Yoon Ki-Yong, Lee Jung-Soo, Kim Kwanghyun, Bak Chang Hong, Kim Sun-I, Kim Jin-Baek, Jang Ji-Hyun
School of Energy and Chemical Engineering, Low Dimensional Carbon Materials Center, Ulsan National Institute of Science and Technology (UNIST) , Ulsan 689-798, Korea.
ACS Appl Mater Interfaces. 2014 Dec 24;6(24):22634-9. doi: 10.1021/am506721a. Epub 2014 Dec 3.
By coupling α-Fe2O3 with a 3D graphene inverse opal (3D-GIO) conducting electrode, the short diffusion length of carriers and low absorption coefficient in α-Fe2O3 for photoelectrochemical applications were successfully addressed. GIO was directly grown on FTO substrate under low temperature conditions, removing the need for a graphene transfer process. α-Fe2O3 nanoparticles (NPs) were hydrothermally deposited on the surface of GIO, creating α-Fe2O3/GIO. The photocurrent density of α-Fe2O3/GIO in water splitting reactions reached 1.62 mA/cm(2) at 1.5 V vs RHE, which is 1.4 times greater than that of optimized α-Fe2O3. The EIS and IPCE data confirm reduced electron-hole recombination and fast electron transfer processes due to the short distance between active materials and the conducting electrode in the α-Fe2O3/GIO system. Our result may pave the way for designing devices in advanced energy conversion applications as well as a high efficiency hematite-based PEC system.
通过将α-Fe2O3与三维石墨烯反蛋白石(3D-GIO)导电电极耦合,成功解决了α-Fe2O3在光电化学应用中载流子扩散长度短和吸收系数低的问题。GIO在低温条件下直接生长在FTO衬底上,无需石墨烯转移过程。α-Fe2O3纳米颗粒(NPs)通过水热法沉积在GIO表面,形成α-Fe2O3/GIO。在相对于可逆氢电极(RHE)为1.5 V的条件下,α-Fe2O3/GIO在水分解反应中的光电流密度达到1.62 mA/cm²,比优化后的α-Fe2O3高1.4倍。电化学阻抗谱(EIS)和入射光电流转换效率(IPCE)数据证实,由于α-Fe2O3/GIO系统中活性材料与导电电极之间的距离较短,电子-空穴复合减少,电子转移过程加快。我们的结果可能为先进能量转换应用中的器件设计以及高效的基于赤铁矿的光电化学系统铺平道路。