期刊文献+
共找到15篇文章
< 1 >
每页显示 20 50 100
Ni,Co基硒化物修饰g-C_(3)N_(4)光催化产氢研究 被引量:4
1
作者 靳治良 李彦兵 郝旭强 《物理化学学报》 SCIE CAS CSCD 北大核心 2021年第10期120-134,共15页
新型高效的催化剂是突破单体光催化材料载流子低分离和转移效率的重要途径。本文将Ni_(3)Se_(4)和CoSe_(2)纳米粒子锚定在具有良好分散性的g-C_(3)N_(4)纳米片表面,合成了两种新的g-C_(3)N_(4)@Ni_(3)Se_(4)和g-C_(3)N_(4)@CoSe_(2)光... 新型高效的催化剂是突破单体光催化材料载流子低分离和转移效率的重要途径。本文将Ni_(3)Se_(4)和CoSe_(2)纳米粒子锚定在具有良好分散性的g-C_(3)N_(4)纳米片表面,合成了两种新的g-C_(3)N_(4)@Ni_(3)Se_(4)和g-C_(3)N_(4)@CoSe_(2)光催化剂并实现了原位光催化析氢。相当严重的载流子的重组导致g-C_(3)N_(4)单体展现了大约只有1.9μmol∙h^(−1)的极差的光催化析氢活性。Ni_(3)Se_(4)和CoSe_(2)纳米颗粒对于加速载流子快速分离和转移的独特作用使得在g-C_(3)N_(4)表面负载Ni_(3)Se_(4)和CoSe_(2)纳米粒子极大地提高了其产氢活性。G-C_(3)N_(4)@Ni_(3)Se_(4)展示了一个大约16.4μmol∙h^(−1)的光催化产氢活性并且g-C_(3)N_(4)@CoSe_(2)展现了一个大约25.6μmol∙h^(−1)的光催化产氢活性,这分别是g-C_(3)N_(4)单体的8倍和13倍。其中,将Ni_(3)Se_(4)和CoSe_(2)与g-C_(3)N_(4)耦合可以显著提高光吸收密度以及扩展光响应范围。激发态EY在g-C_(3)N_(4)@Ni_(3)Se_(4)和g-C_(3)N_(4)@CoSe_(2)存在时比在g-C_(3)N_(4)存在时展现了更低的荧光强度,并且在g-C_(3)N_(4)@Ni_(3)Se_(4)和g-C_(3)N_(4)@CoSe_(2)体系中可观察到最大的电子转移速率。相比g-C_(3)N_(4)@Ni_(3)Se_(4)@FTO和g-C_(3)N_(4)@CoSe_(2)@FTO电极,g-C_(3)N_(4)@@FTO显现了最小的光电流响应密度和最大的电化学,这表明在g-C_(3)N_(4)纳米片表面引入Ni_(3)Se_(4)和CoSe_(2)纳米颗粒增强了光生载流子的分离和转移效率,即基于g-C_(3)N_(4)的金属硒化的合成有效地抑制了光生载流子的复合以及促进了光催化水裂解制氢反应。同时,吸收带边的红移有效地降低了光激电子从价带到导带跃迁的阈值。此外,g-C_(3)N_(4)@Ni_(3)Se_(4)和g-C_(3)N_(4)@CoSe_(2)复合催化剂的zeta电位比g-C_(3)N_(4)的更负,说明样品表面对质子增强的吸附。并且密度泛函理论结果表明:g-C_(3)N_(4)中N位点对H的吸附能为−0.22 eV,还发现氢原子更倾向于吸附在两个硒原子的桥位点上形成Se―H―Se键,并且吸附能为1.53 eV。所有对样品进行的透射电子显微镜(TEM)、扫描电子显微镜(SEM)、X射线光电子能谱(XPS)、X射线衍射(XRD)、紫外可见漫反射光谱(UV-Vis-DRS)、瞬态光电流、傅立叶变换红外光谱(FT-IR)等相关表征都展示了彼此匹配的结果。 展开更多
关键词 Ni3Se4 CoSe2 g-C_(3)N_(4) 析氢
下载PDF
硫化钴改性石墨炔构建S型异质结高效光催化产氢 被引量:1
2
作者 靳治良 李红英 李俊柯 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2022年第2期303-315,共13页
石墨炔(GDY,g-C_(n)H_(2n)-2)作为一种新型的由sp和sp2杂化的碳原子构成的二维碳材料,因其独特的纳米级孔隙、二维层状共轭骨架结构及半导体性质等特性,使之在能源、电化学、光催化、光学、电子学等诸多领域具有显著优势.它作为一种具... 石墨炔(GDY,g-C_(n)H_(2n)-2)作为一种新型的由sp和sp2杂化的碳原子构成的二维碳材料,因其独特的纳米级孔隙、二维层状共轭骨架结构及半导体性质等特性,使之在能源、电化学、光催化、光学、电子学等诸多领域具有显著优势.它作为一种具有良好的层状结构的新型碳材料,其可调节的电子结构弥补了石墨烯无明显带隙的缺点,有望在光催化分解水领域展现出广阔的应用前景.本文报道了以CuI粉末为催化剂制备石墨炔的新方法,并对其进行改性后制备了Co_(9)S_(8)-GDY-CuI新型复合材料;即通过有机合成法和水热法将GDY-CuI片层材料与Co_(9)S_(8)纳米颗粒复合,合理构建了S型异质结,展现出良好的光催化活性.石墨炔的层状结构有利于Co_(9)S_(8)纳米粒子的分散,能够有效避免粒子聚集,从而暴露出更多的活性位点.石墨炔独特的电子转移特性使得它与染料分子之间的相互作用和键合都能表现出良好的电子转移特性.因此,制备的Co_(9)S_(8)-GDY-CuI在染料敏化体系中的产氢活性达到了1411.82μmolg^(-1)h^(-1),是纯石墨炔的10.29倍.通过表征技术深入研究了该复合材料产氢活性提高的内在原因.拉曼光谱研究结果表明材料中存在炔基键,X射线光电子能谱中碳拟合峰以C-C(sp2)和C-C(sp)的形式存在,且两者之间的峰面积之比约为1:2,该结果与理论值吻合.红外光谱结果表明,纯石墨炔和复合材料中存在C≡C.结合紫外可见漫反射和莫特-肖特基表征结果对材料的能带结构进行了深入分析并且提出了该反应的可能机理.结果表明,Co_(9)S_(8)-GDY-CuI样品之间形成了双S型异质结,有效地加速了电子的分离和转移.S型异质结的存在有利于提高材料内部的电荷分离效率,保留了更为有效的氧化还原电位,更有利于该材料光催化分解水反应的进行.此外,复合材料中Co_(9)S_(8)纳米粒子的引入提高了Co_(9)S_(8)-GDY-CuI对可见光的吸收能力,增强了对于可见光的利用率.光致发光光谱和电化学测试结果进一步证明了复合材料中光生电子-空穴对的复合被有效抑制,是Co_(9)S_(8)-GDY-CuI材料产氢活性得以提高的内在原因之一.上述研究表明,Co_(9)S_(8)-GDY-CuI之间异质结的构建为材料光催化反应的进行提供了一条有效的电子转移路径.本文为石墨炔材料在光催化分解水制氢相关领域提供了一个可借鉴的新思路. 展开更多
关键词 石墨炔 Co_(9)S_(8) S型异质结 光催化制氢
下载PDF
CuO修饰改性沸石咪唑框架催化剂的构建及其光催化产氢性能(英文) 被引量:2
3
作者 樊凯 靳治良 +2 位作者 袁红 胡红岩 毕迎普 《Chinese Journal of Catalysis》 CSCD 北大核心 2017年第12期2056-2066,共11页
