作者机构：
[凌灿灿; 李浩; 占光明] School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China;[凌灿灿; 占光明] Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental & Applied Chemistry, Central China Normal University, Wuhan 430079, China;[梁川; 刘修凡; 孙红卫; 赵进才; 周兵; 李亚玲; 李美琪] Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental & Applied Chemistry, Central China Normal University, Wuhan 430079, China;[Li, Hao] School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China. Electronic address: hao_li@sjtu.edu.cn;[李浩] Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental & Applied Chemistry, Central China Normal University, Wuhan 430079, China. Electronic address: zhanglizhi@sjtu.edu.cn
通讯机构：
[Hao Li; Lizhi Zhang] S;School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China<&wdkj&>Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental & Applied Chemistry, Central China Normal University, Wuhan 430079, China<&wdkj&>School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China
摘要：
Heterogeneous peroxysulfates-based advanced oxidation pro-cesses(AOPs)have garnered significant attention for purifying organic wastewater since they offer many advantages like low cost,safe storage,facile activation and reactive species participation[1].
作者：
Chengliang Mao;Jiaxian Wang;Yunjie Zou;Yanbiao Shi;Camilo J. Viasus;...
期刊：
Journal of the American Chemical Society,2023年145(24):13134-13146 ISSN：0002-7863
通讯作者：
Lirong Zheng<&wdkj&>Lizhi Zhang<&wdkj&>Geoffrey A. Ozin
作者机构：
[Yunjie Zou; Meiqi Li; Huan Shang; Zhilin Li] Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental & Applied Chemistry, College of Chemistry, Central China Normal University, Wuhan 430079, P. R. China;[Joel Y. Y. Loh; Nazir P. Kherani] Department of Materials Science and Engineering, University of Toronto, Toronto, Ontario M5S 3E4, Canada;[Yanjiang Liu] Ontario Centre for the Characterization of Advanced Materials, University of Toronto, 200 College Street, Toronto, Ontario M5S 3E5, Canada;[Camilo J. Viasus; Meikun Xia; Shufang Ji; Mireille Ghoussoub; Yang-Fan Xu; Jessica Ye; Geoffrey A. Ozin] Materials Chemistry and Nanochemistry Research Group, Solar Fuels Cluster, Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada;[Lirong Zheng] Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, P. R. China
通讯机构：
[Lirong Zheng] B;[Lizhi Zhang] K;[Geoffrey A. Ozin] M;Materials Chemistry and Nanochemistry Research Group, Solar Fuels Cluster, Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada<&wdkj&>Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, P. R. China<&wdkj&>Key Laboratory of Pesticide & Chemical Biology of Ministry of Education, Institute of Environmental & Applied Chemistry, College of Chemistry, Central China Normal University, Wuhan 430079, P. R. China<&wdkj&>School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China
摘要：
Stable metal nitrides (MN) are promising materials to fit the future "green" ammonia-hydrogen nexus. Either through catalysis or chemical looping, the reductive hydrogenation of MN to MN(1-x) is a necessary step to generate ammonia. However, encumbered by the formation of kinetically stable M-NH(1─3) surface species, this reduction step remains challenging under mild conditions. Herein, we discovered that deleterious Ti-NH(1─3) accumulation on TiN can be circumvented photochemically with supported single atoms and clusters of platinum (Pt(1)-Pt(n)) under N(2)-H(2) conditions. The photochemistry of TiN selectively promoted Ti-NH formation, while Pt(1)-Pt(n) effectively transformed any formed Ti-NH into free ammonia. The generated ammonia was found to originate mainly from TiN reduction with a minor contribution from N(2) activation. The knowledge accrued from this fundamental study could serve as a springboard for the development of MN materials for more efficient ammonia production to potentially disrupt the century-old fossil-powered Haber-Bosch process.
摘要：
Herein, sulfur vacancies in magnetic greigite (SVs-Fe3S4) nanosheets were synthesized by a one-step solvothermal method by adjusting the ethylene glycol: water ratio. Electron paramagnetic resonance spectroscopy (EPR) and X-ray photoelectron spectroscopy (XPS) revealed that SV-rich Fe3S4 and SV-poor Fe3S4 were acquired using 100% ethylene glycol and 100% water as solvent, respectively. A peroxidase-like activity assay demonstrated that maximum reaction rates for H2O2-mediated oxidation of 3,3',5,5'-tetramethyl-benzidine (TMB) catalyzed by the SV-rich Fe3S4 was 2.3 times higher than SV-poor Fe3S4. Density functional theory (DFT) calculations and reactive oxygen species (ROS) detection confirmed that the enhanced peroxidase-like activity by SV-rich Fe3S4 was attributed to efficient adsorption of H2O2 and subsequent decomposition to hydroxyl radicals (center dot OH) on the SVs sites of Fe3S4. The SV-rich Fe3S4 nanozyme was employed to develop a simple, highly sensitive and selective assay for glucose detection with a linear range of 0.5-150 mu M and a detection limit of 0.1 mu M (S/N = 3). A smartphone application (App) was designed and applied to efficiently detect serum glucose with the integrated analytical system based on the SV-rich Fe3S4. These new findings highlight the important role of surface defects in nanozymes on generating peroxidase-like activity for glucose detection in point-of-care diagnosis. (C) 2020 Elsevier B.V. All rights reserved.
