量子点光催化剂与弱 HCHO 吸附及原位生成的 Ni0 合作从生物质 HCO2H 中高效制取 H2

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL
Wen-Ting Niu, Wanghui Zhao, Kai-Wen Feng, Fu-Jia Tang, Tao Wang, Kaixuan Wang, Shaohua Shen and Yang Li*, 
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引用次数: 0

摘要

利用可再生资源(如生物质,地球上最大的可再生资源之一)而不是化石资源高效生产氢气(H2)是非常可取的。将 HCO2H 作为生物质制取氢气的中间体,既有利于高效制取氢气,又能避免氢气储存问题。在此,我们报告了通过 CdS/ZnS-S2- 量子点光催化剂与弱甲醛(HCHO)吸附和原位生成的 Ni0 的合作,在温和条件下利用无惰性金属催化系统从生物质原料甲酸(HCO2H)中高效制取 H2 的过程。在可见光照射下,3.5 小时内 H2 的产率为 94%,选择性为 99.7%,平均速率为 537 ± 14 mol mg-1 h-1。这项研究将促进对催化系统的探索,以简化从可再生生物质制取 H2 的过程,并将其应用于实际应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficient H2 Production from Biomass-Based HCO2H by Cooperation of Quantum Dots Photocatalysts with Weak HCHO Adsorption and In Situ Generated Ni0

Efficient H2 Production from Biomass-Based HCO2H by Cooperation of Quantum Dots Photocatalysts with Weak HCHO Adsorption and In Situ Generated Ni0

Efficient H2 Production from Biomass-Based HCO2H by Cooperation of Quantum Dots Photocatalysts with Weak HCHO Adsorption and In Situ Generated Ni0

Efficient hydrogen (H2) production from renewable resources, such as biomass, one of the largest renewable resources on the earth, instead of fossil resources, is highly desirable. Making it via HCO2H as an intermediate for H2 production from biomass both facilitates efficient H2 production and can avoid the issues of H2 storage. Herein, we report efficient H2 production from raw biomass-based formic acid (HCO2H) by a noble-metal-free catalysis system under mild conditions, enabled by cooperation of CdS/ZnS-S2– quantum dots photocatalysts with weak formaldehyde (HCHO) adsorption and in situ generated Ni0, resulting in H2 with a 94% yield in 3.5 h, with a 99.7% selectivity and a 537 ± 14 mol mg–1 h–1 average rate at 50 °C under visible-light irradiation. This study should promote the exploration of catalytic systems for streamlined H2 production from renewable biomass for practical application.

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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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