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通过掺入二级M(M = Cr、Fe、Co、Ni、Mo)的铂制备的坚固电催化剂进行海水分解以产生氢气。

Seawater splitting for hydrogen evolution by robust electrocatalysts from secondary M (M = Cr, Fe, Co, Ni, Mo) incorporated Pt.

作者信息

Zheng Jingjing, Zhao Yuanyuan, Xi He, Li Changhai

机构信息

Department of Chemical Engineering, Binzhou University Binzhou 256603 China

State Key Laboratory of Crystal Materials, Shandong University Jinan 250100 China.

出版信息

RSC Adv. 2018 Mar 6;8(17):9423-9429. doi: 10.1039/c7ra12112a. eCollection 2018 Feb 28.

Abstract

Water splitting is a promising technique for clean hydrogen energy harvesting. The creation of cost-effective electrocatalysts with improved hydrogen evolution reaction (HER) activity and stability is crucial in realizing persistent hydrogen evolution by reducing the reaction overpotential and minimizing energy consumption. Herein, we present the preparation of alloyed PtM (M = Cr, Fe, Co, Ni, Mo) modified titanium (Ti) mesh by a simple electrodeposition method, aiming at hydrogen generation from seawater splitting. The preliminary results indicate that the Ti/PtM electrodes feature markedly reduced onset overpotentials and Tafel slopes as well as significantly increased exchange current densities compared with pristine Pt electrodes, arising from the incorporation of secondary M atoms into the Pt lattice for alloying effects. Moreover, the competitive dissolution reaction between guest M species to Pt with Cl in seawater is beneficial for enhancing the long-term stability of resultant PtM alloy electrodes. The optimized PtMo alloy electrode maintains 91.13% of the initial current density upon 172 h operation in real seawater, making it promising in practical applications.

摘要

水分解是一种很有前景的清洁氢能获取技术。制备具有改进的析氢反应(HER)活性和稳定性的经济高效的电催化剂对于通过降低反应过电位和最小化能量消耗来实现持续析氢至关重要。在此,我们通过一种简单的电沉积方法展示了合金化的PtM(M = Cr、Fe、Co、Ni、Mo)修饰钛(Ti)网的制备,旨在从海水电解中制氢。初步结果表明,与原始Pt电极相比,Ti/PtM电极具有明显降低的起始过电位和塔菲尔斜率以及显著增加的交换电流密度,这是由于第二M原子掺入Pt晶格中产生了合金化效应。此外,客体M物种与海水中的Cl对Pt的竞争性溶解反应有利于提高所得PtM合金电极的长期稳定性。优化后的PtMo合金电极在实际海水中运行172小时后仍保持初始电流密度的91.13%,使其在实际应用中具有前景。

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