首页> 外文期刊>Advanced Science >Toward Highly Selective Electrochemical CO2 Reduction using Metal‐Free Heteroatom‐Doped Carbon
【24h】

Toward Highly Selective Electrochemical CO2 Reduction using Metal‐Free Heteroatom‐Doped Carbon

机译:朝着使用无金属杂体掺杂碳的高选择性电化学CO2还原

获取原文
           

摘要

There are growing interests in metal‐free heteroatom‐doped carbons for electrochemical CO2 reduction. Previous studies extensively focus on the effect of N‐doping, and their products severely suffer from low current density (mostly 2?mA cm?2) and limited selectivity (90%). Here, it is reported that heteroatom codoping offers a promising solution to the above challenge. As a proof of concept, N,P‐codoped mesoporous carbon is prepared by annealing phytic‐acid‐functionalized ZIF‐8 in NH3. In CO2‐saturated 0.5 m NaHCO3, the catalyst enables CO2 reduction to CO with great selectivity close to 100% and large CO partial current density (≈8?mA cm?2), which are, to the best of knowledge, superior to all other relevant competitors. Theoretical simulations show that the improved activity and selectivity are stemmed from the enhanced surface adsorption of *COOH and *CO intermediates as a result of the synergy of N and P codoping.
机译:在无金属杂体掺杂的碳中,用于电化学二氧化碳的碳的兴趣日益增长。以前的研究广泛地关注n掺杂的影响,并且它们的产品严重遭受低电流密度(大部分<2?mA cm 2)和有限的选择性(<90%)。在这里,据报道,杂原子编码为上述挑战提供了有希望的解决方案。作为概念的证据,通过在NH 3中退火植酸酸官能化ZIF-8来制备N,P型介孔碳。在二氧化碳饱和0.5M NaHCO 3中,催化剂使CO 2降低至CO,其选择性接近100%和大的CO偏电流密度(≈8mm≤2),这是最佳知识,优于所有知识其他相关的竞争对手。理论模拟表明,由于N和P编码的协同作用,改善的活性和选择性源于* COOH和* CO中间体的增强表面吸附。

著录项

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