Lei Yang , Ruyi Wang , Delin Chu , Zhuo Chen , Fangtao Zhong , Xiaoqing Xu , Chonghai Deng , Hai Yu , Jianguo Lv
{"title":"BiVO4 photoelectrodes for unbiased solar water splitting devices enabled by electrodepositing of Cu2O simultaneously as photoanode and photocathode","authors":"Lei Yang , Ruyi Wang , Delin Chu , Zhuo Chen , Fangtao Zhong , Xiaoqing Xu , Chonghai Deng , Hai Yu , Jianguo Lv","doi":"10.1016/j.jallcom.2023.169336","DOIUrl":null,"url":null,"abstract":"<div><p>In this work, BiVO<sub>4</sub> films are firstly synthesized, followed by electrodepositing of Cu<sub>2</sub>O to construct BiVO<sub>4</sub>/Cu<sub>2</sub><span>O heterojunction<span><span> electrodes for photoelectrochemical water splitting. By regulating the </span>electrodeposition potential, it is possible to control that Cu</span></span><sub>2</sub>O is deposited on the surface or inside of BiVO<sub>4</sub><span>, which enables them n-type or p-type semiconductivity behavior for oxygen and hydrogen evolution reactions, respectively. Due to the built-in electric field of p-n heterojunction and the Co-Pi co-catalyst layer, the anodic photocurrent density of optimized BiVO</span><sub>4</sub>/Cu<sub>2</sub>O/Co-Pi photoanode reaches 1.97 mA cm<sup>−2</sup> at 1.23 V vs. RHE. In the meantime, the deposition of Cu<sub>2</sub>O inside BiVO<sub>4</sub> has reversed the arrangement of the BiVO<sub>4</sub>/Cu<sub>2</sub>O heterogeneous structure. The cathodic photocurrent density of the fabricated BiVO<sub>4</sub>/Cu<sub>2</sub>O-C photocathode shows − 2.9 mA cm<sup>−2</sup>. Furthermore, the unbiased solar tandem cell is fabricated using BiVO<sub>4</sub>/Cu<sub>2</sub>O-C photocathode and BiVO<sub>4</sub>/Cu<sub>2</sub>O/Co-Pi photoanode, which exhibits 0.1 mA cm<sup>−2</sup><span> in the photoelectrochemical cell without applying any external voltage.</span></p></div>","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"945 ","pages":"Article 169336"},"PeriodicalIF":5.8000,"publicationDate":"2023-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alloys and Compounds","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0925838823006394","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 7
Abstract
In this work, BiVO4 films are firstly synthesized, followed by electrodepositing of Cu2O to construct BiVO4/Cu2O heterojunction electrodes for photoelectrochemical water splitting. By regulating the electrodeposition potential, it is possible to control that Cu2O is deposited on the surface or inside of BiVO4, which enables them n-type or p-type semiconductivity behavior for oxygen and hydrogen evolution reactions, respectively. Due to the built-in electric field of p-n heterojunction and the Co-Pi co-catalyst layer, the anodic photocurrent density of optimized BiVO4/Cu2O/Co-Pi photoanode reaches 1.97 mA cm−2 at 1.23 V vs. RHE. In the meantime, the deposition of Cu2O inside BiVO4 has reversed the arrangement of the BiVO4/Cu2O heterogeneous structure. The cathodic photocurrent density of the fabricated BiVO4/Cu2O-C photocathode shows − 2.9 mA cm−2. Furthermore, the unbiased solar tandem cell is fabricated using BiVO4/Cu2O-C photocathode and BiVO4/Cu2O/Co-Pi photoanode, which exhibits 0.1 mA cm−2 in the photoelectrochemical cell without applying any external voltage.
本文首先合成BiVO4薄膜,然后电沉积Cu2O,构建BiVO4/Cu2O异质结电极,用于光电化学水分解。通过调节电沉积电位,可以控制Cu2O沉积在BiVO4表面或内部,使其分别具有n型和p型的析氧和析氢半导体行为。由于p-n异质结和Co-Pi共催化剂层的内置电场,优化后的BiVO4/Cu2O/Co-Pi光阳极在1.23 V vs. RHE下的阳极光电流密度达到1.97 mA cm - 2。同时,BiVO4内部Cu2O的沉积改变了BiVO4/Cu2O非均相结构的排列。制备的BiVO4/ cu20 - c光电阴极阴极光电流密度为−2.9 mA cm−2。此外,采用BiVO4/Cu2O- c光电阴极和BiVO4/Cu2O/Co-Pi光电阳极制备了无偏置太阳能串联电池,在不施加任何外部电压的情况下,在光电电池中表现为0.1 mA cm - 2。
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.