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Yin Chen

Yibin University

ORCID: 0000-0002-5968-4713

Publishes on Advanced Photocatalysis Techniques, Crystallization and Solubility Studies, X-ray Diffraction in Crystallography. 215 papers and 10.1k citations.

215Publications
10.1kTotal Citations

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Top publicationsby citations

Low trap-state density and long carrier diffusion in organolead trihalide perovskite single crystals
Cited by 5k

The fundamental properties and ultimate performance limits of organolead trihalide MAPbX3 (MA = CH3NH3(+); X = Br(-) or I(-)) perovskites remain obscured by extensive disorder in polycrystalline MAPbX3 films. We report an antisolvent vapor-assisted crystallization approach that enables us to create sizable crack-free MAPbX3 single crystals with volumes exceeding 100 cubic millimeters. These large single crystals enabled a detailed characterization of their optical and charge transport characteristics. We observed exceptionally low trap-state densities on the order of 10(9) to 10(10) per cubic centimeter in MAPbX3 single crystals (comparable to the best photovoltaic-quality silicon) and charge carrier diffusion lengths exceeding 10 micrometers. These results were validated with density functional theory calculations.

Efficient Peroxydisulfate Activation Process Not Relying on Sulfate Radical Generation for Water Pollutant Degradation
Tao Zhang, Yin Chen, Yuru Wang et al.|Environmental Science & Technology|2014
Cited by 781Open Access

Peroxydisulfate (PDS) is an appealing oxidant for contaminated groundwater and toxic industrial wastewaters. Activation of PDS is necessary for application because of its low reactivity. Present activation processes always generate sulfate radicals as actual oxidants which unselectively oxidize organics and halide anions reducing oxidation capacity of PDS and producing toxic halogenated products. Here we report that copper oxide (CuO) can efficiently activate PDS under mild conditions without producing sulfate radicals. The PDS/CuO coupled process is most efficient at neutral pH for decomposing a model compound, 2,4-dichlorophenol (2,4-DCP). In a continuous-flow reaction with an empty-bed contact time of 0.55 min, over 90% of 2,4-DCP (initially 20 μM) and 90% of adsorbable organic chlorine (AOCl) can be removed at the PDS/2,4-DCP molar ratio of 1 and 4, respectively. Based on kinetic study and surface characterization, PDS is proposed to be first activated by CuO through outer-sphere interaction, the rate-limiting step, followed by a rapid reaction with 2,4-DCP present in the solution. In the presence of ubiquitous chloride ions in groundwater/industrial wastewater, the PDS/CuO oxidation shows significant advantages over sulfate radical oxidation by achieving much higher 2,4-DCP degradation capacity and avoiding the formation of highly chlorinated degradation products. This work provides a new way of PDS activation for contaminant removal.

Synthesis of Hierarchical Graphdiyne-Based Architecture for Efficient Solar Steam Generation
Xin Gao, Huaying Ren, Jingyuan Zhou et al.|Chemistry of Materials|2017
Cited by 238

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTSynthesis of Hierarchical Graphdiyne-Based Architecture for Efficient Solar Steam GenerationXin Gao†§, Huaying Ren†‡§, Jingyuan Zhou†‡, Ran Du†, Chen Yin†‡, Rong Liu†‡, Hailin Peng†, Lianming Tong*†, Zhongfan Liu*†, and Jin Zhang*†View Author Information† Center for Nanochemistry, Beijing Science and Engineering Center for Nanocarbons, Beijing National Laboratory for Molecular Sciences (BNLMS), College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, People's Republic of China‡ Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, People's Republic of China*J. Zhang. E-mail: [email protected]*Z. Liu. E-mail: [email protected]*L. Tong. E-mail: [email protected]Cite this: Chem. Mater. 2017, 29, 14, 5777–5781Publication Date (Web):June 27, 2017Publication History Received4 May 2017Revised27 June 2017Published online29 June 2017Published inissue 25 July 2017https://pubs.acs.org/doi/10.1021/acs.chemmater.7b01838https://doi.org/10.1021/acs.chemmater.7b01838rapid-communicationACS PublicationsCopyright © 2017 American Chemical SocietyRequest reuse permissionsArticle Views4935Altmetric-Citations209LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-AlertscloseSupporting Info (2)»Supporting Information Supporting Information SUBJECTS:Absorption,Copper,Foams,Nanowires,Water Get e-Alerts

Ultrathin Cu<sub>2</sub>O as an efficient inorganic hole transporting material for perovskite solar cells
Weili Yu, Feng Li, Hong Wang et al.|Nanoscale|2016
Cited by 217

We demonstrate that ultrathin P-type Cu2O thin films fabricated by a facile thermal oxidation method can serve as a promising hole-transporting material in perovskite solar cells. Following a two-step method, inorganic-organic hybrid perovskite solar cells were fabricated and a power conversion efficiency of 11.0% was achieved. We found that the thickness and properties of Cu2O layers must be precisely tuned in order to achieve the optimal solar cell performance. The good performance of such perovskite solar cells can be attributed to the unique properties of ultrathin Cu2O, including high hole mobility, good energy level alignment with CH3NH3PbI3, and longer lifetime of photo-excited carriers. Combining the merits of low cost, facile synthesis, and high device performance, ultrathin Cu2O films fabricated via thermal oxidation hold promise for facilitating the developments of industrial-scale perovskite solar cells.