Atomic Ruthenium‐Promoted Cadmium Sulfide for Photocatalytic Production of Amino Acids from Biomass Derivatives

Author:

Li Wulin1,Zheng Xiuhui2,Xu Bei‐Bei34,Yang Yue5,Zhang Yifei1,Cai Lingchao1,Wang Zhu‐Jun5,Yao Ye‐Feng3,Nan Bing6,Li Lina6,Wang Xue‐Lu3,Feng Xiang2,Antonietti Markus7,Chen Zupeng1ORCID

Affiliation:

1. Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources International Innovation Center for Forest Chemicals and Materials Nanjing Forestry University Longpan Road 159 Nanjing 210037 China

2. State Key Laboratory of Heavy Oil Processing China University of Petroleum Changjiang West Road 66 Qingdao 266580 China

3. Physics Department Shanghai Key Laboratory of Magnetic Resonance East China Normal University Shanghai 200062 China

4. School of New Energy Nanjing University of Science and Technology Wu Xi Shi, Jiangyin 214400 China

5. School of Physical Science and Technology Shanghai Tech University Huaxia Middle Road 393 Shanghai 201210 China

6. Shanghai Synchrotron Radiation Facility Shanghai Advanced Research Institute Zhangheng Road 293 Shanghai 201204 China

7. Department of Colloid Chemistry Max-Planck Institute of Colloids and Interfaces, Research Campus Golm Am Mühlenberg 1 Potsdam 14476 Germany

Abstract

AbstractAmino acids are the building blocks of proteins and are widely used as important ingredients for other nitrogen‐containing molecules. Here, we report the sustainable production of amino acids from biomass‐derived hydroxy acids with high activity under visible‐light irradiation and mild conditions, using atomic ruthenium‐promoted cadmium sulfide (Ru1/CdS). On a metal basis, the optimized Ru1/CdS exhibits a maximal alanine formation rate of 26.0 molAla ⋅ gRu−1 ⋅ h−1, which is 1.7 times and more than two orders of magnitude higher than that of its nanoparticle counterpart and the conventional thermocatalytic process, respectively. Integrated spectroscopic analysis and density functional theory calculations attribute the high performance of Ru1/CdS to the facilitated charge separation and O−H bond dissociation of the α‐hydroxy group, here of lactic acid. The operando nuclear magnetic resonance further infers a unique “double activation” mechanism of both the CH−OH and CH3−CH−OH structures in lactic acid, which significantly accelerates its photocatalytic amination toward alanine.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Natural Science Research of Jiangsu Higher Education Institutions of China

Key Technologies Research and Development Program

Publisher

Wiley

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