Department of Chemical System Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 (Japan).
Present address: Department of Chemical Engineering, Fukuoka University, 8-19-1 Nanakuma, Jonan-ku, Fukuoka, 810-0180 (Japan).
Angew Chem Int Ed Engl. 2015 Jun 26;54(27):7877-81. doi: 10.1002/anie.201502586. Epub 2015 May 27.
A photoelectrochemical (PEC) cell consisting of an n-type CdS single-crystal electrode and a Pt counter electrode with the ruthenium-2,2'-bipyridine complex Ru(bpy)3 as the redox shuttle in a non-aqueous electrolyte was studied to obtain a higher open-circuit voltage (V(OC)) than the onset voltage for water splitting. A V(OC) of 1.48 V and a short-circuit current (I(SC)) of 3.88 mA cm(-2) were obtained under irradiation by a 300 W Xe lamp with 420-800 nm visible light. This relatively high voltage was presumably due to the difference between the Fermi level of photo-irradiated n-type CdS and the redox potential of the Ru complex at the Pt electrode. The smooth redox reaction of the Ru complex with one-electron transfer was thought to have contributed to the high V(OC) and I(SC). The obtained V(OC) was more than the onset voltage of water electrolysis for hydrogen and oxygen generation, suggesting prospects for application in water electrolysis.
一种光电化学(PEC)电池,由 n 型 CdS 单晶电极和 Pt 对电极组成,在非水电解质中以钌-2,2'-联吡啶配合物Ru(bpy)3作为氧化还原穿梭体,旨在获得高于水分解起始电压的开路电压(V(OC))。在 300 W Xe 灯照射下,使用 420-800 nm 可见光,获得了 1.48 V 的开路电压(V(OC))和 3.88 mA cm(-2)的短路电流(I(SC))。这种相对较高的电压可能是由于光辐照的 n 型 CdS 的费米能级与 Pt 电极上 Ru 配合物的氧化还原电位之间的差异所致。Ru 配合物具有单电子转移的平滑氧化还原反应,被认为是高 V(OC)和 I(SC)的原因。所得到的 V(OC)高于氢气和氧气生成的水分解起始电压,这表明在水电解中的应用前景。