新型金属有机骨架(MOFs)材料是一类比较新颖的可用作光催化剂的潜在材料.它是由金属离子或金属簇单元与有机配体通过配位作用自组装形成的一类具有周期性多维网络结构的多孔晶态材料.MOFs结构具有高度的有序性、一定程度上的可设计性和... 新型金属有机骨架(MOFs)材料是一类比较新颖的可用作光催化剂的潜在材料.它是由金属离子或金属簇单元与有机配体通过配位作用自组装形成的一类具有周期性多维网络结构的多孔晶态材料.MOFs结构具有高度的有序性、一定程度上的可设计性和可剪裁性,其高度发达的孔结构使得它具有超高的比表面积.MOFs结构中的金属簇被认为可以扮演半导体量子点的角色,同时其有机配体基于'天线效应',在光激发条件下用来活化这些金属簇,从而使得MOFs成为可能的光催化剂.ZIF-9由角共享四面体CoN4单元组成,其中Co2+阳离子和苯并咪唑阴离子之间的配位键是N供体配体,因而具有良好的热稳定性和较高的碳氮含量.本文在一定浓度的甲醇溶液中通过光沉积法将CuO附着于ZIF-9表面上,用于光催化活性测试,并与g-C_3N_4/CuO催化剂进行了比较.结果表明,ZIF-9/CuO催化剂活性是g-C_3N_4/CuO催化剂的19.4倍.这是由于比表面积的不同,导致所吸附的染料与暴露的活性位点的不同.通过SEM,TEM,EDS,XRD,XPS,UV-Vis和稳态瞬态荧光等手段系统研究了催化剂反应动力学行为及内在机理.稳态荧光结果表明,染料的荧光发射峰和ZIF-9的吸收峰之间没有明显的重叠,染料的激发电子可以在该反应系统中从染料分子转移到ZIF-9上.除了一部分电子直接传输到达ZIF-9表面,更多的电子将最终通过CuO到达催化剂表面,最后与反应溶液中的H^+结合生成H_2,EY-ZIF-9/CuO(40%)的荧光衰减可以用双指数荧光衰减动力学即动态淬火机理.表明CuO的引入可以增强染料EY分子的聚集,从而增加该催化剂活性. 展开更多
关键词 ZIF-9 CUO 染料 敏化途径 产氢 反应优化
下载PDF
可控设计Zn-Ni-P修饰g-C_3N_4催化剂光催化产氢性能(英文) 被引量:10
4
作者 李彦兵 靳治良 +1 位作者 张利君 樊凯 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2019年第3期390-402,共13页
光催化分解水制氢是应对能源危机和环境污染问题的途径之一,也是实现太阳能转化和储存的有效方法.其中,应用层面的一个关键制约因素是高效光催化剂的开发和制氢反应体系的构建,理论层面的一个关键科学问题是光生电子-空穴的高效分离及... 光催化分解水制氢是应对能源危机和环境污染问题的途径之一,也是实现太阳能转化和储存的有效方法.其中,应用层面的一个关键制约因素是高效光催化剂的开发和制氢反应体系的构建,理论层面的一个关键科学问题是光生电子-空穴的高效分离及光生电子定向迁移,这两个层面的问题构成当前光催化分解水制氢研究的重大挑战.因此,稳定、高效催化剂的制备成为光催化领域重要的研究目标.类石墨烯氮化碳(g-C_3N_4)的结构与石墨相似,其层与层之间的范德华力使其具有良好的热稳定性和化学稳定性.g-C_3N_4是一种聚合物非金属半导体,由于具有与碳材料相似的层状堆积结构和sp^2杂化的π共轭电子能带结构,因此被认为是最有可能代替碳材料用于光催化分解水制氢的新型光催化材料.g-C_3N_4的室温禁带宽度为2.7eV左右,其价带和导带的位置完全覆盖了水的氧化-还原电位,因此理论上g-C_3N_4不仅能够氧化水为氧气,而且能够将水还原产氢,从而表现出优良的光电特性,成为新型太阳能转换材料.然而, g-C_3N_4在展示了良好研究前景的同时也存在一些缺陷,如比表面积较小及稳定性差等,这制约了g-C_3N_4在光催化领域的应用.为此,通过各种化学修饰对g-C_3N_4进行改性以提高其光催化活性和稳定性成为一个重要的研究方向.本文采用高温煅烧方法成功制备了Zn-Ni-P@g-C_3N_4催化剂.将一定量的g-C_3N_4、乙酸镍、乙酸锌和次亚磷酸钠均匀混合在一起并研磨成粉末,然后以3 oC/min的速率升温至300oC并在此温度下保持2h,自然冷却至室温后即得到Zn-Ni-P@g-C_3N_4催化剂,整个制备过程在氮气环境中进行.研究表明,在Zn与Ni摩尔比为1:3的Zn-Ni-P@g-C_3N_4催化剂上,当反应体系pH=10,在420nm光照下反应5h产氢量可达531.2μmol,是纯g-C_3N_4上的54.7倍.20h循环实验表明催化剂具有较好的光催化稳定性.对催化剂进行了XRD、TEM、SEM、XPS、N_2吸附、UV-vis DRS、瞬态光电流、FT-IR、瞬态荧光和Mott-Schottk等一系列表征,证明Zn-Ni-P的参与有效调变了电荷传输机制.SEM表征表明, Zn-Ni-P@g-C_3N_4为均匀排列的小颗粒,与纯g-C_3N_4相比其结构发生了改变,在Zn-Ni-P@g-C_3N_4结构中未发现g-C_3N_4纳米片的存在,说明Zn-Ni-P和g-C_3N_4成功复合.在上述研究基础上推测了可能的反应机理. 展开更多
关键词 Zn-Ni-P g-C3N4 产氢 可控设计 光催化剂
下载PDF
CoAl LDH@Ni-MOF-74 S-Scheme Heterojunction for Effi cient Hydrogen Evolution 被引量:1
5
作者 zhiliang jin Yanbing Li Qingxiang Ma 《Transactions of Tianjin University》 EI CAS 2021年第2期127-138,共12页
Metal–organic frameworks(MOFs)and layered double hydroxides(LDHs)have been considered to be one of the most promising and worthy hot spot materials to develop advanced catalysts for effi cient hydrogen evolution due ... Metal–organic frameworks(MOFs)and layered double hydroxides(LDHs)have been considered to be one of the most promising and worthy hot spot materials to develop advanced catalysts for effi cient hydrogen evolution due to their prominent characteristics,including unique structures,environmentally friendly nature,high redox activities,and homogeneously eff ective