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In situ preparation of g-C3N4/Bi4O5I2 complex and its elevated photoactivity in Methyl Orange degradation under visible light 被引量:14
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作者 Zhe Feng Lin Zeng +4 位作者 Qingle Zhang shifeng ge Xinyue Zhao Hongjun Lin Yiming He 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2020年第1期149-162,共14页
A graphite carbon nitride(g-C3N4)modified Bi4O5I2 composite was successfully prepared insitu via the thermal treatment of a g-C3N4/Bi OI precursor at 400°C for 3 hr.The as-prepared g-C3N4/Bi4O5I2 showed high phot... A graphite carbon nitride(g-C3N4)modified Bi4O5I2 composite was successfully prepared insitu via the thermal treatment of a g-C3N4/Bi OI precursor at 400°C for 3 hr.The as-prepared g-C3N4/Bi4O5I2 showed high photocatalytic performance in Methyl Orange(MO)degradation under visible light.The best sample presented a degradation rate of 0.164 min^-1,which is 3.2 and 82 times as high as that of Bi4O5I2 and g-C3N4,respectively.The g-C3N4/Bi4O5I2 was characterized by X-ray powder diffractometer(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM),Raman,X-ray photoelectron spectroscopy(XPS),ultraviolet-visible diffuse reflectance spectra(DRS),electrochemical impedance spectroscopy(EIS)and transient photocurrent response in order to explain the enhanced photoactivity.Results indicated that the decoration with a small amount of g-C3N4 influenced the specific surface area only slightly.Nevertheless,the capability for absorbing visible light was improved measurably,which was beneficial to the MO degradation.On top of that,a strong interaction between g-C3N4 and Bi4O5I2 was detected.This interplay promoted the formation of a favorable heterojunction structure and thereby enhanced the charge separation.Thus,the g-C3N4/Bi4O5I2 composite presented greater charge separation efficiency and much better photocatalytic performance than Bi4O5I2.Additionally,g-C3N4/Bi4O5I2 also presented high stability.·O2^- and holes were verified to be the main reactive species. 展开更多
关键词 g-C3N4 Bi4O5I2 Methyl Orange degradation HETEROJUNCTION Visible light
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Design of multifunctional phosphonic acid molecule for highly efficient, stable inverted perovskite solar cells
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作者 Rongmei Zhao Yachao Du +13 位作者 Nan Wu Xinyue Lil Wenbin Yuan shifeng ge Zhaowei Xu Xiaoyang Shen Simin Ma' Ruohao Wang Tinghuan Yang Dengke Wang Xiaodong Ren Jiangzhao Chen Kui Zhao Wen-Hua Zhang 《Science China Materials》 2025年第12期4555-4565,共11页
Inverted perovskite solar cells(PSCs)have emerged as promising photovoltaic candidates because of their high efficiency and cost-effective fabrication.However,abundant defects and inefficient charge transport critical... Inverted perovskite solar cells(PSCs)have emerged as promising photovoltaic candidates because of their high efficiency and cost-effective fabrication.However,abundant defects and inefficient charge transport critically compromise the device efficiency and stability.Phosphonic acid-based multifunctional molecules,mainly as self-assemble monolayer,have recently been demonstrated to be useful in improving the device performance of the inverted PSCs.Herein,we designed and synthesized a new multifunctional molecule,(2-(3,6-bis(trifluoromethoxy)-9H-carbazol-9-yl)ethyl)phosphonic acid(M28)as additive in perovskite precursor solution to fabricate high-efficiency and stable inverted PSCs.Through spontaneous segregation toward the buried interface and grain boundaries(GBs),M28 affords threefold roles in enhancing device performance:(1)slowing the crystallization rate and enlarging the grain sizes to improve the perovskite film quality,(2)passivating the defects at buried interface and GBs to suppress charge recombination,(3)inducing an extra electric field at the buried interface through p-type doping to promote hole transport.The resulting devices thus achieved a remarkable power conversion efficiency of 25.96%and impressive long-term operational stability:maintaining 80%of their initial efficiency after 1500 h tracking at the maximum power point.This work emphasizes the importance of exploration of new types of functional molecules in advancing PSCs. 展开更多
关键词 molecular design crystallization kinetics defect passivation buried interface inverted perovskite solar cell
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