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Title: Synergies between Unsaturated Zn/Cu Doping Sites in Carbon Dots Provide New Pathways for Photocatalytic Oxidation

Journal Article · · ACS Catalysis
ORCiD logo [1];  [2];  [2];  [3];  [2];  [2];  [2];  [4]; ORCiD logo [5]; ORCiD logo [2]
  1. China Univ. of Petroleum, Qingdao (China). State Key Lab. of Heavy Oil Processing, College of Chemical Engineering; Argonne National Lab. (ANL), Argonne, IL (United States). Center for Nanoscale Materials
  2. China Univ. of Petroleum, Qingdao (China). State Key Lab. of Heavy Oil Processing, College of Chemical Engineering
  3. Chinese Academy of Sciences, Beijing (China). Key Lab. of Photochemical Conversion and Optoelectronic Materials, Technical Inst. of Physics and Chemistry
  4. Argonne National Lab. (ANL), Argonne, IL (United States). Center for Nanoscale Materials
  5. Dalian Univ. of Technology, Dalian (China). State Key Lab. of Fine Chemicals, School of Chemical Engineering

Unsaturated metal species (UMS) confined in nanomaterials play important roles for electron transfer in a wide range of catalytic reactions. However, the limited fabrication methods of UMS restrict their wider catalytic applications. Here in this paper, we report on the synergy of unsaturated Zn and Cu dopants confined in carbon dots (ZnCu-CDs) to produce enhanced electron transfer and photooxidation processes in the doped CDs. The Zn/Cu species chelate with the carbon matrix mainly through Cu-O(N)-Zn-O(N)-Cu complexes. Within this structure, Cu2+ acts as a mild oxidizer that facilely increases the unsaturated Zn content and also precisely tunes the unsaturated Zn valence state to Znd+, where d is between 1 and 2, instead of Zn. With the help of UMS, electron-transfer pathways are produced, enhancing both the electron donating (7.0 times) and-accepting (5.3 times) abilities relative to conventional CDs. Because of these synergistic effects, the photocatalytic efficiency of CDs in photooxidation reactions is shown to improve more than 5-fold.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES); National Natural Science Foundation of China (NSFC); China Scholarship Council; China Postdoctoral Science Foundation; Shandong Provincial Natural Science Foundation
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1426233
Journal Information:
ACS Catalysis, Vol. 8, Issue 2; ISSN 2155-5435
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 48 works
Citation information provided by
Web of Science

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Practical Three-Minute Synthesis of Acid-Coated Fluorescent Carbon Dots with Tuneable Core Structure journal August 2018
Lignite-derived carbon quantum dot/TiO 2 heterostructure nanocomposites: photoinduced charge transfer properties and enhanced visible light photocatalytic activity journal January 2019
Two-dimensional-related catalytic materials for solar-driven conversion of CO x into valuable chemical feedstocks journal January 2019
Evolution and Synthesis of Carbon Dots: From Carbon Dots to Carbonized Polymer Dots journal September 2019
Hantzsch ester as hole relay significantly enhanced photocatalytic hydrogen production journal January 2018
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