utilization of transition metal atoms.In this work,the delicate S-scheme heterojunction photocatalyst,CoAl LDH@Ni-MOF-74,was rationally designed and successfully constructed by coupling Ni-MOF-74 with CoAl LDH based on their peculiar structure,excellent electronic properties,and opposite surface potential for enhancing hydrogen generation activity under visible light irradiation.The CoAl LDH nanolayers evenly and dispersedly load on the surface of Ni-MOF-74.The CoAl LDH@Ni-MOF-74 exhibited higher photocatalytic hydrogen evolution activity compared with Ni-MOF-74 and CoAl LDH alone,mainly because the formation of the CoAl LDH@Ni-MOF-74 S-scheme heterojunction accelerated the recombination of several electrons(from conduction band(CB)of Ni-MOF-74)and holes(from valence band(VB)of CoAl LDH)and prevented the recombination of other electrons(from CB of CoAl LDH)and holes(from VB of Ni-MOF-74). 展开更多
关键词 CoAl LDH Ni-MOF-74 S-scheme heterojunction Hydrogen evolution
下载PDF
S-scheme heterojunction in photocatalytic hydrogen production 被引量:1
6
作者 Teng Li Noritatsu Tsubaki zhiliang jin 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2024年第2期82-104,共23页
As an ideal secondary energy source,hydrogen has the title of clean energy and the product of its complete combustion is only water,which is not polluting to the environment.Photocatalytic hydrogen production technolo... As an ideal secondary energy source,hydrogen has the title of clean energy and the product of its complete combustion is only water,which is not polluting to the environment.Photocatalytic hydrogen production technology is an environmentally friendly,safe,and low-cost strategy that requires only an inexhaustible amount of solar energy and water as feedstock.This paper provides a detailed and detailed review of S-scheme heterojunction photocatalysts for photocatalytic hydrogen production,mainly including TiO_(2)-based,Perovskite-based,CdS-based,Graphitic phase carbon nitride-based,COF-based graphdiyne-based,ZnO-based,and ZnIn_(2)S_(4)-based S-scheme heterojunction photocatalysts.The classification of S-scheme heterojunctions is summarized.What’s more,various characterizations for direct verification of the charge migration mechanism of S-scheme heterojunctions are outlined.Based on the present study,the future potential challenges and future research trends for S-scheme heterojunctions in photocatalytic hydrogen evolution technology are pointed out,which provides feasible strategies for the development and design of S-scheme heterojunction photocatalysts in the field of photocatalytic hydrogen evolution. 展开更多
关键词 S-scheme heterojunction Photocatalysis Charges migration Hydrogen evolution
原文传递
Enhanced photocatalytic hydrogen production from Co-MOF/CN by nitrogen and sulfur co-doped coal-based carbon quantum dots
7
作者 Shiyong Xu Mei Li +3 位作者 Yijun Wang Caiyun Gao Rongsheng Xu zhiliang jin 《Journal of Rare Earths》 SCIE EI CAS CSCD 2024年第5期838-850,I0002,共14页