通讯机构：
[Peng, X; Zhang, LZ] C;Cent China Normal Univ, Coll Chem, Inst Environm & Appl Chem, Key Lab Pesticide & Chem Biol,Minist Educ, Wuhan 430079, Peoples R China.
关键词：
Zero-valent iron;FeC2O4 center dot 2H(2)O shell;Cr(VI) removal;Proton transfer;Surface-bound Fe2+
摘要：
In this study, we coated a high proton conducive shell on the zero-valent iron (ZVI) surface by mechanically ball-milling ZVI with oxalic acid dihydrate (OX-ZVI), and demonstrated that the generated FeC2O4 center dot 2H(2)O shell dramatically improved the Cr(VI) removal rate of ZVI by about 15-80 times. Owing to a higher proton conductivity of FeC2O4 center dot 2H(2)O shell than that of Fe2O3 shell, proton could easily transfer through FeC2O4 center dot 2H(2)O shell into iron core and be reduced to center dot H, accompanying with fast surface-bound Fe2+ generation, resulting in high efficiency of Cr(VI) removal in a wide pH range. Meanwhile, the removed Cr(VI) was deposited on OX-ZVI surface in the formation of FexCr1-x(OH)(3) composites, accompanied by the appearance of typical hollow structure derived from iron core dissolution. This study clarifies the significance of proton transfer on the reactivity of zero-valent iron, and also provides a new strategy to prepare highly active zero-valent iron for Cr(VI) removal.
摘要：
Rational engineering of oxygen vacancy (V-O) at atomic precision is the key to comprehensively understanding the oxygen chemistry of oxide materials for catalytic oxidations. Here, we demonstrate that V-O can be spatially confined on the surface through a sophisticated surface hydrogen bond (HB) network. The HB network is constructed between a hydroxyl-rich BiOCl surface and polyprotic phosphoric acid, which remarkably decreases the formation energy of surface V-O by selectively weakening the metal-oxygen bonds in a short range. Thus, surface-confined V-O enables us to unambiguously distinguish the intrafacial and suprafacial oxygen species associated with NO oxidation in two classical catalytic systems. Unlike randomly distributed bulk V-O that benefits the thermocatalytic NO oxidation and lattice O diffusion by the dominant intrafacial mechanism, surface V-O is demonstrated to favor the photocatalytic NO oxidation through a suprafacial scheme by energetically activating surface O-2, which should be attributed to the spatial confinement nature of surface V-O. (C) 2020 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.
摘要：
Developing efficient methods to degrade perfluorochemicals (PFCs), an emerging class of highly recalcitrant contaminants, are urgently needed in recent years, due to their persistence, high toxicity, and resistance to most regular treatment procedures. Here, a UV-photolysis system is reported for efficient mineralization of perfluorooctanoic acid (PFOA) via irradiation of ferric nitrate aqueous solution, where in-situ generating *NO2 and the effective Fe(3+)/Fe(2+) redox cycle synergistically play great roles on rapidly mediating the mineralization of PFOA. A fast PFOA removal kinetics with first-order kinetic constants of 2.262 h(-1) is observed at initial PFOA concentration of 5 ppm (50 mL volume), reaching approximately 92 % removal efficiency within only 0.5-h irradiation. Near-stoichiometric fluoride ions liberation and high total organic carbon (TOC) removal efficiency ( approximately 100 %) further validated the capability for completely destructive removal of PFOA. A tentative pathway for PFOA destruction is proposed. This work, by UV photolysis of abundant existing iron/nitrate-based systems in natural environment, provides an economical, sustainable and highly efficient approach for complete mineralization of perfluorinated chemicals.
作者：
Mao, Chengliang;Wang, Jiaxian;Zou, Yunjie;Qi, Guodong;Loh, Joel Yi Yang;...
期刊：
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,2020年142(41):17403-17412 ISSN：0002-7863
通讯作者：
Zhang, Lizhi;Ozin, Geoffrey A.
