Enhanced Photoelectrochemical Water Splitting using Carbon Cloth Functionalized with ZnO Nanostructures via Polydopamine Assisted Electroless Deposition

分解水 材料科学 纳米结构 沉积(地质) 化学镀 碳纤维 纳米技术 化学工程 催化作用 光催化 化学 冶金 复合材料 复合数 有机化学 古生物学 沉积物 工程类 生物
作者
Ian P. Seetoh,A. Ramesh,Wei Tan,Chang Quan Lai
出处
期刊:Nanoscale [The Royal Society of Chemistry]
标识
DOI:10.1039/d4nr00761a
摘要

ZnO nanorods (ZnO-nr) have been widely studied as a promising nanomaterial for photoelectrochemical water splitting. However, almost all prior studies employed planar electrodes. Here, we investigated the performance of ZnO nanorods on a fibrous carbon cloth (CC) electrode, which offers a larger surface area for functionalization of photocatalysts. ZnO nanorods and Ni nanofilm were deposited on carbon cloth substrates for investigation as the photoanode and cathode of a photoelectrochemical water splitting setup, respectively. The use of polydopamine in the electroless deposition of ZnO ensured a uniform distribution of nanorods that were strongly adherent to the microfiber surface of the carbon cloth. Compared to ZnO nanorods grown on planar ITO/glass substrates, the CC-based ZnO photoanodes exhibited smaller onset potentials (1.1 VRHEvs. 1.8 VRHE), ∼40× larger dark faradaic currents at 1.23 VRHE and 5.5×-9× improvement in photoconversion efficiencies. Ni/CC cathodes were also found to exhibit a lower overpotential@10 mA cm-2 than Ni/Cu by 90 mV. The photocurrent obtained from the ZnO-nr/CC anode was highly stable across an hour and the peak current decreased by only 5% across 5 cycles of illumination, compared to 72% for the planar ZnO-nr/ITO anode. However, the response of the CC-based setups to changes in the illumination conditions was slower, taking hundreds of seconds to reach peak photocurrent, compared to tens of seconds for the planar electrodes. Using cyclic voltammetry, the double-layer capacitance of the electrodes was measured, and it was shown that the increased efficiency of the ZnO-nr/CC anode was due to a 2 order of magnitude increase in electrochemically active sites provided by the copious microfiber surface of the carbon cloth.

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