A novel composite photocatalyst for photocatalytic decomposition of water for hydrogen evolution was successfully synthesized by in-situ growth of nitrogen and sulfur co-doped coal-based carbon quantum dots(NSCQDs)nan... A novel composite photocatalyst for photocatalytic decomposition of water for hydrogen evolution was successfully synthesized by in-situ growth of nitrogen and sulfur co-doped coal-based carbon quantum dots(NSCQDs)nanoparticles on the surface of sheet cobalt-based metal-organic framework(Co-MOF)and graphitic carbon nitride(g-C_(3)N_(4),CN).The structure and properties of the obtained catalysts were systematically analyzed.NSCQDs effectively broaden the absorption of Co-MOF and CN in the visible region.The new composite photocatalyst has high hydrogen production activity and the hydrogen production rate reaches 6254μmol/(g·h)at pH=9.At the same time,NSCQDs synergy Co-MOF/CN composites have good stability.After four cycles of hydrogen production,the performance remains relatively stable.The tran sient photocurrent response and Nyquist plot experimental results further demonstrate the improvement of carrier separation efficiency in composite catalysts.The semiconductor type(n-type semico nductor)of the single-phase catalyst was determined by the Mott-Schottky test,and the band structure was analyzed.The conductive and valence bands of CN are-0.99 and 1.72 eV,respectively,and the conduction and valence bands of Co-MOF are-1.85 and 1.33 eV,respectively.Th e mechanism of the photocatalytic reaction can be inferred,that is,Z-type heterojunction is formed between CN an d Co-MOF,and NSCQDs was used as cocatalyst. 展开更多
关键词 Nitrogen and sulfur co-doped Coal-based carbon quantum dots Co-MOF CN Photocatalytic hydrogen evolution Rare earths
原文传递
Graphdiyne(C_(n)H_(2n-2)based CuI-GDY/ZnAl LDH double S-scheme heterojunction proved with in situ XPS for efficient photocatalytic hydrogen production 被引量:1
8
作者 Tian Wang zhiliang jin 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2023年第24期132-141,共10页
The photocatalytic performance can be significantly improved by constructing suitable heterojunction photocatalysts.It is well known that graphdiyne possesses a unique conjugated carbon network nanostructure,which giv... The photocatalytic performance can be significantly improved by constructing suitable heterojunction photocatalysts.It is well known that graphdiyne possesses a unique conjugated carbon network nanostructure,which gives it ample active sites on its surface and facilitates the reduction of protons.In this study,a unique new double S-scheme heterojunction photocatalyst was constructed by simple self-assembly of GDY prepared via organic synthesis methods and ZnAl-LDH.According to the study,an internal electric field controlling the transfer direction of the electron hole is formed between the interface of CuI-GDY and ZnAl-LDH,which broadens the light absorption range of the catalyst and improves the redox ability of the photocatalytic system.CuI-GDY and ZnAl-LDH