Institution
Shanghai University
Education•Shanghai, Shanghai, China•
About: Shanghai University is a education organization based out in Shanghai, Shanghai, China. It is known for research contribution in the topics: Microstructure & Graphene. The organization has 59583 authors who have published 56840 publications receiving 753549 citations. The organization is also known as: Shànghǎi Dàxué.
Topics: Microstructure, Graphene, Nonlinear system, Catalysis, Thin film
Papers published on a yearly basis
Papers
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TL;DR: The synthesis of a two-dimensional few-layered covalent organic framework trapped by carbon nanotubes as the anode of lithium-ion batteries is reported, paving the way to the development of high-capacity electrodes for organic rechargeable batteries.
Abstract: Conjugated polymeric molecules have been heralded as promising electrode materials for the next-generation energy-storage technologies owing to their chemical flexibility at the molecular level, environmental benefit, and cost advantage. However, before any practical implementation takes place, the low capacity, poor structural stability, and sluggish ion/electron diffusion kinetics remain the obstacles that have to be overcome. Here, we report the synthesis of a few-layered two-dimensional covalent organic framework trapped by carbon nanotubes as the anode of lithium-ion batteries. Remarkably, upon activation, this organic electrode delivers a large reversible capacity of 1536 mAh g−1 and can sustain 500 cycles at 100 mA g−1. Aided by theoretical calculations and electrochemical probing of the electrochemical behavior at different stages of cycling, the storage mechanism is revealed to be governed by 14-electron redox chemistry for a covalent organic framework monomer with one lithium ion per C=N group and six lithium ions per benzene ring. This work may pave the way to the development of high-capacity electrodes for organic rechargeable batteries. Conjugated polymeric molecules are promising electrode materials for batteries. Here the authors show a two-dimensional few-layered covalent organic framework that delivers a large reversible capacity of more than 1500 mAh g−1 with the storage mechanism governed by 14-electron redox chemistry.
417 citations
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TL;DR: In this paper, a competitive complexation strategy has been developed to construct a novel electrocatalyst with Zn-Co atomic pairs coordinated on N doped carbon support (Zn/CoN-C).
Abstract: A competitive complexation strategy has been developed to construct a novel electrocatalyst with Zn-Co atomic pairs coordinated on N doped carbon support (Zn/CoN-C). Such architecture offers enhanced binding ability of O2 , significantly elongates the O-O length (from 1.23 A to 1.42 A), and thus facilitates the cleavage of O-O bond, showing a theoretical overpotential of 0.335 V during ORR process. As a result, the Zn/CoN-C catalyst exhibits outstanding ORR performance in both alkaline and acid conditions with a half-wave potential of 0.861 and 0.796 V respectively. The in situ XANES analysis suggests Co as the active center during the ORR. The assembled zinc-air battery with Zn/CoN-C as cathode catalyst presents a maximum power density of 230 mW cm-2 along with excellent operation durability. The excellent catalytic activity in acid is also verified by H2 /O2 fuel cell tests (peak power density of 705 mW cm-2 ).
414 citations
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TL;DR: Results show that in spite of the extreme reductions in primary emissions, China cannot fully tackle the current air pollution, and re-organisation of the energy and industrial strategy together with trans-regional joint-control for a full long-term air pollution plan need to be further taken into account.
410 citations
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TL;DR: A meta-analysis on 33 time-series and case-crossover studies conducted in China to assess mortality effects of short-term exposure to particulate matter with aerodynamic diameters less than 10 and 2.5 μm found significant associations between air pollution exposure and increased mortality risks.
408 citations
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TL;DR: A fast CU size decision algorithm for HM that can significantly reduce computational complexity while maintaining almost the same RD performance as the original HEVC encoder is proposed.
Abstract: The emerging high efficiency video coding standard (HEVC) adopts the quadtree-structured coding unit (CU). Each CU allows recursive splitting into four equal sub-CUs. At each depth level (CU size), the test model of HEVC (HM) performs motion estimation (ME) with different sizes including 2N × 2N, 2N × N, N × 2N and N × N. ME process in HM is performed using all the possible depth levels and prediction modes to find the one with the least rate distortion (RD) cost using Lagrange multiplier. This achieves the highest coding efficiency but requires a very high computational complexity. In this paper, we propose a fast CU size decision algorithm for HM. Since the optimal depth level is highly content-dependent, it is not efficient to use all levels. We can determine CU depth range (including the minimum depth level and the maximum depth level) and skip some specific depth levels rarely used in the previous frame and neighboring CUs. Besides, the proposed algorithm also introduces early termination methods based on motion homogeneity checking, RD cost checking and SKIP mode checking to skip ME on unnecessary CU sizes. Experimental results demonstrate that the proposed algorithm can significantly reduce computational complexity while maintaining almost the same RD performance as the original HEVC encoder.
406 citations
Authors
Showing all 59993 results
Name | H-index | Papers | Citations |
---|---|---|---|
Zhong Lin Wang | 245 | 2529 | 259003 |
Yang Yang | 171 | 2644 | 153049 |
Yang Liu | 129 | 2506 | 122380 |
Zhen Li | 127 | 1712 | 71351 |
Xin Wang | 121 | 1503 | 64930 |
Jian Liu | 117 | 2090 | 73156 |
Xin Li | 114 | 2778 | 71389 |
Wei Zhang | 112 | 1189 | 93641 |
Jianjun Liu | 112 | 1040 | 71032 |
Liquan Chen | 111 | 689 | 44229 |
Jin-Quan Yu | 111 | 438 | 43324 |
Jonathan L. Sessler | 111 | 997 | 48758 |
Peng Wang | 108 | 1672 | 54529 |
Qian Wang | 108 | 2148 | 65557 |
Wei Zhang | 104 | 2911 | 64923 |