木质素
光催化
生物量(生态学)
氢
制氢
固溶体
基质(水族馆)
化学工程
带隙
化学
材料科学
碳纤维
纳米技术
有机化学
催化作用
光电子学
复合材料
海洋学
工程类
地质学
复合数
作者
Bruna Palma,Xi Cheng,Liyang Liu,Na Zhong,Heng Zhao,Scott Renneckar,Steve Larter,Md Golam Kibria,Jinguang Hu
标识
DOI:10.1002/cptc.202200193
摘要
Abstract Biomass photorefinery for simultaneous production of value‐added chemicals and sustainable hydrogen holds promising perspective to achieve a negative carbon economy. However, insight into lignin valorization by the photorefinery approach is still lacking due to the extremely complex structure and component. In this work, we design a series of Zn 1‐ x Cd x S solid solutions as photocatalyst to reveal the photocatalytic mechanism for model component conversion. Bandgap engineering by changing the Zn/Cd ratio is proven to efficiently regulate the reaction pathway. Specifically, Zn 0.75 Cd 0.25 S (ZCS25) presented the best performance for hydrogen evolution (610±105 μmol h −1 g cat. −1 ) while Zn 0.5 Cd 0.5 S (ZCS50) demonstrated the best substrate conversion to monophenolic compounds. Besides, the well‐designed Zn 1‐x Cd x S solid solutions also show the ability to produce hydrogen and eliminate a methoxy group from real lignin by the photorefinery approach. This present work demonstrates a good example of biomass valorization by careful design of photocatalysts.
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