are tightly bound together,which helps to separate the photogenerated carriers while preserving the strong reduction electrons in the GDY conduction band and the strong oxidation holes in the ZnAl-LDH valence band so that they can fully participate in the redox reaction.The charge-transfer paths on the S-scheme heterojunction interface were analyzed by in situ irradiation XPS.This work provides an effective strategy for the construction of double S-scheme heterojunction photocatalysts. 展开更多
关键词 Conjugated carbon network Graphdiyne S-scheme heterojunction Hydrogen evolution
原文传递
Design and synthesis of ZnCo_(2)O_(4)/CdS for substantially improved photocatalytic hydrogen production
9
作者 Xiaohong Li Youji Li +1 位作者 Xin Guo zhiliang jin 《Frontiers of Chemical Science and Engineering》 SCIE EI CSCD 2023年第5期606-616,共11页
In this study,the hydrogen evolution performance of CdS nanorods is improved using ZnCo_(2)O_(4).ZnCo_(2)O_(4)nanospheres are synthesized using the hydrothermal and calcination methods,and CdS nanorods are synthesized... In this study,the hydrogen evolution performance of CdS nanorods is improved using ZnCo_(2)O_(4).ZnCo_(2)O_(4)nanospheres are synthesized using the hydrothermal and calcination methods,and CdS nanorods are synthesized using the solvothermal method.From the perspective of morphology,numerous CdS nanorods are anchored on the ZnCo_(2)O_(4)microspheres.According to the experimental results of photocatalytic hydrogen evolution,the final hydrogen evolution capacity of 7417.5μmol·g^(-1)·h^(-1)is slightly more than two times that of the single CdS,which proves the feasibility of our study.Through various characterization methods,it is proved that the composite sample has suitable optoelectronic properties.In addition,ZnCo_(2)O_(4)itself exhibits good conductivity and low impedance,which shortens the charge-transfer path.Overall,the introduction of ZnCo_(2)O_(4)expands the adsorption range of light and improves the performance of photocatalytic hydrogen evolution.This design can provide reference for developing high-efficiency photocatalysts. 展开更多
关键词 ZnCo_(2)O_(4)nanosphere CdS nanorods photocatalytic hydrogen evolution
原文传递
Facilitating efficient photocatalytic hydrogen evolution via enhanced carrier migration at MOF-on-MOF S-scheme heterojunction interfaces through a graphdiyne(C_(n)H_(2n-2))electron transport layer
10
作者 Fei jin Bolin Yang +3 位作者 Xuanpu Wang Teng Li Noritatsu Tsubaki zhiliang jin 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2023年第12期11-23,共13页
Interface engineering of photocatalysts is an effective way to enhance their photocatalytic activity.In this work,the MOF-on-MOF strategy was used to construct the ZIF-9(Co)/Cu_(3)BTC_(2) photocatalyst in situ.Moreove... Interface engineering of photocatalysts is an effective way to enhance their photocatalytic activity.In this work,the MOF-on-MOF strategy was used to construct the ZIF-9(Co)/Cu_(3)BTC_(2) photocatalyst in situ.Moreover,graph-diyne,possessing an