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您的检索式：作者名="Xinquan Gong"
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| 1 | High-performance all-solution-processed inverted quantum dot light-emitting diodes enabled by water treatment显示文摘All-solution-processed inverted quantum dot(QD)light-emitting diodes(QLEDs)with transparent bottom cathodes can be directly connected to the n-type thin-film transistors,offering a feasible solution for low-cost active matrix-driven QD displays.However,the subsequent solution-deposition of the hole-transporting layer destroys the underneath QD films,resulting in largely deteriorated device performance.Various strategies have been implemented to prevent QD film from dissolution,but all at a heavy cost of device performance suffering from either reduced efficiency or increased driving voltage.Here,a facile and effective water-treatment approach for QD film to fabricate inverted QLEDs through all solution processing is reported.The water treatment substitutes the long-chain oleate ligands with hydroxyl groups,resulting in significantly improved non-polar solvent resistance of the QD films.Importantly,the QD films reserve their excellent photoluminescence efficiency after water treatment.With the water-treated QD film as the emissive layer,all-solution-processed inverted red QLED with a peak external quantum efficiency of 19.6%,a turn-on voltage of 1.8 V,and a T50 operational lifetime of 150,000 h at 100 cd·m^(-2) was achieved.Furthermore,efficient and low-voltage-driven green and blue QLEDs can also be prepared with this method.This work provides a feasible strategy for the fabrication of high-performance all-solution-processed inverted QLEDs,paving the way toward achieving QLEDs by all ink-jet printing. | Qianqing Hu Junjie Si Desui Chen Xiaoming Hao Rui Xu Yihang Du Zhuopeng Du Xinquan Gong Hong Zhao Peiqing Cai Qi Ai Xin Yao Yu Yan Zenan Zhang Muzhi Cai Wei Liu Yongyin Kang Zugang Liu | 2023 | Nano Research2023，16，7： | 0 |
| 2 | A novel mechanism underlies caspase-dependent conversion of the dicer ribonuclease into a deoxyribonuclease during apoptosis显示文摘在 C 期间。elegans apoptosis, dicer ribonuclease (DCR-1 ) 被房间死亡朊酶 CED-3 劈开与 1.5 ribonuclease III (RNase III ) 产生截断的 DCR-1 (tDCR-1 ) 领域,把它变换成开始 apoptotic 的 deoxyribonuclease (DNase ) 染色体破碎。我们执行了生物化学、功能的分析理解这意外 RNase 到 DNase 变换。在全身的 DCR-1, tDCR-1 DNase 活动被它的 N 终端 DCR-1 顺序压制。然而,不是都,在 N 终端 DCR-1 的顺序元素为这抑制被要求。我们的删除分析揭示那 20 残余 α在 DCR-1 的螺旋顺序看起来为为通过结构依赖者机制压制 tDCR-1 DNase 活动要求的顺序定义一个批评裂缝点。从 tDCR-1 的 N 终端 DCR-1 顺序的移动激活也要求一半 RNase IIIa 域的一项 DNA 有约束力的活动,并且使 tDCR-1 能处理 DNA。一致地, DCR-1 和 tDCR-1 的结构的建模建议由 CED-3 的 DCR-1 的那劈开可以引起允许 tDCR-1 绑并且处理,并且可以移开堵住 DNA 存取到 tDCR-1 的位的阻碍者 DNA 的一个 conformational 变化。而且,新 DNase 能用不同 RNase III 领域被设计,包括从细菌的 RNase III 的。我们的结果显示很远地相关的 RNase III 酶有潜力当解朊地处理了或与便于绑定到 DNA 的一个适当搭挡一起配对时,劈开 DNA。我们建议这现象可以被外推到另外的 ribonucleases 的可能性。 | Xiao Ge Xiang Zhao Akihisa Nakagawa Xinqi Gong Riley Robert Skeen-Gaar Yong Shi Haipeng Gong Xinquan Wang Ding Xue | 2014 | Cell Research2014，24，2： | 0 |
| 3 | 在精确基因由一个改进 CRISPR/Cas9 系统编辑的一步舞 homozygosity显示文摘 | Pei Zhao Zhe Zhang Xiaoying Lv Xiang Zhao Yuji Suehiro Yinan Jiang Xinquan Wang Shohei Mitani Haipeng Gong Ding Xue | 2016 | Cell Research2016，26，5： | 0 |
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