional electron donors as the sacrificial agents to consume photogenerated holes greatly reduces the feasibility of this approach for commercialization. Herein, considering the abundant hydroxyl groups in cellulose, the major component of biomass, we adopted glucose (a component unit of cellulose), cellobiose (a structure unit of cellulose) and dissolving pulp (a pretreated cellulose) as electron donors for photocatalytic hydrogen production over a TiO2-Au-CdS material. The well-designed ternary TiO2-Au-CdS possesses a hierarchical three-dimensional ordered macroporous (3DOM) structure, which not only benefits light harvesting but can also facilitate mass diffusion to boost the reaction kinetics. As expected, the fabricated photocatalyst exhibits considerable hydrogen production from glucose (645.1 μmol·h−1·g−1), while the hydrogen production rates gradually decrease with the increased complexity in structure from cellobiose (273.9 μmol·h−1·g−1) to dissolving pulp (79.7 μmol·h−1·g−1). Other gaseous components such as CO and CH4 are also produced, indicating the partial conversion of biomass during the photoreforming process. This work demonstrates the feasibility of sustainable hydrogen production from biomass by photoreforming with a rational photocatalyst design.
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