inherent capability to facilitate rapid electron transfer at the interface,has been introduced into the ZIF-9(Co)/Cu_(3)BTC_(2) interface to regulate the interfacial carrier migration.The photogenerated carrier transfer capability has been significantly enhanced by the interfacial synergy,while retaining the original active sites and high specific surface area.The exceptional efficiency performance of the composite catalyst under identical conditions could be attributed to the following two key factors:(i)The interfacial S-scheme hetero-junction in ZIF-9(Co)/Cu_(3)BTC_(2) provides the composite catalyst with strong reduction activity,facilitating the involvement of additional electrons in the reduction reaction through bended bands and an internal electric field.(ii)Carrier dynamics analysis shows that graphdiyne,as an electron transport layer,accelerates the charge migration rate at the S-scheme heterojunction interface through the electron relay effect.The incorporation of graphdiyne greatly improves the catalytic activity of MOFs and also demonstrates the great potential of graph-diyne in photocatalysis.This work provides a feasible idea for the interface engineering design of graphdiyne in photocatalysts. 展开更多
关键词 Graphdiyne S-scheme heterojunction MOFS Photocatalytic hydrogen evolution
原文传递
Performance of Ni-Cu bimetallic co-catalyst g-C3N4 nanosheets for improving hydrogen evolution 被引量:4
11
作者 zhiliang jin Lijun Zhang 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2020年第14期144-156,共13页
The Ni-Cu bimetallic nanoparticles were successfully anchorred on the surface of g-C3N4 nanosheets by a simple heat treatment process which was applied to the photocatalytic hydrogen evolution reaction.Insitu introduc... The Ni-Cu bimetallic nanoparticles were successfully anchorred on the surface of g-C3N4 nanosheets by a simple heat treatment process which was applied to the photocatalytic hydrogen evolution reaction.Insitu introduction of Ni-Cu could significantly improve the photocatalytic hydrogen evolution performance compared with pure g-C3N4 in the system sensitized by eosin Y under a visible irradiation condition.The hydrogen production activity of the composite reached 104.4μmol(2088.28μmol g^-1 h^-1)after using the Ni Cu double promoter strategy,which was 24.3 times higher than g-C3N4.The excellent electrical conductivity of the bimetallic Ni-Cu and the close interfacial contact between Ni Cu and g-C3N4 played an important role for increasing the charge transfer rate.They were also the reasons of more efficient charge separation,which ultimately led to a significant promotion on the photocatalytic hydrogen production reaction.Ni-Cu/g-C3N4 coupling with a close Schottky interface between metal and semiconductor which enhanced H2-evolution performance and TEOA oxidation kinetics.This work provided a new way to load Ni Cu bimetallic nanoparticles in situ onto g-C3N4 and a reference on relative semiconductor materials. 展开更多
