Insights into Boosting Photoelectrochemical Performance Over Cu 3 (BTC) 2 Passivated Cu 2 O Nanorod Arrays
Insights into Boosting Photoelectrochemical Performance Over Cu 3 (BTC) 2 Passivated Cu 2 O Nanorod Arrays
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提高 Cu 3 (BTC) 2 钝化 Cu 2 O 纳米棒阵列光电化学性能的见解
DOI:
10.1002/adsu.202200272
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发表时间:
2022
影响因子:
7.1
通讯作者:
Shengwei Liu
中科院分区:
文献类型:
--
作者:
Meng Ye;Xi Wu;Chuanhao Li;Bo Song;Xinzhou Ma;Shengwei Liu
Earth‐abundant Cu2O is a promising photocathode material for photoelectrochemical (PEC) water splitting. However, the serious photocorrosion and low efficiency retard its practical applications. Herein, a porous Cu‐based metal–organic framework material, Cu3(BTC)2, as surface passivation layer is grown on Cu2O nanorod arrays (NRARs) photocathode by in situ surface/interfacial growth. Compared to conventional Cu2O photocathodes, the optimized Cu2O/Cu3(BTC)2NRARs exhibit two times higher photocurrent density, ≈2.73 mA cm−2at 0 VRHEunder visible light irradiation, and the maximum incident photon to converted electron (IPCE) performance reaches 45% (450 nm). It is demonstrated that the Cu3(BTC)2layer synergistically passivates interfacial defects, forms p–n junctions at the Cu2O/Cu3(BTC)2interface, and introduces active sites catalyzing the hydrogen evolution reaction (HER), improving charge separation, transfer, and utilization efficiency. Moreover, the oxidative Cu2O photocorrosion is inhibited owing to the accelerated charge dynamics at the Cu2O/Cu3(BTC)2interface and the hole‐scavenging ability of Cu3(BTC)2, meanwhile, reductive Cu2O photocorrosion at Cu2O/Cu3(BTC)2is also attenuated by catalyzing the water reduction reaction that competes for photoelectrons and sustaining balanced “Cu2+(Cu+)/Cu0” cycles.