题目：

Substitution of native silicon oxide by titanium in Ni-coated silicon photoanodes for water splitting solar cells

作者：

Yuanyuan Shi^1,2, Tingting Han¹, Carolina Gimbert-Suriñach², Xiaoxue Song^1,2, Mario Lanza^1,*, Antoni Llobet^2,3,*

单位：

¹Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, 199 Ren-AiRoad, Suzhou 215123, China.

²Institute of Chemical Research of Catalonia (ICIQ), Avinguda Països Catalans, 16, 43007 Tarragona, Spain.

³Departament de Química, Universitat Autónoma de Barcelona (UAB), 08193 Cerdanyola Del Vallès, Barcelona, Spain.

摘要：

Using an ultrathin (2 nm) evaporated Ti film to replace the native SiO_X of the nSi photoanode and then coating it by thin (2 and 5 nm) Ni layers, the resulting 2 nm Ni/2 nm Ti coated nSi photoanodes (without the native SiO_X) reach a photocurrent onset potential of −42 mV relative to the SCE reference electrode in 1 M KOH under 1 simulated sun illumination (−202 mV relative to the potential for the oxygen evolution reaction). With increasing the thickness of the Ni layer to 5 nm, the 5 nm Ni/2 nm Ti/nSi photoanodes show 50 mV lower onset potential than 5 nm Ni directly coated on native SiO_X/nSi photoanodes and exhibit a very stable photoelectrochemical performance, which keep 100% activity (10 mA cm⁻² at 0.8 V vs. SCE) for ∼6.5 days. These results can be comparable to those of the typical NiO_X coated nSi photoanodes with n�p+ buried homojunctions. Using a Ti layer to replace the native SiO_X of the nSi photoanodes increases the conductivity of the sample and helps the charge transfer process. In addition, the interlayer Ti film absorbs the oxygen from nearby layers or from the atmosphere, making the Ti layer partially oxidized. The in situ TiO_X layer formed from evaporated Ti has more electron defects than the ALD deposited TiO₂, and could be responsible for the improved hole conduction process.

影响因子：

8.262

分区情况：

一区

链接：

http://pubs.rsc.org/en/content/articlelanding/2016/ta/c6ta08774d#!divAbstract

责任编辑：向丹婷 联系方式：dtxiang@suda.edu.cn