关键词 BIMETALLIC NI-CU g-C3N4 Charge separation Hydrogen evolution
原文传递
EDA-assisted synthesis of multifunctional snowflake-Cu_(2)S/CdZnS S-scheme heterojunction for improved the photocatalytic hydrogen evolution 被引量:3
12
作者 Guorong Wang Yongkang Quan +1 位作者 Kaicheng Yang zhiliang jin 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2022年第26期28-39,共12页
The charge separation efficiency is one of the main factors affecting the solar photocatalytic decomposition of water to produce hydrogen.Constructing a unique heterojunction can accelerate the separation and transfer... The charge separation efficiency is one of the main factors affecting the solar photocatalytic decomposition of water to produce hydrogen.Constructing a unique heterojunction can accelerate the separation and transfer of photo-generated charges,and effectively improve the photocatalytic efficiency,which is considered a potential strategy.Accordingly,the 2%Cu_(2)S/CZS step-scheme(S-scheme)heterojunction based on morphology and electronic structure was successfully prepared via simple hydrothermal method.Compared with the monomer Cu_(2)S and Cd Zn S,the hydrogen evolution rate of 2%Cu_(2)S/CZS samples is significantly increased.In particular,the 2%Cu_(2)S/CZS not only shows high hydrogen evolution rate of 5904μmol g^(-1)h^(-1)(3.19 times than original Cd Zn S),but also presents preferable cyclic endurance.According to the characterization,we believe that the introduction of Cu_(2)S has the following three advantages:(i)The snowflake structure of Cu_(2)S reduces the agglomeration of granular Cd Zn S.(ii)The Cu_(2)S with narrow band gap broadens the light response range of the composite catalyst.(iii)The Cu_(2)S was introduced into Cd Zn S to form S-scheme heterojunction,which accelerated the separation and transfer of photo-generated charge.This work broadens the idea of designing efficient photocatalyst of hydrogen evolution. 展开更多
关键词 S-scheme HETEROJUNCTION MULTIFUNCTIONAL Snowflake-Cu_(2)S Photocatalyst
原文传递
Ingenious Design of Co Al-LDH p-n Heterojunction Based on CuI as Holes Receptor for Photocatalytic Hydrogen Evolution 被引量:2
13
作者 Yue Cao Hongqian Gou +1 位作者 Pengfei Zhu zhiliang jin 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2022年第6期79-85,共7页
Reasonable design of heterojunction can greatly improve the photocatalytic hydrogen evolution activity of materials.Herein,p-n heterojunction of 2D/3D structure is constructed by the nanosheet of CoAl-LDH and rock-lik... Reasonable design of heterojunction can greatly improve the photocatalytic hydrogen evolution activity of materials.Herein,p-n heterojunction of 2D/3D structure is constructed by the nanosheet of CoAl-LDH and rock-like CuI.The introduction of CuI can make CoAl-LDH disperse better,which brings more reaction sites for the hydrogen evolution reaction.Meanwhile,the 2D/3D structure is conducive to the construction of p-n heterojunction between the CoAl-LDH and CuI.The optical and electrochemical properties of the material indicate that