光电阴极
材料科学
石墨氮化碳
光电流
分解水
异质结
水溶液
可逆氢电极
光催化
氮化碳
金属
半导体
氮化物
电极
纳米技术
光电子学
催化作用
电化学
参比电极
物理化学
化学
电子
物理
有机化学
冶金
量子力学
图层(电子)
作者
Yingying Han,Xiuli Lu,Shang‐Feng Tang,Xuepeng Yin,Zhen‐Wei Wei,Tong‐Bu Lu
标识
DOI:10.1002/aenm.201702992
摘要
Abstract The design and synthesis of efficient metal‐free photoelectrocatalysts for water splitting are of great significance, as nonmetal elements are generally earth abundant and environment friendly. As a typical metal‐free semiconductor, g‐C3N4 has received much attention in the field of photocatalytic water splitting. However, the poor photoinduced hole mobility of g‐C 3 N 4 restrains its catalytic performance. Herein, for the first time, graphdiyne (GDY) is used to interact with g‐C 3 N 4 to construct a metal‐free 2D/2D heterojunction of g‐C 3 N 4 /GDY as an efficient photoelectrocatalyst for water splitting. The g‐C 3 N 4 /GDY photocathode exhibits enhanced photocarriers separation due to excellent hole transfer nature of graphdiyne and the structure of 2D/2D heterojunction of g‐C 3 N 4 /GDY, realizing a sevenfold increase in electron life time (610 μs) compared to that of g‐C 3 N 4 (88 μs), and a threefold increase in photocurrent density (−98 μA cm −2 ) compared to that of g‐C 3 N 4 photocathode (−32 μA cm −2 ) at a potential of 0 V versus normal hydrogen electrode (NHE) in neutral aqueous solution. The photoelectrocatalytic performance can be further improved by fabricating Pt@g‐C 3 N 4 /GDY, which displays an photocurrent of −133 μA cm −2 at a potential of 0 V versus NHE in neutral aqueous solution. This work provides a new strategy for the design of efficient metal‐free photoelectrocatalysts for water splitting.
科研通智能强力驱动
Strongly Powered by AbleSci AI