首页> 外文期刊>Chemical science >Phase-segregated NiPx@FePyOz core@shell nanoparticles: ready-to-use nanocatalysts for electro- and photo-catalytic water oxidation through in situ activation by structural transformation and spontaneous ligand removal
【24h】

Phase-segregated NiPx@FePyOz core@shell nanoparticles: ready-to-use nanocatalysts for electro- and photo-catalytic water oxidation through in situ activation by structural transformation and spontaneous ligand removal

机译:相分离的NiPx @ FePyOz核壳纳米粒子:即用型纳米催化剂,通过结构转化和自发配体去除原位活化,用于电催化和光催化水氧化

获取原文
           

摘要

The high overpotential of the oxygen evolution reaction is a critical issue to be overcome to realize efficient overall water splitting and enable hydrogen generation powered by sunlight. Homogeneous and stable nanoparticles (NPs) dispersed in solvents are useful as both electrocatalysts and cocatalysts of photocatalysts for the electro- and photo-catalytic oxygen evolution reaction, respectively, through their adsorption on various electrode substrates. Here, phase-segregated NiP _( x ) @FeP _( y ) O _( z ) core@shell NPs are selectively synthesized by the reaction of Fe(CO) _(5) with amorphous NiP _( x ) seed-NPs. The NiP _( x ) @FeP _( y ) O _( z ) NPs on conductive substrates exhibit higher electrocatalytic activity in the oxygen evolution reaction than those of other metal phosphide-based catalysts. The NiP _( x ) @FeP _( y ) O _( z ) NPs can also be used as a cocatalyst of an anodic BiVO _(4) photocatalyst to boost the photocatalytic water oxidation reaction. The excellent catalytic activity and high stability of the NiP _( x ) @FeP _( y ) O _( z ) NPs without any post-treatments are derived from in situ activation through both the structural transformation of NiP _( x ) @FeP _( y ) O _( z ) into mixed hydroxide species, (Ni, Fe)O _( x ) H _( y ) , and the spontaneous removal of the insulating organic ligands from NPs to form a smooth and robust (Ni, Fe)O _( x ) H _( y ) /substrate heterointerface during the oxygen evolution reaction.
机译:氧释放反应的高过电势是要实现有效的整体水分解并实现由阳光驱动的氢气产生所要克服的关键问题。分散在溶剂中的均质且稳定的纳米颗粒(NPs)分别通过在各种电极基材上的吸附而分别用作电催化剂和光催化氧释放反应的光催化剂的电催化剂和助催化剂。在此,通过Fe(CO)_(5)与无定形NiP _(x)种子NP的反应选择性地合成了相分离的NiP _(x)@FeP _(y)O _(z)核壳NPs。 。导电基材上的NiP _(x)@FeP _(y)O _(z)NPs在氧释放反应中比其他基于金属磷化物的催化剂具有更高的电催化活性。 NiP_(x)@FeP_(y)O_(z)NP也可以用作阳极BiVO_(4)光催化剂的助催化剂以促进光催化水氧化反应。 NiP _(x)@FeP _(y)O _(z)NPs的优异催化活性和高稳定性,无需任何后处理,都是通过NiP _(x)@FeP的结构转变而原位活化而得_(y)O _(z)变成混合的氢氧化物(Ni,Fe)O _(x)H _(y),并自发地从NP中去除绝缘有机配体以形成光滑而坚固的(Ni,在氧气析出反应过程中,Fe)O _(x)H _(y)/底物异质界面。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号