the separation and transference of photon-generated carriers are promoted by the p-n heterojunction.The activity of composite catalyst(CI-10)reaches a maximum of 3.59 mmol g^(−1) h^(−1) which is 28.5 times higher than that of CuI.Furthermore,the influence of the amount of CuI and pH value on the hydrogen evolution reaction is explored.Based on the band structures of CoAl-LDH and CuI,the mechanism of photocatalytic reaction of CI-10 is proposed.The p-n heterojunction constructed with the CuI as hole receptor provides a new way to enhance the activity of photocatalytic H_(2) evolution. 展开更多
关键词 CoAl-LDH CUI p-n heterojunction photocatalysis hydrogen production
原文传递
CeO_(2) Particles Anchored to Ni_(2)P Nanoplate for Efficient Photocatalytic Hydrogen Evolution 被引量:2
14
作者 Teng Yan Xiaojie Zhang +1 位作者 Hua Liu zhiliang jin 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2022年第1期47-53,共7页
Photocatalytic hydrogen evolution can convert intermittent and dispersive solar energy into hydrogen with high energy density,which is expected to fundamentally solve the problems of environmental pollution and energy... Photocatalytic hydrogen evolution can convert intermittent and dispersive solar energy into hydrogen with high energy density,which is expected to fundamentally solve the problems of environmental pollution and energy shortages.In this experiment,the performance of the catalyst is modified by introducing cocatalyst and morphology control.Ni(OH)2 nanoflowers are used as substrates to derive nanoplate stack Ni_(2)P by high-temperature phosphating method,and a great many of CeO_(2) nanoparticles are anchored in the Ni_(2)P.This unique 3D/0D combination effectively inhibits the agglomeration of CeO_(2) nanoparticles and shortens the electron transfer path.Secondly,the introduction of metal-like performance of Ni_(2)P broadens the light absorption range of the catalyst and reduces the overpotential of the catalyst,which is a key factor in enhancing the catalytic activity.The design ideas of this experiment have reference significance for the design of efficient and environmentally friendly photocatalysts. 展开更多
关键词 CeO_(2) Ni_(2)P PHOTOCATALYSIS hydrogen evolution
原文传递
Preface to Solar Photocatalysis
15
作者 Jiaguo Yu Xin Li +2 位作者 zhiliang jin Hua Tang Enzhou Liu 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2022年第6期1-2,共2页
Solar energy is the most important clean and renewable energy in the world.However,the unpredictability,seasonal variation day and night,uneven distribution and low energy density limit its practical application.Photo... Solar energy is the most important clean and renewable energy in the world.However,the unpredictability,seasonal variation day and night,uneven distribution and low energy density limit its practical application.Photocatalysis technology has a very broad application prospect in solving energy and environmental problems. 展开更多
关键词 SOLAR CATALYSIS APPLICATION
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部