首页> 外文期刊>Applied Surface Science >Highly dispersed and noble metal-free MP_X (M = Ni, Co, Fe) coupled with g-C_3N_4 nanosheets as 0D/2D photocatalysts for hydrogen evolution
【24h】

Highly dispersed and noble metal-free MP_X (M = Ni, Co, Fe) coupled with g-C_3N_4 nanosheets as 0D/2D photocatalysts for hydrogen evolution

机译:高度分散且不含贵金属的MP_X(M = Ni,Co,Fe)与g-C_3N_4纳米片耦合作为0D / 2D析氢光催化剂

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Developing high-efficiency and low-cost photocatalysts by avoiding expensive noble metals is a great challenge. Here, highly dispersed metal (M = Ni, Co, Fe) phosphides modified g-C3N4 nanosheets (CNNS) were prepared through in situ precipitation and solid/gas-phase phosphorization. The results confirmed that metal phosphides (MPX) nanoparticles with high dispersion were well loaded on CNNS surface. The property well reveals the transfer path of photogenerated charges and the origin of high charge separation efficiency in photocatalytic reaction, thus yielding a remarkable catalytic activity. The apparent quantum efficiency (AQY) based on the NiPx/CNNS-900 is up to 6.61% at 400 nm while the H-2 evolution rate boosts to 4068.84 mu mol.g(-1).h(-1), which is 50 times higher than that of pristine CNNS. The mechanism could be attributed to the highly dispersed MPX nanoparticles on the surface of CNNS, which acted as effective active sites to promote the separation and migration of photogenerated charges, leading to greatly increase in H-2 production. This study is beneficial to further develop the high-efficient, low cost and environmentally-friendly CNNS-based photocatalytic materials for H-2 production.
机译:通过避免使用昂贵的贵金属来开发高效,低成本的光催化剂是一个巨大的挑战。在这里,通过原位沉淀和固/气相磷化制备了高度分散的金属(M = Ni,Co,Fe)磷化物改性的g-C3N4纳米片(CNNS)。结果证实,具有高分散性的金属磷化物(MPX)纳米颗粒很好地负载在CNNS表面上。该性质很好地揭示了光生电荷的转移路径和光催化反应中高电荷分离效率的起因,从而产生了显着的催化活性。基于NiPx / CNNS-900的表观量子效率(AQY)在400 nm时高达6.61%,而H-2的演化速率提高到4068.84 mu mol.g(-1).h(-1),这是比原始CNNS高50倍。该机制可以归因于CNNS表面上高度分散的MPX纳米颗粒,其充当有效的活性位点以促进光生电荷的分离和迁移,从而导致H-2产量大大增加。这项研究对于进一步开发用于H-2生产的高效,低成本和环保的基于CNNS的光催化材料是有益的。

著录项

相似文献

  • 外文文献
  • 中文文献
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