作者机构：
[Zhang, Lizhi; Zou, Yunjie; Liu, Xiao; Ai, Zhihui; Wang, Jiaxian; Mao, Chengliang; Shang, Huan; Zhao, Jincai; Li, Jie; Li, Meiqi] Cent China Normal Univ, Coll Chem, Inst Environm & Appl Chem, Key Lab Pesticide & Chem Biol,Minist Educ, Wuhan 430079, Peoples R China.;[Ghoussoub, Mireille; Mao, Chengliang; Wang, Lu; Xia, Meikun; Ozin, Geoffrey A.] Univ Toronto, Dept Chem, Solar Fuels Cluster, Mat Chem & Nanochem Res Grp, Toronto, ON M5S 3H6, Canada.;[Qi, Guodong; Xu, Jun; Deng, Feng] Chinese Acad Sci, State Key Lab Magnet Resonance & Atom & Mol Phys, Natl Ctr Magnet Resonance Wuhan, Wuhan Inst Phys & Math,Innovat Acad Precis Measur, Wuhan 430071, Peoples R China.;[Loh, Joel Yi Yang; Kherani, Nazir P.] Univ Toronto, Dept Mat Sci & Engn, Toronto, ON M5S 3E4, Canada.;[Zhang, Tianhua] Fuzhou Univ, Natl Engn Res Ctr Chem Fertilizer Catalyst NERC C, Sch Chem Engn, Fuzhou 350002, Fujian, Peoples R China.
通讯机构：
[Zhang, Lizhi] C;[Ozin, Geoffrey A.] U;Cent China Normal Univ, Coll Chem, Inst Environm & Appl Chem, Key Lab Pesticide & Chem Biol,Minist Educ, Wuhan 430079, Peoples R China.;Univ Toronto, Dept Chem, Solar Fuels Cluster, Mat Chem & Nanochem Res Grp, Toronto, ON M5S 3H6, Canada.
摘要：
Optimizing kinetic barriers of ammonia synthesis to reduce the energy intensity has recently attracted significant research interest. The motivation for the research is to discover means by which activation barriers of N-2 dissociation and NHz (z = 1-2, surface intermediates) destabilization can be reduced simultaneously, that is, breaking the "scaling relationship". However, by far only a single success has been reported in 2016 based on the discovery of a strong-weak N-bonding pair: transition metals (nitrides)-LiH. Described herein is a second example that is counterintuitively founded upon a strong-strong N-bonding pair unveiled in a bifunctional nanoscale catalyst TiO2-xHy/Fe (where 0.02 <= x <= 0.03 and 0 < y < 0.03), in which hydrogen spillover (H) from Fe to cascade oxygen vacancies (O-V-O-V) results in the trapped form of O-V-H on the TiO2-xHy component. The Fe component thus enables facile activation of N-2, while the O-V-H in TiO2-xHy hydrogenates the N or NHz to NH3 easily.
期刊：
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,2020年142(15):7036-7046 ISSN：0002-7863
通讯作者：
Zhang, Lizhi;Yu, Jimmy C.
作者机构：
[Xu, Liangpang; Lei, Fengcai; Chan, Alice W. M.; Li, Lejing; Liu, Yang; Yu, Jimmy C.; Li, Jie] Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China.;[Quan, Fengjiao; Zhang, Lizhi; Shi, Yanbiao; Mao, Chengliang; Zhan, Guangming] Cent China Normal Univ, Coll Chem, Inst Environm & Appl Chem, Minist Educ,Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China.;[Wang, Jianfang; Yang, Jianhua] Chinese Univ Hong Kong, Dept Phys, Shatin, Hong Kong, Peoples R China.;[Wong, Po Keung; Wang, Bo] Chinese Univ Hong Kong, Sch Life Sci, Shatin, Hong Kong, Peoples R China.;[Du, Yi; Dou, Shi-Xue] Univ Wollongong, AIIM, ISEM, Wollongong, NSW 2500, Australia.
通讯机构：
[Zhang, Lizhi; Yu, Jimmy C.] C;Cent China Normal Univ, Coll Chem, Inst Environm & Appl Chem, Minist Educ,Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China.;Chinese Univ Hong Kong, Dept Chem, Shatin, Hong Kong, Peoples R China.
摘要：
The limitations of the Haber-Bosch reaction, particularly high-temperature operation, have ignited new interests in low-temperature ammonia-synthesis scenarios. Ambient N-2 electroreduction is a compelling alternative but is impeded by a low ammonia production rate (mostly <10 mmol g(cat)(-1) h(-1)), a small partial current density (<1 mA cm(-2)), and a high-selectivity hydrogen-evolving side reaction. Herein, we report that room-temperature nitrate electroreduction catalyzed by strained ruthenium nanoclusters generates ammonia at a higher rate (5.56 g(cat)(-1) h(-1)) than the Haber- Bosch process. The primary contributor to such performance is hydrogen radicals, which are generated by suppressing hydrogen-hydrogen dimerization during water splitting enabled by the tensile lattice strains. The radicals expedite nitrate-to-ammonia conversion by hydrogenating intermediates of the rate-limiting steps at lower kinetic barriers. The strained nanostructures can maintain nearly 100% ammonia-evolving selectivity at >120 mA cm(-2) current densities for 100 h due to the robust subsurface Ru-O coordination. These findings highlight the potential of nitrate electroreduction in real-world, low-temperature ammonia synthesis.
