High yield of H2O2 and efficient S recovery from toxic H2S splitting through a self-driven photoelectrocatalytic system with a microporous GDE cathode

High yield of H2O2 and efficient S recovery from toxic H2S splitting through a self-driven photoelectrocatalytic system with a microporous GDE cathode
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通过具有微孔 GDE 阴极的自驱动光电催化系统,H2O2 产率高,并从有毒 H2S 分解中高效回收 S

DOI:
10.1016/j.apcatb.2018.07.051
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发表时间:
2018-12
期刊:
Applied Catalysis B: Environmental
影响因子:
--
通讯作者:
Zhou Baoxue
Zhou Baoxue
中科院分区:
其他
文献类型:
--
作者:
Qiao Li;Bai Jing;Luo Tao;Li Jinhua;Zhang Yan;Xia Ligang;Zhou Tingsheng;Xu Qunjie;Zhou Baoxue

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In this paper, the toxic H2S was transformed efficiently into valuable S and H2O2and its chemical reaction energy was converted into electric energy through a self-driven photoelectrocatalytic(PEC) system, which consisted of a microporous gas diffusion electrode(GDE) and a self-bias photoanode. In the cathode region, high yield of H2O2up to 0.8 mmol/L/h, was achieved because of the fast gas diffusion and direct two-electron reduction of molecular oxygen on the microporous GDE cathode. In the anodic region, H2S was completely converted into S without persulfide based on a I−/I3−redox system and the production rate of S recovery was about 0.60 mmol/h, 42 times higher than before. The remarkable catalytic efficiency also benefited from the self-bias design of photoanode, which included a front photoanode of WO3and a rear Si photovoltaic cell (Si PVC). The constituted self-driven PEC system could accelerate the charges separation and increase the electron transfer rate of PEC cell. In addition, electricity was generated simultaneously, with a maximum power density of 0.19 mW/cm2. The proposed self-driven PEC cell system offers an efficient, complete and sustainable way for H2S resourcization.
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