分解水
材料科学
半导体
氧化物
水溶液
电解质
偶极子
GSM演进的增强数据速率
光电子学
纳米技术
无机化学
电极
化学
光催化
物理化学
催化作用
生物化学
计算机科学
冶金
有机化学
电信
作者
Yasuyuki Hikita,Kazunori Nishio,Linsey C. Seitz,Pongkarn Chakthranont,Takashi Tachikawa,Thomas F. Jaramillo,Harold Y. Hwang
标识
DOI:10.1002/aenm.201502154
摘要
One of the crucial parameters dictating the efficiency of photoelectrochemical water‐splitting is the semiconductor band edge alignment with respect to hydrogen and oxygen redox potentials. Despite the importance of metal oxides in their use as photoelectrodes, studies to control the band edge alignment in aqueous solution have been limited predominantly to compound semiconductors with modulation ranges limited to a few hundred mV. The ability to modulate the flat band potential of oxide photoanodes by as much as 1.3 V, using the insertion of subsurface electrostatic dipoles near a Nb‐doped SrTiO 3 /aqueous electrolyte interface is reported. The tunable range achieved far exceeds previous reports in any semiconductor/aqueous electrolyte system and suggests a general design strategy for highly efficient oxide photoelectrodes.
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