Institution
Wuhan University
Education•Wuhan, China•
About: Wuhan University is a education organization based out in Wuhan, China. It is known for research contribution in the topics: Population & Feature extraction. The organization has 92849 authors who have published 92882 publications receiving 1691049 citations. The organization is also known as: WHU & Wuhan College.
Papers published on a yearly basis
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TL;DR: It is illustrated that the roles of nitrogen species in CNT-based persulfate systems are intrinsically different, which provides new insights into the intrinsic roles of heteroatom doping in nanocarbons for persulfates activation and unveils the principles for rational design of reaction-oriented carbocatalysts for pers fulfilment in advanced oxidation processes.
Abstract: Persulfates activation by carbon nanotubes (CNT) has been evidenced as nonradical systems for oxidation of organic pollutants. Peroxymonosulfate (PMS) and peroxydisulfate (PDS) possess discrepant atomic structures and redox potentials, while the nature of their distinct behaviors in carbocatalytic activation has not been investigated. Herein, we illustrated that the roles of nitrogen species in CNT-based persulfate systems are intrinsically different. In PMS activation mediated by nitrogen-doped CNT (N-CNT), surface chemical modification (N-doping) can profoundly promote the adsorption quantity of PMS, consequently elevate potential of derived nonradical N-CNT-PMS* complexes, and boost organic oxidation efficiency via an electron-transfer regime. In contrast, PDS adsorption was not enhanced upon incorporating N into CNT due to the limited equilibrium adsorption quantity of PDS, leading to a relatively lower oxidative potential of PDS/N-CNT system and a mediocre degradation rate. However, with equivalent persulfate adsorption on N-CNT at a low quantity, PDS/N-CNT exhibited a stronger oxidizing capacity than PMS/N-CNT because of the intrinsic higher redox potential of PDS than PMS. The oxidation rates of the two systems were in great linearity with the potentials of carbon-persulfate* complexes, suggesting N-CNT activation of PMS and PDS shared the similar electron-transfer oxidation mechanism. Therefore, this study provides new insights into the intrinsic roles of heteroatom doping in nanocarbons for persulfates activation and unveils the principles for a rational design of reaction-oriented carbocatalysts for persulfate-based advanced oxidation processes.
420 citations
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TL;DR: A large-area graphene-nanomesh/single-walled carbon nanotube (GNM/SWNT) hybrid membrane with excellent mechanical strength while fully capturing the merit of atomically thin membranes is reported.
Abstract: Nanoporous two-dimensional materials are attractive for ionic and molecular nanofiltration but limited by insufficient mechanical strength over large areas. We report a large-area graphene-nanomesh/single-walled carbon nanotube (GNM/SWNT) hybrid membrane with excellent mechanical strength while fully capturing the merit of atomically thin membranes. The monolayer GNM features high-density, subnanometer pores for efficient transport of water molecules while blocking solute ions or molecules to enable size-selective separation. The SWNT network physically separates the GNM into microsized islands and acts as the microscopic framework to support the GNM, thus ensuring the structural integrity of the atomically thin GNM. The resulting GNM/SWNT membranes show high water permeance and a high rejection ratio for salt ions or organic molecules, and they retain stable separation performance in tubular modules.
420 citations
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TL;DR: The use of metal-ion modification to enhance both the stability and transistor performance of BP sheets is described and the strategy can be extended to other metal ions such as Fe3+ , Mg2+ , and Hg2- .
Abstract: Black phosphorus (BP), a burgeoning elemental 2D semiconductor, has aroused increasing scientific and technological interest, especially as a channel material in field-effect transistors (FETs). However, the intrinsic instability of BP causes practical concern and the transistor performance must also be improved. Here, the use of metal-ion modification to enhance both the stability and transistor performance of BP sheets is described. Ag+ spontaneously adsorbed on the BP surface via cation-π interactions passivates the lone-pair electrons of P thereby rendering BP more stable in air. Consequently, the Ag+ -modified BP FET shows greatly enhanced hole mobility from 796 to 1666 cm2 V-1 s-1 and ON/OFF ratio from 5.9 × 104 to 2.6 × 106 . The mechanisms pertaining to the enhanced stability and transistor performance are discussed and the strategy can be extended to other metal ions such as Fe3+ , Mg2+ , and Hg2+ . Such stable and high-performance BP transistors are crucial to electronic and optoelectronic devices. The stability and semiconducting properties of BP sheets can be enhanced tremendously by this novel strategy.
420 citations
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TL;DR: With the consideration of all these parameters, the strong fluorescence and phosphorescence in the aggregated state could be achieved in the rationally designed organic luminogens, providing some guidance for the further development.
Abstract: The strong light emission of organic luminogens in the aggregated state is essential to their applications as optoelectronic materials with good performance. In this review, with respect to the aggregation-induced emission and room-temperature phosphorescence luminogens, the important role of molecular packing modes is highlighted. As demonstrated in the selected examples, the molecular packing status in the aggregate state is affected by many factors, including the molecular configurations, the inherent electronic properties, the special functional groups, and so on. With the consideration of all these parameters, the strong fluorescence and phosphorescence in the aggregated state could be achieved in the rationally designed organic luminogens, providing some guidance for the further development.
420 citations
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TL;DR: Lead thiocyanate in the perovskite precursor can increase the grain size of a perovSkite thin film and reduce the conductivity of the grain boundaries, leading to perovkite solar cells with reduced hysteresis and enhanced fill factor.
Abstract: Lead thiocyanate in the perovskite precursor can increase the grain size of a perovskite thin film and reduce the conductivity of the grain boundaries, leading to perovskite solar cells with reduced hysteresis and enhanced fill factor. A planar perovskite solar cell with grain boundary and interface passivation achieves a steady-state efficiency of 18.42%.
419 citations
Authors
Showing all 93441 results
Name | H-index | Papers | Citations |
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Jing Wang | 184 | 4046 | 202769 |
Jiaguo Yu | 178 | 730 | 113300 |
Lei Jiang | 170 | 2244 | 135205 |
Gang Chen | 167 | 3372 | 149819 |
Omar M. Yaghi | 165 | 459 | 163918 |
Xiang Zhang | 154 | 1733 | 117576 |
Yi Yang | 143 | 2456 | 92268 |
Thomas P. Russell | 141 | 1012 | 80055 |
Jun Chen | 136 | 1856 | 77368 |
Lei Zhang | 135 | 2240 | 99365 |
Chuan He | 130 | 584 | 66438 |
Han Zhang | 130 | 970 | 58863 |
Lei Zhang | 130 | 2312 | 86950 |
Zhen Li | 127 | 1712 | 71351 |
Chao Zhang | 127 | 3119 | 84711 |