Influence of Annealing Temperature of WO3 in Photoelectrochemical Conversion and Energy Storage for Water Splitting

被引:80
|
作者
Ng, Charlene [1 ]
Ng, Yun Hau [1 ]
Iwase, Akihide [1 ]
Amal, Rose [1 ]
机构
[1] Univ New S Wales, Sch Chem Engn, ARC Ctr Excellence Funct Nanomat, Sydney, NSW 2052, Australia
基金
澳大利亚研究理事会;
关键词
crystallinity; hydrogen generation; photoelectrochemical water splitting; self-photorecharge; tungsten oxide; THIN-FILM ELECTRODES; TUNGSTEN TRIOXIDE; SELF-PHOTORECHARGEABILITY; PROTON CONDUCTIVITY; OXIDE; MECHANISM;
D O I
10.1021/am401112q
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The current work demonstrates the importance of WO3 crystallinity in governing both photoenergy conversion efficiency and storage capacity of the flower structured WO3 electrode. The degree of crystallinity of the WO3 electrodes was varied by altering the calcination temperature from 200 to 600 degrees C. For the self-photochargeability phenomenon, the prevailing flexibility of the short-range order structure at low calcination temperature of 200 degrees C favors the intercalation of the positive cations, enabling more photoexcited electrons to be stored within WO3 framework. This leads to a larger amount of stored charges that can be discharged in an on-demand manner under the absence of irradiation for H-2 generation. The stability of the electrodes calcined at 200 degrees C, however, is compromised because of the structural instability caused by the abundance insertion of cations. On the other hand, films that were calcined at 400 degrees C displayed the highest stability toward both intercalation of the cations and photoelectrochemical water splitting performance. Although crystallinty of WO3 was furthered improved at 600 degrees C heat treatment, the worsened contact between the WO3 platelets and the conducting substrate as induced by the significant sintering has been more detrimental toward the charge transport.
引用
收藏
页码:5269 / 5275
页数:7
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