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Abstract
Two-dimensional (2D) materials, as adsorbents, have garnered great attention in removing heavy metal ions (HMIs) from drinking water due to their extensive exposed adsorption sites. Nevertheless, there remains a paucity of experimental research to remarkably unlock their adsorption capabilities and fully elucidate their adsorption mechanisms. In this work, exceptional lead ion (Pb2+) (a common HMI) removal capacity (up to 758 mg g−1) is achieved using our synthesized metallic 1T/1T′ phase 2D transition metal dichalcogenide (TMD, including MoS2, WS2, TaS2, and TiS2) nanosheets, which hold tremendous activated S chemisorption sites. The residual Pb2+ concentration can be reduced from 2 mg L−1 to 2 μg L−1 within 0.5 min, meeting the drinking water standards following World Health Organization guideline (Pb2+ concentrations <10 μg L−1). Atomic-scale characterizations and calculations based on density functional theory unveil that Pb2+ bond to the top positions of transition metal atoms in a single-atom form through the formation of S-Pb bonds. Point-of-use (POU) devices fabricated by our reported metallic phase MoS2 nanosheets exhibit treatment capacity of 55 L-water g−1-adsorbent for feed Pb2+ concentration of 1 mg L−1, which is 1-3 orders of magnitude higher than other 2D materials and commercial activated carbon.
2D materials are known for their ability to remove heavy metal ions from water, however their adsorption mechanism is not well-understood. Here the authors prepared metallic 1T/1T′ phase 2D transition metal dichalcogenide nanosheets, with activated sulfur sites, for rapid removal of Pb2+ ions.
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1 City University of Hong Kong, Department of Materials Science and Engineering, and State Key Laboratory of Marine Pollution, and Center of Super-Diamond and Advanced Films, Hong Kong SAR, China (GRID:grid.35030.35) (ISNI:0000 0004 1792 6846)
2 The Hong Kong Polytechnic University, Department of Applied Biology and Chemical Technology, Hong Kong SAR, China (GRID:grid.16890.36) (ISNI:0000 0004 1764 6123)
3 The Chinese University of Hong Kong, Department of Chemistry, Hong Kong, China (GRID:grid.10784.3a) (ISNI:0000 0004 1937 0482)
4 Chinese Academy of Sciences, Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Beijing, China (GRID:grid.9227.e) (ISNI:0000000119573309)
5 Central South University, School of Materials Science and Engineering, Hunan Provincial Key Laboratory of Electronic Packaging and Advanced Functional Materials, Changsha, PR China (GRID:grid.216417.7) (ISNI:0000 0001 0379 7164)
6 Department of Applied Physics, Research Institute for Smart Energy, The Hong Kong Polytechnic University, Hong Kong, China (GRID:grid.16890.36) (ISNI:0000 0004 1764 6123)
7 State Key Laboratory of Marine Pollution and Department of Chemistry, City University of Hong Kong, Hong Kong SAR, China (GRID:grid.35030.35) (ISNI:0000 0004 1792 6846)
8 Center for 2D Quantum Heterostructures, Institute for Basic Science, Sungkyunkwan University (SKKU), Suwon, Republic of Korea (GRID:grid.410720.0) (ISNI:0000 0004 1784 4496); Department of Energy Science, Sungkyunkwan University (SKKU), Suwon, Republic of Korea (GRID:grid.264381.a) (ISNI:0000 0001 2181 989X)
9 Department of Civil Engineering, The University of Hong Kong, Hong Kong SAR, China (GRID:grid.194645.b) (ISNI:0000 0001 2174 2757)
10 Beijing National Center for Electron Microscopy and Laboratory of Advanced Materials, Department of Materials Science and Engineering, Tsinghua University, Beijing, China (GRID:grid.12527.33) (ISNI:0000 0001 0662 3178)
11 Institut Européen des Membranes, IEM, UMR 5635, Université Montpellier, ENSCM, CNRS, Montpellier, France (GRID:grid.461901.b) (ISNI:0000 0001 2194 0104)
12 City University of Hong Kong, Department of Materials Science and Engineering, and State Key Laboratory of Marine Pollution, and Center of Super-Diamond and Advanced Films, Hong Kong SAR, China (GRID:grid.35030.35) (ISNI:0000 0004 1792 6846); Shenzhen Research Institute, City University of Hong Kong, Shenzhen, China (GRID:grid.35030.35) (ISNI:0000 0004 1792 6846)